Daratumumab-based quadruplet versus triplet induction regimens in transplant-eligible newly diagnosed multiple myeloma: a systematic review and meta-analysis

IF 11.6 1区 医学 Q1 HEMATOLOGY Blood Cancer Journal Pub Date : 2025-03-13 DOI:10.1038/s41408-025-01253-5
João Tadeu Damian Souto Filho, Lucas Oliveira Cantadori, Edvan de Queiroz Crusoe, Vania Hungria, Angelo Maiolino
{"title":"Daratumumab-based quadruplet versus triplet induction regimens in transplant-eligible newly diagnosed multiple myeloma: a systematic review and meta-analysis","authors":"João Tadeu Damian Souto Filho, Lucas Oliveira Cantadori, Edvan de Queiroz Crusoe, Vania Hungria, Angelo Maiolino","doi":"10.1038/s41408-025-01253-5","DOIUrl":null,"url":null,"abstract":"<p>The treatment landscape for transplant-eligible patients with newly diagnosed multiple myeloma (TE-NDMM) has evolved with the introduction of daratumumab-based quadruplet regimens. Adding daratumumab to traditional triplet regimens has demonstrated improved response rates and progression-free survival (PFS). However, the impact on long-term outcomes, particularly overall survival (OS), remains uncertain. This systematic review and meta-analysis aimed to compare the survival outcomes of these quadruplet regimens with triplets. Conducted in adherence to Cochrane Collaboration and PRISMA guidelines and registered on PROSPERO (CRD42024571946), the study involved searching PubMed, Embase, and Cochrane databases, from inception to June 2024. We included randomized clinical trials (RCT) and non-randomized controlled studies (NRCS) that compared daratumumab-based quadruplet regimens to triplets, focusing on OS and PFS, with a minimum follow-up of 18 months. The meta-analysis included 3327 TE-NDMM patients from four studies, comprising three RCT and one NRCS. Daratumumab-based regimens were administered to 1328 (40%) patients. The analysis revealed that daratumumab-based quadruplet regimens significantly improved both OS (pooled HR 0.60; 95% CI 0.48–0.75; <i>P</i> &lt; 0.00001; <i>I</i>² = 0%) and PFS (pooled HR 0.49; 95% CI 0.37–0.65; <i>P</i> &lt; 0.00001; <i>I</i>² = 52%). A per-protocol subgroup analysis comparing D-VRD to VRD further confirmed these benefits, with significant improvements in both OS (pooled HR 0.68; 95% CI 0.48–0.97; <i>P</i> = 0.03; <i>I</i>² = 0%) and PFS (pooled HR 0.41; 95% CI 0.31–0.54; <i>P</i> &lt; 0.00001; <i>I</i>² = 0%). This meta-analysis consolidates evidence that daratumumab-based quadruplet regimens significantly improve OS, compared to triplet regimens for TE-NDMM patients.</p>","PeriodicalId":8989,"journal":{"name":"Blood Cancer Journal","volume":"56 1","pages":""},"PeriodicalIF":11.6000,"publicationDate":"2025-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Blood Cancer Journal","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1038/s41408-025-01253-5","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"HEMATOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

The treatment landscape for transplant-eligible patients with newly diagnosed multiple myeloma (TE-NDMM) has evolved with the introduction of daratumumab-based quadruplet regimens. Adding daratumumab to traditional triplet regimens has demonstrated improved response rates and progression-free survival (PFS). However, the impact on long-term outcomes, particularly overall survival (OS), remains uncertain. This systematic review and meta-analysis aimed to compare the survival outcomes of these quadruplet regimens with triplets. Conducted in adherence to Cochrane Collaboration and PRISMA guidelines and registered on PROSPERO (CRD42024571946), the study involved searching PubMed, Embase, and Cochrane databases, from inception to June 2024. We included randomized clinical trials (RCT) and non-randomized controlled studies (NRCS) that compared daratumumab-based quadruplet regimens to triplets, focusing on OS and PFS, with a minimum follow-up of 18 months. The meta-analysis included 3327 TE-NDMM patients from four studies, comprising three RCT and one NRCS. Daratumumab-based regimens were administered to 1328 (40%) patients. The analysis revealed that daratumumab-based quadruplet regimens significantly improved both OS (pooled HR 0.60; 95% CI 0.48–0.75; P < 0.00001; I² = 0%) and PFS (pooled HR 0.49; 95% CI 0.37–0.65; P < 0.00001; I² = 52%). A per-protocol subgroup analysis comparing D-VRD to VRD further confirmed these benefits, with significant improvements in both OS (pooled HR 0.68; 95% CI 0.48–0.97; P = 0.03; I² = 0%) and PFS (pooled HR 0.41; 95% CI 0.31–0.54; P < 0.00001; I² = 0%). This meta-analysis consolidates evidence that daratumumab-based quadruplet regimens significantly improve OS, compared to triplet regimens for TE-NDMM patients.

