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ID
13502
Beschrijving
Randomized study with a run-in dose-selection phase to assess the added value of Lenalidomide in combination with standard remission-induction chemotherapy and post-remission treatment in patients aged 18-65 years with previously untreated acute myeloid leukemia (AML) or high risk myelodysplasia (MDS) (IPSS-R risk score> 4.5)
Trefwoorden
Versies (3)
- 05-11-15 05-11-15 -
- 02-01-16 02-01-16 -
- 11-02-16 11-02-16 -
Geüploaded op
11 februari 2016
DOI
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Licentie
Creative Commons BY-NC 3.0
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Chemotherapy Evaluation Form HOVON 132 AML/SAKK 30/13 EudraCT 2013-002843-26
Chemotherapy Evaluation Form
- StudyEvent: ODM
Similar models
Chemotherapy Evaluation Form
- StudyEvent: ODM
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
CL Item
induction cycle I (1)
C3179010 (UMLS CUI-1)
CL Item
induction cycle II (2)
C3179010 (UMLS CUI-1)
CL Item
post induction cycle III (3)
C3179010 (UMLS CUI-1)
Nights in hospital
Item
Nights in hospital
float
C0420496 (UMLS CUI [1])
BM sampling date
Item
BM sampling date
date
C0005953 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
BM aspirate done
Item
BM aspirate done
boolean
C0857285 (UMLS CUI [1])
Item
BM aspirate evaluable
integer
C0857285 (UMLS CUI [1,1])
C0220825 (UMLS CUI [1,2])
C0220825 (UMLS CUI [1,2])
CL Item
no (0)
C1298908 (UMLS CUI-1)
CL Item
yes* (1)
C1705108 (UMLS CUI-1)
Blasts
Item
*Blasts
float
C1982687 (UMLS CUI [1])
Auer rods
Item
Auer rods
boolean
C0333828 (UMLS CUI [1])
BM biopsy done
Item
BM biopsy done
boolean
C0005954 (UMLS CUI [1])
Clusters of blasts present
Item
Clusters of blasts present
boolean
C0368761 (UMLS CUI [1])
Date of evaluation
Item
Date of evaluation (preferably date of BM)
date
C2985720 (UMLS CUI [1])
CL Item
no (0)
C1868812 (UMLS CUI-1)
CL Item
skin* (1)
C1123023 (UMLS CUI-1)
CL Item
CNS* (2)
C3714787 (UMLS CUI-1)
CL Item
liver* (3)
C0023884 (UMLS CUI-1)
CL Item
spleen* (4)
C0037993 (UMLS CUI-1)
CL Item
lymphadenopathy* (5)
C0497156 (UMLS CUI-1)
CL Item
other* (8)
C0205394 (UMLS CUI-1)
*specify
Item
*specify
text
C1521902 (UMLS CUI [1])
CL Item
CR (1)
C0677874 (UMLS CUI-1)
CL Item
Death in aplasia (5)
C0243065 (UMLS CUI-1)
CL Item
CRi (2)
C3538993 (UMLS CUI-1)
CL Item
PR (3)
C1521726 (UMLS CUI-1)
CL Item
RD (4)
C3844738 (UMLS CUI-1)
CL Item
Death from indeterminate cause (6)
C0277589 (UMLS CUI-1)
CL Item
Relapse (7)
C0035020 (UMLS CUI-1)
CL Item
alive (0)
C2584946 (UMLS CUI-1)
CL Item
dead (1)
C0011065 (UMLS CUI-1)
CL Item
no further treatment (0)
C0746919 (UMLS CUI-1)
CL Item
induction cycle II (2)
C3179010 (UMLS CUI-1)
CL Item
post induction cycle III (3)
C3179010 (UMLS CUI-1)
CL Item
autoHSCT (4)
C0194037 (UMLS CUI-1)
CL Item
alloHSCT (5)
C1705576 (UMLS CUI-1)
Research Comments
Item
Comments
text
C0947611 (UMLS CUI [1])