Long-term outcomes of rituximab, temozolomide and high-dose methotrexate without consolidation therapy for lymphoma involving the CNS

Author:

Nagle Sarah J1,Shah Nirav N2,Ganetsky Alex3,Landsburg Daniel J1,Nasta Sunita D1,Mato Anthony1,Schuster Stephen J1,Reshef Ran4,Tsai Donald E1,Svoboda Jakub1

Affiliation:

1. Lymphoma Program, Abramson Cancer Center, University of Pennsylvania, Perelman Center for Advanced Medicine, 3400 Civic Center Blvd, 2 West Pavilion, Philadelphia, PA 19104, USA

2. Medical College of Wisconsin, 9200 W. Wisconsin Ave, Milwaukee, WI 53226, USA

3. Department of Pharmacy, Hospital of the University of Pennsylvania, 3400 Spruce Street, Philadelphia, PA 19104, USA

4. Division of Hematology/Oncology & the Columbia Center for Translational Immunology, Department of Medicine, Columbia University Medical Center, New York, NY 10032, USA

Abstract

Aim: To describe the long-term outcomes of patients with lymphoma in the CNS treated with rituximab, temozolomide and high-dose methotrexate without consolidation therapy. Patients & methods: A retrospective cohort study of 46 consecutive patients with primary CNS lymphoma (PCNSL, 27 patients) or secondary CNS involvement of diffuse large B-cell lymphoma (DLBCL, 19 patients) who were treated with rituximab on day 1 in combination with high-dose methotrexate (days 1 and 15) and temozolomide (days 1–5) in 28-day cycles without further consolidation. Results: Median follow-up was 21.2 months. Patients received a median of five cycles (range 1–15). Median overall survival (OS) was 26 months and median progression-free survival was 8.6 months. At 3 years, 37% of patients were alive and without evidence of disease. The patients with PCNSL had a significantly higher response rates (ORR 81 vs 47%; p = 0.015) and longer median OS (55.3 vs 4.8 months; p < 0.01) than those with secondary CNS DLBCL. Toxicities were mild and manageable. Conclusion: The rituximab, temozolomide and methotrexate regimen is an effective therapy for patients with PCNSL without the toxicities typically associated with consolidation therapy.

Publisher

Future Medicine Ltd

Subject

Pharmacology (medical),Oncology,Hematology

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