ID

14230

Beskrivning

DOCUMENTED PATHOGENS for INFECTIOUS RELATED COMPLICATIONS Bacteria: S. pneumoniae, Other gram positive (i.e.: other streptococci, staphylococci, listeria), Haemophilus influenzae, Other gram negative (i.e.: E. coli klebsiella, proteus, serratia, pseudomonas …), Legionella sp, Mycobacteria sp, other Viruses: HSV, VZV, EBV, CMV, HHV-6, RSV, Other respiratory virus, Adenovirus, HBV,HCV,HIV, Papovavirus, Parvovirus, Other Fungi: Candida sp, Aspergillus sp, Pneumocystis carinii, other Parasites: Toxoplasma gondii, other

Nyckelord

  1. 2016-04-05 2016-04-05 -
  2. 2016-07-27 2016-07-27 -
  3. 2021-09-17 2021-09-17 -
Uppladdad den

5 april 2016

DOI

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Creative Commons BY-NC 3.0

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EBMT Solid Tumors

14pp EBMT Solid Tumors 11SoTu

EBMT FORM GENERAL INFORMATION
Beskrivning

EBMT FORM GENERAL INFORMATION

EBMT FORM GENERAL INFORMATION
Beskrivning

EBMT FORM GENERAL INFORMATION

Datatyp

text

Hospital
Beskrivning

Klinik

Datatyp

text

Alias
UMLS CUI [1]
C0019994
Unit
Beskrivning

Unit

Datatyp

text

Name of contact person
Beskrivning

Contact person

Datatyp

text

Alias
UMLS CUI [1]
C0337611
Telephone
Beskrivning

Patient phone number

Datatyp

text

Alias
UMLS CUI [1]
C1515258
Fax
Beskrivning

ContactPersonFaxNumber

Datatyp

text

Alias
UMLS CUI [1,1]
C0237753
UMLS CUI [1,2]
C0027361
UMLS CUI [1,3]
C0337611
UMLS CUI [1,4]
C0085205
E-mail address of contact number
Beskrivning

E-mail

Datatyp

text

Alias
UMLS CUI [1]
C1705961
Date of this report
Beskrivning

Date of this report

Datatyp

date

Alias
UMLS CUI [1]
C1302584
STUDY/TRIAL
Beskrivning

STUDY/TRIAL

Patient following national / international study / trial
Beskrivning

Patient in Trial

Datatyp

integer

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

Name of study / trial

Datatyp

text

PATIENT
Beskrivning

PATIENT

To be entered only if patient previously reported
Beskrivning

Unique Identification Code (UIC)

Datatyp

text

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

Hospital Unique Patient Number or Code

Datatyp

text

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

Initials

Datatyp

text

Alias
UMLS CUI [1]
C2986440
Date of Birth
Beskrivning

PersonBirthDate

Datatyp

date

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

Sex

Datatyp

text

Alias
UMLS CUI [1]
C0079399
ABO Group
Beskrivning

ABO Group

Datatyp

text

Rh factor
Beskrivning

Rh factor

Datatyp

text

DISEASE
Beskrivning

DISEASE

Date of diagnosis
Beskrivning

Diagnose-Datum

Datatyp

date

Alias
UMLS CUI [1,1]
C2316983
UMLS CUI [1,2]
C1274082
Check the disease for which this transplant was performed
Beskrivning

Primary Disease Diagnosis

Datatyp

text

Alias
UMLS CUI [1]
C0277554
SOLID TUMOURS
Beskrivning

SOLID TUMOURS

INITIAL DIAGNOSIS
Beskrivning

INITIAL DIAGNOSIS

Datatyp

integer

if other specify
Beskrivning

INITIAL DIAGNOSIS

Datatyp

text

Clinical TNM classification Tumor
Beskrivning

Clinical TNM classification Tumor

Datatyp

integer

Clinical TNM classification Tumor Nodes
Beskrivning

Clinical TNM classification Tumor Nodes

Datatyp

integer

Clinical TNM classification Metastases
Beskrivning

For metastases, 0 indicates “No metastasis”, 1 indicates “Metastasis” and X indicates “Not evaluable

Datatyp

integer

OR Disease-specific staging
Beskrivning

OR Disease-specific staging

Datatyp

integer

HISTOLOGICAL SUBCLASSIFICATION Describe
Beskrivning

HISTOLOGICAL SUBCLASSIFICATION Describe

Datatyp

text

BREAST CARCINOMA ONLY
Beskrivning

BREAST CARCINOMA ONLY

Datatyp

integer

RECEPTOR STATUS Estrogen (ER)
Beskrivning

RECEPTOR STATUS Estrogen (ER)

Datatyp

integer

Values if RECEPTOR STATUS positive
Beskrivning

RECEPTOR STATUS Estrogen (ER)

Datatyp

float

RECEPTOR STATUS Progesterone (PgR)
Beskrivning

RECEPTOR STATUS Progesterone (PgR)

Datatyp

integer

if Receptor Status positive Values
Beskrivning

RECEPTOR STATUS Progesterone (PgR)

Datatyp

float

RECEPTOR STATUS HER2/neu (c-erb-B2)
Beskrivning

RECEPTOR STATUS HER2/neu (c-erb-B2)

Datatyp

text

if RECEPTOR STATUS HER2/neu (c-erb-B2) positiv Defined by
Beskrivning

RECEPTOR STATUS HER2/neu (c-erb-B2)

Datatyp

integer

HISTOLOGICAL SUBCLASSIFICATION FOR BREAST CARCINOMA
Beskrivning

HISTOLOGICAL SUBCLASSIFICATION FOR BREAST CARCINOMA

Number of positive Axillary lymph nodes
Beskrivning

Axillary lymph nodes

Datatyp

float

Number of examined Axillary lymph nodes
Beskrivning

Axillary lymph nodes

Datatyp

float

Axillary lymph nodes Not evaluated
Beskrivning

Axillary lymph nodes

Datatyp

integer

S.B.R. (Scarff-Bloom-Richardson)
Beskrivning

S.B.R. (Scarff-Bloom-Richardson)

Datatyp

integer

Ductal carcinoma
Beskrivning

Ductal carcinoma

Datatyp

integer

Lobular carcinoma
Beskrivning

Lobular carcinoma

Datatyp

integer

CYTOGENETICS
Beskrivning

CYTOGENETICS

CHROMOSOME ANALYSIS
Beskrivning

CHROMOSOME ANALYSIS

Datatyp

integer

CHROMOSOME ANALYSIS
Beskrivning

If aberrations, notify chromosomal aberrations (e.g. tri/monosomy) and/or other results, in clear

Datatyp

text

Molecular markers
Beskrivning

Molecular markers

Datatyp

integer

Alias
UMLS CUI [1]
C0005516
TREATMENT GIVEN BEFORE THIS HSCT
Beskrivning

TREATMENT GIVEN BEFORE THIS HSCT

Treatment given
Beskrivning

if no: Includes a) Patients who have no surgery and go on to have high dose chemotherapy followed immediately by HSCT, or sequential chemotherapy, as the 1st line treatment; or b) Subsequent HSCT within a multiple/ sequential chemotherapy HSCT procedure if yes: Includes surgery or any other treatment, including chemotherapy, given prior to the HSCT and which is not considered part of the preparative (conditioning) regimen

