Evidence map›Paper›PMID 41972375›Full record

ArticleCancer medicine2026

Comparative Outcomes of Consolidation Strategies After R-MVP Induction in Primary Diffuse Large B-Cell Lymphoma of the Central Nervous System.

Sang-A Kim, Jung Sun Kim, Ji Yun Lee, Joo Ho Lee, Keun-Yong Eom, Chul-Kee Park, Chae-Yong Kim, Dae Seog Heo, Jeong-Ok Lee, Tae Min Kim

Abstract readComparative Study
In one paragraph

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 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

Who cites it

1 citing paper in PubMed.

  1. Article
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.

Sang-A KimDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, Republic of Korea.ORCID https://orcid.org/0000-0002-8529-0232
Jung Sun KimDepartment of Internal Medicine, CHA Bundang Medical Center, CHA University School of Medicine, Seongnam, Republic of Korea.
Ji Yun LeeDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, Republic of Korea.
Joo Ho LeeDepartment of Radiation Oncology, Seoul National University Hospital, Cancer Research Institute, Seoul National University College of Medicine, Seoul, Republic of Korea.
Keun-Yong EomDepartment of Radiation Oncology, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, Republic of Korea.
Chul-Kee ParkDepartment of Neurosurgery, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0002-2350-9876
Chae-Yong KimDepartment of Neurosurgery, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, Republic of Korea.
Dae Seog HeoDepartment of Internal Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Republic of Korea.
Jeong-Ok LeeDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, Republic of Korea.
Tae Min KimDepartment of Internal Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0001-6145-4426

Funding

Seoul National University Bundang Hospital Research Fund 02-2019-00028
6 · The paper itself

Abstract

backgroundThe optimal consolidation strategy following high-dose methotrexate (MTX)-based induction in primary central nervous system lymphoma (PCNSL) remains controversial. This study compared real-world outcomes of different consolidation modalities in patients responsive to rituximab, MTX, vincristine, and procarbazine (R-MVP) induction chemotherapy.

methodsWe retrospectively analyzed 296 newly diagnosed PCNSL patients treated with R-MVP between 2008 and 2023. Among 290 evaluable patients, the overall response rate (ORR) was assessed, and survival outcomes were evaluated by Kaplan-Meier and Cox regression analyses. Propensity score matching (PSM) was performed to compare autologous stem-cell transplantation (ASCT) and whole-brain radiotherapy (WBRT).

resultsThe ORR was 89.7%, with 71.7% achieving complete response (CR) or complete response unconfirmed (CRu) and 17.9% partial response (PR). Of 260 responders, 190 received consolidation: WBRT (40.8%), ASCT (20.0%), or non-myelosuppressive chemotherapy (NMC; 12.3%). After a median follow-up of 45.3 months, median progression-free survival (PFS) and overall survival (OS) for responders were 65.8 (95% CI 50.7-80.8) and 84.6 months (95% CI 66.5-102.7), respectively. ASCT yielded the most favorable survival (median PFS not reached), followed by WBRT (70.8 months), whereas NMC and no-consolidation groups showed significantly inferior PFS (22.9 and 40.1 months, p < 0.001). OS showed a similar trend (p = 0.006). On multivariable analysis, elevated LDH and consolidation type were independent predictors of PFS, whereas age and consolidation type were significant prognostic factors for OS. In the PSM cohort (ASCT vs. WBRT, n = 52 each), median PFS was not reached for ASCT versus 90.0 months for WBRT (p = 0.050); OS was not reached versus 97.9 months (p = 0.160).

conclusionsASCT was associated with the most durable survival among consolidation strategies after R-MVP induction. These findings, derived from a large real-world, multi-institutional cohort, support ASCT as the preferred consolidation for eligible patients while underscoring the heterogeneity of current practice and the need for prospective validation.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCentral Nervous System NeoplasmsConsolidation ChemotherapyLymphoma, Large B-Cell, DiffuseAdultAgedFemaleHumansInduction ChemotherapyMaleMethotrexateMiddle AgedProcarbazineRetrospective StudiesRituximabTransplantation, AutologousMethotrexateProcarbazineRituximabVincristineautologous stem cell transplantationconsolidationmethotrexateprimary central nervous system lymphomaprocarbazineradiation therapyrituximabvincristine

Identifiers

PMID41972375
PMCPMC13072046

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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.