EBMT Code (CIC)
Item
EBMT Code (CIC)
integer
C3826859 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Klinik
Item
Hospital
text
C0019994 (UMLS CUI [1])
Unit
Item
Unit
integer
C1519795 (UMLS CUI [1])
Contact person
Item
Contact person
integer
C0337611 (UMLS CUI [1])
Phone
Item
Phone
integer
C1550483 (UMLS CUI [1])
Fax
Item
Fax
integer
C1549619 (UMLS CUI [1])
e-mail
Item
e-mail
integer
C1705961 (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
Name of study / trial
Item
Name of study / trial
integer
C0008976 (UMLS CUI [1])
Hospital Unique Patient Number
Item
Hospital Unique Patient Number/Code
integer
C2348585 (UMLS CUI [1])
Initials
Item
Initials (first name(s) _family name(s))
integer
C2986440 (UMLS CUI [1])
Date of Birth
Item
Date of Birth
date
C0421451 (UMLS CUI [1])
Item
Sex
text
C0079399 (UMLS CUI [1])
Date of initial diagnosis
Item
Date of initial diagnosis
date
C2316983 (UMLS CUI [1])
PRIMARY DISEASE DIAGNOSIS
Item
PRIMARY DISEASE DIAGNOSIS
integer
C0277554 (UMLS CUI [1])
Item
Performance score (if alive)
integer
C1518965 (UMLS CUI [1])
Code List
Performance score (if alive)
Item
Score achived
text
C1518965 (UMLS CUI [1])
Item
Type of HSCT
integer
C0472699 (UMLS CUI [1])
Item
Patient CMV status (for allografts)
integer
C0582172 (UMLS CUI [1])
Code List
Patient CMV status (for allografts)
CL Item
Negative (Negative )
CL Item
Positive (Positive)
CL Item
Not evaluated (Not evaluated )
CL Item
Unknown (Unknown)
Multiple donors
Item
Multiple donors/products
boolean
C0013018 (UMLS CUI [1])
Multiple donors
Item
Multiple donors: if yes:
integer
C0013018 (UMLS CUI [1])
Item
Source of Stem Cells
integer
C0018956 (UMLS CUI [1])
Code List
Source of Stem Cells
CL Item
Bone Marrow VBMSC (Bone Marrow VBMSC )
CL Item
Peripheral Blood VPBSC (Peripheral Blood VPBSC)
CL Item
Cord Blood VCBSC (Cord Blood VCBSC )
Source of Stem Cells
Item
Source of Stem Cells: if other, please specify
integer
C0018956 (UMLS CUI [1])
Donor ID
Item
Donor ID
text
C1718162 (UMLS CUI [1])
Item
Donor ID
integer
C1718162 (UMLS CUI [1])
Item
HLA match type (for allografts)
integer
C0242318 (UMLS CUI [1])
Code List
HLA match type (for allografts)
CL Item
Syngeneic (monozygotic twin) (Syngeneic (monozygotic twin))
CL Item
HLA-identical sibling (may include non-monozygotic twin) (HLA-identical sibling (may include non-monozygotic twin) )
CL Item
HLA-matched other relative (HLA-matched other relative)
CL Item
HLA-mismatched relative (HLA-mismatched relative)
CL Item
Unrelated donor (Unrelated donor)
Item
Degree of mismatch
integer
C1881865 (UMLS CUI [1])
Code List
Degree of mismatch
CL Item
1 HLA antigen mismatch (1)
CL Item
> 2 HLA antigen mismatch (2)
donor registry
Item
Name of donor registry/CB Bank
integer
C0034975 (UMLS CUI [1])
BMDW/WMDA code
Item
BMDW/WMDA code (up to 4 characters)
integer
C2987198 (UMLS CUI [1])
Item
Number of mismatches A
integer
C1881865 (UMLS CUI [1,1])
C0449788 (UMLS CUI [1,2])
Code List
Number of mismatches A
Item
Number of mismatches B
integer
C1881865 (UMLS CUI [1,1])
C0449788 (UMLS CUI [1,2])
Code List
Number of mismatches B
Item
Number of mismatches C
integer
C1881865 (UMLS CUI [1,1])
C0449788 (UMLS CUI [1,2])
Code List
Number of mismatches C
Item
Number of mismatches DRB1
integer
C1881865 (UMLS CUI [1,1])
C0449788 (UMLS CUI [1,2])