Datatyp

integer

FIRST LINE TREATMENT
Beskrivning

FIRST LINE TREATMENT

1st line treatment started
Beskrivning

Date

Datatyp

date

Did the first-line treatment include HSCT
Beskrivning

Did the first-line treatment include HSCT

Datatyp

integer

if the first-line treatment include HSCT
Beskrivning

Upfront (treatment started with a program including high dose chemotherapy followed by HSCT or high dose sequential chemotherapy; adjuvant excluded) Adjuvant (HSCT done in adjuvant-setting)

Datatyp

integer

Modality
Beskrivning

Modality

Datatyp

text

Drugs
Beskrivning

Drugs

Datatyp

text

if other drugs
Beskrivning

Drugs

Datatyp

text

If breast cancer, type of surgery
Beskrivning

Modality Surgery

Datatyp

text

if other Modality
Beskrivning

Modality

Datatyp

text

Status of disease after first line treatment (best response)
Beskrivning

Status of disease after first line treatment (best response)

Datatyp

text

Criteria used for evaluation
Beskrivning

Criteria used for evaluation

Datatyp

text

ADDITIONAL LINES OF TREATMENT BEFORE THIS HSCT FOR RELAPSED/REFRACTORY DISEASE
Beskrivning

Treatment given

Datatyp

text

TREATMENT HISTORY BEFORE HSCT
Beskrivning

TREATMENT HISTORY BEFORE HSCT

Date of HSCT
Beskrivning

Date of HSCT

Datatyp

date

Alias
UMLS CUI [1]
C2584899
Total number of lines before this HSCT
Beskrivning

TREATMENT SUMMARY

Datatyp

integer

Modality used at least once Chemotherapy
Beskrivning

Modality used at least once Chemotherapy

Datatyp

text

Modality used at least once Surgery
Beskrivning

Modality used at least once Surgery

Datatyp

integer

Modality used at least once Radiotherapy
Beskrivning

Modality used at least once Radiotherapy

Datatyp

text

Modality used at least once other
Beskrivning

Modality used at least once other

Datatyp

text

if used other Modality at least
Beskrivning

Modality used at least once other

Datatyp

text

STATUS OF DISEASE AT HSCT
Beskrivning

STATUS OF DISEASE AT HSCT

STATUS OF DISEASE AT HSCT
Beskrivning

STATUS OF DISEASE AT HSCT

Datatyp

text

if CR please specify
Beskrivning

STATUS OF DISEASE AT HSCT

Datatyp

text

if Relapse please specify
Beskrivning

STATUS OF DISEASE AT HSCT

Datatyp

text

Complete remission (CR) Number
Beskrivning

Complete remission (CR) Number

Datatyp

text

Complete relapse Number
Beskrivning

Complete relapse Number

Datatyp

text

SENSITIVITY TO CHEMOTHERAPY
Beskrivning

(complete only for relapse)

Datatyp

text

Organ(s) involved
Beskrivning

Organ(s) involved

Datatyp

text

if other Organ(s) involved please specify
Beskrivning

Organ(s) involved

Datatyp

text

Primary site affected
Beskrivning

Primary site affected

Datatyp

integer

ADDITIONAL TREATMENT POST-HSCT
Beskrivning

ADDITIONAL TREATMENT POST-HSCT

Additional Disease Treatment
Beskrivning

Additional Disease Treatment

Datatyp

text

Alias
UMLS CUI [1]
C1706712
if ADDITIONAL DISEASE TREATMENT
Beskrivning

ADDITIONAL DISEASE TREATMENT

Datatyp

integer

BEST DISEASE RESPONSE AT 100 DAYS POST-HSCT
Beskrivning

BEST DISEASE RESPONSE AT 100 DAYS POST-HSCT

BEST RESPONSE AT 100 DAYS AFTER HSCT
Beskrivning

BEST RESPONSE AT 100 DAYS AFTER HSCT

Datatyp

text

Date of Evaluation
Beskrivning

LesionAssessmentDate

Datatyp

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C0221198
UMLS CUI [1,3]
C0031809
FORMS TO BE FILLED IN
Beskrivning

FORMS TO BE FILLED IN

TYPE OF TRANSPLANT
Beskrivning

TYPE OF TRANSPLANT

Datatyp

text

it other type of transplant contact the EBMT Central Registry Office for instructions
Beskrivning

TYPE OF TRANSPLANT

Datatyp

text

FOLLOW UP SOLID TUMOURS
Beskrivning

FOLLOW UP SOLID TUMOURS

Unique Identification Code (UIC) (if known)
Beskrivning

Unique Identification Code (UIC)

Datatyp

text

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

Date of this report

Datatyp

date

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

Patient in Trial

Datatyp

integer

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

Name of study / trial

Datatyp

text

Hospital Unique Patient Number
Beskrivning

Hospital Unique Patient Number

Datatyp

text

Alias
UMLS CUI [1]
C2348585
First name(s)_surname(s)
Beskrivning

Initials

Datatyp

text

Alias
UMLS CUI [1]
C2986440
Date of birth
Beskrivning

Date of birth

Datatyp

date

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

Date of last HSCT for this patient

Datatyp

date

Alias
UMLS CUI [1,1]
C0472699
UMLS CUI [1,2]
C0011008
Date of Last Contact or Death
Beskrivning

Date last contact

Datatyp

date

Alias
UMLS CUI [1]
C0805839
GRAFT VERSUS HOST DISEASE (GvHD) SINCE LAST REPORT
Beskrivning

GRAFT VERSUS HOST DISEASE (GvHD) SINCE LAST REPORT

ACUTE GRAFT VERSUS HOST DISEASE (AGVHD)
Beskrivning

Maximum grade

Datatyp

text

If ACUTE GRAFT VERSUS HOST DISEASE (AGVHD) present
Beskrivning

ACUTE GRAFT VERSUS HOST DISEASE (AGVHD)

Datatyp

text

Reason for ACUTE GRAFT VERSUS HOST DISEASE (AGVHD)
Beskrivning

ACUTE GRAFT VERSUS HOST DISEASE (AGVHD)

Datatyp

text

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

Date onset of this episode

Datatyp

date

Måttenheter
  • yyyy/mm/dd
Alias
UMLS CUI [1]
C0574845
yyyy/mm/dd
Date onset of this episode
Beskrivning

Date onset of this episode

Datatyp

integer

Stage skin
Beskrivning

Stage skin

Datatyp

integer

Stage liver
Beskrivning

Stage liver

Datatyp

integer

Stage gut
Beskrivning

Stage gut

Datatyp

integer

Resolution
Beskrivning

aGvHD Resolution

Datatyp

integer

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

aGvHD Date of resolution

Datatyp

date

Måttenheter
  • yyyy/mm/dd
Alias
UMLS CUI [1,1]
C0856825
UMLS CUI [1,2]
C1514893
UMLS CUI [1,3]
C0011008
yyyy/mm/dd
CHRONIC GRAFT VERSUS HOST DISEASE (CGVHD)
Beskrivning

CHRONIC GRAFT VERSUS HOST DISEASE (CGVHD)

Presence of cGvHD
Beskrivning

Chronic Graft versus Host Disease (cGvHD)

