ID

16099

Description

DOCUMENTED PATHOGENS (Use this table for guidance on the pathogens of interest) Bacteria:S. pneumoniae,OHaemophilus influenzaether gram positive (i.e.: other streptococci, staphylococci, listeria …), Other gram negative (i.e.: E. coli klebsiella, proteus, serratia, pseudomonas …), Legionella sp,Mycobacteria sp, Other Fungi:Candida sp, Aspergillus sp, Pneumocystis carinii, Other Parasites: Toxoplasma gondii, Other Viruses: HSV, VZV, EBV,CMV,HHV-6, RSV,Other respiratory virus (influenza, parainfluenza, rhinovirus),Adenovirus, HBV, HCV, HIV,Papovavirus, Parvovirus, Other

Keywords

  1. 4/26/16 4/26/16 -
  2. 6/29/16 6/29/16 - Julian Varghese
Uploaded on

June 29, 2016

DOI

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License

Creative Commons BY-NC 3.0

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EBMT Multiple Myeloma General Information

16pp EBMT Multiple Myeloma 10PCD

GENERAL INFORMATION Team
Description

GENERAL INFORMATION Team

EBMT Centre Identification Code (CIC)
Description

EBMT Centre Identification Code (CIC)

Data type

text

Alias
UMLS CUI [1]
C2348585
Hospital
Description

Hospital

Data type

text

Alias
UMLS CUI [1]
C0019994
Unit
Description

Unit

Data type

text

Name of contact person
Description

Contact person

Data type

text

Alias
UMLS CUI [1]
C0337611
Telephone
Description

Patient phone number

Data type

text

Alias
UMLS CUI [1]
C1515258
Fax
Description

ContactPersonFaxNumber

Data type

text

Alias
UMLS CUI [1,1]
C0237753
UMLS CUI [1,2]
C0027361
UMLS CUI [1,3]
C0337611
UMLS CUI [1,4]
C0085205
E-mail
Description

ContactPersonE-mailText

Data type

text

Alias
UMLS CUI [1,1]
C1527021
UMLS CUI [1,2]
C0027361
UMLS CUI [1,3]
C0013849
UMLS CUI [1,4]
C0337611
Date of this report
Description

Date of this report

Data type

date

Alias
UMLS CUI [1]
C1302584
Patient following national / international study / trial
Description

Patient in Trial

Data type

integer

Alias
UMLS CUI [1]
C1997894
Name of study trial
Description

Name of study trial

Data type

text

Alias
UMLS CUI [1]
C2348560
PATIENT
Description

PATIENT

To be entered only if patient previously reported
Description

Unique Identification Code (UIC)

Data type

text

Alias
UMLS CUI [1]
C2348585
Hospital Unique Patient Number or Code
Description

Hospital Unique Patient Number or Code

Data type

text

Alias
UMLS CUI [1]
C1827636
First name(s)_surname(s)
Description

Initials

Data type

text

Alias
UMLS CUI [1]
C2986440
Date of Birth
Description

PersonBirthDate

Data type

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C0027361
UMLS CUI [1,3]
C0005615
Sex
Description

Sex

Data type

integer

ABO Group
Description

ABO Group

Data type

text

Rh factor
Description

Rh factor

Data type

text

DISEASE
Description

DISEASE

Date of Diagnosis
Description

Date of Diagnosis

Data type

date

Alias
UMLS CUI [1]
C2316983
Check the disease for which this transplant was performed
Description

Primary Disease Diagnosis

Data type

text

Alias
UMLS CUI [1]
C0277554
If other diagnosis, specify:
Description

Primary Disease Diagnosis

Data type

text

Alias
UMLS CUI [1,1]
C0277554
UMLS CUI [1,2]
C2348235
PLASMA CELL DISORDERS (INCLUDING MULTIPLE MYELOMA)
Description

PLASMA CELL DISORDERS (INCLUDING MULTIPLE MYELOMA)

Has the information requested in this section been submitted with a previous HSCT registration for this patient?
Description

SubmittedPreviously

Data type

integer

SUBCLASSIFICATION
Description

SUBCLASSIFICATION

Data type

text

if Multiple myeloma
Description

Multiple myeloma

Data type

integer

Heavy chain and light chain
Description

Heavy Chain

Data type

integer

Heavy chain and light chain
Description

Light Chain

Data type

integer

Light chain only
Description

Light chain only

Data type

integer

SALMON AND DURIE Stage at diagnosis
Description

SALMON AND DURIE Stage at diagnosis

Data type

integer

Alias
UMLS CUI [1]
C3846373
ISS (Multiple Myeloma Prognosis) (Stage 1-3)
Description

ISS (Multiple Myeloma Prognosis Score)

Data type

integer

Alias
UMLS CUI [1]
C2346508
Chromosome analysis
Description

Chromosome analysis

Data type

text

Alias
UMLS CUI [1]
C0200867
Number of metaphases with anomalies:
Description

Number of abnormal metaphases

Data type

float

Alias
UMLS CUI [1,1]
C1621812
UMLS CUI [1,2]
C0237753
Number of metaphases examined
Description

Number of examined metaphases

Data type

float

Alias
UMLS CUI [1,1]
C1621812
UMLS CUI [1,2]
C0237753
UMLS CUI [1,3]
C0260877
IF ABNORMAL, INDICATE ABNORMALITIES FOUND Del 13q14
Description

Chromosome analysis

Data type

text

IF ABNORMAL, INDICATE ABNORMALITIES FOUND t(11;14)
Description

Chromosome analysis

Data type

integer

IF ABNORMAL, INDICATE ABNORMALITIES FOUND abn 17q
Description

Chromosome analysis

Data type

integer

IF ABNORMAL, INDICATE ABNORMALITIES FOUND 17p del
Description

Chromosome analysis

Data type

integer

IF ABNORMAL, INDICATE ABNORMALITIES FOUND t(4:14)
Description

Chromosome analysis

Data type

integer

IF ABNORMAL, INDICATE ABNORMALITIES FOUND (14:16)
Description

Chromosome analysis

Data type

integer

IF ABNORMAL, INDICATE ABNORMALITIES FOUND 1q amplification
Description

Chromosome analysis

Data type

integer

IF ABNORMAL, INDICATE ABNORMALITIES FOUND c-myc
Description

Chromosome analysis

Data type

integer

IF Other ABNORMAL, INDICATE ABNORMALITIES FOUND, please specify
Description

Chromosome analysis

Data type

integer

Other or associated abnormalities (specify) please specify
Description

Chromosome analysis

Data type

text

Molecular Analysis
Description

Molecular Analysis

Data type

integer

Alias
UMLS CUI [1]
C1513380
Hb (g/dL)
Description

CLINICAL AND LABORATORY DATA

Data type

float

Hb (g/dL)
Description

CLINICAL AND LABORATORY DATA

Data type

integer

Serum creatinine (mol/L)
Description

CLINICAL AND LABORATORY DATA

Data type

float

Serum creatinine (mol/L)
Description

CLINICAL AND LABORATORY DATA

Data type

text

Serum calcium (mmol/L)
Description

CLINICAL AND LABORATORY DATA

Data type

float

Serum calcium (mmol/L)
Description

CLINICAL AND LABORATORY DATA

Data type

integer

Serum albumin (g/L)
Description

CLINICAL AND LABORATORY DATA

Data type

float

Serum albumin (g/L)
Description

CLINICAL AND LABORATORY DATA

Data type

integer

BM aspirate: % plasmacytosis
Description

CLINICAL AND LABORATORY DATA

Data type

float

BM aspirate: % plasmacytosis
Description

CLINICAL AND LABORATORY DATA

Data type

integer

BM trephine: % plasmacytosis
Description

CLINICAL AND LABORATORY DATA

Data type

float

BM trephine: % plasmacytosis
Description

CLINICAL AND LABORATORY DATA

Data type

integer

Monoclonal Ig in serum (g/L)
Description

CLINICAL AND LABORATORY DATA

Data type

float

Monoclonal Ig in serum (g/L)
Description

CLINICAL AND LABORATORY DATA

Data type

integer

Monoclonal Ig in urine (g/24 h)
Description

CLINICAL AND LABORATORY DATA

Data type

float

Monoclonal Ig in urine (g/24 h)
Description

CLINICAL AND LABORATORY DATA

Data type

integer

Serum ß2 microglobulin (mg/L)
Description

CLINICAL AND LABORATORY DATA

Data type

float

Serum ß2 microglobulin (mg/L)
Description

CLINICAL AND LABORATORY DATA

Data type

integer

INVOLVEMENT AT DIAGNOSIS, Bone structure
Description

Lytic lesions

Data type

integer

INVOLVEMENT AT DIAGNOSIS, Bone structure
Description

Extramedullary involvement

Data type

integer

if yes, specify location
Description

Extramedullary involvement

Data type

text

PRE-HSCT TREATMENT
Description

PRE-HSCT TREATMENT

Was the patient treated before the HSCT procedure?
Description

Previous treatment

Data type

text

Alias
UMLS CUI [1]
C0087111
(counted from diagnosis, or last HSCT if applicable)
Description

Sequential number of this treatment

Data type

text

Chemo/Drugs
Description

Modality

Data type

text

Alias
UMLS CUI [1]
C0695347
Radiotherapy
Description

Modality

Data type

integer

Alias
UMLS CUI [1]
C0695347
see manual for full definition of each response
Description

Response

Data type

integer

Additional Pre-HSCT treatment
Description

Additional Pre-HSCT treatment

Data type

text

Alias
UMLS CUI [1,1]
C1706712
UMLS CUI [1,2]
C2709094
(counted from diagnosis, or last HSCT if applicable)
Description

Sequential number of this treatment

Data type

text

Chemo/Drugs
Description

Modality

Data type

integer

Radiotherapy
Description

Modality

Data type

integer

(see manual for full definition of each response)
Description

Response

Data type

integer

ADDITIONAL PRE-HSCT TREATMENT?
Description

ADDITIONAL PRE-HSCT TREATMENT?

