Trial Search Results

Rituximab, Combination Chemotherapy, and 90-Yttrium Ibritumomab Tiuxetan for Patients With Stage I or II Non-Hodgkin's Lymphoma

This phase II trial is studying how well giving rituximab together with combination chemotherapy and 90-Yttrium ibritumomab tiuxetan works in treating patients with stage I or stage II lymphoma. Drugs used in chemotherapy, such as prednisone, cyclophosphamide, doxorubicin, and vincristine, work in different ways to stop cancer cells from dividing so they stop growing or die. Monoclonal antibodies such as rituximab and yttrium 90-Yttrium ibritumomab tiuxetan can locate cancer cells and either kill them or deliver radioactive cancer-killing substances to them without harming normal cells. Combining a monoclonal antibody with combination chemotherapy and a radiolabeled monoclonal antibody may kill more cancer cells.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

National Cancer Institute (NCI)


  • Biological: rituximab
  • Drug: prednisone
  • Drug: cyclophosphamide
  • Drug: doxorubicin
  • Drug: vincristine
  • Radiation: indium In 111 ibritumomab tiuxetan
  • Radiation: radiation therapy
  • Procedure: positron emission tomography


Phase 2


Inclusion Criteria:

   - Patients must have histologically confirmed diagnosis of diffuse large cell lymphoma

   - Patients must be stage I or II (Modified Ann Arbor staging)

   - Baseline measurements and evaluations must be obtained within 4 weeks of registration
   to the study; abnormal PET scans will not constitute evaluable disease unless verified
   by CT scan or other appropriate imaging; patients must have at least one objective
   measurable disease parameter (a lesion with at least 1 dimension > 1.5 cm); or if they
   are stage 1

   - Stage I patients must have at least one of the following risk factors:

      - Age >= 60 years

      - Bulky disease (>= 5 cm in at least one dimension)

      - Elevated Lactate Dehydrogenase (LDH) above institutional upper limit of normal

      - Eastern Cooperative Oncology Group (ECOG) performance status = 2

   - Eastern Cooperative Oncology Group (ECOG) performance status 0-2

   - Absolute neutrophil count >= 1500/mm^3 (includes neutrophils and bands)

   - Platelet count >= 100,000/mm^3

   - Creatinine < 2.0 mg/dl

   - Total bilirubin < 2 mg/dl (may be up to 3.0 mg/dl if due to liver involvement by
   lymphoma); patients with elevated total bilirubin should have a direct bilirubin
   checked; if the direct bilirubin is normal there is no need for a dose reduction

   - Patients must have left ventricular ejection fraction (LVEF) of > 45%

   - Patients must be tested for hepatitis B (HBV) surface antigen within 2 weeks of

      - NOTE: Patients who test positive will be allowed to participate but must be
      followed closely for clinical and laboratory signs of active HBV infection and
      for signs of hepatitis

Exclusion Criteria:

   - Prior chemotherapy, radiation therapy, radioimmunotherapy, or immunotherapy; a short
   course (=< 14 days prior to registration) of corticosteroids is allowed

   - Evidence of other malignancy:

      - Prior chemotherapy or prior radiation therapy for other malignancies

      - Currently receiving hormone therapy or chemotherapy for another malignancy even
      if the treatment is being provided in the adjuvant treatment setting, i.e. with
      no evidence of the original other malignancy

      - Adjuvant hormonal therapy must have been discontinued > 3 months before entering
      this study

      - Patients are eligible if they meet the following conditions: (a) treated
      carcinoma-in-situ of the cervix; (b) treated squamous cell or basal cell skin
      cancer; or (c) any other surgically cured malignancy from which the patient has
      been disease free for at least 3 years

   - Pregnant or breast feeding, as there would be radiation exposure to the fetus or
   child; a negative pregnancy test is required =< 1 week prior to registration for women
   of childbearing potential (WOCBP). Women of childbearing potential and sexually active
   males must be strongly advised to use an accepted and effective method of

   - Known central nervous system (CNS) lymphoma, testicular lymphoma, or vitreous lymphoma

   - Known HIV infection. The safety of Zevalin™ in this population has not been tested at
   this time

   - Serious coexisting medical condition or active infection which would compromise the
   ability to deliver standard R-CHOP chemotherapy

   - Evidence of myelodysplasia on bone marrow aspiration and biopsy

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study


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
Not Recruiting