Important note: Information in this article was accurate in 1994. The state of the art may have changed since the publication date.
Preirradiation chemotherapy (CTX) with cytoxan, Adriamycin, vincristine, and decadron (CHOD) for primary CNS lymphomas (PCNSL): initial report of Radiation Therapy Oncology Group (RTOG) protocol 88-06 (Meeting abstract).
Proc Annu Meet Am Soc Clin Oncol; 13:A485 1994. Unique Identifier : AIDSLINE ICDB/94600481 Schultz C; Scott C; Wasserman T; Fisher B; Abrams R; Sherman W; Fetell M; Nelson J; No affiliation given
Abstract:
From 1988 to 1992, a prospective Phase I/II trial was carried out by the RTOG to test the tolerance and efficacy of preirradiation (RT) CHOD CTX followed by large vol, high-dose brain RT for patients (pts) with PCNSL. Fifty-four (51 evaluable) HIV-negative pts with PCNSL were entered and received 2 (19 pts) or 3 (32 pts) cycles of CHOD (6 pts with positive CSF cytology received intrathecal methotrexate in addition to CHOD). Whole brain RT to 41.4 Gy and tumor boost to 18 Gy (total dose 59.4 Gy) followed CTX. Grade 4 neutropenia during CTX developed in 28/51 pts. Worst toxicity during RT was less than or equal to grade 2 for all but 2 pts. There was 1 septic death. One pt died of encephalomalacia 3 mo following RT. All pts were potentially followed for 1 yr. Survival from registration was calculated using the Kaplan-Meier technique. Survival compared to RTOG 83-15 (IJROBP 23:9-17, 1992), which tested RT alone to 59.4 Gy, is given in a table. Age remains a powerful prognostic factor for pts with PCNSL independent of therapy. These early results suggest that the rate of 2-yr survival is increased with pre-RT CHOD CTX compared to RT alone, particularly for pts less than 60 yr of age.
Keywords: Antineoplastic Agents, Combined/ADVERSE EFFECTS/*THERAPEUTIC USE Brain Neoplasms/DRUG THERAPY/MORTALITY/*RADIOTHERAPY Combined Modality Therapy Cranial Irradiation Female Follow-Up Studies Human Lymphoma/DRUG THERAPY/MORTALITY/*RADIOTHERAPY Male Middle Age Prospective Studies Radiotherapy Dosage Survival Analysis Survival Rate ABSTRACT CLINICAL TRIAL, PHASE I CLINICAL TRIAL, PHASE II CLINICAL TRIAL 941030
M94A0893
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