Data type

integer

Sequential number of this treatment
Description

(counted from diagnosis, or last HSCT if applicable)

Data type

text

Chemo/Drugs
Description

Modality

Data type

text

Radiotherapy
Description

Modality

Data type

integer

Response
Description

see manual for full definition of each response)

Data type

integer

HSCT
Description

HSCT

Date of HSCT
Description

Date of HSCT

Data type

date

Alias
UMLS CUI [1]
C2584899
HSCT type
Description

HSCT type

Data type

integer

Alias
UMLS CUI [1]
C0472699
Autologous
Description

Date of 1st collection or pheresis

Data type

date

STATUS OF DISEASE AT COLLECTION
Description

STATUS OF DISEASE AT COLLECTION

STATUS OF DISEASE AT COLLECTION
Description

IMMEDIATELY PRIOR TO MOBILISING CHEMOTHERAPY AND/OR GROWTH FACTOR IF USED

Data type

integer

If sCR or CR: NUMBER OF THIS COMPLETE REMISSION
Description

STATUS OF DISEASE AT COLLECTION

Data type

integer

If VGPR or PR: NUMBER OF THIS PARTIAL REMISSION
Description

STATUS OF DISEASE AT COLLECTION

Data type

integer

Relapse from CR, NUMBER OF THIS RELAPSE
Description

STATUS OF DISEASE AT COLLECTION

Data type

integer

Relapse from CR, NUMBER OF THIS RELAPSE
Description

STATUS OF DISEASE AT COLLECTION

Data type

integer

Plateau
Description

Plateau

Data type

integer

Hb (g/dL)
Description

CLINICAL AND LABORATORY DATA

Data type

float

Hb (g/dL)
Description

CLINICAL AND LABORATORY DATA

Data type

integer

Serum creatinine (mol/L)
Description

CLINICAL AND LABORATORY DATA

Data type

float

Serum creatinine (mol/L)
Description

CLINICAL AND LABORATORY DATA

Data type

integer

Serum calcium (mmol/L)
Description

CLINICAL AND LABORATORY DATA

Data type

float

Serum calcium (mmol/L)
Description

CLINICAL AND LABORATORY DATA

Data type

integer

Serum albumin (g/L)
Description

CLINICAL AND LABORATORY DATA

Data type

float

Serum albumin (g/L)
Description

albumin

Data type

integer

Alias
UMLS CUI [1]
C0201838
BM aspirate: % plasmacytosis
Description

CLINICAL AND LABORATORY DATA

Data type

float

BM aspirate: % plasmacytosis
Description

CLINICAL AND LABORATORY DATA

Data type

integer

BM trephine: % plasmacytosis
Description

CLINICAL AND LABORATORY DATA

Data type

float

BM trephine: % plasmacytosis
Description

CLINICAL AND LABORATORY DATA

Data type

integer

Monoclonal Ig in serum (g/L)
Description

CLINICAL AND LABORATORY DATA

Data type

float

Monoclonal Ig in serum (g/L)
Description

CLINICAL AND LABORATORY DATA

Data type

integer

Immunofixation of serum
Description

CLINICAL AND LABORATORY DATA

Data type

integer

Monoclonal Ig in urine (g/24 h)
Description

CLINICAL AND LABORATORY DATA

Data type

float

Monoclonal Ig in urine (g/24 h)
Description

CLINICAL AND LABORATORY DATA

Data type

integer

Immunofixation of urine
Description

CLINICAL AND LABORATORY DATA

Data type

integer

Serum 2 microglobulin (mg/L)
Description

CLINICAL AND LABORATORY DATA

Data type

float

Serum 2 microglobulin (mg/L)
Description

CLINICAL AND LABORATORY DATA

Data type

integer

Bone structure, Lytic lesions
Description

Bone structure

Data type

text

DISEASE STATUS AT HSCT
Description

DISEASE STATUS AT HSCT

DISEASE STATUS AT HSCT
Description

DISEASE STATUS AT HSCT

Data type

integer

NUMBER OF THIS COMPLETE REMISSION
Description

If sCR or CR

Data type

integer

NUMBER OF THIS PARTIAL REMISSION
Description

If VGPR or PR

Data type

integer

NUMBER OF THIS RELAPSE
Description

Relapse from CR

Data type

integer

(not applicable for non secretory myelona)
Description

Plateau

Data type

integer

Hb (g/dL)
Description

CLINICAL AND LABORATORY DATA

Data type

float

Hb (g/dL)
Description

CLINICAL AND LABORATORY DATA

Data type

text

Serum creatinine (mol/L)
Description

CLINICAL AND LABORATORY DATA

Data type

float

Serum creatinine (mol/L)
Description

CLINICAL AND LABORATORY DATA

Data type

integer

Serum calcium (mmol/L)
Description

CLINICAL AND LABORATORY DATA

Data type

float

Serum calcium (mmol/L)
Description

CLINICAL AND LABORATORY DATA

Data type

integer

Serum albumin (g/L)
Description

CLINICAL AND LABORATORY DATA

Data type

float

Serum albumin (g/L)
Description

CLINICAL AND LABORATORY DATA

Data type

integer

BM aspirate: % plasmacytosis
Description

CLINICAL AND LABORATORY DATA

Data type

float

BM aspirate: % plasmacytosis
Description

CLINICAL AND LABORATORY DATA

Data type

integer

Monoclonal Ig in serum (g/L)
Description

CLINICAL AND LABORATORY DATA

Data type

float

Monoclonal Ig in serum (g/L)
Description

CLINICAL AND LABORATORY DATA

Data type

integer

Immunofixation of serum
Description

CLINICAL AND LABORATORY DATA

Data type

integer

Monoclonal Ig in urine (g/24 h)
Description

CLINICAL AND LABORATORY DATA

Data type

float

Monoclonal Ig in urine (g/24 h)
Description

CLINICAL AND LABORATORY DATA

Data type

integer

Immunofixation of urine
Description

CLINICAL AND LABORATORY DATA

Data type

text

Serum 2 microglobulin (mg/L)
Description

CLINICAL AND LABORATORY DATA

Data type

float

Serum 2 microglobulin (mg/L)
Description

CLINICAL AND LABORATORY DATA

Data type

integer

Lytic lesions
Description

Bone structure

Data type

integer

ADDITIONAL TREATMENT POST-HSCT
Description

ADDITIONAL TREATMENT POST-HSCT

Additional Disease Treatment
Description

Additional Disease Treatment

Data type

text

Alias
UMLS CUI [1]
C1706712
if yes
Description

ADDITIONAL DISEASE TREATMENT

Data type

text

Date started
Description

ADDITIONAL DISEASE TREATMENT

Data type

date

Chemo/drug/agen
Description

(including MoAB, etc.)

Data type

text

Alias
UMLS CUI [1]
C1706712
if other
Description

ADDITIONAL DISEASE TREATMENT

Data type

text

Radiotherapy
Description

ADDITIONAL DISEASE TREATMENT

Data type

text

Other treatment
Description

ADDITIONAL DISEASE TREATMENT

Data type

integer

Alias
UMLS CUI [1]
C1706712
if other treatment please specify
Description

ADDITIONAL DISEASE TREATMENT

Data type

text

STATUS OF DISEASE AT 100 DAYS AFTER HSCT
Description

STATUS OF DISEASE AT 100 DAYS AFTER HSCT

BEST RESPONSE TO HSCT AT 100 DAYS
Description

(see manual for full definition of each response)

Data type

text

If sCR or CR: NUMBER OF THIS COMPLETE REMISSION
Description

BEST RESPONSE TO HSCT AT 100 DAYS

Data type

integer

If VGPR or PR: NUMBER OF THIS PARTIAL REMISSION
Description

BEST RESPONSE TO HSCT AT 100 DAYS

Data type

integer

If complete response: Date of CR
Description

BEST RESPONSE TO HSCT AT 100 DAYS

Data type

date

Otherwise: date of evaluation
Description

BEST RESPONSE TO HSCT AT 100 DAYS

Data type

date

(COMPLETE ONLY IF STATUS IS STABLE DISEASE OR PR)
Description

Plateau

Data type

text

BM aspirate: % plasmacytosis
Description

CLINICAL AND LABORATORY DATA

Data type

float

BM aspirate: % plasmacytosis
Description

CLINICAL AND LABORATORY DATA

Data type

integer

BM trephine: % plasmacytosis
Description

CLINICAL AND LABORATORY DATA

Data type

float

Monoclonal Ig in serum (g/L)
Description

CLINICAL AND LABORATORY DATA

Data type

float

Monoclonal Ig in serum (g/L)
Description

CLINICAL AND LABORATORY DATA

Data type

integer

Immunofixation of serum
Description

CLINICAL AND LABORATORY DATA

Data type

text

Monoclonal Ig in urine (g/24 h)
Description

CLINICAL AND LABORATORY DATA

Data type

float

Monoclonal Ig in urine (g/24 h)
Description

CLINICAL AND LABORATORY DATA

Data type

integer

Immunofixation of urine
Description

CLINICAL AND LABORATORY DATA

Data type

integer

Serum 2 microglobulin (mg/L)
Description

CLINICAL AND LABORATORY DATA

Data type

float

Serum 2 microglobulin (mg/L)
Description

CLINICAL AND LABORATORY DATA

Data type

integer

Lytic lesions
Description

Bone structure

Data type

integer

FORMS TO BE FILLED IN
Description

FORMS TO BE FILLED IN

Type of Transplant
Description

Type of Transplant

Data type

text

Alias
UMLS CUI [1,1]
C0559189
UMLS CUI [1,2]
C0040739
If Other contact the EBMT Central Registry Office for instructions
Description

TYPE OF TRANSPLANT

Data type

text

PLASMA CELL DISORDERS (INCLUDING MULTIPLE MYELOMA)
Description

PLASMA CELL DISORDERS (INCLUDING MULTIPLE MYELOMA)

Unique Identification Code (UIC) (if known)
Description

Unique Identification Code (UIC)

Data type

text

Alias
UMLS CUI [1]
C2348585
Hospital Unique Patient Number
Description

Hospital Unique Patient Number

Data type

text

Alias
UMLS CUI [1]
C2348585
Date of this report
Description

Date of this report

Data type

date

Alias
UMLS CUI [1]
C1302584
Patient following national / international study / trial
Description

Patient in Trial

Data type

integer

Alias
UMLS CUI [1]
C1997894
Name of study / trial
Description

Name of study / trial

Data type

text

Alias
UMLS CUI [1]
C0008976
First name(s)_surname(s)
Description

Initials

Data type

text

Alias
UMLS CUI [1]
C2986440
Date of birth
Description

Date of birth

Data type

date

Alias
UMLS CUI [1]
C0421451
Date of last HSCT for this patient
Description

Date of last HSCT for this patient

Data type

date

Alias
UMLS CUI [1,1]
C0472699
UMLS CUI [1,2]
C0011008
PATIENT LAST SEEN
Description

PATIENT LAST SEEN

Date of Last Contact or Death
Description

Date last contact

Data type

date

Alias
UMLS CUI [1]
C0805839
Complete haematological remission obtained after the HSCT in the absence of additional disease treatment
Description

Complete haematological remission obtained after the HSCT in the absence of additional disease treatment

Data type

integer

if yes, date
Description

Complete haematological remission obtained after the HSCT in the absence of additional disease treatment

Data type

date

GRAFT VERSUS HOST DISEASE (GvHD) SINCE LAST REPORT
Description

GRAFT VERSUS HOST DISEASE (GvHD) SINCE LAST REPORT

Acute Graft versus Host Disease (aGvHD) - Grade
Description

aGvHD Grade

Data type

integer

Alias
UMLS CUI [1,1]
C0856825
UMLS CUI [1,2]
C0441800
if present
Description

Maximum grade

Data type

integer

Alias
UMLS CUI [1,1]
C0856825
UMLS CUI [1,2]
C0806909
UMLS CUI [1,3]
C0441800
UMLS CUI [1,4]
C1561607
Reason
Description

Maximum grade

Data type

integer

Date onset of this episode (if new or recurrent)
Description

Date onset of this episode

Data type

date

Measurement units
  • yyyy/mm/dd
Alias
UMLS CUI [1]
C0574845
yyyy/mm/dd
Date onset of this episode
Description

Date onset of this episode

Data type

integer

Stage skin
Description

aGvHD Stage Skin

Data type

integer

Alias
UMLS CUI [1,1]
C0856825
UMLS CUI [1,2]
C1306673
UMLS CUI [1,3]
C1306673
Stage liver
Description

aGvHD Stage liver

Data type

integer

Alias
UMLS CUI [1,1]
C0856825
UMLS CUI [1,2]
C1306673
UMLS CUI [1,3]
C0023884
Stage gut
Description

aGvHD stage gut

Data type

integer

Alias
UMLS CUI [1,1]
C0856825
UMLS CUI [1,2]
C1306673
UMLS CUI [1,3]
C0021853
aGvHD Resolution
Description

