Rituximab, methotrexate, procarbazine and lomustine (R-MPL) for the treatment of primary Central nervous system lymphoma

  • Eyal Lebel*
  • , Neta Goldschmidt
  • , Tali Siegal
  • , Alexander Lossos
  • , Shai Rosenberg
  • , Chen Makranz
  • , Eduard Linetski
  • , Moshe E. Gatt
  • , Alexander Gural
  • , Revital Saban
  • , David Lavie
  • , Vladimir Vainstein
  • , Eran Zimran
  • , Batia Avni
  • , Sigal Grisaro
  • , Adir Shaulov
  • , Boaz Nachmias
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

3 Scopus citations

Abstract

The optimal high-dose methotrexate (HDMTX)-based combination therapy for primary central nervous system lymphoma is unknown. We report our experience with rituximab, HDMTX, procarbazine and lomustine (R-MPL) given as first-line treatment in our center. Fifty-two patients between 2006 and 2019 were included. Eighteen patients proceeded to autologous transplant or two cycles of intermediate-dose cytarabine. The median age was 62 y (range 28–94) and the Eastern Cooperative Oncology Group performance status (ECOG-PS) was ≥2 in 62% (32/52). The overall/complete response rates were 79% (41/52) and 52% (27/52), respectively. The median progression-free/overall survival was 19 m/84m, respectively. Grade 3–4 adverse events included infections (17%) and kidney injury (13%). Ten patients (19%) discontinued therapy for toxicity. There were no treatment-related deaths. In summary, in a cohort enriched in frail patients, R-MPL achieved good responses and OS and was safe for all ages. The PFS was sub-optimal, possibly explained by a low proportion of consolidation. This regimen should be evaluated prospectively.

Original languageEnglish
Pages (from-to)2102-2108
Number of pages7
JournalLeukemia and Lymphoma
Volume63
Issue number9
DOIs
StatePublished - Sep 2022

Bibliographical note

Publisher Copyright:
© 2022 Informa UK Limited, trading as Taylor & Francis Group.

Keywords

  • Primary CNS lymphoma
  • lomustine
  • methotrexate
  • procarbazine

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