Department of Hematology and Medical Oncology, Winship Cancer Institute, Emory University, Atlanta, GA.
J Clin Oncol. 2020 Jun 10;38(17):1928-1937. doi: 10.1200/JCO.19.02515. Epub 2020 Apr 16.
The combination of lenalidomide, bortezomib, and dexamethasone (RVD) is a highly effective and convenient induction regimen for both transplantation-eligible and -ineligible patients with myeloma. Here, we present the largest cohort of patients consecutively treated with RVD induction therapy followed by risk-adapted maintenance therapy with the longest follow-up and important information on long-term outcomes.
We describe 1,000 consecutive patients with newly diagnosed myeloma treated with RVD induction therapy from January 2007 until August 2016. Demographic and clinical characteristics and outcomes data were obtained from our institutional review board-approved myeloma database. Responses and progression were evaluated per International Myeloma Working Group Uniform Response Criteria.
The overall response rate was 97.1% after induction therapy and 98.5% after transplantation, with 89.9% of patients achieving a very good partial response (VGPR) or better and 33.3% achieving stringent complete response after transplantation at a median follow-up time of 67 months. The estimated median progression-free survival time was 65 months (95% CI, 58.7 to 71.3 months) for the entire cohort, 40.3 months (95% CI, 33.5 to 47 months) for high-risk patients, and 76.5 months (95% CI, 66.9 to 86.2 months) for standard-risk patients. The median overall survival (OS) time for the entire cohort was 126.6 months (95% CI, 113.3 to 139.8 months). The median OS for high-risk patients was 78.2 months (95% CI, 62.2 to 94.2 months), whereas it has not been reached for standard-risk patients. Five-year OS rates for high-risk and standard-risk patients were 57% and 81%, respectively, and the 10-year OS rates were 29% and 58%, respectively.
RVD is an induction regimen that delivers high response rates (VGPR or better) in close to 90% of patients after transplantation, and risk-adapted maintenance can deliver unprecedented long-term outcomes. This study includes the largest cohort of patients treated with RVD reported to date with long follow-up and demonstrates the ability of 3-drug induction regimens in patients with newly diagnosed multiple myeloma to result in a substantial survival benefit.
来那度胺、硼替佐米和地塞米松(RVD)联合方案是一种对适合移植和不适合移植的骨髓瘤患者都非常有效且方便的诱导方案。在这里,我们报告了最大的一组连续接受 RVD 诱导治疗的患者队列,随后进行了适应风险的维持治疗,随访时间最长,并提供了有关长期结果的重要信息。
我们描述了 1000 例新诊断骨髓瘤患者,他们在 2007 年 1 月至 2016 年 8 月期间接受了 RVD 诱导治疗。从我们机构审查委员会批准的骨髓瘤数据库中获得人口统计学和临床特征以及结局数据。根据国际骨髓瘤工作组统一反应标准评估反应和进展。
诱导治疗后总缓解率为 97.1%,移植后为 98.5%,89.9%的患者达到非常好的部分缓解(VGPR)或更好,33.3%的患者在中位随访时间为 67 个月时达到严格完全缓解。整个队列的估计中位无进展生存期为 65 个月(95%CI,58.7 至 71.3 个月),高危患者为 40.3 个月(95%CI,33.5 至 47 个月),标准风险患者为 76.5 个月(95%CI,66.9 至 86.2 个月)。整个队列的中位总生存期(OS)时间为 126.6 个月(95%CI,113.3 至 139.8 个月)。高危患者的中位 OS 为 78.2 个月(95%CI,62.2 至 94.2 个月),而标准风险患者的中位 OS 尚未达到。高危和标准风险患者的 5 年 OS 率分别为 57%和 81%,10 年 OS 率分别为 29%和 58%。
RVD 是一种诱导方案,在移植后近 90%的患者中可达到高缓解率(VGPR 或更好),适应性维持治疗可提供前所未有的长期结局。本研究包括迄今为止报道的接受 RVD 治疗的最大患者队列,随访时间长,并证明了新诊断多发性骨髓瘤患者使用 3 药诱导方案可显著获益。