Resolution

Data type

boolean

Alias
UMLS CUI [1,1]
C0856825
UMLS CUI [1,2]
C1514893
Date of resolution
Description

aGvHD Date of resolution

Data type

date

Measurement units
  • yyyy/mm/dd
Alias
UMLS CUI [1,1]
C0856825
UMLS CUI [1,2]
C1514893
UMLS CUI [1,3]
C0011008
yyyy/mm/dd
Presence of cGvHD
Description

Chronic Graft versus Host Disease (cGvHD)

Data type

text

Alias
UMLS CUI [1]
C0867389
Presence of cGVHD, if yes
Description

CHRONIC GRAFT VERSUS HOST DISEASE (CGVHD)

Data type

integer

Date of onset
Description

Date of onset

Data type

date

Alias
UMLS CUI [1]
C0574845
If present continously since last report, specify cGvHD gade:
Description

cGvHD grade

Data type

text

Alias
UMLS CUI [1,1]
C0867389
UMLS CUI [1,2]
C0441799
Organs affected
Description

Organs affected

Data type

integer

Alias
UMLS CUI [1]
C0449642
if Other please specify
Description

Organs affected

Data type

text

If Resolved: Date of resolution
Description

Presence of cGVHD

Data type

date

OTHER COMPLICATIONS SINCE LAST REPORT
Description

OTHER COMPLICATIONS SINCE LAST REPORT

Infection related complications
Description

Infection related complications

Data type

boolean

Alias
UMLS CUI [1,1]
C0009450
UMLS CUI [1,2]
C0009566
Pathogen Use the list of pathogens listed after this table for guidance. Use “unknown” if necessary.
Description

Bacteremia / fungemia / viremia / parasites

Data type

text

Pathogen Use the list of pathogens listed after this table for guidance. Use “unknown” if necessary.
Description

Septic shock

Data type

text

Pathogen Use the list of pathogens listed after this table for guidance. Use “unknown” if necessary.
Description

ARDS

Data type

text

Pathogen Use the list of pathogens listed after this table for guidance. Use “unknown” if necessary.
Description

Multiorgan failure due to infection

Data type

text

Pathogen Use the list of pathogens listed after this table for guidance. Use “unknown” if necessary.
Description

Pneumonia

Data type

text

Pathogen Use the list of pathogens listed after this table for guidance. Use “unknown” if necessary.
Description

Hepatitis

Data type

text

Pathogen Use the list of pathogens listed after this table for guidance. Use “unknown” if necessary.
Description

CNS infection

Data type

text

Pathogen Use the list of pathogens listed after this table for guidance. Use “unknown” if necessary.
Description

Gut infection

Data type

text

Pathogen Use the list of pathogens listed after this table for guidance. Use “unknown” if necessary.
Description

Skin infection

Data type

text

Pathogen Use the list of pathogens listed after this table for guidance. Use “unknown” if necessary.
Description

Cystitis

Data type

text

Pathogen Use the list of pathogens listed after this table for guidance. Use “unknown” if necessary.
Description

Retinitis

Data type

text

Pathogen Use the list of pathogens listed after this table for guidance. Use “unknown” if necessary.
Description

Other

Data type

text

Date Provide different dates for different episodes of the same complication if applicable.
Description

Bacteremia / fungemia / viremia / parasites

Data type

date

Date Provide different dates for different episodes of the same complication if applicable.
Description

Septic shock

Data type

date

Date Provide different dates for different episodes of the same complication if applicable.
Description

Multiorgan failure due to infection

Data type

date

Date Provide different dates for different episodes of the same complication if applicable.
Description

Pneumonia

Data type

date

Date Provide different dates for different episodes of the same complication if applicable.
Description

Hepatitis

Data type

date

Date Provide different dates for different episodes of the same complication if applicable
Description

CNS infection

Data type

date

Date Provide different dates for different episodes of the same complication if applicable
Description

Gut infection

Data type

date

Date Provide different dates for different episodes of the same complication if applicable.
Description

Skin infection

Data type

date

Date Provide different dates for different episodes of the same complication if applicable.
Description

Cystitis

Data type

date

Date Provide different dates for different episodes of the same complication if applicable.
Description

Retinitis

Data type

date

Date Provide different dates for different episodes of the same complication if applicable.
Description

Other

Data type

date

Non infection related complications
Description

Non infection related complications

Data type

boolean

Alias
UMLS CUI [1]
C0009566
(Check all that are applicable for this period)
Description

Idiopathic pneumonia syndrome

Data type

integer

Idiopathic pneumonia syndrome
Description

Idiopathic pneumonia syndrome

Data type

date

(Check all that are applicable for this period)
Description

VOD

Data type

integer

Alias
UMLS CUI [1]
C0948441
VOD
Description

VOD

Data type

date

(Check all that are applicable for this period)
Description

Cataract

Data type

integer

Alias
UMLS CUI [1]
C0086543
Cataract
Description

Cataract

Data type

date

Check all that are applicable for this period Haemorrhagic cystitis, non infectious
Description

Haemorrhagic cystitis, non infectious

Data type

text

Alias
UMLS CUI [1]
C0085692
Haemorrhagic cystitis, non infectious
Description

Haemorrhagic cystitis, non infectious

Data type

date

ARDS, non infectious ARDS, non infectious
Description

ARDS, non infectious

Data type

integer

Alias
UMLS CUI [1]
C0035222
ARDS, non infectious
Description

ARDS, non infectious

Data type

date

Check all that are applicable for this period)
Description

Multiorgan failure, non infectious

Data type

integer

Multiorgan failure, non infectious
Description

Multiorgan failure, non infectious

Data type

date

(Check all that are applicable for this period HSCT-associated microangiopathy
Description

HSCT-associated microangiopathy

Data type

text

Alias
UMLS CUI [1]
C0155765
HSCT-associated microangiopathy
Description

HSCT-associated microangiopathy

Data type

date

(Check all that are applicable for this period) Renal failure requiring dialysis
Description

Renal failure requiring dialysis

Data type

text

Alias
UMLS CUI [1]
C0035078
Renal failure requiring dialysis
Description

Renal failure requiring dialysis

Data type

date

(Check all that are applicable for this period) Haemolytic anaemia due to blood group
Description

Haemolytic anaemia due to blood group

Data type

integer

Alias
UMLS CUI [1]
C0002878
Haemolytic anaemia due to blood group
Description

Haemolytic anaemia due to blood group

Data type

date

Check all that are applicable for this period) Aseptic bone necrosis
Description

Aseptic bone necrosis

Data type

text

Alias
UMLS CUI [1]
C0158452
Aseptic bone necrosis
Description

Aseptic bone necrosis

Data type

date

Other type of complication > CTCAE grade 2
Description

Other type of complication

Data type

boolean

Graft loss
Description

GRAFT ASSESSMENT AND HAEMOPOIETIC CHIMAERISM

Data type

integer

Overall chimaerism
Description

Overall chimaerism

Data type

text

Alias
UMLS CUI [1]
C0333678
Date of Test
Description

Date of Test

Data type

date

Alias
UMLS CUI [1,1]
C0024671
UMLS CUI [1,2]
C0011008
Identification of donor or Cord Blood Unit given by the centre
Description

Identification

Data type

text

Alias
UMLS CUI [1]
C1718162
Number in the infusion order (if applicable)
Description

Number in the infusion order

Data type

text

Alias
UMLS CUI [1]
C0237753
Cell type on which test was performed (% Donor Cells): BM
Description

Bone marrow

Data type

float

Measurement units
  • %
Alias
UMLS CUI [1]
C0005953
%
Cell type on which test was performed (% Donor cells): PB mononuclear cells (PBMC)
Description

PB mononuclear cells (PBMC)

Data type

float

Measurement units
  • %
Alias
UMLS CUI [1]
C1321301
%
Cell type on which test was performed (% Donor cells): T-Cells
Description

T-Cells

Data type

float

Measurement units
  • %
Alias
UMLS CUI [1]
C0039194
%
Cell type on which test was performed (% Donor cells): B-Cells
Description

B-Cells

Data type

float

Measurement units
  • %
Alias
UMLS CUI [1]
C0004561
%
Cell type on which test was performed (% Donor cells): Red blood cells
Description

Red blood cells

Data type

float

Measurement units
  • %
Alias
UMLS CUI [1]
C0014772
%
Cell type on which test was performed (% Donor cells): Monocytes
Description

Monocytes

Data type

float

Measurement units
  • %
Alias
UMLS CUI [1]
C0026473
%
Cell type on which test was performed (% Donor cells): PMNs (neutrophils)
Description

PMNs (neutrophils)

Data type

float

Measurement units
  • %
Alias
UMLS CUI [1]
C0200633
%
Cell type on which test was performed (% Donor cells): Lymphocytes, NOS
Description

Lymphocytes, NOS

Data type

float

Measurement units
  • %
Alias
UMLS CUI [1]
C0024264
%
Cell type on which test was performed (% Donor cells): Myeloid cells, NOS
Description

Myeloid cells, NOS

Data type

float

Measurement units
  • %
Alias
UMLS CUI [1]
C0887899
%
Cell type on which test was performed % Donor cells
Description

Other

Data type

float

Test used:
Description

Laboratory tests

Data type

text

Alias
UMLS CUI [1]
C0022885
SECONDARY MALIGNANCY, LYMPHOPROLIFERATIVE OR MYELOPROLIFRATIVE DISORDER DIAGNOSED
Description

SECONDARY MALIGNANCY, LYMPHOPROLIFERATIVE OR MYELOPROLIFRATIVE DISORDER DIAGNOSED

Data type

integer

Date of Diagnosis
Description

Date of Diagnosis

Data type

date

Alias
UMLS CUI [1]
C2316983
Diagnosis
Description

Diagnosis

Data type

text

Alias
UMLS CUI [1]
C0011900
if other, please specify
Description

diagnosis

Data type

text

ADDITIONAL THERAPIES SINCE LAST FOLLOW UP
Description

ADDITIONAL THERAPIES SINCE LAST FOLLOW UP

Treatment given since last report
Description

Additional treatment

Data type

text

Alias
UMLS CUI [1]
C1706712
If yes: CELLULAR THERAPY One cell therapy regimen is defined as any number of infusions given within 10 weeks for the same indication. If more than one regimen of cell therapy has been given since last report, copy this section and complete it as many times as necessary.
Description

ADDITIONAL TREATMENT

Data type

integer

Disease status before this cellular therapy
Description

Disease status before this cellular therapy

Data type

text

If yes: Type of cells
Description

Type of cells

Data type

integer

Alias
UMLS CUI [1]
C0302189
Number of Nucleated cells infused (DLI only)
Description

Nucleated cells

Data type

integer

Measurement units
  • 10^8/kg
Alias
UMLS CUI [1]
C1180059
If DLI, specify the number of cells infused by type: CD 34+
Description

CD 34+

Data type

text

Alias
UMLS CUI [1]
C3538723
If DLI, specify the number of cells infused by type: CD 3+
Description

CD 3+

Data type

text

Alias
UMLS CUI [1]
C3542405
Total number of cells infused (non DLI only)
Description

All cells

Data type

integer

Measurement units
  • x10^6/kg
Alias
UMLS CUI [1]
C0007584
Chronological number of this cell therapy for this patient
Description

Chronological number

Data type

float

Alias
UMLS CUI [1]
C2348184
Indication (check all that apply)
Description

Indication

Data type

text

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C0302189
If Other, please specify
Description