Code List
Number of mismatches DRB1
Item
Number of mismatches DQB1
integer
C1881865 (UMLS CUI [1,1])
C0449788 (UMLS CUI [1,2])
Code List
Number of mismatches DQB1
Item
Number of mismatches DPB1
integer
C1881865 (UMLS CUI [1,1])
C0449788 (UMLS CUI [1,2])
Code List
Number of mismatches DPB1
Item
Donor Sex
integer
C0079399 (UMLS CUI [1])
Item
Donor age
integer
C0013018 (UMLS CUI [1,1])
C0421451 (UMLS CUI [1,2])
CL Item
Not evaluated (3)
Graft manipulation ex-vivo (including T-cell depletion) other than for RBC removal or volume reduction
Item
Graft manipulation ex-vivo (including T-cell depletion) other than for RBC removal or volume reduction
boolean
C0677960 (UMLS CUI [1])
Chronological number of HSCT
Item
Chronological number of HSCT for this patient?
integer
C1318453 (UMLS CUI [1,1])
C0449788 (UMLS CUI [1,2])
If >1, date of last HSCT before this one
Item
If >1, date of last HSCT before this one
date
C0018956 (UMLS CUI [1,1])
C0029216 (UMLS CUI [1,2])
C2745955 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,4])
HSCT part of a planned multiple graft protocol?
Item
HSCT part of a planned multiple graft protocol?
boolean
Preparative (conditioning) regimen given?
Item
Preparative (conditioning) regimen given?
boolean
C1882454 (UMLS CUI [1])
Was this intended to be myeloablative?
Item
Was this intended to be myeloablative?
boolean
C1831742 (UMLS CUI [1])
Item
Reason
integer
C0392360 (UMLS CUI [1])
CL Item
Age of recipient (Age of recipient)
CL Item
Comorbid conditions (Comorbid conditions)
CL Item
Prior HSCT (Prior HSCT)
CL Item
Protocol driven REASRIOT (Protocol driven REASRIOT)
Ara-C
Item
Ara-C (cytarabine)
float
C0733521 (UMLS CUI [1])
Item
Ara-C (cytarabine): Unit of dosing
integer
C0733521 (UMLS CUI [1,1])
C1321095 (UMLS CUI [1,2])
Code List
Ara-C (cytarabine): Unit of dosing
ALS
Item
ALG, ATG (ALS, ATS)
float
C0002736 (UMLS CUI [1])
Item
AST: Unit of dosing
integer
C1321095 (UMLS CUI [1,1])
C0004002 (UMLS CUI [1,2])
Code List
AST: Unit of dosing
Item
Animal origin
integer
C3494749 (UMLS CUI [1])
Bleomycin
Item
Bleomycin
float
C0005740 (UMLS CUI [1])
Item
Unit of dosing
integer
C1321095 (UMLS CUI [1])
Busulfan
Item
Busulfan
float
C0006463 (UMLS CUI [1])
Item
Busulfan Unit of dosing:
integer
C0869039 (UMLS CUI [1,1])
C0006463 (UMLS CUI [1,2])
Code List
Busulfan Unit of dosing:
BCNU
Item
BCNU
float
C0007257 (UMLS CUI [1])
Item
BCNU Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0007257 (UMLS CUI [1,2])
Code List
BCNU Unit of dosing
Bexar (radiolabelled MoAB)
Item
Bexar (radiolabelled MoAB)
float
C3831356 (UMLS CUI [1])
Item
Bexar Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C3831356 (UMLS CUI [1,2])
Code List
Bexar Unit of dosing
CCNU
Item
CCNU
float
C0687700 (UMLS CUI [1])
Item
CCNU Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0687700 (UMLS CUI [1,2])
Code List
CCNU Unit of dosing
Campath
Item
Campath (antiCD52)
float
C0939276 (UMLS CUI [1])
Item
Campath Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0939276 (UMLS CUI [1,2])
Code List
Campath Unit of dosing
Carboplatin
Item
Carboplatin
float
C0079083 (UMLS CUI [1])
Item
Carboplatin Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0079083 (UMLS CUI [1,2])
Code List
Carboplatin Unit of dosing
Cisplatin
Item
Cisplatin
float
C0008838 (UMLS CUI [1])
Item
