<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(20)</volume><submitter>Camus V</submitter><pubmed_abstract>&lt;h4>Abstract&lt;/h4>Tafasitamab plus lenalidomide (TAFA-LEN) treatment relevance pre- or post-anti-CD19 chimeric antigen receptor (CAR) T-cell therapy is debated. We analyzed patients with large B-cell lymphoma in the DESCAR-T registry treated with axi[1]cel or tisa-cel in ≥3rd line and TAFA-LEN before (n = 15, "TL-pre-CAR-T" set) or directly after (n = 52, "TL-post-CAR-T" set) CAR T-cell therapy. We compared TAFA-LEN v. other treatments using inverse probability weighting in the TL-post-CAR[1]T set. In the TL-post-CAR-T set, the median progression-free survival (mPFS), overall survival (mOS), and duration of response (mDOR) since the first treatment for progression (mPFS2/mOS2/mDOR2) were 3, 4.7, and 8.1 months, respectively. The best overall response rate (bORR) and best complete response r</pubmed_abstract><journal>Blood advances</journal><pagination>5371-5381</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11568786</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Outcome of patients with large B-cell lymphoma treated with tafasitamab plus lenalidomide either before or after CAR T-cell therapy.</pubmed_title><pmcid>PMC11568786</pmcid><pubmed_authors>Carras S</pubmed_authors><pubmed_authors>Castilla-Llorente C</pubmed_authors><pubmed_authors>Chauchet A</pubmed_authors><pubmed_authors>Abraham J</pubmed_authors><pubmed_authors>Houot R</pubmed_authors><pubmed_authors>Drieu La Rochelle L</pubmed_authors><pubmed_authors>Casasnovas O</pubmed_authors><pubmed_authors>Marquet A</pubmed_authors><pubmed_authors>Tounes L</pubmed_authors><pubmed_authors>Oberic L</pubmed_authors><pubmed_authors>Damaj GL</pubmed_authors><pubmed_authors>Bailly S</pubmed_authors><pubmed_authors>Decroocq J</pubmed_authors><pubmed_authors>Jardin F</pubmed_authors><pubmed_authors>Guidez S</pubmed_authors><pubmed_authors>Dupont V</pubmed_authors><pubmed_authors>Fornecker LM</pubmed_authors><pubmed_authors>Lemonnier F</pubmed_authors><pubmed_authors>Herbaux C</pubmed_authors><pubmed_authors>Hermine O</pubmed_authors><pubmed_authors>Morschhauser F</pubmed_authors><pubmed_authors>Le Gouill S</pubmed_authors><pubmed_authors>Sesques P</pubmed_authors><pubmed_authors>Campidelli A</pubmed_authors><pubmed_authors>Joris M</pubmed_authors><pubmed_authors>Brisou G</pubmed_authors><pubmed_authors>Bouabdallah K</pubmed_authors><pubmed_authors>Paillassa J</pubmed_authors><pubmed_authors>Choquet S</pubmed_authors><pubmed_authors>Tessoulin B</pubmed_authors><pubmed_authors>Krzisch D</pubmed_authors><pubmed_authors>Camus V</pubmed_authors></additional><is_claimable>false</is_claimable><name>Outcome of patients with large B-cell lymphoma treated with tafasitamab plus lenalidomide either before or after CAR T-cell therapy.</name><description>&lt;h4>Abstract&lt;/h4>Tafasitamab plus lenalidomide (TAFA-LEN) treatment relevance pre- or post-anti-CD19 chimeric antigen receptor (CAR) T-cell therapy is debated. We analyzed patients with large B-cell lymphoma in the DESCAR-T registry treated with axi[1]cel or tisa-cel in ≥3rd line and TAFA-LEN before (n = 15, "TL-pre-CAR-T" set) or directly after (n = 52, "TL-post-CAR-T" set) CAR T-cell therapy. We compared TAFA-LEN v. other treatments using inverse probability weighting in the TL-post-CAR[1]T set. In the TL-post-CAR-T set, the median progression-free survival (mPFS), overall survival (mOS), and duration of response (mDOR) since the first treatment for progression (mPFS2/mOS2/mDOR2) were 3, 4.7, and 8.1 months, respectively. The best overall response rate (bORR) and best complete response r</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Oct</publication><modification>2026-06-03T03:12:10.748Z</modification><creation>2025-04-06T22:45:57.644Z</creation></dates><accession>S-EPMC11568786</accession><cross_references><pubmed>39163620</pubmed><doi>10.1182/bloodadvances.2024013726</doi></cross_references></HashMap>