Datatyp

text

Alias
UMLS CUI [1]
C0867389
If Presence of cGVHD
Beskrivning

Presence of cGVHD

Datatyp

text

Date of onset
Beskrivning

Date of onset

Datatyp

date

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

cGvHD grade

Datatyp

text

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

Organs affected

Datatyp

integer

Alias
UMLS CUI [1]
C0449642
If other Organs affected please specify
Beskrivning

Organs affected

Datatyp

text

Resolved: Date of resolution
Beskrivning

Resolved: Date of resolution

Datatyp

date

OTHER COMPLICATIONS SINCE LAST REPORT
Beskrivning

OTHER COMPLICATIONS SINCE LAST REPORT

INFECTIOUS RELATED COMPLICATIONS
Beskrivning

INFECTIOUS RELATED COMPLICATIONS

Datatyp

integer

Bacteremia / fungemia / viremia / parasites Pathogen
Beskrivning

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

Datatyp

text

Bacteremia / fungemia / viremia / parasites Pathogen
Beskrivning

Bacteremia / fungemia / viremia / parasites Pathogen

Datatyp

date

SYSTEMIC SYMPTOMS OF INFECTION: Septic shock
Beskrivning

SYSTEMIC SYMPTOMS OF INFECTION: Septic shock

Datatyp

text

SYSTEMIC SYMPTOMS OF INFECTION: Septic shock
Beskrivning

SYSTEMIC SYMPTOMS OF INFECTION: Septic shock

Datatyp

date

SYSTEMIC SYMPTOMS OF INFECTION ARDS Pathogen
Beskrivning

SYSTEMIC SYMPTOMS OF INFECTION ARDS Pathogen

Datatyp

text

SYSTEMIC SYMPTOMS OF INFECTION ARDS Pathogen
Beskrivning

SYSTEMIC SYMPTOMS OF INFECTION ARDS Pathogen

Datatyp

date

SYSTEMIC SYMPTOMS OF INFECTION Multiorgan failure due to infection Pathogen
Beskrivning

SYSTEMIC SYMPTOMS OF INFECTION Multiorgan failure due to infection Pathogen

Datatyp

text

SYSTEMIC SYMPTOMS OF INFECTION Multiorgan failure due to infection Pathogen
Beskrivning

SYSTEMIC SYMPTOMS OF INFECTION Multiorgan failure due to infection Pathogen

Datatyp

date

Endorgan diseases
Beskrivning

Endorgan diseases

Datatyp

text

Alias
UMLS CUI [1,1]
C0349410
UMLS CUI [1,2]
C0009450
ENDORGAN DISEASES
Beskrivning

ENDORGAN DISEASES

Datatyp

date

NON INFECTIOUS RELATED COMPLICATIONS
Beskrivning

NON INFECTIOUS RELATED COMPLICATIONS

Datatyp

text

Specify: Idiopathic pneumonia syndrome
Beskrivning

Idiopathic pneumonia syndrome

Datatyp

text

Alias
UMLS CUI [1]
C1504431
Specify: VOD
Beskrivning

VOD

Datatyp

text

Alias
UMLS CUI [1]
C0948441
Specify: Cataract
Beskrivning

Cataract

Datatyp

text

Alias
UMLS CUI [1]
C0086543
Specify: Haemorrhagic cystitis, non infectious
Beskrivning

Haemorrhagic cystitis, non infectious

Datatyp

text

Alias
UMLS CUI [1]
C0085692
Specify: ARDS, non infectious
Beskrivning

ARDS, non infectious

Datatyp

text

Alias
UMLS CUI [1]
C0035222
Multiorgan failure, non infectious
Beskrivning

Multiorgan failure, non infectious

Datatyp

text

Specify: HSCT-associated microangiopathy
Beskrivning

HSCT-associated microangiopathy

Datatyp

text

Alias
UMLS CUI [1]
C0155765
Specify: Renal failure requiring dialysis
Beskrivning

Renal failure requiring dialysis

Datatyp

text

Alias
UMLS CUI [1]
C0035078
Specify: Haemolytic anaemia due to blood group
Beskrivning

Haemolytic anaemia due to blood group

Datatyp

text

Alias
UMLS CUI [1]
C0002878
Specify: Aseptic bone necrosis
Beskrivning

Aseptic bone necrosis

Datatyp

text

Alias
UMLS CUI [1]
C0158452
Other NON INFECTIOUS RELATED COMPLICATIONS
Beskrivning

Other NON INFECTIOUS RELATED COMPLICATIONS

Datatyp

text

Idiopathic pneumonia syndrome
Beskrivning

Idiopathic pneumonia syndrome

Datatyp

date

VOD
Beskrivning

VOD

Datatyp

date

Cataract
Beskrivning

Cataract

Datatyp

date

Haemorrhagic cystitis, non infectious
Beskrivning

Haemorrhagic cystitis, non infectious

Datatyp

date

ARDS, non infectious
Beskrivning

ARDS, non infectious

Datatyp

date

Multiorgan failure, non infectious
Beskrivning

Multiorgan failure, non infectious

Datatyp

date

HSCT-associated microangiopathy
Beskrivning

HSCT-associated microangiopathy

Datatyp

date

Renal failure requiring dialysis
Beskrivning

Renal failure requiring dialysis

Datatyp

date

Haemolytic anaemia due to blood group
Beskrivning

Haemolytic anaemia due to blood group

Datatyp

date

Aseptic bone necrosis
Beskrivning

Aseptic bone necrosis

Datatyp

date

if Other NON INFECTIOUS RELATED COMPLICATIONS
Beskrivning

Other NON INFECTIOUS RELATED COMPLICATIONS

Datatyp

date

GRAFT ASSESSMENT AND HAEMOPOIETIC CHIMAERISM
Beskrivning

GRAFT ASSESSMENT AND HAEMOPOIETIC CHIMAERISM

Graft loss
Beskrivning

Graft loss

Datatyp

text

Alias
UMLS CUI [1]
C0877042
Overall chimaerism
Beskrivning

Overall chimaerism

Datatyp

text

Alias
UMLS CUI [1]
C0333678
Date of test
Beskrivning

Date of test

Datatyp

date

Alias
UMLS CUI [1]
C2826247
Identification of donor or Cord Blood Unit given by the centre
Beskrivning

Identification

Datatyp

text

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

Number in the infusion order (if applicable)

Datatyp

integer

Alias
UMLS CUI [1]
C2348184
Cell type on which test was performed (% Donor Cells): BM
Beskrivning

Bone marrow

Datatyp

float

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

PB mononuclear cells (PBMC)

Datatyp

float

Måttenheter
  • %
Alias
UMLS CUI [1]
C1321301
%
Cell type on which test was performed (% Donor cells):
Beskrivning

T-Cell

Datatyp

float

Måttenheter
  • %
%
Cell type on which test was performed (% Donor cells): B-Cells
Beskrivning

B-Cells

Datatyp

float

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

Red blood cells

Datatyp

float

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

Monocytes

Datatyp

float

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

PMNs (neutrophils)

Datatyp

float

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

Lymphocytes, NOS

Datatyp

float

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

Myeloid cells, NOS

Datatyp

float

Måttenheter
  • %
Alias
UMLS CUI [1]
C0887899
%
Cell type on which test was performed (% Donor cells): Other
Beskrivning

Other cell type - value

Datatyp

float

Måttenheter
  • %
Alias
UMLS CUI [1,1]
C0449475
UMLS CUI [1,2]
C1522609
%
Test used:
Beskrivning

