<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(5)</volume><submitter>Tivey A</submitter><pubmed_abstract>&lt;h4>Abstract&lt;/h4>During the COVID-19 pandemic, ibrutinib with or without rituximab was approved in England for initial treatment of mantle cell lymphoma (MCL) instead of immunochemotherapy. Because limited data are available in this setting, we conducted an observational cohort study evaluating safety and efficacy. Adults receiving ibrutinib with or without rituximab for untreated MCL were evaluated for treatment toxicity, response, and survival, including outcomes in high-risk MCL (TP53 mutation/deletion/p53 overexpression, blastoid/pleomorphic, or Ki67 ≥ 30%). A total of 149 patients from 43 participating centers were enrolled: 74.1% male, median age 75 years, 75.2% Eastern Cooperative Oncology Group status of 0 to 1, 36.2% high-risk, and 8.9% autologous transplant candidates. All patien</pubmed_abstract><journal>Blood advances</journal><pagination>1209-1219</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10912842</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Ibrutinib as first-line therapy for mantle cell lymphoma: a multicenter, real-world UK study.</pubmed_title><pmcid>PMC10912842</pmcid><pubmed_authors>Fowler N</pubmed_authors><pubmed_authors>Dukka V</pubmed_authors><pubmed_authors>Goddard J</pubmed_authors><pubmed_authors>Rees C</pubmed_authors><pubmed_authors>Sharpley F</pubmed_authors><pubmed_authors>Santarsieri A</pubmed_authors><pubmed_authors>Wilson J</pubmed_authors><pubmed_authors>Protheroe S</pubmed_authors><pubmed_authors>Talbot G</pubmed_authors><pubmed_authors>Wilson M</pubmed_authors><pubmed_authors>Lambert J</pubmed_authors><pubmed_authors>Wrench D</pubmed_authors><pubmed_authors>Crosbie N</pubmed_authors><pubmed_authors>Swe W</pubmed_authors><pubmed_authors>Moule S</pubmed_authors><pubmed_authors>Knott C</pubmed_authors><pubmed_authors>Owen M</pubmed_authors><pubmed_authors>Pillai A</pubmed_authors><pubmed_authors>Ediriwickrema K</pubmed_authors><pubmed_authors>Sutton T</pubmed_authors><pubmed_authors>Wright J</pubmed_authors><pubmed_authors>Mohamedbhai S</pubmed_authors><pubmed_authors>Walter H</pubmed_authors><pubmed_authors>Prahladan M</pubmed_authors><pubmed_authors>Chaturvedi A</pubmed_authors><pubmed_authors>Stern S</pubmed_authors><pubmed_authors>Tivey A</pubmed_authors><pubmed_authors>Qureshi I</pubmed_authors><pubmed_authors>Flont M</pubmed_authors><pubmed_authors>Nga E</pubmed_authors><pubmed_authors>Willimott V</pubmed_authors><pubmed_authors>Bailey J</pubmed_authors><pubmed_authors>Everden A</pubmed_authors><pubmed_authors>Davies E</pubmed_authors><pubmed_authors>Lewis D</pubmed_authors><pubmed_authors>Miall F</pubmed_authors><pubmed_authors>Jones S</pubmed_authors><pubmed_authors>Bishton M</pubmed_authors><pubmed_authors>McCulloch R</pubmed_authors><pubmed_authors>Tucker D</pubmed_authors><pubmed_authors>Burney C</pubmed_authors><pubmed_authors>Reeve M</pubmed_authors><pubmed_authors>Thomas N</pubmed_authors><pubmed_authors>Stanton L</pubmed_authors><pubmed_authors>Zhao R</pubmed_authors><pubmed_authors>Norman J</pubmed_authors><pubmed_authors>Virchis A</pubmed_authors><pubmed_authors>Jackson B</pubmed_authors><pubmed_authors>Maddox J</pubmed_authors><pubmed_authors>Hildyard C</pubmed_authors><pubmed_authors>Beech A</pubmed_authors><pubmed_authors>Eyre TA</pubmed_authors><pubmed_authors>Lowry L</pubmed_authors><pubmed_authors>Camacho RG</pubmed_authors><pubmed_authors>Hodson A</pubmed_authors><pubmed_authors>Allchin R</pubmed_authors><pubmed_authors>Shotton R</pubmed_authors><pubmed_authors>Marr H</pubmed_authors><pubmed_authors>Phillips N</pubmed_authors><pubmed_authors>Koppana M</pubmed_authors><pubmed_authors>Nicholson T</pubmed_authors><pubmed_authors>Paneesha S</pubmed_authors><pubmed_authors>Bedford C</pubmed_authors><pubmed_authors>Smith S</pubmed_authors><pubmed_authors>Lord A</pubmed_authors><pubmed_authors>Webb A</pubmed_authors><pubmed_authors>Gibb A</pubmed_authors><pubmed_authors>Linton K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Ibrutinib as first-line therapy for mantle cell lymphoma: a multicenter, real-world UK study.</name><description>&lt;h4>Abstract&lt;/h4>During the COVID-19 pandemic, ibrutinib with or without rituximab was approved in England for initial treatment of mantle cell lymphoma (MCL) instead of immunochemotherapy. Because limited data are available in this setting, we conducted an observational cohort study evaluating safety and efficacy. Adults receiving ibrutinib with or without rituximab for untreated MCL were evaluated for treatment toxicity, response, and survival, including outcomes in high-risk MCL (TP53 mutation/deletion/p53 overexpression, blastoid/pleomorphic, or Ki67 ≥ 30%). A total of 149 patients from 43 participating centers were enrolled: 74.1% male, median age 75 years, 75.2% Eastern Cooperative Oncology Group status of 0 to 1, 36.2% high-risk, and 8.9% autologous transplant candidates. All patien</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2026-06-17T06:31:33.138Z</modification><creation>2026-06-17T03:06:56.198Z</creation></dates><accession>S-EPMC10912842</accession><cross_references><pubmed>38127279</pubmed><doi>10.1182/bloodadvances.2023011152</doi></cross_references></HashMap>