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Treatment of Relapsed Central Nervous System Lymphoma with High-Dose Methotrexate
Purpose: Over the past decade, high-dose methotrexate has emerged as the single most effective agent in the initial treatment of primary nervous system lymphoma. However, the majority of patients who respond initially to treatment relapse. The optimal management of these patients has not been determ...
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Published in: | Clinical cancer research 2004-09, Vol.10 (17), p.5643-5646 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Purpose: Over the past decade, high-dose methotrexate has emerged as the single most effective agent in the initial treatment of primary
nervous system lymphoma. However, the majority of patients who respond initially to treatment relapse. The optimal management
of these patients has not been determined. We performed a multicenter, retrospective study of high-dose methotrexate in patients
with relapsed central nervous system lymphoma.
Experimental Design: Patients with relapsed disease were eligible if they achieved a complete response to initial treatment with methotrexate-based
chemotherapy or received methotrexate after gross total resection or interstitial radiation. All of the patients were retreated
with a regimen containing high-dose methotrexate (≥3 g/m 2 ).
Results: Twenty-two patients with a median age of 58 years were included in the study. Overall response rates were 91% to first salvage
(20 of 22 patients) and 100% to second salvage (4 of 4 patients). Median survival was 61.9 months after first relapse (95%
confidence interval, 42.1–∞) and 91.9 months overall (95% confidence interval, 47.2–∞). Toxicity was primarily hematologic
with 10 episodes of grade 3 or 4 toxicity during 566 cycles of chemotherapy.
Conclusions: These results indicate that high-dose methotrexate remains effective for relapsed central nervous system lymphoma in patients
who initially respond to methotrexate and raise the possibility of deferring more toxic salvage regimens in this select group
of patients. |
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ISSN: | 1078-0432 1557-3265 |
DOI: | 10.1158/1078-0432.CCR-04-0159 |