Laboratory tests

Datatyp

text

Alias
UMLS CUI [1]
C0022885
Test used: If other, specify: (Indicate the date(s) and results of all tests done for all donors. Split the results by donor and by the cell type on which the test was performed if applicable. Copy this table as many times as necessary.)
Beskrivning

Specification other labaratory tests

Datatyp

text

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C2348235
SECONDARY MALIGNANCY, LYMPHOPROLIFERATIVE OR MYELOPROLIFRATIVE DISORDER DIAGNOSED
Beskrivning

SECONDARY MALIGNANCY, LYMPHOPROLIFERATIVE OR MYELOPROLIFRATIVE DISORDER DIAGNOSED

Datatyp

text

date of diagnosis
Beskrivning

date of diagnosis

Datatyp

date

Diagnosis:
Beskrivning

Diagnosis:

Datatyp

text

Diagnosis, other
Beskrivning

Other diagnosis

Datatyp

text

Alias
UMLS CUI [1]
C0205394
Treatment given since last report
Beskrivning

Additional treatment

Datatyp

text

Alias
UMLS CUI [1]
C1706712
Date started ADDITIONAL TREATMENT
Beskrivning

Date started ADDITIONAL TREATMENT

Datatyp

date

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.)
Beskrivning

Cellular therapy

Datatyp

integer

Alias
UMLS CUI [1]
C0302189
Disease status before this cellular therapy
Beskrivning

Disease status before this cellular therapy

Datatyp

text

If yes: Type of cells
Beskrivning

Type of cells

Datatyp

integer

Alias
UMLS CUI [1]
C0302189
If other type of cells, please specify
Beskrivning

Type of cells

Datatyp

text

Number of cells infused
Beskrivning

Nucleated cells (/kg*)

Datatyp

integer

Måttenheter
  • x 10^8
x 10^8
Number of cells infused
Beskrivning

Nucleated cells (/kg*)

Datatyp

text

Number of cells infused
Beskrivning

CD 34+ (cells/kg*)

Datatyp

integer

Måttenheter
  • x10^6
x10^6
Number of cells infused
Beskrivning

CD 34+ (cells/kg*)

Datatyp

text

Number of cells infused
Beskrivning

CD 3+ (cells/kg*)

Datatyp

integer

Måttenheter
  • x 10^6
x 10^6
Number of cells infused
Beskrivning

CD 3+ (cells/kg*)

Datatyp

text

Total number of cells infused
Beskrivning

All cells (cells/kg*)

Datatyp

integer

Måttenheter
  • x 10^6
x 10^6
Total number of cells infused
Beskrivning

All cells (cells/kg*)

Datatyp

text

Chronological number of this cell therapy for this patient
Beskrivning

Chronological number of this cell therapy for this patient

Datatyp

integer

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

Indication

Datatyp

text

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C0302189
If other Indication, please specify
Beskrivning

Indication

Datatyp

text

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

Number of Infusions

Datatyp

float

Alias
UMLS CUI [1,1]
C2348184
UMLS CUI [1,2]
C1289919
Hospital Unique Patient Number (UPN):
Beskrivning

Hospital Unique Patient Number (UPN)

Datatyp

text

HSCT date
Beskrivning

HSCT date

Datatyp

date

Acute Graft versus Host Disease (after this infusion but before any further infusion/ transplant) Maximum grade:
Beskrivning

Acute Graft versus Host Disease

Datatyp

text

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

Disease treatment

Datatyp

integer

Alias
UMLS CUI [1]
C0087111
Relapse or progression
Beskrivning

Relapse or progression

Datatyp

integer

Alias
UMLS CUI [1,1]
C0035020
UMLS CUI [1,2]
C1704632
if yes, date diagnosed
Beskrivning

RELAPSE OR PROGRESSION

Datatyp

date

Organs involved at relapse or progression
Beskrivning

Organs involved at relapse or progression

Datatyp

text

Organs distant involved at relapse or progression
Beskrivning

Organs distant involved at relapse or progression

Datatyp

text

If Other Distant Organs involved at relapse or progression
Beskrivning

Other Distant Organs involved at relapse or progression

Datatyp

text

LAST DISEASE AND PATIENT STATUS
Beskrivning

LAST DISEASE AND PATIENT STATUS

Last Disease Status
Beskrivning

Disease response

Datatyp

text

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

Conception

Datatyp

text

Alias
UMLS CUI [1]
C0032961
Survival Status
Beskrivning

Survival Status

Datatyp

integer

Alias
UMLS CUI [1]
C1148433
If alive: Type of score used:
Beskrivning

Performance Score

Datatyp

text

Alias
UMLS CUI [1]
C1518965
Score
Beskrivning

Performance score

Datatyp

integer

Alias
UMLS CUI [1]
C1518965
CAUSE OF DEATH
Beskrivning

CAUSE OF DEATH

Datatyp

text

If dead and HSCT related cause of death, specify (check as many as apppropriate): GvHD
Beskrivning

GvHD

Datatyp

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
Beskrivning

Interstitial Pneumonitis

Datatyp

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
Beskrivning

Pulmonary toxicity

Datatyp

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
Beskrivning

Infection

Datatyp

text

Alias
UMLS CUI [1,1]
C0007465
UMLS CUI [1,2]
C0009450
HSCT related cause: .. (check as many as appropriate)
Beskrivning

Rejection / poor graft function

Datatyp

text

If dead and HSCT related cause of death, specify (check as many as apppropriate): Veno-Occlusive disease (VOD)
Beskrivning

Veno-Occlusive disease (VOD)

Datatyp

text

Alias
UMLS CUI [1,1]
C0007465
UMLS CUI [1,2]
C0948441
If dead and HSCT related cause of death, specify (check as many as apppropriate): Haemorrhage
Beskrivning

Haemorrhage

Datatyp

text

Alias
UMLS CUI [1,1]
C0007465
UMLS CUI [1,2]
C0019080
If dead and HSCT related cause of death, specify (check as many as apppropriate): Cardiac toxicity
Beskrivning

Cardiac toxicity

Datatyp

text

Alias
UMLS CUI [1,1]
C0007465
UMLS CUI [1,2]
C0876994
If dead and HSCT related cause of death, specify (check as many as apppropriate): Central nervous system t8oxicity
Beskrivning

Central nervous system t8oxicity

Datatyp

text

If dead and HSCT related cause of death, specify (check as many as apppropriate): Gastro intestinal toxicity
Beskrivning

Gastro intestinal toxicity

Datatyp

text

Alias
UMLS CUI [1,1]
C0007465
UMLS CUI [1,2]
C1142499
If dead and HSCT related cause of death, specify (check as many as apppropriate): Skin toxicity
Beskrivning

Skin toxicity

Datatyp

text

Alias
UMLS CUI [1,1]
C0007465
UMLS CUI [1,2]
C1167791
If dead and HSCT related cause of death, specify (check as many as apppropriate): Renal failure
Beskrivning

Renal failure

Datatyp

text

Alias
UMLS CUI [1,1]
C0007465
UMLS CUI [1,2]
C0035078
If dead and HSCT related cause of death, specify (check as many as apppropriate): Multiple organ failure
Beskrivning

