Trial Search Results

Rituximab in Treating Patients With Low Tumor Burden Indolent Non-Hodgkin's Lymphoma

RATIONALE: Monoclonal antibodies such as rituximab can locate cancer cells and either kill them or deliver cancer-killing substances to them without harming normal cells. It is not yet known which rituximab regimen is more effective in treating indolent non-Hodgkin's lymphoma.

PURPOSE: This randomized phase III trial is studying two different schedules of rituximab and comparing them to see how well they work in treating patients with low tumor burden indolent stage III non-Hodgkin's lymphoma or stage IV non-Hodgkin's lymphoma.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

Eastern Cooperative Oncology Group

Collaborator: National Cancer Institute (NCI)

Stanford Investigator(s):

Intervention(s):

  • Biological: rituximab

Phase:

Phase 3

Eligibility


INCLUSION CRITERIA:

   - Histologically confirmed non-Hodgkin's lymphoma, including 1 of the following:

      - Follicular grade 1 or 2

      - Small lymphocytic

      - Marginal zone (nodal)

      - Marginal zone (splenic)

      - Mucosa-associated lymphoid tissue (MALT)

   - Stage III or IV disease

   - Must meet the following criteria for low tumor burden:

      - No nodal or extranodal mass at least 7 cm

      - Less than 3 nodal masses greater than 3 cm in diameter

      - No systemic symptoms or B symptoms

      - No splenomegaly greater than 16 cm by a computed tomography (CT) scan

      - No evidence of risk of compression of a vital organ (i.e., ureteral or epidural)

      - No leukemic phase with greater than 5,000/mm^3 circulating lymphocytes

      - No cytopenias, defined as any of the following:

         - Platelet count less than 100,000/mm^3

         - Hemoglobin less than 10 g/dL

         - Absolute neutrophil count less than 1,500/mm^3

   - At least 1 objective measurable disease parameter

      - Abnormal positron emission tomography (PET) scans will not constitute evaluable
      disease unless verified by CT scan or other appropriate imaging

   - Age: 18 and over

   - Eastern Cooperative Oncology Group (ECOG) performance status 0-1

   - Must meet the following criteria for labs:

      - Hematopoietic

         - Absolute neutrophil count at least 1,500/mm^3*

         - Hemoglobin at least 10 g/dL*

         - Platelet count at least 100,000/mm^3*

         - NOTE: *Without growth factor and/or transfusion support

      - Hepatic

         - Bilirubin no greater than 2 times upper limit of normal (ULN) OR direct
         bilirubin normal for patients with Gilbert's Syndrome

         - The aspartate transaminase (AST) and alanine transaminase (ALT) ratio
         (AST/ALT) no greater than 5 times ULN

         - Hepatitis B surface antigen negative

      - Renal

         - Creatinine no greater than 2 times ULN

EXCLUSION CRITERIA:

   - Evidence of transformation to a large cell histology

   - Pregnant or nursing. Fertile patients must use effective contraception

   - HIV positive

   - Uncontrolled active infection

   - Other malignancy within the past 2 years except adequately treated basal cell or
   squamous cell skin cancer or carcinoma in situ of the cervix

   - Prior immunotherapy for lymphoma

   - Prior chemotherapy for lymphoma

   - Concurrent chemotherapy

   - Prior radiotherapy for lymphoma

   - Concurrent radiotherapy

   - Concurrent radioimmunotherapy

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

All

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Cancer Clinical Trials Office
6504987061
Not Recruiting