Cisplatin Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0008838 (UMLS CUI [1,2])
Code List
Cisplatin Unit of dosing
Corticosteroids
Item
Corticosteroids
float
C0001617 (UMLS CUI [1])
Item
Corticosteroids Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0001617 (UMLS CUI [1,2])
Code List
Corticosteroids Unit of dosing
Cyclophosphamide
Item
Cyclophosphamide
float
C0010583 (UMLS CUI [1])
Item
Cyclophosphamide Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0010583 (UMLS CUI [1,2])
Code List
Cyclophosphamide Unit of dosing
Daunorubicin
Item
Daunorubicin
float
C0011015 (UMLS CUI [1])
Item
Unit of dosing Daunorubicin
integer
C0869039 (UMLS CUI [1,1])
C0011015 (UMLS CUI [1,2])
Code List
Unit of dosing Daunorubicin
Doxorubicin
Item
Doxorubicin (adriamycine)
float
C0013089 (UMLS CUI [1])
Item
Doxorubicin Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0013089 (UMLS CUI [1,2])
Code List
Doxorubicin Unit of dosing
Etoposide
Item
Etoposide (VP16)
float
C0015133 (UMLS CUI [1])
Item
Etoposide Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0015133 (UMLS CUI [1,2])
Code List
Etoposide Unit of dosing
Fludarabine
Item
Fludarabine
float
C0059985 (UMLS CUI [1])
Item
Fludarabine Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0059985 (UMLS CUI [1,2])
Code List
Fludarabine Unit of dosing
Gemtuzumab
Item
Gemtuzumab
float
C0872968 (UMLS CUI [1])
Item
Gemtuzumab Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0872968 (UMLS CUI [1,2])
Code List
Gemtuzumab Unit of dosing
Idarubicin
Item
Idarubicin
float
C0020789 (UMLS CUI [1])
Item
Idarubicin Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0020789 (UMLS CUI [1,2])
Code List
Idarubicin Unit of dosing
Ifosfamide
Item
Ifosfamide
float
C0020823 (UMLS CUI [1])
Item
Ifosfamide Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0020823 (UMLS CUI [1,2])
Code List
Ifosfamide Unit of dosing
Imatinib mesylate
Item
Imatinib mesylate
float
C0939537 (UMLS CUI [1])
Item
Imatinib mesylate Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0939537 (UMLS CUI [1,2])
Code List
Imatinib mesylate Unit of dosing
Melphalan
Item
Melphalan
float
C0025241 (UMLS CUI [1])
Item
Melphalan Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0025241 (UMLS CUI [1,2])
Code List
Melphalan Unit of dosing
Mitoxantrone
Item
Mitoxantrone
float
C0026259 (UMLS CUI [1])
Item
Mitoxantrone Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0026259 (UMLS CUI [1,2])
Code List
Mitoxantrone Unit of dosing
Paclitaxel
Item
Paclitaxel
float
C0144576 (UMLS CUI [1])
Item
Paclitaxel Unit of dosing
integer
C0869039 (UMLS CUI [1])
Code List
Paclitaxel Unit of dosing
Rituximab
Item
Rituximab (mabthera, antiCD20)
float
C0393022 (UMLS CUI [1])
Item
Rituximab Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0393022 (UMLS CUI [1,2])
Code List
Rituximab Unit of dosing
Teniposide
Item
Teniposide
float
C0039512 (UMLS CUI [1])
Item
Teniposide Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0039512 (UMLS CUI [1,2])
Code List
Teniposide Unit of dosing
Thiotepa
Item
Thiotepa
float
C0039871 (UMLS CUI [1])
Item
Thiotepa Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0039871 (UMLS CUI [1,2])
Code List
Thiotepa Unit of dosing
Zevalin
Item
Zevalin (radiolabelled MoAB)
float
C0919274 (UMLS CUI [1])
Item