Indication

Data type

text

Number of infusions within 10 weeks (count only infusions that are part of same regimen and given for the same indication)
Description

Infusion count

Data type

float

Alias
UMLS CUI [1,1]
C0574032
UMLS CUI [1,2]
C0750480
Acute Graft versus Host Disease (after this infusion but before any further infusion/ transplant) Maximum grade:
Description

Acute Graft versus Host Disease

Data type

text

Alias
UMLS CUI [1]
C0856825
Disease treatment (apart from donor cell infusion or other type of cell therapy)
Description

Disease treatment

Data type

integer

Alias
UMLS CUI [1]
C0087111
FIRST EVIDENCE OF RELAPSE OR PROGRESSION SINCE LAST HSCT
Description

FIRST EVIDENCE OF RELAPSE OR PROGRESSION SINCE LAST HSCT

Relapse or Progression
Description

Relapse or Progression

Data type

text

Alias
UMLS CUI [1,1]
C0277556
UMLS CUI [1,2]
C0242656
if yes, date diagnosed
Description

RELAPSE OR PROGRESSION

Data type

date

LAST DISEASE AND PATIENT STATUS
Description

LAST DISEASE AND PATIENT STATUS

Last Disease Status
Description

Disease response

Data type

text

Alias
UMLS CUI [1]
C1704632
Has patient or partner become pregnant after this HSCT?
Description

Conception

Data type

text

Alias
UMLS CUI [1]
C0032961
Survival Status
Description

Survival Status

Data type

integer

Alias
UMLS CUI [1]
C1148433
Type of score used
Description

Type of score used

Data type

text

Score
Description

Performance score

Data type

integer

Alias
UMLS CUI [1]
C1518965
If dead, specify cause of death:
Description

Cause of Death

Data type

text

Alias
UMLS CUI [1]
C0007465
If dead and HSCT related cause of death, specify (check as many as apppropriate): GvHD
Description

GvHD

Data type

text

Alias
UMLS CUI [1,1]
C0007465
UMLS CUI [1,2]
C0018133
If dead and HSCT related cause of death, specify (check as many as apppropriate): Interstitial Pneumonitis
Description

Interstitial Pneumonitis

Data type

text

Alias
UMLS CUI [1,1]
C0007465
UMLS CUI [1,2]
C0206061
If dead and HSCT related cause of death, specify (check as many as apppropriate): Pulmonary toxicity
Description

Pulmonary toxicity

Data type

text

Alias
UMLS CUI [1,1]
C0007465
UMLS CUI [1,2]
C0919924
If dead and HSCT related cause of death, specify (check as many as apppropriate): Infection
Description

Infection

Data type

text

Alias
UMLS CUI [1,1]
C0007465
UMLS CUI [1,2]
C0009450
check as many as appropriate
Description

