{"title":"来那度胺和利妥昔单抗联合brentuximab vedotin可改善R/R DLBCL的OS","authors":"David Killock","doi":"10.1038/s41571-025-00988-1","DOIUrl":null,"url":null,"abstract":"<p>Haematopoietic stem cell transplantation (HSCT) and CD19-targeted chimeric antigen receptor (CAR) T cells are potentially curative therapies for relapsed and/or refractory diffuse large B cell lymphoma (R/R DLBCL); however, many patients are unable to receive or have further relapse following these treatments. New data from the phase III ECHELON-3 trial demonstrate the promise of a novel combination regimen incorporating the anti-CD30 antibody–drug conjugate brentuximab vedotin (BV) for such patients.</p><p>In ECHELON-3, 230 patients with R/R DLBCL who had received ≥2 prior lines of therapy and were ineligible for HSCT or CAR T cell therapy were randomly assigned (1:1) to received lenalidomide and rituximab plus either BV or placebo. The primary end point was overall survival (OS).</p>","PeriodicalId":19079,"journal":{"name":"Nature Reviews Clinical Oncology","volume":"23 1","pages":""},"PeriodicalIF":81.1000,"publicationDate":"2025-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Adding brentuximab vedotin to lenalidomide and rituximab improves OS in R/R DLBCL\",\"authors\":\"David Killock\",\"doi\":\"10.1038/s41571-025-00988-1\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Haematopoietic stem cell transplantation (HSCT) and CD19-targeted chimeric antigen receptor (CAR) T cells are potentially curative therapies for relapsed and/or refractory diffuse large B cell lymphoma (R/R DLBCL); however, many patients are unable to receive or have further relapse following these treatments. New data from the phase III ECHELON-3 trial demonstrate the promise of a novel combination regimen incorporating the anti-CD30 antibody–drug conjugate brentuximab vedotin (BV) for such patients.</p><p>In ECHELON-3, 230 patients with R/R DLBCL who had received ≥2 prior lines of therapy and were ineligible for HSCT or CAR T cell therapy were randomly assigned (1:1) to received lenalidomide and rituximab plus either BV or placebo. The primary end point was overall survival (OS).</p>\",\"PeriodicalId\":19079,\"journal\":{\"name\":\"Nature Reviews Clinical Oncology\",\"volume\":\"23 1\",\"pages\":\"\"},\"PeriodicalIF\":81.1000,\"publicationDate\":\"2025-01-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nature Reviews Clinical Oncology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1038/s41571-025-00988-1\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ONCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature Reviews Clinical Oncology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1038/s41571-025-00988-1","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ONCOLOGY","Score":null,"Total":0}
Adding brentuximab vedotin to lenalidomide and rituximab improves OS in R/R DLBCL
Haematopoietic stem cell transplantation (HSCT) and CD19-targeted chimeric antigen receptor (CAR) T cells are potentially curative therapies for relapsed and/or refractory diffuse large B cell lymphoma (R/R DLBCL); however, many patients are unable to receive or have further relapse following these treatments. New data from the phase III ECHELON-3 trial demonstrate the promise of a novel combination regimen incorporating the anti-CD30 antibody–drug conjugate brentuximab vedotin (BV) for such patients.
In ECHELON-3, 230 patients with R/R DLBCL who had received ≥2 prior lines of therapy and were ineligible for HSCT or CAR T cell therapy were randomly assigned (1:1) to received lenalidomide and rituximab plus either BV or placebo. The primary end point was overall survival (OS).
期刊介绍:
Nature Reviews publishes clinical content authored by internationally renowned clinical academics and researchers, catering to readers in the medical sciences at postgraduate levels and beyond. Although targeted at practicing doctors, researchers, and academics within specific specialties, the aim is to ensure accessibility for readers across various medical disciplines. The journal features in-depth Reviews offering authoritative and current information, contextualizing topics within the history and development of a field. Perspectives, News & Views articles, and the Research Highlights section provide topical discussions, opinions, and filtered primary research from diverse medical journals.