<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Omuro A</submitter><funding>National Cancer Institute/National Institute of Health</funding><funding>NCI NIH HHS</funding><pubmed_abstract>&lt;h4>Background&lt;/h4>Methotrexate-based chemoradiotherapy is effective in primary central nervous system lymphoma (PCNSL) but carries a risk of severe neurotoxicity. In a single-arm study, a regimen with methotrexate, procarbazine, vincristine and cytarabine was combined with rituximab (R-MPV-A) and substantially reduced doses of whole-brain radiotherapy (LD-WBRT), resulting in excellent progression-free survival (PFS) and overall survival (OS). Because R-MPV-A had never been tested without radiation, we sought to evaluate the efficacy of R-MPV-A with and without LD-WBRT, as well as determining if such low radiotherapy doses influenced disease control and/or neurotoxicity.&lt;h4>Methods&lt;/h4>Patients were randomized to receive R-MPV-A alone (Chemo arm) or combined with LD-WBRT (ChemoRT arm), giv</pubmed_abstract><journal>Neuro-oncology</journal><pagination>noaf221</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12904153</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Multicenter Randomized Phase II Study of R-MPV-A Chemoimmunotherapy With or Without Low-Dose Whole-Brain Radiotherapy for Newly-Diagnosed Primary CNS Lymphoma.</pubmed_title><pmcid>PMC12904153</pmcid><funding_grant_id>U10 CA180868</funding_grant_id><funding_grant_id>U10 CA180822</funding_grant_id><funding_grant_id>U10CA180868</funding_grant_id><funding_grant_id>U10CA180822</funding_grant_id><pubmed_authors>Wefel JS</pubmed_authors><pubmed_authors>Werner-Wasik M</pubmed_authors><pubmed_authors>Bovi JA</pubmed_authors><pubmed_authors>Lallana EC</pubmed_authors><pubmed_authors>Omuro A</pubmed_authors><pubmed_authors>Corn BW</pubmed_authors><pubmed_authors>Aneja S</pubmed_authors><pubmed_authors>Rogers CL</pubmed_authors><pubmed_authors>Donnelly ED</pubmed_authors><pubmed_authors>Correa D</pubmed_authors><pubmed_authors>Iwamoto FM</pubmed_authors><pubmed_authors>Struve TD</pubmed_authors><pubmed_authors>Rosenblum M</pubmed_authors><pubmed_authors>Grommes C</pubmed_authors><pubmed_authors>Mehta MP</pubmed_authors><pubmed_authors>Yu HM</pubmed_authors><pubmed_authors>DeAngelis LM</pubmed_authors><pubmed_authors>Peereboom DM</pubmed_authors><pubmed_authors>Polley MC</pubmed_authors><pubmed_authors>Won M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Multicenter Randomized Phase II Study of R-MPV-A Chemoimmunotherapy With or Without Low-Dose Whole-Brain Radiotherapy for Newly-Diagnosed Primary CNS Lymphoma.</name><description>&lt;h4>Background&lt;/h4>Methotrexate-based chemoradiotherapy is effective in primary central nervous system lymphoma (PCNSL) but carries a risk of severe neurotoxicity. In a single-arm study, a regimen with methotrexate, procarbazine, vincristine and cytarabine was combined with rituximab (R-MPV-A) and substantially reduced doses of whole-brain radiotherapy (LD-WBRT), resulting in excellent progression-free survival (PFS) and overall survival (OS). Because R-MPV-A had never been tested without radiation, we sought to evaluate the efficacy of R-MPV-A with and without LD-WBRT, as well as determining if such low radiotherapy doses influenced disease control and/or neurotoxicity.&lt;h4>Methods&lt;/h4>Patients were randomized to receive R-MPV-A alone (Chemo arm) or combined with LD-WBRT (ChemoRT arm), giv</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Nov</publication><modification>2026-07-15T18:02:21.858Z</modification><creation>2026-07-08T03:08:24.488Z</creation></dates><accession>S-EPMC12904153</accession><cross_references><pubmed>41189315</pubmed><doi>10.1093/neuonc/noaf221</doi></cross_references></HashMap>