Multiple organ failure

Datatyp

text

Alias
UMLS CUI [1,1]
C0007465
UMLS CUI [1,2]
C0026766
If dead and HSCT related cause of death, specify (check as many as apppropriate): other
Beskrivning

Other

Datatyp

text

ADDITIONAL NOTES IF APPLICABLE
Beskrivning

ADDITIONAL NOTES IF APPLICABLE

COMMENTS
Beskrivning

COMMENTS

Datatyp

text

Identification
Beskrivning

Identification

Datatyp

text

Alias
UMLS CUI [1]
C0205396

Similar models

14pp EBMT Solid Tumors 11SoTu

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
EBMT FORM GENERAL INFORMATION
EBMT FORM GENERAL INFORMATION
Item
EBMT FORM GENERAL INFORMATION
text
Klinik
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])
E-mail
Item
E-mail address of contact number
text
C1705961 (UMLS CUI [1])
Date of this report
Item
Date of this report
date
C1302584 (UMLS CUI [1])
Item Group
STUDY/TRIAL
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
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
text
C0079399 (UMLS CUI [1])
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 (1)
CL Item
Present (2)
CL Item
Not evaluated (3)
Item Group
DISEASE
Diagnose-Datum
Item
Date of diagnosis
date
C2316983 (UMLS CUI [1,1])
C1274082 (UMLS CUI [1,2])
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)
Item Group
SOLID TUMOURS
Item
INITIAL DIAGNOSIS
integer
Code List
INITIAL DIAGNOSIS
CL Item
Bone sarcoma (excluding Ewing sarcoma/PNET) (1)
CL Item
Central nervous system tumors (include CNS PNET) (2)
CL Item
Colorectal (3)
CL Item
Ewing sarcoma/PNET, extra-skeletal (4)
CL Item
Ewing sarcoma/PNET, skeletal (5)
CL Item
Germ cell tumour, extragonadal only (6)
CL Item
Hepatobiliary (7)
CL Item
Lung cancer, non-small cell (8)
CL Item
Lung cancer, small cell (9)
CL Item
Medulloblastoma (10)
CL Item
Melanoma (11)
CL Item
Other, specify (12)
CL Item
Breas (13)
CL Item
Neuroblastoma (14)
CL Item
Ovarian (15)
CL Item
Pancreas (16)
CL Item
Prostate (17)
CL Item
Renal cell (18)
CL Item
Retinoblastoma (19)
CL Item
Rhabdomyosarcoma (20)
CL Item
Soft tissue sarcoma (21)
CL Item
Testicular (22)
CL Item
Thymoma (23)
CL Item
Wilms tumour (24)
INITIAL DIAGNOSIS
Item
if other specify
text
Item
Clinical TNM classification Tumor
integer
Code List
Clinical TNM classification Tumor
CL Item
0 (1)
CL Item
1 (2)
CL Item
2 (3)
CL Item
3 (4)
CL Item
4 (5)
CL Item
X (6)
CL Item
not evaluated (7)
Item
Clinical TNM classification Tumor Nodes
integer
Code List
Clinical TNM classification Tumor Nodes
CL Item
0 (1)
CL Item
1 (2)
CL Item
2 (3)
CL Item
3 (4)
CL Item
X (5)
CL Item
not evaluated (6)
CL Item
unknown (7)
Item
Clinical TNM classification Metastases
integer
Code List
Clinical TNM classification Metastases
CL Item
0 (1)
CL Item
1 (2)
CL Item
X (3)
CL Item
not evaluated (4)
CL Item
unknown (5)
Item
OR Disease-specific staging
integer
Code List
OR Disease-specific staging
CL Item
1 (1)
CL Item
2 (2)
CL Item
3 (3)
CL Item
4 (4)
HISTOLOGICAL SUBCLASSIFICATION Describe
Item
HISTOLOGICAL SUBCLASSIFICATION Describe
text
Item
BREAST CARCINOMA ONLY
integer
Code List
BREAST CARCINOMA ONLY
CL Item
Inflammatory (1)
CL Item
Non-inflammatory (2)
Item
RECEPTOR STATUS Estrogen (ER)
integer
Code List
RECEPTOR STATUS Estrogen (ER)
CL Item
Negative (1)
CL Item
Not evaluated (2)
CL Item
Positive (3)
CL Item
Unknown (4)
CL Item
Not evaluated (5)
CL Item
Unknown (6)
RECEPTOR STATUS Estrogen (ER)
Item
Values if RECEPTOR STATUS positive
float
Item
RECEPTOR STATUS Progesterone (PgR)
integer
Code List
RECEPTOR STATUS Progesterone (PgR)
CL Item
Negative (1)
CL Item
Not evaluated (2)
CL Item
Positive (3)
CL Item
Unknown (4)
CL Item
Not evaluated (5)
CL Item
Unknown (6)
RECEPTOR STATUS Progesterone (PgR)
Item
if Receptor Status positive Values
float
Item
RECEPTOR STATUS HER2/neu (c-erb-B2)
text
Code List
RECEPTOR STATUS HER2/neu (c-erb-B2)
CL Item
Negative (1)
CL Item
Positive (2)
CL Item
Not evaluated (3)
CL Item
Unknown (4)
Item
if RECEPTOR STATUS HER2/neu (c-erb-B2) positiv Defined by
integer
Code List
if RECEPTOR STATUS HER2/neu (c-erb-B2) positiv Defined by
CL Item
IHC 3+ (1)
CL Item
IHC 2+ and FISH + (2)
CL Item
Unknown (3)
Item Group
HISTOLOGICAL SUBCLASSIFICATION FOR BREAST CARCINOMA
Axillary lymph nodes
Item
Number of positive Axillary lymph nodes
float
Axillary lymph nodes
Item
Number of examined Axillary lymph nodes
float
Axillary lymph nodes
Item
Axillary lymph nodes Not evaluated
integer
Item
S.B.R. (Scarff-Bloom-Richardson)
integer
Code List
S.B.R. (Scarff-Bloom-Richardson)
CL Item
1 (1)
CL Item
2 (2)
CL Item
3 (3)
CL Item
not evaluated (4)
CL Item
unknown (5)
Item
Ductal carcinoma
integer
Code List
Ductal carcinoma
CL Item
yes (1)
CL Item
no (2)
CL Item
not evaluated (3)
CL Item
unknown (4)
Item
Lobular carcinoma
integer
Code List
Lobular carcinoma
CL Item
yes (1)
CL Item
no (2)
CL Item
not evaluated (3)
CL Item
unknown (4)
Item Group
CYTOGENETICS
Code List
CHROMOSOME ANALYSIS
CL Item
Normal (1)
CL Item
Abnormal (2)
CL Item
Not done (3)
CL Item
Unknown (4)
CHROMOSOME ANALYSIS
Item
CHROMOSOME ANALYSIS
text
Item
Molecular markers
integer
C0005516 (UMLS CUI [1])
Code List
Molecular markers
CL Item
Evaluated: Absent  (1)
CL Item
Evaluated: Present (2)
CL Item
Not evaluated (3)
CL Item
unknown (4)
Item Group
TREATMENT GIVEN BEFORE THIS HSCT
Item
Treatment given
integer
Code List
Treatment given
CL Item
no (1)
CL Item
yes (2)
Item Group
FIRST LINE TREATMENT
Date
Item
1st line treatment started
date
Item
Did the first-line treatment include HSCT
integer
Code List
Did the first-line treatment include HSCT
CL Item
yes (1)
CL Item
no (2)
Item
if the first-line treatment include HSCT
integer
Code List
if the first-line treatment include HSCT
CL Item
Upfront (1)
CL Item
Adjuvant (2)
Item
Modality
text
Code List
Modality
CL Item
Chemotherapy (1)
CL Item
Adjuvant Chemotherapy (2)
CL Item
Neoadjuvant Chemotherapy (3)
CL Item
Surgery (4)
CL Item
Radiotherapy (5)
CL Item
Other (6)
Item
Drugs
text
Code List
Drugs
CL Item
Anthracyclines (1)
CL Item
Taxanes (2)
CL Item
Platinum compounds (3)
CL Item
Antimetabolites (4)