Zevalin Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0919274 (UMLS CUI [1,2])
Code List
Zevalin Unit of dosing
other radiolabelled MoAB
Item
Other radiolabelled MoAB
float
C0003250 (UMLS CUI [1,1])
C0454110 (UMLS CUI [1,2])
Item
other radiolabelled MoAB Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0003250 (UMLS CUI [1,2])
C0454110 (UMLS CUI [1,3])
Code List
other radiolabelled MoAB Unit of dosing
Other radiolabelled MoAB: if other, please specify
Item
Other radiolabelled MoAB: if other, please specify
integer
C0205394 (UMLS CUI [1,1])
C0003250 (UMLS CUI [1,2])
C0454110 (UMLS CUI [1,3])
Other MoAB
Item
Other MoAB
float
C0003250 (UMLS CUI [1])
Item
MoAB Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0003250 (UMLS CUI [1,2])
Code List
MoAB Unit of dosing
Total body irradiation
Item
Total body irradiation
boolean
C0043162 (UMLS CUI [1])
Total Body Irradiation: if yes, please specify value
Item
Total Body Irradiation: if yes, please specify value
integer
C4035158 (UMLS CUI [1,1])
C0043162 (UMLS CUI [1,2])
TLI, TNI, TAI
Item
TLI, TNI, TAI
boolean
C4035158 (UMLS CUI [1])
C0043162 (UMLS CUI [2])
GvHD prophylaxis
Item
GvHD prophylaxis or preventive treatment (Allografts only)
boolean
C0278845 (UMLS CUI [1])
Item
GvHD prophylaxis or preventive treatment: if yes, please specify
integer
C0278845 (UMLS CUI [1,1])
C4035158 (UMLS CUI [1,2])
Code List
GvHD prophylaxis or preventive treatment: if yes, please specify
CL Item
Drugs (Immunosuppressive chemo) VAGVHDP5 (1)
CL Item
ALG, ALS, ATG, ATS (given after day 0) (2)
CL Item
Anti CD25 (MoAB in vivo) (3)
CL Item
Campath (MoAB in vivo; can be "in the bag") (4)
CL Item
Corticosteroids (5)
CL Item
Cyclophosphamide (given after day 0) (7)
CL Item
Etanercept (MoAB in vivo) (8)
CL Item
FK 506 (Tacrolimus, Prograf) (9)
CL Item
Infliximab (MoAB in vivo) (10)
CL Item
Methotrexate (11)
CL Item
Mycophenolate (MMF) (12)
CL Item
Other monoclonal antibody (in vivo), (14)
CL Item
Other agent (in vivo), specify (16)
CL Item
Extracorporeal photopheresis (ECP) (17)
CL Item
Other, specify (18)
GvHD prophylaxis or preventive treatment: if other, please specify
Item
GvHD prophylaxis or preventive treatment: if other, please specify
integer
C4035158 (UMLS CUI [1,1])
C4035158 (UMLS CUI [1,2])
GvHD prophylaxis or preventive treatment: if Other monoclonal antibody, please specify
Item
GvHD prophylaxis or preventive treatment: if Other monoclonal antibody, please specify
integer
C4035158 (UMLS CUI [1,1])
C4035158 (UMLS CUI [1,2])
C0003250 (UMLS CUI [1,3])
Item
Absolute neutrophil count (ANC) recovery (engraftment) (Neutrophils >0.5X109 /L)
integer
C0948762 (UMLS CUI [1])
Code List
Absolute neutrophil count (ANC) recovery (engraftment) (Neutrophils >0.5X109 /L)
Date of last assessment
Item
Date of last assessment
date
C0011008 (UMLS CUI [1,1])
C1516048 (UMLS CUI [1,2])
Date of ANC recovery
Item
Date of ANC recovery
date
C0948762 (UMLS CUI [1,1])
C2004454 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Date of last assessment
Item
Date of last assessment
date
C0011008 (UMLS CUI [1,1])
C1516048 (UMLS CUI [1,2])
Item
Maximum Grade
integer
C0856825 (UMLS CUI [1,1])
C0441800 (UMLS CUI [1,2])
CL Item
Present but grade unknown (6)
CL Item
Not evaluated (7)
Cell infusion
Item
Cell infusion (CI)
boolean
C2145394 (UMLS CUI [1])
Date of first infusion
