<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(20)</volume><submitter>Hawkes EA</submitter><pubmed_abstract>&lt;h4>Abstract&lt;/h4>Diffuse large B-cell lymphoma (DLBCL) and follicular lymphoma (FL) are highly radiosensitive with immune-driven abscopal responses reported. Programmed cell death 1/programmed cell death ligand 1 (PD-L1) inhibitors are relatively ineffective in DLBCL/FL; however, evidence suggests synergy with radiotherapy (RT), but no clear biomarkers. This phase 1 study examined the safety of escalating RT dose and treated volumes with durvalumab (PD-L1 inhibitor) in 34 adults with relapsed/refractory DLBCL and relapsed/refractory FL, and the role of immune-cell subsets on outcomes. Patients received external-beam RT (2.5-30 Gray [Gy], 5 or 10 fractions up to 3 target sites) plus durvalumab from RT day 2, until progression. Novel positron emission tomography (PET) biodistribution studies</pubmed_abstract><journal>Blood advances</journal><pagination>5263-5273</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12552934</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>T-cell dysregulation informs radiotherapy-immunotherapy response in B-cell lymphoma: results from a phase 1 trial.</pubmed_title><pmcid>PMC12552934</pmcid><pubmed_authors>Palmer JB</pubmed_authors><pubmed_authors>Manos K</pubmed_authors><pubmed_authors>Scott AM</pubmed_authors><pubmed_authors>Barraclough A</pubmed_authors><pubmed_authors>Chong G</pubmed_authors><pubmed_authors>Gandhi MK</pubmed_authors><pubmed_authors>Smith C</pubmed_authors><pubmed_authors>Martynchyk A</pubmed_authors><pubmed_authors>Chowdhury R</pubmed_authors><pubmed_authors>Scott FE</pubmed_authors><pubmed_authors>Hawkes EA</pubmed_authors><pubmed_authors>Churilov L</pubmed_authors><pubmed_authors>Shortt J</pubmed_authors><pubmed_authors>MacManus M</pubmed_authors><pubmed_authors>Law SC</pubmed_authors><pubmed_authors>Burgess M</pubmed_authors><pubmed_authors>Swain F</pubmed_authors><pubmed_authors>Keane C</pubmed_authors><pubmed_authors>Khor R</pubmed_authors><pubmed_authors>Lee ST</pubmed_authors></additional><is_claimable>false</is_claimable><name>T-cell dysregulation informs radiotherapy-immunotherapy response in B-cell lymphoma: results from a phase 1 trial.</name><description>&lt;h4>Abstract&lt;/h4>Diffuse large B-cell lymphoma (DLBCL) and follicular lymphoma (FL) are highly radiosensitive with immune-driven abscopal responses reported. Programmed cell death 1/programmed cell death ligand 1 (PD-L1) inhibitors are relatively ineffective in DLBCL/FL; however, evidence suggests synergy with radiotherapy (RT), but no clear biomarkers. This phase 1 study examined the safety of escalating RT dose and treated volumes with durvalumab (PD-L1 inhibitor) in 34 adults with relapsed/refractory DLBCL and relapsed/refractory FL, and the role of immune-cell subsets on outcomes. Patients received external-beam RT (2.5-30 Gray [Gy], 5 or 10 fractions up to 3 target sites) plus durvalumab from RT day 2, until progression. Novel positron emission tomography (PET) biodistribution studies</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Oct</publication><modification>2026-06-05T05:17:29.421Z</modification><creation>2026-06-04T03:06:03.344Z</creation></dates><accession>S-EPMC12552934</accession><cross_references><pubmed>40540795</pubmed><doi>10.1182/bloodadvances.2025016505</doi></cross_references></HashMap>