Infection

Data type

text

COMMENTS
Description

ADDITIONAL NOTES IF APPLICABLE

Data type

text

IDENTIFICATION & SIGNATURE
Description

IDENTIFICATION & SIGNATURE

Data type

text

Similar models

16pp EBMT Multiple Myeloma 10PCD

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
GENERAL INFORMATION Team
EBMT Centre Identification Code (CIC)
Item
EBMT Centre Identification Code (CIC)
text
C2348585 (UMLS CUI [1])
Hospital
Item
Hospital
text
C0019994 (UMLS CUI [1])
Unit
Item
Unit
text
Contact person
Item
Name of contact person
text
C0337611 (UMLS CUI [1])
Patient phone number
Item
Telephone
text
C1515258 (UMLS CUI [1])
ContactPersonFaxNumber
Item
Fax
text
C0237753 (UMLS CUI [1,1])
C0027361 (UMLS CUI [1,2])
C0337611 (UMLS CUI [1,3])
C0085205 (UMLS CUI [1,4])
ContactPersonE-mailText
Item
E-mail
text
C1527021 (UMLS CUI [1,1])
C0027361 (UMLS CUI [1,2])
C0013849 (UMLS CUI [1,3])
C0337611 (UMLS CUI [1,4])
Date of this report
Item
Date of this report
date
C1302584 (UMLS CUI [1])
Item
Patient following national / international study / trial
integer
C1997894 (UMLS CUI [1])
Code List
Patient following national / international study / trial
CL Item
No (1)
CL Item
Yes (2)
CL Item
Not evaluated (3)
CL Item
Unknown (4)
Name of study trial
Item
Name of study trial
text
C2348560 (UMLS CUI [1])
Item Group
PATIENT
Unique Identification Code (UIC)
Item
To be entered only if patient previously reported
text
C2348585 (UMLS CUI [1])
Hospital Unique Patient Number or Code
Item
Hospital Unique Patient Number or Code
text
C1827636 (UMLS CUI [1])
Initials
Item
First name(s)_surname(s)
text
C2986440 (UMLS CUI [1])
PersonBirthDate
Item
Date of Birth
date
C0011008 (UMLS CUI [1,1])
C0027361 (UMLS CUI [1,2])
C0005615 (UMLS CUI [1,3])
Item
Sex
integer
Code List
Sex
CL Item
Male (1)
CL Item
Female (2)
ABO Group
Item
ABO Group
text
Item
Rh factor
text
Code List
Rh factor
CL Item
Absent (Absent)
CL Item
Present (Present)
CL Item
Not evaluated (Not evaluated)
Item Group
DISEASE
Date of Diagnosis
Item
Date of Diagnosis
date
C2316983 (UMLS CUI [1])
Item
Check the disease for which this transplant was performed
text
C0277554 (UMLS CUI [1])
Code List
Check the disease for which this transplant was performed
CL Item
Acute Leukaemia (Acute Leukaemia)
CL Item
Acute Myelogenous Leukaemia (AML) (Acute Myelogenous Leukaemia (AML))
CL Item
Acute Lymphoblastic Leukaemia (ALL) (Acute Lymphoblastic Leukaemia (ALL))
CL Item
Secondary Acute Leukaemia (do not use if transformed from MDS/MPN) (Secondary Acute Leukaemia (do not use if transformed from MDS/MPN))
CL Item
Chronic Leukaemia (Chronic Leukaemia)
CL Item
Chronic Myeloid Leukaemia (CML) (Chronic Myeloid Leukaemia (CML))
CL Item
Chronic Lymphocytic Leukaemia (Chronic Lymphocytic Leukaemia)
CL Item
Lymphoma (Lymphoma)
CL Item
Non Hodgkin (Non Hodgkin)
CL Item
Hodgkin´s Disease (Hodgkin´s Disease)
CL Item
Myeloma/ Plasma cell disorder (Myeloma/ Plasma cell disorder)
CL Item
Solid Tumour (Solid Tumour)
CL Item
Myelodysplastic syndromes (Myelodysplastic syndromes)
CL Item
MDS (MDS)
CL Item
MD/ MPN (MD/ MPN)
CL Item
Myeloproliferative neoplasm (Myeloproliferative neoplasm)
CL Item
Bone marrow failure including Aplastic anaemia (Bone marrow failure including Aplastic anaemia)
CL Item
Inherited disorders (Inherited disorders)
CL Item
Primary immune deficiencies (Primary immune deficiencies)
CL Item
Metabolic disorders (Metabolic disorders)
CL Item
Histiocytic disorders (Histiocytic disorders)
CL Item
Autoimmune disease (Autoimmune disease)
CL Item
Juvenile Idiopathic Arthritis (Juvenile Idiopathic Arthritis)
CL Item
Multiple Sclerosis (Multiple Sclerosis)
CL Item
Systemic Lupus (Systemic Lupus)
CL Item
Systemic Sclerosis (Systemic Sclerosis)
CL Item
Haemoglobinopathiy (Haemoglobinopathiy)
CL Item
Other diagnosis (Other diagnosis)
Primary Disease Diagnosis
Item
If other diagnosis, specify:
text
C0277554 (UMLS CUI [1,1])
C2348235 (UMLS CUI [1,2])
Item Group
PLASMA CELL DISORDERS (INCLUDING MULTIPLE MYELOMA)
Item
Has the information requested in this section been submitted with a previous HSCT registration for this patient?
integer
Code List
Has the information requested in this section been submitted with a previous HSCT registration for this patient?
CL Item
Yes: go to page 2, Pre HSCT Treatment (1)
CL Item
No: proceed with this section (2)
Code List
SUBCLASSIFICATION
CL Item
Multiple myeloma (Multiple myeloma)
CL Item
Plasma Cell Leukaemia (Plasma Cell Leukaemia)
CL Item
Solitary plasmacytoma of bone (Solitary plasmacytoma of bone)
CL Item
POEMS (POEMS)
CL Item
Monoclonal light and heavy chain deposition disease (LCDD/HCDD) (Monoclonal light and heavy chain deposition disease (LCDD/HCDD))
CL Item
Other (Other)
Item
if Multiple myeloma
integer
Code List
if Multiple myeloma
CL Item
Heavy chain and light chain (check light and heavy chain types) (1)
CL Item
Light chain only (check light chain type only)  (2)
CL Item
Non secretory (3)
Item
Heavy chain and light chain
integer
Code List
Heavy chain and light chain
CL Item
IgG (1)
CL Item
IgA (2)
CL Item
IgD (3)
CL Item
IgE (4)
CL Item
IgM (5)
Item
Heavy chain and light chain
integer
Code List
Heavy chain and light chain
CL Item
Kappa (1)
CL Item
Lambda (2)
Item
Light chain only
integer
Code List
Light chain only
CL Item
Kappa (1)
CL Item
Lambda (2)
Item
SALMON AND DURIE Stage at diagnosis
integer
C3846373 (UMLS CUI [1])
Code List
SALMON AND DURIE Stage at diagnosis
CL Item
A I (1)
CL Item
A II (2)
CL Item
A III (3)
CL Item
B I (4)
CL Item
B II (5)
CL Item
B III (6)
Item
ISS (Multiple Myeloma Prognosis) (Stage 1-3)
integer
C2346508 (UMLS CUI [1])
Code List
ISS (Multiple Myeloma Prognosis) (Stage 1-3)
Item
Chromosome analysis
text
C0200867 (UMLS CUI [1])
Code List
Chromosome analysis
CL Item
Not Done or failed (Not Done or failed)
CL Item
Done: normal (Done: normal)
CL Item
Done: abnormal (Done: abnormal)
CL Item
Unknown (Unknown)
Number of abnormal metaphases
Item
Number of metaphases with anomalies:
float
C1621812 (UMLS CUI [1,1])
C0237753 (UMLS CUI [1,2])
Number of examined metaphases
Item
Number of metaphases examined
float
C1621812 (UMLS CUI [1,1])
C0237753 (UMLS CUI [1,2])
C0260877 (UMLS CUI [1,3])
Item
IF ABNORMAL, INDICATE ABNORMALITIES FOUND Del 13q14
text
Code List
IF ABNORMAL, INDICATE ABNORMALITIES FOUND Del 13q14
CL Item
Absent (Absent)
CL Item
Present (Present)
CL Item
Not evaluated (Not evaluated)
Item
IF ABNORMAL, INDICATE ABNORMALITIES FOUND t(11;14)
integer
Code List
IF ABNORMAL, INDICATE ABNORMALITIES FOUND t(11;14)
CL Item
Absent (Absent)
CL Item
Present (Present)
CL Item
Not evaluated (Not evaluated)
Item
IF ABNORMAL, INDICATE ABNORMALITIES FOUND abn 17q
integer
Code List
IF ABNORMAL, INDICATE ABNORMALITIES FOUND abn 17q
CL Item
Absent (Absent)
CL Item
Present (Present)
CL Item
Not evaluated (Not evaluated)
Item
IF ABNORMAL, INDICATE ABNORMALITIES FOUND 17p del
integer
Code List
IF ABNORMAL, INDICATE ABNORMALITIES FOUND 17p del
CL Item
Absent (Absent)
CL Item
Present (Present)
CL Item
Not evaluated (Not evaluated)
Item
IF ABNORMAL, INDICATE ABNORMALITIES FOUND t(4:14)
integer
Code List
IF ABNORMAL, INDICATE ABNORMALITIES FOUND t(4:14)
CL Item
Absent (Absent)
CL Item
Present (Present)
CL Item
Not evaluated (Not evaluated)
Item
IF ABNORMAL, INDICATE ABNORMALITIES FOUND (14:16)
integer
Code List
IF ABNORMAL, INDICATE ABNORMALITIES FOUND (14:16)
CL Item
Absent (Absent)
CL Item
Present (Present)
CL Item
Not evaluated (Not evaluated)
Item
IF ABNORMAL, INDICATE ABNORMALITIES FOUND 1q amplification
integer
Code List
IF ABNORMAL, INDICATE ABNORMALITIES FOUND 1q amplification
CL Item
Absent (Absent)
CL Item
Present (Present)
CL Item
Not evaluated (Not evaluated)
Item
IF ABNORMAL, INDICATE ABNORMALITIES FOUND c-myc
integer
Code List
IF ABNORMAL, INDICATE ABNORMALITIES FOUND c-myc
CL Item
Absent (Absent)
CL Item
Present (Present)
CL Item
Not evaluated (Not evaluated)
Item
IF Other ABNORMAL, INDICATE ABNORMALITIES FOUND, please specify
integer
Code List
IF Other ABNORMAL, INDICATE ABNORMALITIES FOUND, please specify
CL Item
Absent (Absent)
CL Item
Present (Present)
CL Item
Not evaluated (Not evaluated)
Chromosome analysis
Item
Other or associated abnormalities (specify) please specify
text
Item
Molecular Analysis
integer
C1513380 (UMLS CUI [1])
Code List
Molecular Analysis
CL Item
Done but failed (1)
CL Item
Done, successful (2)
CL Item
Not evaluated (3)
CL Item
Unknown (4)
CLINICAL AND LABORATORY DATA
Item
Hb (g/dL)
float
Item
Hb (g/dL)
integer
Code List
Hb (g/dL)
CL Item
Not evaluated (1)
CLINICAL AND LABORATORY DATA
Item
Serum creatinine (mol/L)
float
Item
Serum creatinine (mol/L)
text
Code List
Serum creatinine (mol/L)
CL Item
Not evaluated (1)
CLINICAL AND LABORATORY DATA
Item
Serum calcium (mmol/L)
float
Item
Serum calcium (mmol/L)
integer
Code List
Serum calcium (mmol/L)
CL Item
Not evaluated (1)
CLINICAL AND LABORATORY DATA
Item
Serum albumin (g/L)
float
Item
Serum albumin (g/L)
integer
Code List
Serum albumin (g/L)
CL Item
Not evaluated (1)
CLINICAL AND LABORATORY DATA
Item
BM aspirate: % plasmacytosis
float
Item
BM aspirate: % plasmacytosis
integer
Code List
BM aspirate: % plasmacytosis
CL Item
Not evaluated (1)
CLINICAL AND LABORATORY DATA
Item
BM trephine: % plasmacytosis
float
Item
BM trephine: % plasmacytosis
integer
Code List
BM trephine: % plasmacytosis
CL Item
Not evaluated (1)
CLINICAL AND LABORATORY DATA
Item
Monoclonal Ig in serum (g/L)
float
Item
Monoclonal Ig in serum (g/L)
integer
Code List
Monoclonal Ig in serum (g/L)
CL Item
Not evaluated (1)
CLINICAL AND LABORATORY DATA
Item
Monoclonal Ig in urine (g/24 h)
float
Item
Monoclonal Ig in urine (g/24 h)
integer
Code List
Monoclonal Ig in urine (g/24 h)
CL Item
Not evaluated (1)
CLINICAL AND LABORATORY DATA
Item
Serum ß2 microglobulin (mg/L)
float
Item
Serum ß2 microglobulin (mg/L)
integer
Code List
Serum ß2 microglobulin (mg/L)
CL Item
Not evaluated (1)
Item
INVOLVEMENT AT DIAGNOSIS, Bone structure
integer
Code List
INVOLVEMENT AT DIAGNOSIS, Bone structure
CL Item
Normal (1)
CL Item
Minor (2)
CL Item
Major (3)
CL Item
Not evaluated (4)
Item
INVOLVEMENT AT DIAGNOSIS, Bone structure
integer
Code List
INVOLVEMENT AT DIAGNOSIS, Bone structure
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Extramedullary involvement
Item
if yes, specify location
text
Item Group
PRE-HSCT TREATMENT
Item
Was the patient treated before the HSCT procedure?
text
C0087111 (UMLS CUI [1])
Code List
Was the patient treated before the HSCT procedure?
CL Item
No (proceed to `Date of HSCT`) (No (proceed to `Date of HSCT`))
CL Item
Yes (Yes)
CL Item
Unknown (Unknown)
Sequential number of this treatment
Item
(counted from diagnosis, or last HSCT if applicable)
text
Item
Chemo/Drugs
text
C0695347 (UMLS CUI [1])
Code List
Chemo/Drugs
CL Item
No (No)
CL Item
Yes, Chemo/Drug regimen (Yes, Chemo/Drug regimen)
Item
Radiotherapy
integer
C0695347 (UMLS CUI [1])
