Chemotherapy and Whole-Brain Radiation Therapy in Treating Patients With Primary Central Nervous System Non- Hodgkin's Lymphoma
Status: | Completed |
---|---|
Conditions: | Lymphoma, Lymphoma |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - 70 |
Updated: | 4/21/2016 |
Start Date: | July 1995 |
End Date: | October 2006 |
PHASE II TRIAL OF CHEMOTHERAPY PLUS RADIOTHERAPY FOR MANAGEMENT OF PRIMARY CENTRAL NERVOUS SYSTEM NON-HODGKIN'S LYMPHOMA (PCNSL)
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing
so they stop growing or die. Radiation therapy uses high-energy x-rays to damage tumor
cells. Combining radiation therapy with chemotherapy may kill more tumor cells and may be an
effective treatment for non-Hodgkin's lymphoma.
PURPOSE: Phase II trial to study the effectiveness of combination chemotherapy and
whole-brain radiation therapy in patients with primary central nervous system non-Hodgkin's
lymphoma.
so they stop growing or die. Radiation therapy uses high-energy x-rays to damage tumor
cells. Combining radiation therapy with chemotherapy may kill more tumor cells and may be an
effective treatment for non-Hodgkin's lymphoma.
PURPOSE: Phase II trial to study the effectiveness of combination chemotherapy and
whole-brain radiation therapy in patients with primary central nervous system non-Hodgkin's
lymphoma.
OBJECTIVES: I. Assess the response to CHOD (cyclophosphamide/doxorubicin/vincristine/
dexamethasone) and BVAM (carmustine/vincristine/cytarabine/methotrexate) plus whole-brain
radiotherapy in patients with primary central nervous system non-Hodgkin's lymphoma (PCNSL).
II. Assess the toxic effects associated with this treatment. III. Assess the survival of
patients with PCNSL receiving this treatment. IV. Investigate the frequency of systemic
involvement at follow-up. V. Identify factors that appear to be associated with outcome.
dexamethasone) and BVAM (carmustine/vincristine/cytarabine/methotrexate) plus whole-brain
radiotherapy in patients with primary central nervous system non-Hodgkin's lymphoma (PCNSL).
II. Assess the toxic effects associated with this treatment. III. Assess the survival of
patients with PCNSL receiving this treatment. IV. Investigate the frequency of systemic
involvement at follow-up. V. Identify factors that appear to be associated with outcome.
DISEASE CHARACTERISTICS: Primary central nervous system non-Hodgkin's lymphoma (PCNSL)
Clinically diagnosed intracranial space-occupying lesion Pathology consistent with
non-Hodgkin's lymphoma and reviewed by NCCTG Biopsy optional if characteristic history,
pathognomonic neuroimaging, and cytology are consistent with malignant lymphocytes from
vitrectomy, CSF, or both No occult systemic lymphoma or prior lymphoma No post-transplant
lymphoproliferative disorder Disease measurable or evaluable on postoperative
contrast-enhanced CT or MRI Postoperative therapy must start within 6 weeks of definitive
diagnosis
PATIENT CHARACTERISTICS: Age: 18 to 70 Performance status: ECOG 0-3 Hematopoietic: WBC at
least 4,000/mm3 Platelet count at least 120,000/mm3 Hepatic: Bilirubin no greater than 2
times normal AST no greater than 2 times normal Renal: Creatinine no greater than 1.5
times normal Cardiovascular: No heart failure No uncontrolled arrhythmia Pulmonary: No
severe pulmonary failure Other: No serious uncontrolled infection No active bleeding No
AIDS or HIV-positive serology No prior organ transplant No pregnant or nursing women
Negative pregnancy test required of fertile women Adequate contraception required of
fertile patients
PRIOR CONCURRENT THERAPY: Biologic therapy: Not specified Chemotherapy: No prior
chemotherapy Endocrine therapy: Corticosteroids allowed if dose fixed or decreasing for at
least 1 week prior to baseline scan Radiotherapy: No prior radiotherapy Surgery: Not
specified
We found this trial at
21
sites
300 East Locust St., Ste 350
Des Moines, Iowa 50309
Des Moines, Iowa 50309
(515) 244-7586
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