Evidence map›Paper›PMID 41906256›Full record

ArticleCancer medicine2026

Nationwide Incidence, Treatment Pattern, and Prognosis of Primary CNS Lymphoma in Taiwan, 2012-2020: A Retrospective Cohort Study.

Fei-Yuan Hsiao, Hung-Yu Lin, Ho-Min Chen, Wan-Hsuan Hsu, Bor-Sheng Ko

Abstract read
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Article in Cancer medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Fei-Yuan HsiaoGraduate Institute of Clinical Pharmacy, College of Medicine, National Taiwan University, Taipei, Taiwan.ORCID https://orcid.org/0000-0003-1660-9120
Hung-Yu LinSchool of Pharmacy, College of Medicine, National Taiwan University, Taipei, Taiwan.
Ho-Min ChenHealth Data Research Center, National Taiwan University, Taipei, Taiwan.
Wan-Hsuan HsuDepartment of Medical Affairs, Ono Pharma Taiwan Co., Ltd., Taipei, Taiwan.
Bor-Sheng KoDivision of Hematology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.

Funding

Ono Pharmaceutical
6 · The paper itself

Abstract

backgroundPrimary central nervous system lymphoma (PCNSL) is a rare but devastating form of non-Hodgkin lymphoma with persistently poor outcomes despite treatment advances. This nationwide population-based study evaluated real-world epidemiology, treatment patterns, and survival outcomes in Asian PCNSL patients.

methodsPatients with newly diagnosed PCNSL (2012-2020) were identified from the Taiwan Cancer Registry Database and linked with the National Health Insurance Research Database. Incidence, treatment patterns, survival outcomes, healthcare costs, and adverse events were analyzed for identified PCNSL patients. Specifically, median survival times (MSTs), with 95% confidence intervals (CIs), were estimated using the Kaplan-Meier method.

resultsAmong 820 PCNSL patients (median age 65 [IQR 56-74] years; 53.5% male; 94.4% DLBCL subtype), age-standardized incidence was 0.39 per 100,000 person-years (2012-2020) with male predominance (0.44 vs. 0.34) and elderly burden (1.62 in ≥ 75 years vs. 0.28 in < 65 years). Despite 89.5% receiving induction therapy within median 24 days, outcomes remained poor: median survival 1.85 (95% CI 1.53-2.27) years, with 1-, 2-, and 3-year survival rates of 61.5%, 48.3%, and 40.2%, respectively. All-cause survival deteriorated markedly with age-median survival of 5.71, 3.29, 2.32, 0.97, and 0.69 years for ages < 50, 50-59, 60-69, 70-79, and ≥ 80 years, respectively. MTX-based chemotherapy with rituximab adoption increased (22.2% to 55.3%), achieving superior survival (3.44 years) versus WBRT alone (1.24 years). However, 46.2% developed relapsed/refractory disease at median 156 (89-339) days. Consolidation therapy was administered in 52.5% at median 53 days post-induction. Infection (87.9%), nausea/vomiting (81.1%), and neutropenia (54.4%) dominated adverse events, with first-year costs averaging $35,472 (SD $20,816) USD.

conclusionPCNSL demonstrates persistently poor prognosis, with elderly patients experiencing disproportionately worse outcomes. High relapse rates, substantial treatment-related adverse events, and considerable healthcare burden underscore the urgent need for novel therapeutic approaches.

Indexed as

Central Nervous System NeoplasmsLymphoma, Non-HodgkinAgedAntineoplastic Combined Chemotherapy ProtocolsFemaleHumansIncidenceMaleMiddle AgedPrognosisRegistriesRetrospective StudiesTaiwan

Identifiers

PMID41906256
PMCPMC13140827

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