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Rituximab Anti-CD20 Monoclonal Antibody and Dexamethasone in the Treatment of Relapsed Indolent Lymphoma (NCT00003663)

Cancer Biotherapy Research Group
RATIONALE: Monoclonal antibodies can locate tumor cells and either kill them or deliver tumor-killing substances to them without harming normal cells. Combining the monoclonal antibody rituximab with dexamethasone may kill more cancer cells. PURPOSE: Phase II trial to study the effectiveness of rituximab and dexamethasone in treating patients with recurrent or refractory indolent non-Hodgkin's lymphoma.
  • Biological: rituximab
    • Drug: dexamethasone
      Ages eligible for Study
      18 Years and older
      Genders eligible for Study
      All
      Accepts Healthy Volunteers
      No
      OBJECTIVES: I. Determine the toxic effects of rituximab and dexamethasone in patients with recurrent or refractory indolent non-Hodgkin's lymphoma. II. Determine the objective tumor response rate and duration of response at 2 months after initiation of therapy, and the percentage of patients with progressive disease. III. Determine the maximum response, duration of response, and progression free interval for patients who have not progressed after 4 weeks of therapy. IV. Determine the failure-free and overall survival of these patients on this regimen. V. Compare the response rate and survival rates to results for similar patients (historical and concurrent) who have received 4 weeks of rituximab without dexamethasone, and patients who did not receive maintenance rituximab.

      OUTLINE: Patients receive dexamethasone IV followed by rituximab IV on days 1, 8, 15, and 22 for one course. Two months after initiating treatment, patients are evaluated for disease progression. Patients with stable or responding disease may receive monthly dexamethasone and rituximab therapy for up to 10 additional months. Patients are followed every 3 months for 2 years, then every 6 months for years 3-4, and then yearly for up to 5 years.

      PROJECTED ACCRUAL: A total of 20-40 patients will be accrued for this study.

      3 locations

      United States (3)
      • Hoag Memorial Hospital Presbyterian
        Not specified
        Newport Beach, California, United States, 92658
      • Cancer Care Center for Southern Indiana
        Not specified
        Bloomington, Indiana, United States, 47403
      • St. Joseph Regional Cancer Center
        Not specified
        Bryan, Texas, United States, 77802
      Status:
      withdrawn
      Type:
      Interventional
      Phase:
      Start:
      31 May, 1998
      Updated:
      16 August, 2015
      Participants:
      0
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