CL Item
Cyclophosphamide or other alkylating agents (5)
CL Item
Vinca alcaloids (6)
CL Item
Etoposide (7)
CL Item
Other (8)
Drugs
Item
if other drugs
text
Item
If breast cancer, type of surgery
text
Code List
If breast cancer, type of surgery
CL Item
Mastectomy (1)
CL Item
Conservative (2)
Modality
Item
if other Modality
text
Item
Status of disease after first line treatment (best response)
text
Code List
Status of disease after first line treatment (best response)
CL Item
Complete Remission (1)
CL Item
Partial Remission (2)
CL Item
Not Evaluable (3)
CL Item
Stable Disease (4)
CL Item
Refractory Disease (5)
Item
Criteria used for evaluation
text
Code List
Criteria used for evaluation
CL Item
WHO criteria (1)
CL Item
RECIST criteria (2)
Item
ADDITIONAL LINES OF TREATMENT BEFORE THIS HSCT FOR RELAPSED/REFRACTORY DISEASE
text
Code List
ADDITIONAL LINES OF TREATMENT BEFORE THIS HSCT FOR RELAPSED/REFRACTORY DISEASE
CL Item
no (1)
CL Item
yes (2)
Item Group
TREATMENT HISTORY BEFORE HSCT
Date of HSCT
Item
Date of HSCT
date
C2584899 (UMLS CUI [1])
Item
Total number of lines before this HSCT
integer
Code List
Total number of lines before this HSCT
CL Item
1 (1)
CL Item
2 (2)
CL Item
3 (3)
CL Item
4 (4)
CL Item
>4 (5)
CL Item
unknown (6)
Item
Modality used at least once Chemotherapy
text
Code List
Modality used at least once Chemotherapy
CL Item
no (1)
CL Item
yes (2)
CL Item
unknown (3)
Item
Modality used at least once Surgery
integer
Code List
Modality used at least once Surgery
CL Item
no (1)
CL Item
yes (2)
CL Item
unknown (3)
Item
Modality used at least once Radiotherapy
text
Code List
Modality used at least once Radiotherapy
CL Item
no (1)
CL Item
yes (2)
CL Item
unknown (3)
Item
Modality used at least once other
text
Code List
Modality used at least once other
CL Item
no (1)
CL Item
yes (2)
CL Item
unknown (3)
Modality used at least once other
Item
if used other Modality at least
text
Item Group
STATUS OF DISEASE AT HSCT
Item
STATUS OF DISEASE AT HSCT
text
Code List
STATUS OF DISEASE AT HSCT
CL Item
Adjuvant (1)
CL Item
Never treated (upfront) (2)
CL Item
Primary refractory (3)
CL Item
Complete remission (CR) (4)
CL Item
1st Partial remission (PR1) (5)
CL Item
Relapse (6)
CL Item
Progressive disease (PD) (7)
Item
if CR please specify
text
Code List
if CR please specify
CL Item
Confirmed (1)
CL Item
Unconfirmed (CRU*) (2)
CL Item
Unknown (3)
Item
if Relapse please specify
text
Code List
if Relapse please specify
CL Item
Local (1)
CL Item
Metastatic (2)
Item
Complete remission (CR) Number
text
Code List
Complete remission (CR) Number
CL Item
1st (1)
CL Item
2nd (2)
CL Item
3rd or higher (3)
Item
Complete relapse Number
text
Code List
Complete relapse Number
CL Item
1st (1)
CL Item
2nd (2)
CL Item
3rd or higher (3)
Item
SENSITIVITY TO CHEMOTHERAPY
text
Code List
SENSITIVITY TO CHEMOTHERAPY
CL Item
Sensitive (SR:>50% response) (1)
CL Item
Resistant (RR:<50% response) (2)
CL Item
Untreated (3)
Item
Organ(s) involved
text
Code List
Organ(s) involved
CL Item
Nodes Below Diaphragm (1)
CL Item
Bone marrow (2)
CL Item
CNS (3)
CL Item
Mediastinum (4)
CL Item
Soft Tissue (5)
CL Item
Gastrointestinal tract (6)
CL Item
Liver (7)
CL Item
Nodes Above Diaphragm (8)
CL Item
Bone (9)
CL Item
Lungs (10)
CL Item
Heart (11)
CL Item
Skin (12)
CL Item
Urogenital tract (13)
CL Item
Ovaries/Testes (14)
Organ(s) involved
Item
if other Organ(s) involved please specify
text
Item
Primary site affected
integer
Code List
Primary site affected
CL Item
yes (1)
CL Item
no (2)
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)
Item
if ADDITIONAL DISEASE TREATMENT
integer
Code List
if ADDITIONAL DISEASE TREATMENT
CL Item
Planned (planned before HSCT took place) (1)
CL Item
Not planned (for relapse/progression or persistent disease) (2)
Item Group
BEST DISEASE RESPONSE AT 100 DAYS POST-HSCT
Item
BEST RESPONSE AT 100 DAYS AFTER HSCT
text
Code List
BEST RESPONSE AT 100 DAYS AFTER HSCT
CL Item
Complete Remission (1)
CL Item
Very Good Partial Remission (2)
CL Item
Partial Remission (>50%) (3)
CL Item
Not Evaluable (4)
CL Item
Stable Disease (5)
CL Item
Progressive Disease (6)
CL Item
Minor Response (>25% and <50%) (7)
LesionAssessmentDate
Item
Date of Evaluation
date
C0011008 (UMLS CUI [1,1])
C0221198 (UMLS CUI [1,2])
C0031809 (UMLS CUI [1,3])
Item Group
FORMS TO BE FILLED IN
Item
TYPE OF TRANSPLANT
text
Code List
TYPE OF TRANSPLANT
CL Item
AUTOgraft, proceed to Autograft form (1)
CL Item
ALLOgraft or Syngeneic graft, proceed to Allograft form (2)
CL Item
Other (3)
TYPE OF TRANSPLANT
Item
it other type of transplant contact the EBMT Central Registry Office for instructions
text
Item Group
FOLLOW UP SOLID TUMOURS
Unique Identification Code (UIC)
Item
Unique Identification Code (UIC) (if known)
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
Hospital Unique Patient Number
Item
Hospital Unique Patient Number
text
C2348585 (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])
Date last contact
Item
Date of Last Contact or Death
date
C0805839 (UMLS CUI [1])
Item Group
GRAFT VERSUS HOST DISEASE (GvHD) SINCE LAST REPORT
Item
ACUTE GRAFT VERSUS HOST DISEASE (AGVHD)
text
Code List
ACUTE GRAFT VERSUS HOST DISEASE (AGVHD)
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 ACUTE GRAFT VERSUS HOST DISEASE (AGVHD) present
text
Code List
If ACUTE GRAFT VERSUS HOST DISEASE (AGVHD) present
CL Item
New onset (1)
CL Item
Recurrent (2)
CL Item
Persistent (3)
Item
Reason for ACUTE GRAFT VERSUS HOST DISEASE (AGVHD)
text
Code List
Reason for ACUTE GRAFT VERSUS HOST DISEASE (AGVHD)
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
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
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
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)
Item
Resolution
integer
C0856825 (UMLS CUI [1,1])
C1514893 (UMLS CUI [1,2])
Code List
Resolution
CL Item
No  (1)
CL Item
Yes (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 Group
CHRONIC GRAFT VERSUS HOST DISEASE (CGVHD)