Code List
Radiotherapy
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Item
see manual for full definition of each response
integer
Code List
see manual for full definition of each response
CL Item
sCR (1)
CL Item
CR (2)
CL Item
VGPR (3)
CL Item
PR (4)
CL Item
Stable disease (5)
CL Item
Progression (6)
CL Item
Not evaluated (7)
CL Item
Unknown (8)
Item
Additional Pre-HSCT treatment
text
C1706712 (UMLS CUI [1,1])
C2709094 (UMLS CUI [1,2])
Code List
Additional Pre-HSCT treatment
CL Item
No (No)
CL Item
Yes (Yes)
CL Item
Unknown (Unknown)
Sequential number of this treatment
Item
(counted from diagnosis, or last HSCT if applicable)
text
Item
Chemo/Drugs
integer
Code List
Chemo/Drugs
CL Item
No (1)
CL Item
Yes, Chemo/Drug regimen (2)
Item
Radiotherapy
integer
Code List
Radiotherapy
CL Item
No (1)
CL Item
Yes (2)
Item
(see manual for full definition of each response)
integer
Code List
(see manual for full definition of each response)
CL Item
sCR (1)
CL Item
CR (2)
CL Item
VGPR (3)
CL Item
PR (4)
CL Item
Stable disease (5)
CL Item
Progression (6)
CL Item
Not evaluated (7)
CL Item
Unknown (8)
Item
ADDITIONAL PRE-HSCT TREATMENT?
integer
Code List
ADDITIONAL PRE-HSCT TREATMENT?
CL Item
No (1)
CL Item
Yes, Date started (2)
Sequential number of this treatment
Item
Sequential number of this treatment
text
Item
Chemo/Drugs
text
Code List
Chemo/Drugs
CL Item
No (No)
CL Item
Yes: Chemo/Drug regimen (Yes: Chemo/Drug regimen)
Item
Radiotherapy
integer
Code List
Radiotherapy
CL Item
No (1)
CL Item
Yes (2)
Item
Response
integer
Code List
Response
CL Item
sCR (1)
CL Item
CR (2)
CL Item
VGPR (3)
CL Item
PR (4)
CL Item
Stable disease (5)
CL Item
Progression (6)
CL Item
Not evaluated (7)
CL Item
Unknown (8)
Item Group
HSCT
Date of HSCT
Item
Date of HSCT
date
C2584899 (UMLS CUI [1])
Item
HSCT type
integer
C0472699 (UMLS CUI [1])
Code List
HSCT type
CL Item
Autologous (1)
CL Item
Allogeneic (2)
Date of 1st collection or pheresis
Item
Autologous
date
Item Group
STATUS OF DISEASE AT COLLECTION
Item
STATUS OF DISEASE AT COLLECTION
integer
Code List
STATUS OF DISEASE AT COLLECTION
CL Item
At diagnosis (untreated) (1)
CL Item
Stringent complete remission (sCR) (2)
CL Item
Complete remission (CR) (3)
CL Item
Very good PR (VGPR) (4)
CL Item
PR (5)
CL Item
Relapse from CR (6)
CL Item
Stable disease (7)
CL Item
Progression (8)
CL Item
Unknown (9)
Item
If sCR or CR: NUMBER OF THIS COMPLETE REMISSION
integer
Code List
If sCR or CR: NUMBER OF THIS COMPLETE REMISSION
CL Item
1st (1)
CL Item
2nd (2)
CL Item
3rd or higher (3)
Item
If VGPR or PR: NUMBER OF THIS PARTIAL REMISSION
integer
Code List
If VGPR or PR: NUMBER OF THIS PARTIAL REMISSION
CL Item
1st (1)
CL Item
2nd (2)
CL Item
3rd or higher (3)
Item
Relapse from CR, NUMBER OF THIS RELAPSE
integer
Code List
Relapse from CR, NUMBER OF THIS RELAPSE
CL Item
1st (1)
CL Item
2nd (2)
CL Item
3rd or higher (3)
Item
Relapse from CR, NUMBER OF THIS RELAPSE
integer
Code List
Relapse from CR, NUMBER OF THIS RELAPSE
CL Item
1st (1)
CL Item
2nd (2)
CL Item
3rd or higher (3)
Item
Plateau
integer
Code List
Plateau
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
CLINICAL AND LABORATORY DATA
Item
Hb (g/dL)
float
Item
Hb (g/dL)
integer
Code List
Hb (g/dL)
CL Item
Not evaluated (1)
CLINICAL AND LABORATORY DATA
Item
Serum creatinine (mol/L)
float
Item
Serum creatinine (mol/L)
integer
Code List
Serum creatinine (mol/L)
CL Item
Not evaluated (1)
CLINICAL AND LABORATORY DATA
Item
Serum calcium (mmol/L)
float
Item
Serum calcium (mmol/L)
integer
Code List
Serum calcium (mmol/L)
CL Item
Not evaluated (1)
CLINICAL AND LABORATORY DATA
Item
Serum albumin (g/L)
float
Item
Serum albumin (g/L)
integer
C0201838 (UMLS CUI [1])
Code List
Serum albumin (g/L)
CL Item
Not evaluated (1)
CLINICAL AND LABORATORY DATA
Item
BM aspirate: % plasmacytosis
float
Item
BM aspirate: % plasmacytosis
integer
Code List
BM aspirate: % plasmacytosis
CL Item
Not evaluated (1)
CLINICAL AND LABORATORY DATA
Item
BM trephine: % plasmacytosis
float
Item
BM trephine: % plasmacytosis
integer
Code List
BM trephine: % plasmacytosis
CL Item
Not evaluated (1)
CLINICAL AND LABORATORY DATA
Item
Monoclonal Ig in serum (g/L)
float
Item
Monoclonal Ig in serum (g/L)
integer
Code List
Monoclonal Ig in serum (g/L)
CL Item
Not evaluated (1)
Item
Immunofixation of serum
integer
Code List
Immunofixation of serum
CL Item
Negative (1)
CL Item
Positive (2)
CL Item
Not evaluated (3)
CL Item
Unknown (4)
CLINICAL AND LABORATORY DATA
Item
Monoclonal Ig in urine (g/24 h)
float
Item
Monoclonal Ig in urine (g/24 h)
integer
Code List
Monoclonal Ig in urine (g/24 h)
CL Item
Not evaluated (1)
Item
Immunofixation of urine
integer
Code List
Immunofixation of urine
CL Item
Negative (1)
CL Item
Positive (2)
CL Item
Not evaluated (3)
CL Item
Unknown (4)
CLINICAL AND LABORATORY DATA
Item
Serum 2 microglobulin (mg/L)
float
Item
Serum 2 microglobulin (mg/L)
integer
Code List
Serum 2 microglobulin (mg/L)
CL Item
Not evaluated (1)
Item
Bone structure, Lytic lesions
text
Code List
Bone structure, Lytic lesions
CL Item
Normal (Normal)
CL Item
Minor (Minor)
CL Item
Major (Major)
CL Item
Not evaluated (Not evaluated)
Item Group
DISEASE STATUS AT HSCT
Item
DISEASE STATUS AT HSCT
integer
Code List
DISEASE STATUS AT HSCT
CL Item
At diagnosis (1)
CL Item
Stringent complete remission (sCR) (2)
CL Item
Complete remission (CR) (3)
CL Item
Very good PR (VGPR) (4)
CL Item
PR (5)
CL Item
Relapse from CR (6)
CL Item
Stable disease (no change, includes old MR) (7)
CL Item
Progression (8)
CL Item
Unknown (9)
Item
NUMBER OF THIS COMPLETE REMISSION
integer
Code List
NUMBER OF THIS COMPLETE REMISSION
CL Item
1st (1)
CL Item
2nd (2)
CL Item
3rd or higher (3)
Item
NUMBER OF THIS PARTIAL REMISSION
integer
Code List
NUMBER OF THIS PARTIAL REMISSION
CL Item
1st (1)
CL Item
2nd (2)
CL Item
3rd or higher (3)
Item
NUMBER OF THIS RELAPSE
integer
Code List
NUMBER OF THIS RELAPSE
CL Item
1st (1)
CL Item
2nd (2)
CL Item
3rd or higher (3)
Item
(not applicable for non secretory myelona)
integer
Code List
(not applicable for non secretory myelona)
CL Item
No (1)
CL Item
Yes  (2)
CL Item
Unknown (3)
CLINICAL AND LABORATORY DATA
Item
Hb (g/dL)
float
Item
Hb (g/dL)
text
Code List
Hb (g/dL)
CL Item
Not evaluated (Not evaluated)
CLINICAL AND LABORATORY DATA
Item
Serum creatinine (mol/L)
float
Item
Serum creatinine (mol/L)
integer
Code List
Serum creatinine (mol/L)
CL Item
Not evaluated (Not evaluated)
CLINICAL AND LABORATORY DATA
Item
Serum calcium (mmol/L)
float
Item
Serum calcium (mmol/L)
integer
Code List
Serum calcium (mmol/L)
CL Item
Not evaluated (Not evaluated)
CLINICAL AND LABORATORY DATA
Item
Serum albumin (g/L)
float
Item
Serum albumin (g/L)
integer
Code List
Serum albumin (g/L)
CL Item
Not evaluated (Not evaluated)
CLINICAL AND LABORATORY DATA
Item
BM aspirate: % plasmacytosis
float
Item
BM aspirate: % plasmacytosis
integer
Code List
BM aspirate: % plasmacytosis
CL Item
Not evaluated (Not evaluated)
CLINICAL AND LABORATORY DATA
Item
Monoclonal Ig in serum (g/L)
float
Item
Monoclonal Ig in serum (g/L)
integer
Code List
Monoclonal Ig in serum (g/L)
CL Item
Not evaluated (Not evaluated)
Item
Immunofixation of serum
integer
Code List
Immunofixation of serum
CL Item
Negative (1)
CL Item
Positive (2)
CL Item
Not evaluated (3)
CL Item
Unknown (4)
CLINICAL AND LABORATORY DATA
Item
Monoclonal Ig in urine (g/24 h)
float
Item
Monoclonal Ig in urine (g/24 h)
integer
Code List
Monoclonal Ig in urine (g/24 h)
CL Item
Negative (1)
CL Item
Positive (2)
CL Item
Not evaluated (3)
CL Item
Unknown (4)
Item
Immunofixation of urine
text
Code List
Immunofixation of urine
CL Item
Negative (Negative)
CL Item
Positive (Positive)
CL Item
Not evaluated (Not evaluated)
CL Item
Unknown (Unknown)
CLINICAL AND LABORATORY DATA
Item
Serum 2 microglobulin (mg/L)
float
Item
Serum 2 microglobulin (mg/L)
integer
Code List
Serum 2 microglobulin (mg/L)
CL Item
Not evaluated (1)
Item
Lytic lesions
integer
Code List
Lytic lesions
CL Item
Normal (1)
CL Item
Minor (2)
CL Item
Major (3)
CL Item
Not evaluated (4)
Item Group
ADDITIONAL TREATMENT POST-HSCT
Item
Additional Disease Treatment
text
C1706712 (UMLS CUI [1])
Code List
Additional Disease Treatment
CL Item
No (No)
CL Item
Yes (Yes)
CL Item
Unknown (Unknown)
CL Item
Planned (planned before HSCT took place) (Planned (planned before HSCT took place))
CL Item
Not planned (for relapse/progression or persistent disease) (Not planned (for relapse/progression or persistent disease))
ADDITIONAL DISEASE TREATMENT
Item
Date started
date
Item
Chemo/drug/agen
text
C1706712 (UMLS CUI [1])
Code List
Chemo/drug/agen
CL Item
Thalidomide (Thalidomide)
CL Item
Other (Other)
CL Item
Unknown (Unknown)
ADDITIONAL DISEASE TREATMENT
Item
if other
text
Item
Radiotherapy
text
Code List
Radiotherapy
CL Item
No (No)
CL Item
Yes (Yes)
CL Item
Unknown (Unknown)
Item
Other treatment
integer
C1706712 (UMLS CUI [1])
Code List
Other treatment
CL Item
No  (1)
CL Item
Yes (2)
CL Item
Unknown (3)
ADDITIONAL DISEASE TREATMENT
Item
if other treatment please specify
text
Item Group
STATUS OF DISEASE AT 100 DAYS AFTER HSCT
Code List
BEST RESPONSE TO HSCT AT 100 DAYS
CL Item
Stringent complete remission (sCR) (Stringent complete remission (sCR))
CL Item
Complete remission (CR) (Complete remission (CR))
CL Item
Very good PR (VGPR) (Very good PR (VGPR))
CL Item
PR (PR)
CL Item
Stable disease (no change, includes old MR) (Stable disease (no change, includes old MR))
CL Item
Progression (Progression)
CL Item
Unknown (Unknown)
Item
If sCR or CR: NUMBER OF THIS COMPLETE REMISSION
integer
Code List
If sCR or CR: NUMBER OF THIS COMPLETE REMISSION
CL Item
1st (1)
CL Item
2nd (2)
CL Item
3rd or higher (3)
Item
If VGPR or PR: NUMBER OF THIS PARTIAL REMISSION
integer
Code List
If VGPR or PR: NUMBER OF THIS PARTIAL REMISSION
CL Item
1st (1)
CL Item
2nd (2)
CL Item
3rd or higher (3)
BEST RESPONSE TO HSCT AT 100 DAYS
Item
If complete response: Date of CR
date
BEST RESPONSE TO HSCT AT 100 DAYS
Item
Otherwise: date of evaluation
date
Item
(COMPLETE ONLY IF STATUS IS STABLE DISEASE OR PR)
text
Code List
(COMPLETE ONLY IF STATUS IS STABLE DISEASE OR PR)
CL Item
No (No)
CL Item
Yes (Yes)
CL Item
Unknown (Unknown)
CLINICAL AND LABORATORY DATA
Item
BM aspirate: % plasmacytosis
float
Item
BM aspirate: % plasmacytosis
integer
Code List
BM aspirate: % plasmacytosis
CL Item
Not evaluated (1)
CLINICAL AND LABORATORY DATA
Item
BM trephine: % plasmacytosis
float
CLINICAL AND LABORATORY DATA
Item
Monoclonal Ig in serum (g/L)
float
Item
Monoclonal Ig in serum (g/L)
integer
Code List
Monoclonal Ig in serum (g/L)
CL Item
Not evaluated (1)
Item
Immunofixation of serum
text
Code List
Immunofixation of serum
CL Item
Negative (Negative)
CL Item
Positive (Positive)
CL Item
Not evaluated (Not evaluated)
CL Item
Unknown (Unknown)
CLINICAL AND LABORATORY DATA
Item
Monoclonal Ig in urine (g/24 h)
float
Item
Monoclonal Ig in urine (g/24 h)
