Eligibility T-Cell Lymphoma NCT00161590

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients must have a diagnosis of non-b-cell, non-hodgkin's lymphoma (including t-cell, null-cell, or nk-cell lymphoma, but excluding lymphoblastic lymphoma)
Description

Lymphoma, Non-Hodgkin | T-Cell Lymphoma | NK-cell lymphoma | lymphoblastic lymphoma

Data type

boolean

Alias
UMLS CUI [1]
C0024305
UMLS CUI [2]
C0079772
UMLS CUI [3]
C3647364
UMLS CUI [4]
C0079748
stage ii, iii, or iv disease requiring chemotherapy
Description

Ann Arbor lymphoma staging system | Chemotherapy Patient need for

Data type

boolean

Alias
UMLS CUI [1]
C0432516
UMLS CUI [2,1]
C0392920
UMLS CUI [2,2]
C0686904
at least one site of measurable disease, 1.5 cm in diameter or greater
Description

Anatomic Site Quantity Measurable Disease | Diameter size

Data type

boolean

Alias
UMLS CUI [1,1]
C1515974
UMLS CUI [1,2]
C1265611
UMLS CUI [1,3]
C1513041
UMLS CUI [2,1]
C1301886
UMLS CUI [2,2]
C0456389
age > or = 18 years
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
absolute granulocyte count of at least 1500 cells/mm3, unless neutropenia is due to marrow infiltration by the tumor
Description

Absolute neutrophil count | Neutropenia Due to Bone marrow tumour cell infiltration

Data type

boolean

Alias
UMLS CUI [1]
C0948762
UMLS CUI [2,1]
C0027947
UMLS CUI [2,2]
C0678226
UMLS CUI [2,3]
C0877254
platelet count of at least 100,000 cells/mm3 unless thrombocytopenia is due to marrow infiltration by tumor
Description

Platelet Count measurement | Thrombocytopenia Due to Bone marrow tumour cell infiltration

Data type

boolean

Alias
UMLS CUI [1]
C0032181
UMLS CUI [2,1]
C0040034
UMLS CUI [2,2]
C0678226
UMLS CUI [2,3]
C0877254
creatinine less than 2 x upper limits of normal (uln)
Description

Creatinine measurement, serum

Data type

boolean

Alias
UMLS CUI [1]
C0201976
total bilirubin less than 2 x uln (dose reduced vincristine and adriamycin required for bilirubin > 1.2 mg/dl)
Description

Serum total bilirubin measurement | Vincristine Dose Reduced | Adriamycin Dose Reduced

Data type

boolean

Alias
UMLS CUI [1]
C1278039
UMLS CUI [2,1]
C0042679
UMLS CUI [2,2]
C1707814
UMLS CUI [3,1]
C0085752
UMLS CUI [3,2]
C1707814
echocardiogram (echo) or multiple gate acquisition scan (muga) documenting a normal ejection fraction prior to chemotherapy
Description

Ejection fraction normal Echocardiography | Multiple gated acquisition scanning | Chemotherapy

Data type

boolean

Alias
UMLS CUI [1,1]
C1535947
UMLS CUI [1,2]
C0013516
UMLS CUI [2]
C0521317
UMLS CUI [3]
C0392920
able to give informed consent
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
known central nervous system (cns) involvement
Description

Central Nervous System Involvement

Data type

boolean

Alias
UMLS CUI [1]
C4050309
known hiv disease
Description

HIV Infection

Data type

boolean

Alias
UMLS CUI [1]
C0019693
patients who are pregnant or nursing
Description

Pregnancy | Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
any factor which might limit the patient's ability to provide informed consent
Description

Informed Consent Ability Limited

Data type

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0085732
UMLS CUI [1,3]
C0439801
life expectancy < 3 months
Description

Life Expectancy

Data type

boolean

Alias
UMLS CUI [1]
C0023671
patients who are unwilling to agree to use an effective means of birth control while on treatment
Description

