<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>43(36)</volume><submitter>Hutchings M</submitter><pubmed_abstract>&lt;h4>Purpose&lt;/h4>An unmet need remains for more effective therapies for relapsed/refractory (R/R) large B-cell lymphoma (LBCL), especially high-grade B-cell lymphoma (HGBCL). We present the primary analysis of a phase Ib/II study (ClinicalTrials.gov identifier: NCT03533283) investigating efficacy and safety of glofitamab plus polatuzumab vedotin (Glofit-Pola) in patients with R/R LBCL, including HGBCL and those who received previous chimeric antigen receptor (CAR) T-cell therapy.&lt;h4>Methods&lt;/h4>Patients received 1,000 mg obinutuzumab on Cycle (C)1 Day (D)1 (once daily). Polatuzumab vedotin (1.8 mg/kg) was given on C1D2 and D1 of C2-6 (21-day cycles; once daily). Glofitamab was given as step-up doses in C1 (D8, 2.5 mg; D15, 10 mg) followed by 30 mg on D1 of C2-12 (21-day cycles; once daily).</pubmed_abstract><journal>Journal of clinical oncology : official journal of the American Society of Clinical Oncology</journal><pagination>3788-3798</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12711264</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Efficacy and Safety of Glofitamab Plus Polatuzumab Vedotin in Relapsed/Refractory Large B-Cell Lymphoma Including High-Grade B-Cell Lymphoma: Results From a Phase Ib/II Trial.</pubmed_title><pmcid>PMC12711264</pmcid><pubmed_authors>Cordoba R</pubmed_authors><pubmed_authors>Avigdor A</pubmed_authors><pubmed_authors>Skarbnik A</pubmed_authors><pubmed_authors>Sellam G</pubmed_authors><pubmed_authors>Li D</pubmed_authors><pubmed_authors>Dominguez AR</pubmed_authors><pubmed_authors>Tandon M</pubmed_authors><pubmed_authors>Hutchings M</pubmed_authors><pubmed_authors>Larsen TS</pubmed_authors><pubmed_authors>Jorgensen JM</pubmed_authors><pubmed_authors>Corradini P</pubmed_authors><pubmed_authors>Gritti G</pubmed_authors><pubmed_authors>Terol MJ</pubmed_authors><pubmed_authors>Sureda A</pubmed_authors><pubmed_authors>Pinto A</pubmed_authors><pubmed_authors>Bottos A</pubmed_authors><pubmed_authors>Relf J</pubmed_authors><pubmed_authors>Bosch F</pubmed_authors><pubmed_authors>Zinzani PL</pubmed_authors><pubmed_authors>Leung W</pubmed_authors></additional><is_claimable>false</is_claimable><name>Efficacy and Safety of Glofitamab Plus Polatuzumab Vedotin in Relapsed/Refractory Large B-Cell Lymphoma Including High-Grade B-Cell Lymphoma: Results From a Phase Ib/II Trial.</name><description>&lt;h4>Purpose&lt;/h4>An unmet need remains for more effective therapies for relapsed/refractory (R/R) large B-cell lymphoma (LBCL), especially high-grade B-cell lymphoma (HGBCL). We present the primary analysis of a phase Ib/II study (ClinicalTrials.gov identifier: NCT03533283) investigating efficacy and safety of glofitamab plus polatuzumab vedotin (Glofit-Pola) in patients with R/R LBCL, including HGBCL and those who received previous chimeric antigen receptor (CAR) T-cell therapy.&lt;h4>Methods&lt;/h4>Patients received 1,000 mg obinutuzumab on Cycle (C)1 Day (D)1 (once daily). Polatuzumab vedotin (1.8 mg/kg) was given on C1D2 and D1 of C2-6 (21-day cycles; once daily). Glofitamab was given as step-up doses in C1 (D8, 2.5 mg; D15, 10 mg) followed by 30 mg on D1 of C2-12 (21-day cycles; once daily).</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Dec</publication><modification>2026-07-15T14:29:44.594Z</modification><creation>2026-07-06T03:08:56.508Z</creation></dates><accession>S-EPMC12711264</accession><cross_references><pubmed>41115257</pubmed><doi>10.1200/JCO-25-00992</doi></cross_references></HashMap>