integer
Code List
Monoclonal Ig in urine (g/24 h)
CL Item
Not evaluated (1)
Item
Immunofixation of urine
integer
Code List
Immunofixation of urine
CL Item
Negative (1)
CL Item
Positive (2)
CL Item
Not evaluated (3)
CL Item
Unknown (4)
CLINICAL AND LABORATORY DATA
Item
Serum 2 microglobulin (mg/L)
float
Item
Serum 2 microglobulin (mg/L)
integer
Code List
Serum 2 microglobulin (mg/L)
CL Item
Not evaluated (1)
Item
Lytic lesions
integer
Code List
Lytic lesions
CL Item
Normal (1)
CL Item
Minor (2)
CL Item
Major (3)
CL Item
Not evaluated (4)
Item Group
FORMS TO BE FILLED IN
Item
Type of Transplant
text
C0559189 (UMLS CUI [1,1])
C0040739 (UMLS CUI [1,2])
Code List
Type of Transplant
CL Item
AUTOgraft (proceed to Autograft form) (AUTOgraft (proceed to Autograft form))
CL Item
ALLOgraft or Syngeneic graft (proceed to Allograft form) (ALLOgraft or Syngeneic graft (proceed to Allograft form))
CL Item
Other (contact the EBMT Central Registry for instructions) (Other (contact the EBMT Central Registry for instructions))
TYPE OF TRANSPLANT
Item
If Other contact the EBMT Central Registry Office for instructions
text
Item Group
PLASMA CELL DISORDERS (INCLUDING MULTIPLE MYELOMA)
Unique Identification Code (UIC)
Item
Unique Identification Code (UIC) (if known)
text
C2348585 (UMLS CUI [1])
Hospital Unique Patient Number
Item
Hospital Unique Patient Number
text
C2348585 (UMLS CUI [1])
Date of this report
Item
Date of this report
date
C1302584 (UMLS CUI [1])
Item
Patient following national / international study / trial
integer
C1997894 (UMLS CUI [1])
Code List
Patient following national / international study / trial
CL Item
No (1)
CL Item
Yes (2)
CL Item
Not evaluated (3)
CL Item
Unknown (4)
Name of study / trial
Item
Name of study / trial
text
C0008976 (UMLS CUI [1])
Initials
Item
First name(s)_surname(s)
text
C2986440 (UMLS CUI [1])
Date of birth
Item
Date of birth
date
C0421451 (UMLS CUI [1])
Date of last HSCT for this patient
Item
Date of last HSCT for this patient
date
C0472699 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item Group
PATIENT LAST SEEN
Date last contact
Item
Date of Last Contact or Death
date
C0805839 (UMLS CUI [1])
Item
Complete haematological remission obtained after the HSCT in the absence of additional disease treatment
integer
Code List
Complete haematological remission obtained after the HSCT in the absence of additional disease treatment
CL Item
Previously reported (1)
CL Item
Yes (2)
CL Item
No (3)
CL Item
Unknown (4)
Complete haematological remission obtained after the HSCT in the absence of additional disease treatment
Item
if yes, date
date
Item Group
GRAFT VERSUS HOST DISEASE (GvHD) SINCE LAST REPORT
Item
Acute Graft versus Host Disease (aGvHD) - Grade
integer
C0856825 (UMLS CUI [1,1])
C0441800 (UMLS CUI [1,2])
Code List
Acute Graft versus Host Disease (aGvHD) - Grade
CL Item
grade 0 (Absent) (1)
CL Item
grade I (2)
CL Item
grade II (3)
CL Item
grade III (4)
CL Item
grade IV (5)
CL Item
Not evaluated (6)
Item
if present
integer
C0856825 (UMLS CUI [1,1])
C0806909 (UMLS CUI [1,2])
C0441800 (UMLS CUI [1,3])
C1561607 (UMLS CUI [1,4])
Code List
if present
CL Item
New onset (1)
CL Item
Recurrent (2)
CL Item
Persistent (3)
Item
Reason
integer
Code List
Reason
CL Item
Tapering (1)
CL Item
DLI (2)
CL Item
Unexplained (3)
Date onset of this episode
Item
Date onset of this episode (if new or recurrent)
date
C0574845 (UMLS CUI [1])
Item
Date onset of this episode
integer
Code List
Date onset of this episode
CL Item
Not applicable (1)
Item
Stage skin
integer
C0856825 (UMLS CUI [1,1])
C1306673 (UMLS CUI [1,2])
C1306673 (UMLS CUI [1,3])
Code List
Stage skin
CL Item
0 (1)
CL Item
1 (2)
CL Item
2 (3)
CL Item
3 (4)
CL Item
4 (5)
CL Item
Not evaluated (6)
CL Item
unknown (7)
Item
Stage liver
integer
C0856825 (UMLS CUI [1,1])
C1306673 (UMLS CUI [1,2])
C0023884 (UMLS CUI [1,3])
Code List
Stage liver
CL Item
0 (1)
CL Item
1 (2)
CL Item
2 (3)
CL Item
3 (4)
CL Item
4 (5)
CL Item
Not evaluated (6)
CL Item
unknown (7)
Item
Stage gut
integer
C0856825 (UMLS CUI [1,1])
C1306673 (UMLS CUI [1,2])
C0021853 (UMLS CUI [1,3])
Code List
Stage gut
CL Item
0 (1)
CL Item
1 (2)
CL Item
2 (3)
CL Item
3 (4)
CL Item
4 (5)
CL Item
Not evaluated (6)
CL Item
unknown (7)
Resolution
Item
aGvHD Resolution
boolean
C0856825 (UMLS CUI [1,1])
C1514893 (UMLS CUI [1,2])
aGvHD Date of resolution
Item
Date of resolution
date
C0856825 (UMLS CUI [1,1])
C1514893 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Item
Presence of cGvHD
text
C0867389 (UMLS CUI [1])
CL Item
No (No)
CL Item
Yes (Yes)
CL Item
Present continuously since last reported episode (Present continuously since last reported episode)
CL Item
Resolved (Resolved)
Item
Presence of cGVHD, if yes
integer
Code List
Presence of cGVHD, if yes
CL Item
First episode (1)
CL Item
Recurrence (2)
Date of onset
Item
Date of onset
date
C0574845 (UMLS CUI [1])
Item
If present continously since last report, specify cGvHD gade:
text
C0867389 (UMLS CUI [1,1])
C0441799 (UMLS CUI [1,2])
Code List
If present continously since last report, specify cGvHD gade:
CL Item
Limited (Limited)
CL Item
Extensive (Extensive)
Item
Organs affected
integer
C0449642 (UMLS CUI [1])
Code List
Organs affected
CL Item
Skin (1)
CL Item
Gut (2)
CL Item
Liver (3)
CL Item
Mouth (4)
CL Item
Eyes (5)
CL Item
Lung (6)
CL Item
Other, specify (7)
CL Item
Unknown (8)
Organs affected
Item
if Other please specify
text
Presence of cGVHD
Item
If Resolved: Date of resolution
date
Item Group
OTHER COMPLICATIONS SINCE LAST REPORT
Infection related complications
Item
Infection related complications
boolean
C0009450 (UMLS CUI [1,1])
C0009566 (UMLS CUI [1,2])
Bacteremia / fungemia / viremia / parasites
Item
Pathogen Use the list of pathogens listed after this table for guidance. Use “unknown” if necessary.
text
Septic shock
Item
Pathogen Use the list of pathogens listed after this table for guidance. Use “unknown” if necessary.
text
ARDS
Item
Pathogen Use the list of pathogens listed after this table for guidance. Use “unknown” if necessary.
text
Multiorgan failure due to infection
Item
Pathogen Use the list of pathogens listed after this table for guidance. Use “unknown” if necessary.
text
Pneumonia
Item
Pathogen Use the list of pathogens listed after this table for guidance. Use “unknown” if necessary.
text
Hepatitis
Item
Pathogen Use the list of pathogens listed after this table for guidance. Use “unknown” if necessary.
text
CNS infection
Item
Pathogen Use the list of pathogens listed after this table for guidance. Use “unknown” if necessary.
text
Gut infection
Item
Pathogen Use the list of pathogens listed after this table for guidance. Use “unknown” if necessary.
text
Skin infection
Item
Pathogen Use the list of pathogens listed after this table for guidance. Use “unknown” if necessary.
text
Cystitis
Item
Pathogen Use the list of pathogens listed after this table for guidance. Use “unknown” if necessary.
text
Retinitis
Item
Pathogen Use the list of pathogens listed after this table for guidance. Use “unknown” if necessary.
text
Other
Item
Pathogen Use the list of pathogens listed after this table for guidance. Use “unknown” if necessary.
text
Bacteremia / fungemia / viremia / parasites
Item
Date Provide different dates for different episodes of the same complication if applicable.
date
Septic shock
Item
Date Provide different dates for different episodes of the same complication if applicable.
date
Multiorgan failure due to infection
Item
Date Provide different dates for different episodes of the same complication if applicable.
date
Pneumonia
Item
Date Provide different dates for different episodes of the same complication if applicable.
date
Hepatitis
Item
Date Provide different dates for different episodes of the same complication if applicable.
date
CNS infection
Item
Date Provide different dates for different episodes of the same complication if applicable
date
Gut infection
Item
Date Provide different dates for different episodes of the same complication if applicable
date
Skin infection
Item
Date Provide different dates for different episodes of the same complication if applicable.
date
Cystitis
Item
Date Provide different dates for different episodes of the same complication if applicable.
date
Retinitis
Item
Date Provide different dates for different episodes of the same complication if applicable.
date
Other
Item
Date Provide different dates for different episodes of the same complication if applicable.
date
Non infection related complications
Item
Non infection related complications
boolean
C0009566 (UMLS CUI [1])
Item
(Check all that are applicable for this period)
integer
Code List
(Check all that are applicable for this period)
CL Item
Yes (Yes)
CL Item
No  (No )
CL Item
Unknown (Unknown)
Idiopathic pneumonia syndrome
Item
Idiopathic pneumonia syndrome
date
Item
(Check all that are applicable for this period)
integer
C0948441 (UMLS CUI [1])
Code List
(Check all that are applicable for this period)
CL Item
Yes (Yes)
CL Item
No  (No )
CL Item
Unknown (Unknown)
VOD
Item
VOD
date
Item
(Check all that are applicable for this period)
integer
C0086543 (UMLS CUI [1])
Code List
(Check all that are applicable for this period)
CL Item
Yes (Yes)
CL Item
No (No)
CL Item
Unknown (Unknown)
Cataract
Item
Cataract
date
Item
Check all that are applicable for this period Haemorrhagic cystitis, non infectious
text
C0085692 (UMLS CUI [1])
Code List
Check all that are applicable for this period Haemorrhagic cystitis, non infectious
CL Item
Yes  (Yes )
CL Item
No  (No )
CL Item
Unknown (Unknown)
Haemorrhagic cystitis, non infectious
Item
Haemorrhagic cystitis, non infectious
date
Item
ARDS, non infectious ARDS, non infectious
integer
C0035222 (UMLS CUI [1])
Code List
ARDS, non infectious ARDS, non infectious
CL Item
Yes (Yes)
CL Item
No (No)
CL Item
Unknown (Unknown)
ARDS, non infectious
Item
ARDS, non infectious
date
Item
Check all that are applicable for this period)
integer
Code List
Check all that are applicable for this period)
CL Item
Yes (1)
CL Item
No  (2)
CL Item
Unknown (3)
Multiorgan failure, non infectious
Item
Multiorgan failure, non infectious
date
Item
(Check all that are applicable for this period HSCT-associated microangiopathy
text
C0155765 (UMLS CUI [1])
Code List
(Check all that are applicable for this period HSCT-associated microangiopathy
CL Item
Yes (Yes)
CL Item
No (No)
CL Item
Unknown (Unknown)
HSCT-associated microangiopathy
Item
HSCT-associated microangiopathy
date
Item
(Check all that are applicable for this period) Renal failure requiring dialysis
text
C0035078 (UMLS CUI [1])
Code List
(Check all that are applicable for this period) Renal failure requiring dialysis
CL Item
Yes (Yes)
CL Item
No (No)
CL Item
Unknown (Unknown)
Renal failure requiring dialysis
Item
Renal failure requiring dialysis
date
Item
