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Combination of rituximab and methotrexate followed by rituximab and cytarabine in elderly patients with primary central nervous system lymphoma

Authors
Yi, Jun HoKim, Seok JinYang, Deok-HwanDo, Young RokWon, Jong HoBaek, DongwonShin, Ho JinKim, Dae SikKim, Hyo JungKang, Ka-wonBae, Sung HwaKwon, Ji-HyunKwon, Jung HyePark, Byeong BaeKim, Won Seog
Issue Date
5-Aug-2024
Publisher
WILEY
Keywords
cytarabine; elderly patients; methotrexate; primary central nervous system lymphoma; rituximab
Citation
BRITISH JOURNAL OF HAEMATOLOGY
Indexed
SCIE
SCOPUS
Journal Title
BRITISH JOURNAL OF HAEMATOLOGY
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/199464
DOI
10.1111/bjh.19659
ISSN
0007-1048
1365-2141
Abstract
The optimal treatment strategy for newly diagnosed primary central nervous system lymphoma (PCNSL) has yet to be established, especially in the elderly. In the current study, we conducted a phase II study to evaluate the efficacy and safety of rituximab plus high-dose MTX followed by rituximab plus cytarabine in patients aged >= 60 years newly diagnosed with PCNSL. Patients received an induction treatment of high-dose methotrexate plus rituximab followed by two cycles of a consolidation treatment of cytarabine plus rituximab. The primary end-point was a 2-year progression-free survival (PFS) rate. A total of 35 patients were recruited, and their median age was 73 (range: 60-81). After induction treatment, the complete and partial responses (PRs) were 56% and 20% respectively. Twenty-six patients proceeded to the consolidation treatment; the complete and PRs were 59% and 9% respectively. After a median follow-up duration of 36.0 months, the 2-year PFS rate was 58.7%. Treatment was generally well-tolerated as only three patients were withdrawn from the study due to toxicity, and no treatment-related mortality was reported. The 2-year overall survival rate was 77.9%. The current study may suggest the feasibility of administering high-dose MTX plus cytarabine in PCNSL patients aged >= 60 years and the potential role of additive rituximab.
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