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
If Presence of cGVHD
text
Code List
If Presence of cGVHD
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 Organs affected please specify
text
Resolved: Date of resolution
Item
Resolved: Date of resolution
date
Item Group
OTHER COMPLICATIONS SINCE LAST REPORT
Item
INFECTIOUS RELATED COMPLICATIONS
integer
Code List
INFECTIOUS RELATED COMPLICATIONS
CL Item
No complications (1)
CL Item
Yes (2)
Bacteremia / fungemia / viremia / parasites Pathogen
Item
Bacteremia / fungemia / viremia / parasites Pathogen
text
Bacteremia / fungemia / viremia / parasites Pathogen
Item
Bacteremia / fungemia / viremia / parasites Pathogen
date
SYSTEMIC SYMPTOMS OF INFECTION: Septic shock
Item
SYSTEMIC SYMPTOMS OF INFECTION: Septic shock
text
SYSTEMIC SYMPTOMS OF INFECTION: Septic shock
Item
SYSTEMIC SYMPTOMS OF INFECTION: Septic shock
date
SYSTEMIC SYMPTOMS OF INFECTION ARDS Pathogen
Item
SYSTEMIC SYMPTOMS OF INFECTION ARDS Pathogen
text
SYSTEMIC SYMPTOMS OF INFECTION ARDS Pathogen
Item
SYSTEMIC SYMPTOMS OF INFECTION ARDS Pathogen
date
SYSTEMIC SYMPTOMS OF INFECTION Multiorgan failure due to infection Pathogen
Item
SYSTEMIC SYMPTOMS OF INFECTION Multiorgan failure due to infection Pathogen
text
SYSTEMIC SYMPTOMS OF INFECTION Multiorgan failure due to infection Pathogen
Item
SYSTEMIC SYMPTOMS OF INFECTION Multiorgan failure due to infection Pathogen
date
Item
Endorgan diseases
text
C0349410 (UMLS CUI [1,1])
C0009450 (UMLS CUI [1,2])
Code List
Endorgan diseases
CL Item
Pneumonia (Pneumonia)
CL Item
Hepatits (Hepatits)
CL Item
CNS infection (CNS infection)
CL Item
Gut infection (Gut infection)
CL Item
Skin infection (Skin infection)
CL Item
Cystitis (Cystitis)
CL Item
Retinitis (Retinitis)
CL Item
Other (Other)
ENDORGAN DISEASES
Item
ENDORGAN DISEASES
date
Item
NON INFECTIOUS RELATED COMPLICATIONS
text
Code List
NON INFECTIOUS RELATED COMPLICATIONS
CL Item
No complications (1)
CL Item
yes (2)
Item
Specify: Idiopathic pneumonia syndrome
text
C1504431 (UMLS CUI [1])
Code List
Specify: Idiopathic pneumonia syndrome
CL Item
Yes (Yes)
CL Item
No  (No )
CL Item
Unknown (Unknown)
Item
Specify: VOD
text
C0948441 (UMLS CUI [1])
Code List
Specify: VOD
CL Item
Yes (Yes)
CL Item
No  (No )
CL Item
Unknown (Unknown)
Item
Specify: Cataract
text
C0086543 (UMLS CUI [1])
Code List
Specify: Cataract
CL Item
Yes (Yes)
CL Item
No (No)
CL Item
Unknown (Unknown)
Item
Specify: Haemorrhagic cystitis, non infectious
text
C0085692 (UMLS CUI [1])
Code List
Specify: Haemorrhagic cystitis, non infectious
CL Item
Yes  (Yes )
CL Item
No  (No )
CL Item
Unknown (Unknown)
Item
Specify: ARDS, non infectious
text
C0035222 (UMLS CUI [1])
Code List
Specify: ARDS, non infectious
CL Item
Yes (Yes)
CL Item
No (No)
CL Item
Unknown (Unknown)
Item
Multiorgan failure, non infectious
text
Code List
Multiorgan failure, non infectious
CL Item
yes (yes)
CL Item
no  (no )
CL Item
unknown (unknown)
Item
Specify: HSCT-associated microangiopathy
text
C0155765 (UMLS CUI [1])
Code List
Specify: HSCT-associated microangiopathy
CL Item
Yes (Yes)
CL Item
No (No)
CL Item
Unknown (Unknown)
Item
Specify: Renal failure requiring dialysis
text
C0035078 (UMLS CUI [1])
Code List
Specify: Renal failure requiring dialysis
CL Item
Yes (Yes)
CL Item
No (No)
CL Item
Unknown (Unknown)
Item
Specify: Haemolytic anaemia due to blood group
text
C0002878 (UMLS CUI [1])
Code List
Specify: Haemolytic anaemia due to blood group
CL Item
Yes (Yes)
CL Item
No (No)
CL Item
Unknown (Unknown)
Item
Specify: Aseptic bone necrosis
text
C0158452 (UMLS CUI [1])
Code List
Specify: Aseptic bone necrosis
CL Item
Yes (Yes)
CL Item
No (No)
CL Item
Unknown (Unknown)
Other NON INFECTIOUS RELATED COMPLICATIONS
Item
Other NON INFECTIOUS RELATED COMPLICATIONS
text
Idiopathic pneumonia syndrome
Item
Idiopathic pneumonia syndrome
date
VOD
Item
VOD
date
Cataract
Item
Cataract
date
Haemorrhagic cystitis, non infectious
Item
Haemorrhagic cystitis, non infectious
date
ARDS, non infectious
Item
ARDS, non infectious
date
Multiorgan failure, non infectious
Item
Multiorgan failure, non infectious
date
HSCT-associated microangiopathy
Item
HSCT-associated microangiopathy
date
Renal failure requiring dialysis
Item
Renal failure requiring dialysis
date
Haemolytic anaemia due to blood group
Item
Haemolytic anaemia due to blood group
date
Aseptic bone necrosis
Item
Aseptic bone necrosis
date
Other NON INFECTIOUS RELATED COMPLICATIONS
Item
if Other NON INFECTIOUS RELATED COMPLICATIONS
date
Item Group
GRAFT ASSESSMENT AND HAEMOPOIETIC CHIMAERISM
Item
Graft loss
text
C0877042 (UMLS CUI [1])
Code List
Graft loss
CL Item
No (No)
CL Item
Yes (Yes)
CL Item
Not evaluated (Not evaluated)
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
C2826247 (UMLS CUI [1])
Identification
Item
Identification of donor or Cord Blood Unit given by the centre
text
C1718162 (UMLS CUI [1])
Item
Number in the infusion order (if applicable)
integer
C2348184 (UMLS CUI [1])
Code List
Number in the infusion order (if applicable)
CL Item
......... (1)
CL Item
N/A (2)
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-Cell
Item
Cell type on which test was performed (% Donor cells):
float
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 cell type - value
Item
Cell type on which test was performed (% Donor cells): Other
float
C0449475 (UMLS CUI [1,1])
C1522609 (UMLS CUI [1,2])
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)
Specification other labaratory tests
Item
Test used: If other, specify: (Indicate the date(s) and results of all tests done for all donors. Split the results by donor and by the cell type on which the test was performed if applicable. Copy this table as many times as necessary.)
text
C0022885 (UMLS CUI [1,1])
C2348235 (UMLS CUI [1,2])
Item
SECONDARY MALIGNANCY, LYMPHOPROLIFERATIVE OR MYELOPROLIFRATIVE DISORDER DIAGNOSED
text
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
Item
Diagnosis:
text
Code List
Diagnosis:
CL Item
AML (1)
CL Item
MDS (2)
CL Item
Lymphoproliferative disorder (3)
CL Item
Other (4)
