<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(18)</volume><submitter>Stephan P</submitter><pubmed_abstract>&lt;h4>Abstract&lt;/h4>Anti-CD19 chimeric antigen receptor (CAR) T cells have shown impressive results in the treatment of relapsed/refractory aggressive large B-cell lymphomas (LBCLs). However, the prognostic value of the LBCL histological subtype in the context of CAR T-cell therapy is unclear. Here, we report the prognostic value of transformed indolent non-Hodgkin lymphoma (TriNHL; N = 110) confirmed by an expert pathological review (LYMPHOPATH) vs de novo LBCL (N = 391) in the context of CAR T-cell therapy from 4 centers of the French DESCAR-T registry. After 1:1 propensity score matching (n = 170, 85 patients with TriNHL and 85 patients with de novo LBCL), the median follow-up was 19.4 months (95% confidence interval [CI], 12.0-25.1) for patients with TriNHL and 18.5 months (95% CI, 13.8-2</pubmed_abstract><journal>Blood advances</journal><pagination>4693-4704</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12466217</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>TRANSCAR: real-world outcomes of CD19 CAR T-cell therapy in relapsed/refractory transformed indolent lymphomas.</pubmed_title><pmcid>PMC12466217</pmcid><pubmed_authors>Parrens M</pubmed_authors><pubmed_authors>Le Gouill S</pubmed_authors><pubmed_authors>Sesques P</pubmed_authors><pubmed_authors>Di Blasi R</pubmed_authors><pubmed_authors>Galtier J</pubmed_authors><pubmed_authors>Stephan P</pubmed_authors><pubmed_authors>Houot R</pubmed_authors><pubmed_authors>Meignin V</pubmed_authors><pubmed_authors>Poullot E</pubmed_authors><pubmed_authors>Gros FX</pubmed_authors><pubmed_authors>Thieblemont C</pubmed_authors><pubmed_authors>Marquet A</pubmed_authors><pubmed_authors>Donzel M</pubmed_authors><pubmed_authors>Roulin L</pubmed_authors><pubmed_authors>Dupont V</pubmed_authors><pubmed_authors>Calvani J</pubmed_authors><pubmed_authors>Traverse-Glehen A</pubmed_authors><pubmed_authors>Lemonnier F</pubmed_authors><pubmed_authors>Bachy E</pubmed_authors></additional><is_claimable>false</is_claimable><name>TRANSCAR: real-world outcomes of CD19 CAR T-cell therapy in relapsed/refractory transformed indolent lymphomas.</name><description>&lt;h4>Abstract&lt;/h4>Anti-CD19 chimeric antigen receptor (CAR) T cells have shown impressive results in the treatment of relapsed/refractory aggressive large B-cell lymphomas (LBCLs). However, the prognostic value of the LBCL histological subtype in the context of CAR T-cell therapy is unclear. Here, we report the prognostic value of transformed indolent non-Hodgkin lymphoma (TriNHL; N = 110) confirmed by an expert pathological review (LYMPHOPATH) vs de novo LBCL (N = 391) in the context of CAR T-cell therapy from 4 centers of the French DESCAR-T registry. After 1:1 propensity score matching (n = 170, 85 patients with TriNHL and 85 patients with de novo LBCL), the median follow-up was 19.4 months (95% confidence interval [CI], 12.0-25.1) for patients with TriNHL and 18.5 months (95% CI, 13.8-2</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-06-03T21:24:10.365Z</modification><creation>2026-05-01T03:11:11.282Z</creation></dates><accession>S-EPMC12466217</accession><cross_references><pubmed>40311067</pubmed><doi>10.1182/bloodadvances.2025015834</doi></cross_references></HashMap>