符合移植条件的R/R DLBCL患者使用格列菲坦单抗加化疗可获益

IF 81.1 1区 医学 Q1 ONCOLOGY Nature Reviews Clinical Oncology Pub Date : 2024-11-28 DOI:10.1038/s41571-024-00975-y
Diana Romero
{"title":"符合移植条件的R/R DLBCL患者使用格列菲坦单抗加化疗可获益","authors":"Diana Romero","doi":"10.1038/s41571-024-00975-y","DOIUrl":null,"url":null,"abstract":"<p>Chimeric antigen receptor (CAR) T cells have emerged as an effective treatment option for patients with relapsed and/or refractory (R/R) diffuse large B cell lymphoma (DLBCL) who are ineligible for autologous stem-cell transplantation (ASCT), although owing to manufacturing and access-related limitations many patients receive rituximab plus gemcitabine–oxaliplatin. Now, data from the phase III STARGLO trial show that addition of the CD20 × CD3 bispecific T cell engager glofitamab to chemotherapy provides an overall survival (OS) benefit over the rituximab regimen in this setting.</p><p>Patients were randomly allocated to receive gemcitabine–oxaliplatin plus either glofitamab (<i>n</i> = 183) or rituximab (<i>n</i> = 91). Most patients (63%) had received only one prior line of therapy. OS was the primary end point.</p>","PeriodicalId":19079,"journal":{"name":"Nature Reviews Clinical Oncology","volume":"8 1","pages":""},"PeriodicalIF":81.1000,"publicationDate":"2024-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Benefit with glofitamab plus chemotherapy in transplant-ineligible R/R DLBCL\",\"authors\":\"Diana Romero\",\"doi\":\"10.1038/s41571-024-00975-y\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Chimeric antigen receptor (CAR) T cells have emerged as an effective treatment option for patients with relapsed and/or refractory (R/R) diffuse large B cell lymphoma (DLBCL) who are ineligible for autologous stem-cell transplantation (ASCT), although owing to manufacturing and access-related limitations many patients receive rituximab plus gemcitabine–oxaliplatin. Now, data from the phase III STARGLO trial show that addition of the CD20 × CD3 bispecific T cell engager glofitamab to chemotherapy provides an overall survival (OS) benefit over the rituximab regimen in this setting.</p><p>Patients were randomly allocated to receive gemcitabine–oxaliplatin plus either glofitamab (<i>n</i> = 183) or rituximab (<i>n</i> = 91). Most patients (63%) had received only one prior line of therapy. OS was the primary end point.</p>\",\"PeriodicalId\":19079,\"journal\":{\"name\":\"Nature Reviews Clinical Oncology\",\"volume\":\"8 1\",\"pages\":\"\"},\"PeriodicalIF\":81.1000,\"publicationDate\":\"2024-11-28\",\"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/s41571-024-00975-y\",\"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/s41571-024-00975-y","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

嵌合抗原受体(CAR)T细胞已成为不符合自体干细胞移植(ASCT)条件的复发和/或难治性弥漫大B细胞淋巴瘤(DLBCL)患者的一种有效治疗选择,但由于生产和获取方面的限制,许多患者接受利妥昔单抗加吉西他滨-奥沙利铂治疗。现在,来自III期STARGLO试验的数据显示,在化疗中加入CD20 × CD3双特异性T细胞吞噬因子格洛菲他单抗,比利妥昔单抗方案更能提高总生存期(OS)。患者被随机分配接受吉西他滨-奥沙利铂+格洛菲他单抗(n = 183)或利妥昔单抗(n = 91)。大多数患者(63%)之前只接受过一种疗法。OS是主要终点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Benefit with glofitamab plus chemotherapy in transplant-ineligible R/R DLBCL

Chimeric antigen receptor (CAR) T cells have emerged as an effective treatment option for patients with relapsed and/or refractory (R/R) diffuse large B cell lymphoma (DLBCL) who are ineligible for autologous stem-cell transplantation (ASCT), although owing to manufacturing and access-related limitations many patients receive rituximab plus gemcitabine–oxaliplatin. Now, data from the phase III STARGLO trial show that addition of the CD20 × CD3 bispecific T cell engager glofitamab to chemotherapy provides an overall survival (OS) benefit over the rituximab regimen in this setting.

Patients were randomly allocated to receive gemcitabine–oxaliplatin plus either glofitamab (n = 183) or rituximab (n = 91). Most patients (63%) had received only one prior line of therapy. OS was the primary end point.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
99.40
自引率
0.40%
发文量
114
审稿时长
6-12 weeks
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.
期刊最新文献
Synthetic lethal strategies for the development of cancer therapeutics Perioperative nivolumab results in favourable long-term outcomes in patients with locally advanced resectable non-small-cell lung cancer Getting the right combination to break the epigenetic code The changing treatment landscape of EGFR-mutant non-small-cell lung cancer Benefit with glofitamab plus chemotherapy in transplant-ineligible R/R DLBCL
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1