Haematology Department, University Hospital of Salamanca/IBSAL, Salamanca, Spain.
Clínica Universidad de Navarra-CIMA, IDISNA, CIBERONC, Pamplona, Spain.
Leuk Lymphoma. 2020 Mar;61(3):680-690. doi: 10.1080/10428194.2019.1675881. Epub 2019 Nov 5.
For patients with newly diagnosed multiple myeloma (NDMM) who are transplant ineligible, bortezomib-melphalan-prednisone (VMP) demonstrated superior efficacy based on the VISTA trial. In subsequent trials, twice-weekly bortezomib was limited to the first cycle or completely replaced with once-weekly bortezomib to reduce toxicity. Following a systematic literature review, the efficacy and safety of modified VMP schedules (pooled data from the once-weekly bortezomib VMP arm of the GIMEMA trial and the VMP arm of the ALCYONE trial) were compared to the VISTA schedule using naïve and unanchored matching-adjusted indirect comparison (MAIC). Median progression-free survival was similar between VISTA and modified VMP (20.7 months [95% CI, 18.4-24.3] vs 19.6 months [95% CI, 18.8-21.0]). Peripheral neuropathy was significantly reduced with modified VMP versus VISTA VMP (all grades: naïve, 32.1% vs 46.8% and MAIC, 32.1% vs 46.7%; both < .0001). These findings support a modified VMP dosing schedule for patients with NDMM who are transplant ineligible.
对于不适合移植的新诊断多发性骨髓瘤(NDMM)患者,硼替佐米-美法仑-泼尼松(VMP)方案在 VISTA 试验中显示出更好的疗效。在随后的试验中,为了降低毒性,每周两次的硼替佐米限制在第一个周期或完全被每周一次的硼替佐米替代。通过系统文献回顾,使用未调整和锚定匹配调整间接比较(MAIC),比较了改良 VMP 方案(来自 GIMEMA 试验每周一次硼替佐米 VMP 臂和 ALCYONE 试验 VMP 臂的合并数据)与 VISTA 方案的疗效和安全性。VISTA 和改良 VMP 之间的中位无进展生存期相似(20.7 个月[95%CI,18.4-24.3]与 19.6 个月[95%CI,18.8-21.0])。与 VISTA-VMP 相比,改良 VMP 方案外周神经病变显著减少(所有级别:未调整,32.1% vs 46.8%和 MAIC,32.1% vs 46.7%;均 < 0.0001)。这些发现支持为不适合移植的 NDMM 患者选择改良 VMP 剂量方案。