Item
Date of first infusion
date
C0574032 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item
Type of cell(s): (check all that apply)
integer
Code List
Type of cell(s): (check all that apply)
CL Item
Lymphocyte (DLI) (1)
CL Item
Dendritic cells (4)
Type of cell(s): (check all that apply)
Item
if other, please specify
text
Chronological no. of CI for this patient
Item
Chronological no. of CI for this patient
text
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
Loss/decreased chimaerism (Loss/decreased chimaerism)
CL Item
Mixed chimaerism (Mixed chimaerism)
CL Item
Planned/ protocol (Planned/ protocol)
CL Item
Prophylactic (Prophylactic)
CL Item
Treatment for disease (Treatment for disease)
CL Item
Treatment of GvHD (Treatment of GvHD)
CL Item
Treatment PTLD, EBV, lymphoma (Treatment PTLD, EBV, lymphoma)
CL Item
Treatment viral infection (Treatment viral infection)
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
Disease treatment
integer
C0087111 (UMLS CUI [1])
Code List
Disease treatment
CL Item
Yes: Planned (planned before HSCT took place) (2)
CL Item
Yes: Not planned (for relapse/progression or persistent disease) (3)
Item
Best disease status (response) after HSCT (prior to treatment modification in response to a post HSCT disease assessment)
integer
Code List
Best disease status (response) after HSCT (prior to treatment modification in response to a post HSCT disease assessment)
CL Item
Continued complete remission (CCR) (1)
CL Item
CR achieved: Date achieved (2)
CL Item
Never in CR: Date assessed (3)
CL Item
Not evaluated (4)
CR achieved: Date achieved
Item
CR achieved: Date achieved
date
Never in CR: Date assessed
Item
Never in CR: Date assessed
date
Date of last follow up or death
Item
Date of last follow up or death
date
C3694716 (UMLS CUI [1,1])
C0011065 (UMLS CUI [1,2])
Was disease detected by clinical/haematological method?:
Item
Was disease detected by clinical/haematological method?:
date
Last date assessed
Item
Last date assessed
date
Item
Was disease detected by cytogenetic/FISH method?:
integer
Code List
Was disease detected by cytogenetic/FISH method?:
CL Item
Not evaluated (3)
Considered disease relapse/progression
Item
Considered disease relapse/progression
boolean
Last date assessed
Item
Last date assessed
date
Item
Survival Status
text
Code List
Survival Status
CL Item
Died before HSCT (Died before HSCT)
Check here if patient lost to follow up
Item
Check here if patient lost to follow up
boolean
Item
Main Cause of Death
integer
C0007465 (UMLS CUI [1])
Code List
Main Cause of Death
CL Item
Relapse or Progression (if indication: primary disease) (1)
CL Item
HSCT related (if applicable) (2)
Item
HSCT related cause
integer
Code List
HSCT related cause
CL Item
Cardiac Toxicity CTX (2)
CL Item
Rejection/Poor graft function REJ (3)
CL Item
Infection INF (4)
CL Item
Pulmonary toxicity PTX (5)
CL Item
Veno occlusive disorder (6)
DATE OF NEXT HSCT
Item
Date of this HSCT
date
EBMT Code (CIC):
Item
EBMT Code (CIC):
text
Hospital
Item
Name of the hospital
text
C0019994 (UMLS CUI [1])
Contact person
Item
Contact person
text
Has the HSCT been registered in the EBMT database ?
Item
Has the HSCT been registered in the EBMT database ?
boolean
C0421512 (UMLS CUI [1])
Has the HSCT been registered in the EBMT database ?
