Eligibility Acute Myelogenous Leukemia NCT01902329

Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
acute myeloid leukemia, positive for cd33
Descrição

AML

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0023467
eastern cooperative oncology group status of 0 or 1
Descrição

ECOG

Tipo de dados

boolean

Alias
UMLS CUI [1]
C1520224
adequate baseline renal and hepatic function
Descrição

renal and hepatic function

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0232804
UMLS CUI [1,2]
C0232741
central venous access
Descrição

central venous access

Tipo de dados

boolean

Alias
UMLS CUI [1]
C1145640
either achieved complete remission (greater than 12 weeks in duration) with initial induction/consolidation and have experienced relapse of disease or declined treatment with high-dose induction/consolidation
Descrição

remission or relapse

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0544452
UMLS CUI [2]
C0277556
bone marrow blasts greater than or equal to 5% for relapsed patients, or greater than or equal to 20% for untreated patients
Descrição

bone marrow blasts

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0368761
Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
inadequate lung function
Descrição

pulmonary function

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0231921
prior allogeneic stem cell transplant, except for a specific cohort
Descrição

stem cell transplant

Tipo de dados

boolean

Alias
UMLS CUI [1]
C1504389
high-dose chemotherapy within 4 weeks of study drug
Descrição

chemotherapy

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0392920
antileukemia treatment within 14 days of study drug (other than hydroxyurea or 6-mercaptopurine)
Descrição

antileukemia treatment

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0087111

Similar models

Eligibility Acute Myelogenous Leukemia NCT01902329

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
AML
Item
acute myeloid leukemia, positive for cd33
boolean
C0023467 (UMLS CUI [1])
ECOG
Item
eastern cooperative oncology group status of 0 or 1
boolean
C1520224 (UMLS CUI [1])
renal and hepatic function
Item
adequate baseline renal and hepatic function
boolean
C0232804 (UMLS CUI [1,1])
C0232741 (UMLS CUI [1,2])
central venous access
Item
central venous access
boolean
C1145640 (UMLS CUI [1])
remission or relapse
Item
either achieved complete remission (greater than 12 weeks in duration) with initial induction/consolidation and have experienced relapse of disease or declined treatment with high-dose induction/consolidation
boolean
C0544452 (UMLS CUI [1])
C0277556 (UMLS CUI [2])
bone marrow blasts
Item
bone marrow blasts greater than or equal to 5% for relapsed patients, or greater than or equal to 20% for untreated patients
boolean
C0368761 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
pulmonary function
Item
inadequate lung function
boolean
C0231921 (UMLS CUI [1])
stem cell transplant
Item
prior allogeneic stem cell transplant, except for a specific cohort
boolean
C1504389 (UMLS CUI [1])
chemotherapy
Item
high-dose chemotherapy within 4 weeks of study drug
boolean
C0392920 (UMLS CUI [1])
antileukemia treatment
Item
antileukemia treatment within 14 days of study drug (other than hydroxyurea or 6-mercaptopurine)
boolean
C0087111 (UMLS CUI [1])