Evidence map›Paper›PMID 40166831›Full record

ArticleCancer medicine2025

Central Nervous System Prophylaxis Approach in High-Risk Diffuse Large B-Cell Lymphoma Patients: A Retrospectively Collected, Single-Center Cohort Analysis.

Yanli Wang, Xiaolian Wen, Tao Guan, Hongwei Zhang, Wei'e Han, Min Bai, Xiaolan Liu, Min Zhang, Liping Su, Weihua Zhang

Abstract read
In one paragraph

Article in Cancer medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

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0 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

10 authors.

Yanli WangShanxi Medical University Affiliated Cancer Hospital/Shanxi Provincial Cancer Hospital/Chinese Academy of Medical Sciences Cancer Hospital Affiliated Shanxi Hospital, Hematology Department, Taiyuan, China.
Xiaolian WenShanxi Medical University Affiliated Cancer Hospital/Shanxi Provincial Cancer Hospital/Chinese Academy of Medical Sciences Cancer Hospital Affiliated Shanxi Hospital, Hematology Department, Taiyuan, China.
Tao GuanShanxi Medical University Affiliated Cancer Hospital/Shanxi Provincial Cancer Hospital/Chinese Academy of Medical Sciences Cancer Hospital Affiliated Shanxi Hospital, Hematology Department, Taiyuan, China.
Hongwei ZhangShanxi Medical University Affiliated Cancer Hospital/Shanxi Provincial Cancer Hospital/Chinese Academy of Medical Sciences Cancer Hospital Affiliated Shanxi Hospital, Hematology Department, Taiyuan, China.ORCID https://orcid.org/0000-0002-6819-5225
Wei'e HanShanxi Medical University Affiliated Cancer Hospital/Shanxi Provincial Cancer Hospital/Chinese Academy of Medical Sciences Cancer Hospital Affiliated Shanxi Hospital, Hematology Department, Taiyuan, China.
Min BaiShanxi Medical University Affiliated Cancer Hospital/Shanxi Provincial Cancer Hospital/Chinese Academy of Medical Sciences Cancer Hospital Affiliated Shanxi Hospital, Hematology Department, Taiyuan, China.
Xiaolan LiuShanxi Medical University Affiliated Cancer Hospital/Shanxi Provincial Cancer Hospital/Chinese Academy of Medical Sciences Cancer Hospital Affiliated Shanxi Hospital, Hematology Department, Taiyuan, China.
Min ZhangShanxi Medical University Affiliated Cancer Hospital/Shanxi Provincial Cancer Hospital/Chinese Academy of Medical Sciences Cancer Hospital Affiliated Shanxi Hospital, Hematology Department, Taiyuan, China.
Liping SuShanxi Medical University Affiliated Cancer Hospital/Shanxi Provincial Cancer Hospital/Chinese Academy of Medical Sciences Cancer Hospital Affiliated Shanxi Hospital, Hematology Department, Taiyuan, China.
Weihua ZhangFirst Hospital of Shanxi Medical University, Taiyuan, China.

Funding

Beijing Xisike Clinical Oncology Research Foundation Y-HR2019-0456
6 · The paper itself

Abstract

objectivesRecent advances in the prevention of diffuse large B-cell lymphoma (DLBCL) have considerably focused on optimal strategies for preventing its recurrence in the central nervous system (CNS) in patients. This retrospective study aimed to assess the protective efficacy of intravenous high-dose methotrexate (HD-MTX) regimens in newly diagnosed patients with DLBCL presenting a high risk for CNS recurrence.

methodsA total of 136 newly diagnosed high-risk DLBCL patients (HD-MTX group: n = 46; non-HD-MTX group: n = 90) were enrolled in this retrospective study. The primary endpoints included CNS recurrence rate, progression-free survival (PFS), overall survival (OS), and toxicity.

resultsThe 2-year CNS recurrence rates (median follow-up period: 25.5 months; 95% confidence interval: 21.0-30.0) were 4.3% and 11.1% in the HD-MTX and non-HD-MTX groups (p = 0.337), respectively. Additionally, the 2-year progression-free survival (PFS) and overall survival (OS) rates were 70.7% versus 60.8% and 72.9% versus 60.8% (p = 0.013 and p = 0.024), respectively. The subgroup analysis for PFS and OS revealed that patients classified as the National Comprehensive Cancer Network (NCCN)-International Prognostic Index (IPI) low- or intermediate-risk, at a younger age, and without B symptoms demonstrated potential benefits from the HD-MTX treatment. In total, 46 patients completed 92 cycles of HD-MTX treatment, of which, 49 cycles were administered on day 6 of the R-CHOP regimen, with an average delay of no more than 4 days. In contrast, the remaining 43 cycles were initiated on days 10-14 following the completion of the R-CHOP regimen, with an average delay of 15 days. Interestingly, the incidence of hematological or non-hematological toxicity did not differ significantly among the groups.

conclusionOwing to the lack of robust evidence, the role of HD-MTX in preventing CNS recurrence could not be conclusively determined. Nevertheless, some patients could tolerate the treatment, such as younger individuals and those at NCCN-IPI low or intermediate risk, suggesting the efficacy of intravenous HD-MTX administration on day 6 as an optimal strategy for preventing CNS recurrence of DLBCL.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCentral Nervous System NeoplasmsLymphoma, Large B-Cell, DiffuseMethotrexateNeoplasm Recurrence, LocalAdultAgedAged, 80 and overCyclophosphamideDoxorubicinFemaleHumansMaleMiddle AgedPrednisoneProgression-Free SurvivalCyclophosphamideDoxorubicinMethotrexatePrednisoneRituximabVincristineCNS prophylaxisCNS relapsediffuse large B‐cell lymphomasystemic high‐dose methotrexate

Identifiers

PMID40166831
PMCPMC11959301

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.