Consecutive single-institution case series of primary central nervous system lymphoma treated by R-MPV or high-dose methotrexate monotherapy

Author:

Sasaki Nobuyoshi123,Kobayashi Keiichi4,Saito Kuniaki4,Shimizu Saki4,Suzuki Kaori4,Lee Jeunghun5,Yamagishi Yuki12,Shibahara Junji6,Takayama Nobuyuki7,Shiokawa Yoshiaki4,Nagane Motoo4ORCID

Affiliation:

1. Department of Neurosurgery, Kyorin University Graduate School of Medicine, Tokyo, Japan

2. Department of Brain Tumor Translational Research, National Cancer Center Research Institute, Tokyo, Japan

3. Department of Neurosurgery, Koyama Memorial Hospital, Kashima, Japan

4. Department of Neurosurgery, Kyorin University Faculty of Medicine, Tokyo, Japan

5. Department of Neurosurgery, Kanto Central Hospital, Tokyo, Japan

6. Department of Pathology, Kyorin University Faculty of Medicine, Tokyo, Japan

7. Department of Hematology, Kyorin University Faculty of Medicine, Tokyo, Japan

Abstract

Abstract Objective The optimal regimen for use of high dose-methotrexate-based chemotherapy in primary central nervous system lymphoma is still under debate. We conducted a retrospective study to evaluate the treatment outcome of a combination immunochemotherapy consisting of rituximab, methotrexate, procarbazine and vincristine followed by with or without whole brain radiotherapy and consolidation cytarabine, in comparison with high dose-methotrexate monotherapy followed by full dose whole brain radiotherapy. Methods Newly diagnosed primary central nervous system lymphoma patients treated with either rituximab, methotrexate, procarbazine and vincristine or high dose-methotrexate in Kyorin University Hospital were identified, and the response rates and survival were compared. Toxicities, post-treatment transition of Mini-Mental State Examination, Karnofsky performance status score, Fazekas scale and prognostic factors were analysed in the rituximab, methotrexate, procarbazine and vincristine group. Results Ninety-five patients treated with rituximab, methotrexate, procarbazine and vincristine (n = 39) or high dose-methotrexate (n = 56) were analysed. The complete response/complete response unconfirmed rate was significantly higher in the rituximab, methotrexate, procarbazine and vincristine group (74.4 vs. 15.4%, P < 0.001). Accordingly, both median progression-free survival and overall survival were significantly longer in the rituximab, methotrexate, procarbazine and vincristine group (median progression-free survival: unreached vs. 14.75 months, P < 0.001) (median overall survival: unreached vs. 63.15 months, P = 0.005). Although the rate of grade 3/4 hematologic toxicities was high both during rituximab, methotrexate, procarbazine and vincristine and consolidation cytarabine, the rate of grade 3/4 infections was low, and no treatment related deaths were observed. Deterioration in Karnofsky performance status or Mini-Mental State Examination was rare, except on disease recurrence. Although whole brain radiotherapy was associated with Fazekas scale deterioration, its association with Karnofsky performance status or Mini-Mental State Examination deterioration was not significant. Conclusions Rituximab, methotrexate, procarbazine and vincristine was apparently promising in comparison with high dose-methotrexate monotherapy with manageable toxicity in this retrospective study, and further investigation is warranted.

Funder

Grant-in-Aid for Scientific Research

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Radiology Nuclear Medicine and imaging,Oncology,General Medicine

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