Eligibility Myelogenous Leukemia, Acute NCT00130702

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients must have pathologically documented acute myelogenous leukemia and either not be a candidate for myelosuppressive chemotherapy due to age or comorbid disease; or have relapsed acute myelogenous leukemia or be refractory to standard therapy and not likely to require cytoreductive therapy within 30 days.
Description

Leukemia, Myelocytic, Acute | Myelosuppressive Chemotherapy | Age | Comorbidity | Acute Myelocytic Leukemia Relapse | Standard therapy refractory | Cytoreductive Therapeutic procedure Unlikely

Data type

boolean

Alias
UMLS CUI [1]
C0023467
UMLS CUI [2,1]
C1513793
UMLS CUI [2,2]
C0392920
UMLS CUI [3]
C0001779
UMLS CUI [4]
C0009488
UMLS CUI [5,1]
C0023467
UMLS CUI [5,2]
C0035020
UMLS CUI [6,1]
C2936643
UMLS CUI [6,2]
C0205269
UMLS CUI [7,1]
C0864494
UMLS CUI [7,2]
C0087111
UMLS CUI [7,3]
C0750558
ecog performance status 0, 1 or 2
Description

ECOG performance status

Data type

boolean

Alias
UMLS CUI [1]
C1520224
age > 18 years
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
adequate kidney and hepatic function
Description

Renal function | Liver function

Data type

boolean

Alias
UMLS CUI [1]
C0232804
UMLS CUI [2]
C0232741
greater than 4 weeks from any chemotherapy, radiotherapy, immunotherapy, or systemic steroid therapy with the exception of hydroxyurea.
Description

Chemotherapy | Therapeutic radiology procedure | Immunotherapy | Steroid therapy Systemic | hydroxyurea

Data type

boolean

Alias
UMLS CUI [1]
C0392920
UMLS CUI [2]
C1522449
UMLS CUI [3]
C0021083
UMLS CUI [4,1]
C0149783
UMLS CUI [4,2]
C0205373
UMLS CUI [5]
C0020402
greater than 2 months following bone marrow or peripheral blood stem cell transplantation or donor lymphocyte infusion.
Description

Bone Marrow Transplantation | Peripheral Stem Cell Transplantation | Donor Lymphocyte Infusion

Data type

boolean

Alias
UMLS CUI [1]
C0005961
UMLS CUI [2]
C0242602
UMLS CUI [3]
C1512034
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
uncontrolled active infection
Description

Communicable Disease Uncontrolled

Data type

boolean

Alias
UMLS CUI [1,1]
C0009450
UMLS CUI [1,2]
C0205318
urgent need for cytoreductive chemotherapy, surgery, or radiotherapy
Description

Cytoreductive Chemotherapy Patient need for Urgent | Cytoreductive surgery Patient need for Urgent | Cytoreductive Therapeutic radiology procedure Patient need for Urgent

Data type

boolean

Alias
UMLS CUI [1,1]
C0864494
UMLS CUI [1,2]
C0392920
UMLS CUI [1,3]
C0686904
UMLS CUI [1,4]
C0439609
UMLS CUI [2,1]
C1112438
UMLS CUI [2,2]
C0686904
UMLS CUI [2,3]
C0439609
UMLS CUI [3,1]
C0864494
UMLS CUI [3,2]
C1522449
UMLS CUI [3,3]
C0686904
UMLS CUI [3,4]
C0439609
current chemotherapy or chemotherapy within the last 4 weeks.
Description

Chemotherapy

Data type

boolean

Alias
UMLS CUI [1]
C0392920
pregnancy or nursing mothers
Description

Pregnancy | Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
infection with hiv
Description

HIV Infection

Data type

boolean

Alias
UMLS CUI [1]
C0019693

Similar models

Eligibility Myelogenous Leukemia, Acute NCT00130702

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Leukemia, Myelocytic, Acute | Myelosuppressive Chemotherapy | Age | Comorbidity | Acute Myelocytic Leukemia Relapse | Standard therapy refractory | Cytoreductive Therapeutic procedure Unlikely
Item
patients must have pathologically documented acute myelogenous leukemia and either not be a candidate for myelosuppressive chemotherapy due to age or comorbid disease; or have relapsed acute myelogenous leukemia or be refractory to standard therapy and not likely to require cytoreductive therapy within 30 days.
boolean
C0023467 (UMLS CUI [1])
C1513793 (UMLS CUI [2,1])
C0392920 (UMLS CUI [2,2])
C0001779 (UMLS CUI [3])
C0009488 (UMLS CUI [4])
C0023467 (UMLS CUI [5,1])
C0035020 (UMLS CUI [5,2])
C2936643 (UMLS CUI [6,1])
C0205269 (UMLS CUI [6,2])
C0864494 (UMLS CUI [7,1])
C0087111 (UMLS CUI [7,2])
C0750558 (UMLS CUI [7,3])
ECOG performance status
Item
ecog performance status 0, 1 or 2
boolean
C1520224 (UMLS CUI [1])
Age
Item
age > 18 years
boolean
C0001779 (UMLS CUI [1])
Renal function | Liver function
Item
adequate kidney and hepatic function
boolean
C0232804 (UMLS CUI [1])
C0232741 (UMLS CUI [2])
Chemotherapy | Therapeutic radiology procedure | Immunotherapy | Steroid therapy Systemic | hydroxyurea
Item
greater than 4 weeks from any chemotherapy, radiotherapy, immunotherapy, or systemic steroid therapy with the exception of hydroxyurea.
boolean
C0392920 (UMLS CUI [1])
C1522449 (UMLS CUI [2])
C0021083 (UMLS CUI [3])
C0149783 (UMLS CUI [4,1])
C0205373 (UMLS CUI [4,2])
C0020402 (UMLS CUI [5])
Bone Marrow Transplantation | Peripheral Stem Cell Transplantation | Donor Lymphocyte Infusion
Item
greater than 2 months following bone marrow or peripheral blood stem cell transplantation or donor lymphocyte infusion.
boolean
C0005961 (UMLS CUI [1])
C0242602 (UMLS CUI [2])
C1512034 (UMLS CUI [3])
Item Group
C0680251 (UMLS CUI)
Communicable Disease Uncontrolled
Item
uncontrolled active infection
boolean
C0009450 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
Cytoreductive Chemotherapy Patient need for Urgent | Cytoreductive surgery Patient need for Urgent | Cytoreductive Therapeutic radiology procedure Patient need for Urgent
Item
urgent need for cytoreductive chemotherapy, surgery, or radiotherapy
boolean
C0864494 (UMLS CUI [1,1])
C0392920 (UMLS CUI [1,2])
C0686904 (UMLS CUI [1,3])
C0439609 (UMLS CUI [1,4])
C1112438 (UMLS CUI [2,1])
C0686904 (UMLS CUI [2,2])
C0439609 (UMLS CUI [2,3])
C0864494 (UMLS CUI [3,1])
C1522449 (UMLS CUI [3,2])
C0686904 (UMLS CUI [3,3])
C0439609 (UMLS CUI [3,4])
Chemotherapy
Item
current chemotherapy or chemotherapy within the last 4 weeks.
boolean
C0392920 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
pregnancy or nursing mothers
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
HIV Infection
Item
infection with hiv
boolean
C0019693 (UMLS CUI [1])