<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>6(3)</volume><submitter>Kim WS</submitter><funding>Regeneron Pharmaceuticals</funding><pubmed_abstract>The phase 2, multicohort, ongoing ELM-2 study evaluates odronextamab, a CD20×CD3 bispecific antibody, in patients with relapsed/refractory (R/R) B cell non-Hodgkin lymphoma after ≥2 lines of therapy. Here primary analysis of the diffuse large B cell lymphoma (DLBCL) cohort is reported. Patients received intravenous odronextamab in 21-day cycles until progression or unacceptable toxicity, with cycle 1 step-up dosing to mitigate cytokine release syndrome (CRS) risk. The primary endpoint was objective response rate (ORR). Secondary endpoints included complete response (CR) rate, duration of response, progression-free survival (PFS) and overall survival. A total of 127 patients were enrolled. At the 29.9-month efficacy follow-up, the ORR was 52.0% and CR rate was 31.5%. Median durations of res</pubmed_abstract><journal>Nature cancer</journal><pagination>528-539</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12003196</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Odronextamab monotherapy in patients with relapsed/refractory diffuse large B cell lymphoma: primary efficacy and safety analysis in phase 2 ELM-2 trial.</pubmed_title><pmcid>PMC12003196</pmcid><pubmed_authors>Rossi F</pubmed_authors><pubmed_authors>Cunningham D</pubmed_authors><pubmed_authors>Zhang H</pubmed_authors><pubmed_authors>Poon LM</pubmed_authors><pubmed_authors>Zhang M</pubmed_authors><pubmed_authors>Carpio C</pubmed_authors><pubmed_authors>Miqueleiz S</pubmed_authors><pubmed_authors>Zhang Q</pubmed_authors><pubmed_authors>Venugopal P</pubmed_authors><pubmed_authors>Ke X</pubmed_authors><pubmed_authors>Kim WS</pubmed_authors><pubmed_authors>Uchida T</pubmed_authors><pubmed_authors>Magnano 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TM</pubmed_authors><pubmed_authors>Knopinska-Posluszny W</pubmed_authors><pubmed_authors>Luminari S</pubmed_authors><pubmed_authors>Huang H</pubmed_authors><pubmed_authors>Ambati S</pubmed_authors><pubmed_authors>Tobai T</pubmed_authors><pubmed_authors>Tsukasaki K</pubmed_authors><pubmed_authors>Chen TY</pubmed_authors><pubmed_authors>Tan TD</pubmed_authors><pubmed_authors>Villasboas JC</pubmed_authors><pubmed_authors>Jo JC</pubmed_authors><pubmed_authors>Brouwer-Visser J</pubmed_authors><pubmed_authors>Kim BS</pubmed_authors><pubmed_authors>Keating MM</pubmed_authors><pubmed_authors>Battistini R</pubmed_authors><pubmed_authors>La Rosee PG</pubmed_authors><pubmed_authors>Chen Y</pubmed_authors><pubmed_authors>Elmusharaf N</pubmed_authors><pubmed_authors>Capochiani E</pubmed_authors><pubmed_authors>Ayyappan S</pubmed_authors><pubmed_authors>Cordoba R</pubmed_authors><pubmed_authors>Minami Y</pubmed_authors><pubmed_authors>Li C</pubmed_authors><pubmed_authors>Li 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G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Odronextamab monotherapy in patients with relapsed/refractory diffuse large B cell lymphoma: primary efficacy and safety analysis in phase 2 ELM-2 trial.</name><description>The phase 2, multicohort, ongoing ELM-2 study evaluates odronextamab, a CD20×CD3 bispecific antibody, in patients with relapsed/refractory (R/R) B cell non-Hodgkin lymphoma after ≥2 lines of therapy. Here primary analysis of the diffuse large B cell lymphoma (DLBCL) cohort is reported. Patients received intravenous odronextamab in 21-day cycles until progression or unacceptable toxicity, with cycle 1 step-up dosing to mitigate cytokine release syndrome (CRS) risk. The primary endpoint was objective response rate (ORR). Secondary endpoints included complete response (CR) rate, duration of response, progression-free survival (PFS) and overall survival. A total of 127 patients were enrolled. At the 29.9-month efficacy follow-up, the ORR was 52.0% and CR rate was 31.5%. Median durations of res</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Mar</publication><modification>2026-06-01T14:48:58.47Z</modification><creation>2026-04-08T13:31:08.217Z</creation></dates><accession>S-EPMC12003196</accession><cross_references><pubmed>40097657</pubmed><doi>10.1038/s43018-025-00921-6</doi></cross_references></HashMap>