Suppr超能文献

达雷妥尤单抗、来那度胺、硼替佐米和地塞米松用于适合移植的新诊断多发性骨髓瘤:GRIFFIN 试验。

Daratumumab, lenalidomide, bortezomib, and dexamethasone for transplant-eligible newly diagnosed multiple myeloma: the GRIFFIN trial.

机构信息

Levine Cancer Institute, Atrium Health, Charlotte, NC.

Winship Cancer Institute, Emory University, Atlanta, GA.

出版信息

Blood. 2020 Aug 20;136(8):936-945. doi: 10.1182/blood.2020005288.

Abstract

Lenalidomide, bortezomib, and dexamethasone (RVd) followed by autologous stem cell transplantation (ASCT) is standard frontline therapy for transplant-eligible patients with newly diagnosed multiple myeloma (NDMM). The addition of daratumumab (D) to RVd (D-RVd) in transplant-eligible NDMM patients was evaluated. Patients (N = 207) were randomized 1:1 to D-RVd or RVd induction (4 cycles), ASCT, D-RVd or RVd consolidation (2 cycles), and lenalidomide or lenalidomide plus D maintenance (26 cycles). The primary end point, stringent complete response (sCR) rate by the end of post-ASCT consolidation, favored D-RVd vs RVd (42.4% vs 32.0%; odds ratio, 1.57; 95% confidence interval, 0.87-2.82; 1-sided P = .068) and met the prespecified 1-sided α of 0.10. With longer follow-up (median, 22.1 months), responses deepened; sCR rates improved for D-RVd vs RVd (62.6% vs 45.4%; P = .0177), as did minimal residual disease (MRD) negativity (10-5 threshold) rates in the intent-to-treat population (51.0% vs 20.4%; P < .0001). Four patients (3.8%) in the D-RVd group and 7 patients (6.8%) in the RVd group progressed; respective 24-month progression-free survival rates were 95.8% and 89.8%. Grade 3/4 hematologic adverse events were more common with D-RVd. More infections occurred with D-RVd, but grade 3/4 infection rates were similar. Median CD34+ cell yield was 8.2 × 106/kg for D-RVd and 9.4 × 106/kg for RVd, although plerixafor use was more common with D-RVd. Median times to neutrophil and platelet engraftment were comparable. Daratumumab with RVd induction and consolidation improved depth of response in patients with transplant-eligible NDMM, with no new safety concerns. This trial was registered at www.clinicaltrials.gov as #NCT02874742.

摘要

来那度胺、硼替佐米和地塞米松(RVd)联合自体干细胞移植(ASCT)是适合移植的新发多发性骨髓瘤(NDMM)患者的标准一线治疗方法。评估了达雷妥尤单抗(D)联合 RVd(D-RVd)在适合移植的 NDMM 患者中的应用。患者(N=207)按 1:1 随机分为 D-RVd 或 RVd 诱导(4 个周期)、ASCT、D-RVd 或 RVd 巩固(2 个周期)、以及来那度胺或来那度胺加 D 维持(26 个周期)。主要终点是 ASCT 巩固后结束时严格完全缓解(sCR)率,D-RVd 优于 RVd(42.4% vs. 32.0%;优势比,1.57;95%置信区间,0.87-2.82;单侧 P=0.068),符合预定的单侧α=0.10。随着随访时间的延长(中位数,22.1 个月),缓解程度加深;D-RVd 组的 sCR 率高于 RVd 组(62.6% vs. 45.4%;P=0.0177),意向治疗人群的微小残留病灶(MRD)阴性率(10-5 界值)也更高(51.0% vs. 20.4%;P<.0001)。D-RVd 组有 4 例(3.8%)和 RVd 组有 7 例(6.8%)患者进展;相应的 24 个月无进展生存率分别为 95.8%和 89.8%。D-RVd 组更常见 3/4 级血液学不良事件。D-RVd 组发生更多感染,但 3/4 级感染发生率相似。D-RVd 组的中位 CD34+细胞产量为 8.2×106/kg,RVd 组为 9.4×106/kg,尽管 D-RVd 组更常使用普乐沙福。中性粒细胞和血小板植入的中位时间相当。RVd 诱导和巩固联合达雷妥尤单抗可提高适合移植的 NDMM 患者的缓解深度,且无新的安全性问题。该试验在 www.clinicaltrials.gov 上注册为#NCT02874742。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1db2/7441167/03f048e60393/bloodBLD2020005288absf1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验