Item
If Yes: UIC number
text
Hospital Unique Patient Number/ Code
Item
Hospital Unique Patient Number/ Code
text
Initials
Item
Initials
text
Date of Birth
Item
Date of Birth
date
Date of HSCT
Item
Date of HSCT
date
Donor ID
Item
Donor ID
text
Item
Agents involved Tick all that apply:
text
Code List
Agents involved Tick all that apply:
CL Item
Alkylating agent/radiation-related (Alkylating agent/radiation-related)
CL Item
Topoisomerase II inhibitor-related (Topoisomerase II inhibitor-related)
CL Item
Unknown (Unknown)
Item
MOLECULAR BIOLOGYCompulsory for CIBMTR Research centres. Fill only for MPS. Janus kinase 2 (jak2)
integer
Code List
MOLECULAR BIOLOGYCompulsory for CIBMTR Research centres. Fill only for MPS. Janus kinase 2 (jak2)
THERAPY GIVEN PRIOR TO THIS HSCT
Item
THERAPY GIVEN PRIOR TO THIS HSCT
boolean
THERAPY GIVEN PRIOR TO THIS HSCT
Item
Date started
date
Tyrosine kinase receptor antagonist given
Item
Tyrosine kinase receptor antagonist given
boolean
Item
if yes, please specify
integer
Code List
if yes, please specify
CL Item
Imatinib mesylate (Gleevec, Glivec) (1)
CL Item
Dasatinib (Sprycel) (2)
CL Item
Nilotinib (Tasigna) (3)
Item
Other agent, Fill only for CML
text
Code List
Other agent, Fill only for CML
CL Item
Combination chemotherapy (Combination chemotherapy )
CL Item
Hydroxyurea (Hydroxyurea)
CL Item
Interferon (Interferon)
Were there any clinically significant co-existing disease or organ impairment at time of patient assessment prior to preparative (conditioning) regimen?
Item
Were there any clinically significant co-existing disease or organ impairment at time of patient assessment prior to preparative (conditioning) regimen?
boolean
Item
(Platelets >20X109 /L; first of 3 consecutive days)
text
Code List
(Platelets >20X109 /L; first of 3 consecutive days)
CL Item
Never below this lever (Never below this lever)
CL Item
Unknown (Unknown)
Date Platelets > 20 x 10 9 /l
Item
Date Platelets > 20 x 10 9 /l
date
Item
Platelet reconstitution (Platelets >20X109 /L; first of 3 consecutive days)
text
Code List
Platelet reconstitution (Platelets >20X109 /L; first of 3 consecutive days)
CL Item
Never below this lever (Never below this lever)
CL Item
Unknown (Unknown)
Date Platelets > 20 x 10 9 /l
Item
Date Platelets > 20 x 10 9 /l
date
PLANNED THERAPY GIVEN AFTER THIS HSCT
Item
PLANNED THERAPY GIVEN AFTER THIS HSCT, Date started
date
Chemo/drug
Item
Chemo/drug
boolean
CL Item
Imatinib mesylate (Gleevec, Glivec) (Imatinib mesylate (Gleevec, Glivec))
CL Item
Dasatinib (Sprycel) (Dasatinib (Sprycel))
CL Item
Nilotinib (Tasigna) (Nilotinib (Tasigna))
CL Item
Bortezomib (Velcade) (Bortezomib (Velcade))
CL Item
Intrathecal chemotherapy (Intrathecal chemotherapy)
CL Item
Lenalidomide (Revlimid) (Lenalidomide (Revlimid))
CL Item
Rituximab (Rituxan, mabthera) (Rituximab (Rituxan, mabthera))
CL Item
Velafermin (FGF) (Velafermin (FGF))
CL Item
Lepivance (KGF, palifermin) (Lepivance (KGF, palifermin))
CL Item
Thalidomide (Thalidomide)
Radiotherapy
Item
Radiotherapy
boolean
EBMT Centre Identification Code (CIC)
Item
EBMT Centre Identification Code (CIC)
text
C2348585 (UMLS CUI [1])
Hospital Unique Patient Number/Code (UPN)
Item
Hospital Unique Patient Number/Code (UPN)
text
Date of Initial Diagnosis
Item
Date of Initial Diagnosis
date