Department of Medicine and Biosystemic Sciences, Kyushu University Graduate School of Medicine, Fukuoka, Japan.
Division of Hematology, Graduate School of Medical and Dental Sciences, Niigata University, Niigata, Japan.
Cancer Sci. 2024 Jun;115(6):2002-2011. doi: 10.1111/cas.16158. Epub 2024 Mar 18.
Triplet regimen comprising proteasome inhibitors, immunomodulatory drugs, and dexamethasone (DEX) is a recommended induction/consolidation therapy for multiple myeloma (MM) patients eligible for transplant. In this Japanese phase II study conducted from 2017 to 2019, newly diagnosed MM patients aged 20-65 received four induction cycles with bortezomib (Bor), lenalidomide (Len), and DEX (VRD), followed by Bor and high-dose melphalan with autologous stem cell rescue. Subsequently, they underwent four consolidation cycles with carfilzomib, Len, and DEX (KRD), followed by Len maintenance until disease progression. A total of 141 patients were analyzed. In an intent-to-treat population, the complete or better response post induction was 19.9%, rising to 39.7%, 58.9%, and 62.4% after transplant, consolidation, and 1-year maintenance, respectively. With a median follow-up of 38 months, the 3-year progression-free survival (PFS) rate was 83.5% and the 3-year overall survival rate was 92.5%. Severe adverse events (≥grade 3) occurred in ~30% of patients; however, there was no treatment-related mortality. These findings clearly showed the tolerability and effectiveness of this protocol. Nevertheless, patients with high-risk cytogenetics showed a trend toward lower 3-year PFS than those without (77.8% vs. 89.4%, p = 0.051), and ultra-high-risk cytogenetics (≥2 high-risk cytogenetics) had an even worse prognosis, with 61.2% 3-year PFS. To overcome this situation, a more potent treatment strategy incorporating novel agents such as the CD38-antibody should be assessed in future studies.
三药联合方案(蛋白酶体抑制剂、免疫调节剂和地塞米松)是适合移植的多发性骨髓瘤(MM)患者的推荐诱导/巩固治疗方案。在这项于 2017 年至 2019 年进行的日本 II 期研究中,年龄在 20-65 岁的新发 MM 患者接受了四个硼替佐米(Bor)、来那度胺(Len)和地塞米松(VRD)诱导周期治疗,随后接受了 Bor 和大剂量马法兰联合自体干细胞挽救。随后,他们接受了四个卡非佐米、来那度胺和地塞米松(KRD)巩固周期治疗,随后进行来那度胺维持治疗,直至疾病进展。共分析了 141 例患者。在意向治疗人群中,诱导后完全或更好缓解率为 19.9%,移植后、巩固后和 1 年维持后分别上升至 39.7%、58.9%和 62.4%。中位随访 38 个月时,3 年无进展生存(PFS)率为 83.5%,3 年总生存率为 92.5%。约 30%的患者发生严重不良事件(≥3 级);然而,无治疗相关死亡。这些发现清楚地表明了该方案的耐受性和有效性。然而,具有高危细胞遗传学的患者 3 年 PFS 率低于无高危细胞遗传学的患者(77.8%比 89.4%,p=0.051),超高危细胞遗传学(≥2 种高危细胞遗传学)预后更差,3 年 PFS 率为 61.2%。为了克服这种情况,未来的研究应评估更有效的治疗策略,包括新型药物,如 CD38 抗体。