Clinical Trial Eligibility Criteria Fulfill
Item
to be included in this study, you must meet the following criteria:
boolean
C1516637 (UMLS CUI [1,1])
C1550543 (UMLS CUI [1,2])
Intermediate Grade B-Cell Non-Hodgkin's Lymphoma positive for CD20 antigen
Item
intermediate grade cd20-positive b-cell non-hodgkin's lymphoma
boolean
C1512858 (UMLS CUI [1,1])
C0882818 (UMLS CUI [1,2])
Chemotherapy Regimen Quantity | Lymphoma persistent
Item
persistent lymphoma after one or two previous chemotherapy regimens
boolean
C0392920 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0024299 (UMLS CUI [2,1])
C0205322 (UMLS CUI [2,2])
Indication high-dose chemotherapy
Item
patients should not be considered candidates for high-dose chemotherapy
boolean
C3146298 (UMLS CUI [1,1])
C1328050 (UMLS CUI [1,2])
Ability to perform activities of everyday life Assisted
Item
ability to perform activities of daily living with assistance
boolean
C0562507 (UMLS CUI [1,1])
C1269765 (UMLS CUI [1,2])
Measurable Disease | Evaluable Disease
Item
measurable or evaluable disease
boolean
C1513041 (UMLS CUI [1])
C1516986 (UMLS CUI [2])
Age
Item
age > 18 years
boolean
C0001779 (UMLS CUI [1])
Bone Marrow function | Liver function | Renal function
Item
adequate bone marrow, liver and kidney function
boolean
C0005953 (UMLS CUI [1,1])
C0031843 (UMLS CUI [1,2])
C0232741 (UMLS CUI [2])
C0232804 (UMLS CUI [3])
Clinical Trial Eligibility Criteria Fulfill
Item
you cannot participate in this study if any of the following apply to you:
boolean
C1516637 (UMLS CUI [1,1])
C1550543 (UMLS CUI [1,2])
Few mature neutrophils in the bone marrow
Item
patients with impaired bone marrow reserve
boolean
C2748959 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
female patients who are pregnant or lactating
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Communicable Disease Serious
Item
serious active infection at the time of treatment
boolean
C0009450 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
Comorbidity Serious
Item
any other serious underlying condition
boolean
C0009488 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
Primary cerebral lymphoma | Meningeal Lymphoma
Item
brain or meningeal) with lymphoma
boolean
C0240803 (UMLS CUI [1])
C2213017 (UMLS CUI [2])
lymphoma; resulting from HIV disease | Lymphoma, AIDS-Related
Item
hiv or aids-related lymphoma
boolean
C1399703 (UMLS CUI [1])
C0085090 (UMLS CUI [2])
External Beam Radiation Therapy Bone Marrow Percentage
Item
received external beam radiation therapy to > 25% of active bone marrow.
boolean
C1517033 (UMLS CUI [1,1])
C0005953 (UMLS CUI [1,2])
C0439165 (UMLS CUI [1,3])
Malignant Neoplasms | Malignant Neoplasms Treated
Item
history of other cancers, either active or treated
boolean
C0006826 (UMLS CUI [1])
C0006826 (UMLS CUI [2,1])
C1522326 (UMLS CUI [2,2])
Clinical Trial Eligibility Criteria Additional
Item
please note: there are additional inclusion/exclusion criteria. the study center will determine if you meet all of the criteria. if you do not qualify for the trial, study personnel will explain the reasons. if you do qualify, study personnel will explain the trial in detail and answer any questions you may have.
boolean
C1516637 (UMLS CUI [1,1])
C1524062 (UMLS CUI [1,2])