Abstract Image

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
基于daratumumab的四联体与三联体诱导方案治疗符合移植条件的新诊断多发性骨髓瘤:系统回顾和荟萃分析
新诊断的符合移植条件的多发性骨髓瘤(TE-NDMM)患者的治疗前景随着基于daratumumab的四联体方案的引入而发生了变化。将daratumumab添加到传统的三联方案中已证明可改善缓解率和无进展生存期(PFS)。然而,对长期预后的影响,特别是总生存期(OS)仍不确定。本系统综述和荟萃分析旨在比较这些四胞胎方案与三胞胎方案的生存结果。该研究遵循Cochrane Collaboration和PRISMA指南,在PROSPERO上注册(CRD42024571946),从研究开始到2024年6月,检索PubMed、Embase和Cochrane数据库。我们纳入了随机临床试验(RCT)和非随机对照研究(NRCS),比较了基于daratumumab的四胞胎方案和三胞胎方案,重点关注OS和PFS,至少随访18个月。荟萃分析纳入了来自4项研究的3327例TE-NDMM患者,包括3项RCT和1项NRCS。1328例(40%)患者接受了以daratumumab为基础的方案。分析显示,基于daratumumab的四联体方案显着改善了OS(合并HR 0.60;95% ci 0.48-0.75;P < 0.00001;I²= 0%)和PFS(合并HR 0.49;95% ci 0.37-0.65;P < 0.00001;i²= 52%)。比较D-VRD和VRD的每协议亚组分析进一步证实了这些益处,两种OS均有显著改善(总HR 0.68;95% ci 0.48-0.97;p = 0.03;I²= 0%)和PFS(合并HR 0.41;95% ci 0.31-0.54;P < 0.00001;i²= 0%)。该荟萃分析证实,与TE-NDMM患者的三联体方案相比,基于daratumumab的四联体方案可显著改善OS。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
16.70
自引率
2.30%
发文量
153
审稿时长
>12 weeks
期刊介绍: Blood Cancer Journal is dedicated to publishing high-quality articles related to hematologic malignancies and related disorders. The journal welcomes submissions of original research, reviews, guidelines, and letters that are deemed to have a significant impact in the field. While the journal covers a wide range of topics, it particularly focuses on areas such as: Preclinical studies of new compounds, especially those that provide mechanistic insights Clinical trials and observations Reviews related to new drugs and current management of hematologic malignancies Novel observations related to new mutations, molecular pathways, and tumor genomics Blood Cancer Journal offers a forum for expedited publication of novel observations regarding new mutations or altered pathways.
期刊最新文献
Aberrant glycosylation in hematologic malignancies: mechanisms, immune evasion, and therapeutic targeting. Association of ciltacabtagene autoleucel with immune effector cell-associated enterocolitis: insights from a large national database. Dietary intake and the risk of monoclonal gammopathy of undetermined significance: results from the population-based iStopMM screening study Correction: Exploiting PRMT5 as a target for combination therapy in mantle cell lymphoma characterized by frequent ATM and TP53 mutations. Association between treatment-emergent cytopenias and clinical responses to imetelstat in lower-risk myelodysplastic syndromes.
×
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:604180095
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