(Check all that are applicable for this period) Haemolytic anaemia due to blood group
integer
C0002878 (UMLS CUI [1])
Code List
(Check all that are applicable for this period) Haemolytic anaemia due to blood group
CL Item
Yes (Yes)
CL Item
No (No)
CL Item
Unknown (Unknown)
Haemolytic anaemia due to blood group
Item
Haemolytic anaemia due to blood group
date
Item
Check all that are applicable for this period) Aseptic bone necrosis
text
C0158452 (UMLS CUI [1])
Code List
Check all that are applicable for this period) Aseptic bone necrosis
CL Item
Yes (Yes)
CL Item
No (No)
CL Item
Unknown (Unknown)
Aseptic bone necrosis
Item
Aseptic bone necrosis
date
Other type of complication
Item
Other type of complication > CTCAE grade 2
boolean
CL Item
No (1)
CL Item
Yes (2)
CL Item
Not evaluated (3)
Item
Overall chimaerism
text
C0333678 (UMLS CUI [1])
Code List
Overall chimaerism
CL Item
95%) (Full (donor >)
CL Item
Mixed (partial) (Mixed (partial))
CL Item
95%) (Autologuos reconstitution (recipient >)
CL Item
Aplasia (Aplasia)
CL Item
Not evaluated (Not evaluated)
Date of Test
Item
Date of Test
date
C0024671 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Identification
Item
Identification of donor or Cord Blood Unit given by the centre
text
C1718162 (UMLS CUI [1])
Number in the infusion order
Item
Number in the infusion order (if applicable)
text
C0237753 (UMLS CUI [1])
Bone marrow
Item
Cell type on which test was performed (% Donor Cells): BM
float
C0005953 (UMLS CUI [1])
PB mononuclear cells (PBMC)
Item
Cell type on which test was performed (% Donor cells): PB mononuclear cells (PBMC)
float
C1321301 (UMLS CUI [1])
T-Cells
Item
Cell type on which test was performed (% Donor cells): T-Cells
float
C0039194 (UMLS CUI [1])
B-Cells
Item
Cell type on which test was performed (% Donor cells): B-Cells
float
C0004561 (UMLS CUI [1])
Red blood cells
Item
Cell type on which test was performed (% Donor cells): Red blood cells
float
C0014772 (UMLS CUI [1])
Monocytes
Item
Cell type on which test was performed (% Donor cells): Monocytes
float
C0026473 (UMLS CUI [1])
PMNs (neutrophils)
Item
Cell type on which test was performed (% Donor cells): PMNs (neutrophils)
float
C0200633 (UMLS CUI [1])
Lymphocytes, NOS
Item
Cell type on which test was performed (% Donor cells): Lymphocytes, NOS
float
C0024264 (UMLS CUI [1])
Myeloid cells, NOS
Item
Cell type on which test was performed (% Donor cells): Myeloid cells, NOS
float
C0887899 (UMLS CUI [1])
Other
Item
Cell type on which test was performed % Donor cells
float
Item
Test used:
text
C0022885 (UMLS CUI [1])
Code List
Test used:
CL Item
FISH (FISH)
CL Item
Molecular (Molecular)
CL Item
Cytogenetic (Cytogenetic)
CL Item
ABO group (ABO group)
CL Item
Other (Other)
CL Item
unknown (unknown)
Item
SECONDARY MALIGNANCY, LYMPHOPROLIFERATIVE OR MYELOPROLIFRATIVE DISORDER DIAGNOSED
integer
Code List
SECONDARY MALIGNANCY, LYMPHOPROLIFERATIVE OR MYELOPROLIFRATIVE DISORDER DIAGNOSED
CL Item
Previously reported (1)
CL Item
Yes (2)
CL Item
No at date of this follow-up (3)
Date of Diagnosis
Item
Date of Diagnosis
date
C2316983 (UMLS CUI [1])
Item
text
C0011900 (UMLS CUI [1])
Code List
Diagnosis
CL Item
AML (AML)
CL Item
MDS (MDS)
CL Item
Lymphoproliferative disorder (Lymphoproliferative disorder)
CL Item
Other (Other)
diagnosis
Item
if other, please specify
text
Item Group
ADDITIONAL THERAPIES SINCE LAST FOLLOW UP
Item
Treatment given since last report
text
C1706712 (UMLS CUI [1])
Code List
Treatment given since last report
CL Item
No (No)
CL Item
Yes (Yes)
CL Item
Unknown (Unknown)
Item
If yes: CELLULAR THERAPY One cell therapy regimen is defined as any number of infusions given within 10 weeks for the same indication. If more than one regimen of cell therapy has been given since last report, copy this section and complete it as many times as necessary.
integer
Code List
If yes: CELLULAR THERAPY One cell therapy regimen is defined as any number of infusions given within 10 weeks for the same indication. If more than one regimen of cell therapy has been given since last report, copy this section and complete it as many times as necessary.
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Code List
Disease status before this cellular therapy
CL Item
CR (CR)
CL Item
Not in CR (Not in CR)
CL Item
Not evaluated (Not evaluated)
Item
If yes: Type of cells
integer
C0302189 (UMLS CUI [1])
Code List
If yes: Type of cells
CL Item
Donor lymphocyte infusion (DLI) (1)
CL Item
Mesenchymal cells (2)
CL Item
Other (3)
CL Item
Unknown (4)
Item
Number of Nucleated cells infused (DLI only)
integer
C1180059 (UMLS CUI [1])
Code List
Number of Nucleated cells infused (DLI only)
CL Item
Number (1)
CL Item
Not evaluated (2)
CL Item
Unknown (3)
Item
If DLI, specify the number of cells infused by type: CD 34+
text
C3538723 (UMLS CUI [1])
Code List
If DLI, specify the number of cells infused by type: CD 34+
CL Item
Evaluated (Evaluated)
CL Item
Not Evaluated (Not Evaluated)
CL Item
Unknown (Unknown)
Item
If DLI, specify the number of cells infused by type: CD 3+
text
C3542405 (UMLS CUI [1])
Code List
If DLI, specify the number of cells infused by type: CD 3+
CL Item
Evaluated  (Evaluated )
CL Item
Not evaluated (Not evaluated)
CL Item
Unknown (Unknown)
Item
Total number of cells infused (non DLI only)
integer
C0007584 (UMLS CUI [1])
Code List
Total number of cells infused (non DLI only)
CL Item
Number (1)
CL Item
Not evaluated (2)
CL Item
Unknown (3)
Chronological number
Item
Chronological number of this cell therapy for this patient
float
C2348184 (UMLS CUI [1])
Item
Indication (check all that apply)
text
C3146298 (UMLS CUI [1,1])
C0302189 (UMLS CUI [1,2])
Code List
Indication (check all that apply)
CL Item
Planned/ protocol (Planned/ protocol)
CL Item
Treatment for disease (Treatment for disease)
CL Item
Prophylactic (Prophylactic)
CL Item
Mixed chimaerism (Mixed chimaerism)
CL Item
Treatment of GvHD (Treatment of GvHD)
CL Item
Treatment viral infection (Treatment viral infection)
CL Item
Loss/decreased chimaerism (Loss/decreased chimaerism)
CL Item
Treatment PTLD, EBV, lymphoma (Treatment PTLD, EBV, lymphoma)
CL Item
Other (Other)
Indication
Item
If Other, please specify
text
Infusion count
Item
Number of infusions within 10 weeks (count only infusions that are part of same regimen and given for the same indication)
float
C0574032 (UMLS CUI [1,1])
C0750480 (UMLS CUI [1,2])
Item
Acute Graft versus Host Disease (after this infusion but before any further infusion/ transplant) Maximum grade:
text
C0856825 (UMLS CUI [1])
Code List
Acute Graft versus Host Disease (after this infusion but before any further infusion/ transplant) Maximum grade:
CL Item
grade 0 (absent) (grade 0 (absent))
CL Item
grade 1 (grade 1)
CL Item
grade 2 (grade 2)
CL Item
grade 3 (grade 3)
CL Item
grade 4 (grade 4)
CL Item
present, grade unknown (present, grade unknown)
Item
Disease treatment (apart from donor cell infusion or other type of cell therapy)
integer
C0087111 (UMLS CUI [1])
Code List
Disease treatment (apart from donor cell infusion or other type of cell therapy)
CL Item
No (1)
CL Item
Yes: Planned (planned before HSCT took place) (2)
CL Item
Yes: Not planned (for relapse/progression or persistent disease) (3)
Item Group
FIRST EVIDENCE OF RELAPSE OR PROGRESSION SINCE LAST HSCT
Item
Relapse or Progression
text
C0277556 (UMLS CUI [1,1])
C0242656 (UMLS CUI [1,2])
Code List
Relapse or Progression
CL Item
Previously reported (Previously reported)
CL Item
No (No)
CL Item
Yes (Yes)
CL Item
Continous progression since transplant (Continous progression since transplant)
CL Item
Unknown (Unknown)
RELAPSE OR PROGRESSION
Item
if yes, date diagnosed
date
Item Group
LAST DISEASE AND PATIENT STATUS
Item
Last Disease Status
text
C1704632 (UMLS CUI [1])
Code List
Last Disease Status
CL Item
Complete Remission (Complete Remission)
CL Item
Stable disease (Stable disease)
CL Item
Relapse (Relapse)
CL Item
Progression (Progression)
Item
Has patient or partner become pregnant after this HSCT?
text
C0032961 (UMLS CUI [1])
Code List
Has patient or partner become pregnant after this HSCT?
CL Item
No (No)
CL Item
Yes (Yes)
CL Item
Unknown (Unknown)
Item
Survival Status
integer
C1148433 (UMLS CUI [1])
Code List
Survival Status
CL Item
alive (0)
CL Item
dead (1)
Item
Type of score used
text
Code List
Type of score used
CL Item
Karnofsky (Karnofsky)
CL Item
Lansky (Lansky)
Item
Score
integer
C1518965 (UMLS CUI [1])
Code List
Score
CL Item
100 (Normal, NED) (1)
CL Item
90 (Normal activity)  (2)
CL Item
80 (Normal with effort) (3)
CL Item
70 (Cares for self) (4)
CL Item
60 (Requires occasional assistance) (5)
CL Item
50 (Requires assistance) (6)
CL Item
40 (Disabled) (7)
CL Item
30 (Severely disabled) (8)
CL Item
20 (Very sick) (9)
CL Item
10 (Moribund) (10)
CL Item
Not evaluated (11)
CL Item
Unknown (12)
Item
If dead, specify cause of death:
text
C0007465 (UMLS CUI [1])
Code List
If dead, specify cause of death:
CL Item
Relapse or progression (Relapse or progression)
CL Item
Secondary malignancy (including lymphoproliferative disease) (Secondary malignancy (including lymphoproliferative disease))
CL Item
HSCT related cause  (HSCT related cause )
CL Item
Unknown  (Unknown )
CL Item
Other (Other)
Item
If dead and HSCT related cause of death, specify (check as many as apppropriate): GvHD
text
C0007465 (UMLS CUI [1,1])
C0018133 (UMLS CUI [1,2])
Code List
If dead and HSCT related cause of death, specify (check as many as apppropriate): GvHD
CL Item
Yes (Yes)
CL Item
No  (No )
CL Item
Unknown (Unknown)
Item
If dead and HSCT related cause of death, specify (check as many as apppropriate): Interstitial Pneumonitis
text
C0007465 (UMLS CUI [1,1])
C0206061 (UMLS CUI [1,2])
Code List
If dead and HSCT related cause of death, specify (check as many as apppropriate): Interstitial Pneumonitis
CL Item
Yes (Yes)
CL Item
No  (No )
CL Item
Unknown (Unknown)
Item
If dead and HSCT related cause of death, specify (check as many as apppropriate): Pulmonary toxicity
text
C0007465 (UMLS CUI [1,1])
C0919924 (UMLS CUI [1,2])
Code List
If dead and HSCT related cause of death, specify (check as many as apppropriate): Pulmonary toxicity
CL Item
Yes (Yes)
CL Item
No  (No )
CL Item
Unknown (Unknown)
Item
If dead and HSCT related cause of death, specify (check as many as apppropriate): Infection
text
C0007465 (UMLS CUI [1,1])
C0009450 (UMLS CUI [1,2])
Code List
If dead and HSCT related cause of death, specify (check as many as apppropriate): Infection
CL Item
Yes (Yes)
CL Item
No  (No )
CL Item
Unknown (Unknown)
Item
check as many as appropriate
text
Code List
check as many as appropriate
CL Item
bacterial (bacterial)
CL Item
viral (viral)
CL Item
fungal (fungal)
CL Item
parasitic (parasitic)
CL Item
unknown (unknown)
ADDITIONAL NOTES IF APPLICABLE
Item
COMMENTS
text
IDENTIFICATION & SIGNATURE
Item
IDENTIFICATION & SIGNATURE
text

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