Contraceptive methods Unwilling

Data type

boolean

Alias
UMLS CUI [1,1]
C0700589
UMLS CUI [1,2]
C0558080

Similar models

Eligibility T-Cell Lymphoma NCT00161590

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Lymphoma, Non-Hodgkin | T-Cell Lymphoma | NK-cell lymphoma | lymphoblastic lymphoma
Item
patients must have a diagnosis of non-b-cell, non-hodgkin's lymphoma (including t-cell, null-cell, or nk-cell lymphoma, but excluding lymphoblastic lymphoma)
boolean
C0024305 (UMLS CUI [1])
C0079772 (UMLS CUI [2])
C3647364 (UMLS CUI [3])
C0079748 (UMLS CUI [4])
Ann Arbor lymphoma staging system | Chemotherapy Patient need for
Item
stage ii, iii, or iv disease requiring chemotherapy
boolean
C0432516 (UMLS CUI [1])
C0392920 (UMLS CUI [2,1])
C0686904 (UMLS CUI [2,2])
Anatomic Site Quantity Measurable Disease | Diameter size
Item
at least one site of measurable disease, 1.5 cm in diameter or greater
boolean
C1515974 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C1513041 (UMLS CUI [1,3])
C1301886 (UMLS CUI [2,1])
C0456389 (UMLS CUI [2,2])
Age
Item
age > or = 18 years
boolean
C0001779 (UMLS CUI [1])
Absolute neutrophil count | Neutropenia Due to Bone marrow tumour cell infiltration
Item
absolute granulocyte count of at least 1500 cells/mm3, unless neutropenia is due to marrow infiltration by the tumor
boolean
C0948762 (UMLS CUI [1])
C0027947 (UMLS CUI [2,1])
C0678226 (UMLS CUI [2,2])
C0877254 (UMLS CUI [2,3])
Platelet Count measurement | Thrombocytopenia Due to Bone marrow tumour cell infiltration
Item
platelet count of at least 100,000 cells/mm3 unless thrombocytopenia is due to marrow infiltration by tumor
boolean
C0032181 (UMLS CUI [1])
C0040034 (UMLS CUI [2,1])
C0678226 (UMLS CUI [2,2])
C0877254 (UMLS CUI [2,3])
Creatinine measurement, serum
Item
creatinine less than 2 x upper limits of normal (uln)
boolean
C0201976 (UMLS CUI [1])
Serum total bilirubin measurement | Vincristine Dose Reduced | Adriamycin Dose Reduced
Item
total bilirubin less than 2 x uln (dose reduced vincristine and adriamycin required for bilirubin > 1.2 mg/dl)
boolean
C1278039 (UMLS CUI [1])
C0042679 (UMLS CUI [2,1])
C1707814 (UMLS CUI [2,2])
C0085752 (UMLS CUI [3,1])
C1707814 (UMLS CUI [3,2])
Ejection fraction normal Echocardiography | Multiple gated acquisition scanning | Chemotherapy
Item
echocardiogram (echo) or multiple gate acquisition scan (muga) documenting a normal ejection fraction prior to chemotherapy
boolean
C1535947 (UMLS CUI [1,1])
C0013516 (UMLS CUI [1,2])
C0521317 (UMLS CUI [2])
C0392920 (UMLS CUI [3])
Informed Consent
Item
able to give informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Central Nervous System Involvement
Item
known central nervous system (cns) involvement
boolean
C4050309 (UMLS CUI [1])
HIV Infection
Item
known hiv disease
boolean
C0019693 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
patients who are pregnant or nursing
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Informed Consent Ability Limited
Item
any factor which might limit the patient's ability to provide informed consent
boolean
C0021430 (UMLS CUI [1,1])
C0085732 (UMLS CUI [1,2])
C0439801 (UMLS CUI [1,3])
Life Expectancy
Item
life expectancy < 3 months
boolean
C0023671 (UMLS CUI [1])
Contraceptive methods Unwilling
Item
patients who are unwilling to agree to use an effective means of birth control while on treatment
boolean
C0700589 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])