Other diagnosis
Item
Diagnosis, other
text
C0205394 (UMLS CUI [1])
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)
Date started ADDITIONAL TREATMENT
Item
Date started ADDITIONAL TREATMENT
date
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
C0302189 (UMLS CUI [1])
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 (Mark disease status before this cellular therapy) (2)
CL Item
Unknown (3)
Item
Disease status before this cellular therapy
text
Code List
Disease status before this cellular therapy
CL Item
CR (1)
CL Item
Not in CR (2)
CL Item
Not evaluated (3)
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)
Type of cells
Item
If other type of cells, please specify
text
Nucleated cells (/kg*)
Item
Number of cells infused
integer
Item
Number of cells infused
text
Code List
Number of cells infused
CL Item
Not evaluated (1)
CL Item
unknown (2)
CD 34+ (cells/kg*)
Item
Number of cells infused
integer
Item
Number of cells infused
text
Code List
Number of cells infused
CL Item
Not evaluated (1)
CL Item
unknown (2)
CD 3+ (cells/kg*)
Item
Number of cells infused
integer
Item
Number of cells infused
text
Code List
Number of cells infused
CL Item
Not evaluated (1)
CL Item
unknown (2)
All cells (cells/kg*)
Item
Total number of cells infused
integer
Item
Total number of cells infused
text
Code List
Total number of cells infused
CL Item
Not evaluated (1)
CL Item
unknown (2)
Chronological number of this cell therapy for this patient
Item
Chronological number of this cell therapy for this patient
integer
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 Indication, please specify
text
Number of Infusions
Item
Number of Infusions (within 10 weeks) (count only infusions that are part of same regimen and given for the same indication)
float
C2348184 (UMLS CUI [1,1])
C1289919 (UMLS CUI [1,2])
Hospital Unique Patient Number (UPN)
Item
Hospital Unique Patient Number (UPN):
text
HSCT date
Item
HSCT date
date
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
Relapse or progression
integer
C0035020 (UMLS CUI [1,1])
C1704632 (UMLS CUI [1,2])
Code List
Relapse or progression
CL Item
Previously reported (1)
CL Item
No (2)
CL Item
yes (3)
CL Item
Continuous progression since HSCT (4)
CL Item
Unknown (5)
RELAPSE OR PROGRESSION
Item
if yes, date diagnosed
date
Item
Organs involved at relapse or progression
text
Code List
Organs involved at relapse or progression
CL Item
Local (1)
CL Item
Distant (2)
Item
Organs distant involved at relapse or progression
text
Code List
Organs distant involved at relapse or progression
CL Item
CNS (1)
CL Item
liver (2)
CL Item
nodes (3)
CL Item
bone marrow (4)
CL Item
bone (5)
CL Item
soft tissue (6)
CL Item
lung (7)
CL Item
pleura (8)
CL Item
other (9)
Other Distant Organs involved at relapse or progression
Item
If Other Distant Organs involved at relapse or progression
text
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
If alive: Type of score used:
text
C1518965 (UMLS CUI [1])
Code List
If alive: Type of score used:
CL Item
Karnofsky (Karnofsky)
CL Item
Lansky (Lansky)
CL Item
Not evaluated (Not evaluated)
CL Item
Unknown (Unknown)
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)
Item
CAUSE OF DEATH
text
Code List
CAUSE OF DEATH
CL Item
Relapse or progression (1)
CL Item
Secondary malignancy (2)
CL Item
HSCT related cause (3)
CL Item
Unknown (4)
CL Item
Other (5)
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
HSCT related cause: .. (check as many as appropriate)
text
Code List
HSCT related cause: .. (check as many as appropriate)
CL Item
yes (1)
CL Item
no (2)
CL Item
unknown (3)
Item
If dead and HSCT related cause of death, specify (check as many as apppropriate): Veno-Occlusive disease (VOD)
text
C0007465 (UMLS CUI [1,1])
C0948441 (UMLS CUI [1,2])
Code List
If dead and HSCT related cause of death, specify (check as many as apppropriate): Veno-Occlusive disease (VOD)
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): Haemorrhage
text
C0007465 (UMLS CUI [1,1])
C0019080 (UMLS CUI [1,2])
Code List
If dead and HSCT related cause of death, specify (check as many as apppropriate): Haemorrhage
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): Cardiac toxicity
text
C0007465 (UMLS CUI [1,1])
C0876994 (UMLS CUI [1,2])
Code List
If dead and HSCT related cause of death, specify (check as many as apppropriate): Cardiac 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): Central nervous system t8oxicity
text
Code List
If dead and HSCT related cause of death, specify (check as many as apppropriate): Central nervous system t8oxicity
CL Item
yes (1)
CL Item
no (2)
CL Item
unknown (3)
Item
If dead and HSCT related cause of death, specify (check as many as apppropriate): Gastro intestinal toxicity
text
C0007465 (UMLS CUI [1,1])
C1142499 (UMLS CUI [1,2])
Code List
If dead and HSCT related cause of death, specify (check as many as apppropriate): Gastro intestinal 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): Skin toxicity
text
C0007465 (UMLS CUI [1,1])
C1167791 (UMLS CUI [1,2])
Code List
If dead and HSCT related cause of death, specify (check as many as apppropriate): Skin 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): Renal failure
text
C0007465 (UMLS CUI [1,1])
C0035078 (UMLS CUI [1,2])
Code List
If dead and HSCT related cause of death, specify (check as many as apppropriate): Renal failure
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): Multiple organ failure
text
C0007465 (UMLS CUI [1,1])
C0026766 (UMLS CUI [1,2])
Code List
If dead and HSCT related cause of death, specify (check as many as apppropriate): Multiple organ failure
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): other
text
Code List
If dead and HSCT related cause of death, specify (check as many as apppropriate): other
CL Item
yes (1)
CL Item
no (2)
CL Item
unknown (3)
Item Group
ADDITIONAL NOTES IF APPLICABLE
COMMENTS
Item
COMMENTS
text
Identification
Item
Identification
text
C0205396 (UMLS CUI [1])

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