Tanimura Akira, Hirai Risen, Nakamura Miki, Takeshita Masataka, Togano Tomiteru, Sekine Rieko, Hagiwara Shotaro, Miwa Akiyoshi
Dept. of Hematology, Tokyo-Kita Medical Center.
Gan To Kagaku Ryoho. 2020 May;47(5):789-796.
Autologous stem cell transplantation(ASCT)for newly-diagnosed multiple myeloma(NDMM)has underwent recent improvements in combination with novel agents-containing induction and post-ASCT therapy. Since the approval of bortezomib for NDMM in Japan, we conducted the following regimen(BD arm)in transplant-eligible patients with NDMM: BD (bortezomib and dexamethasone)induction, ASCT, VRD consolidation, and maintenance therapy with immunomodulatory drugs(IMIDs). The efficacy and safety of the BD arm were compared to those of patients treated with vincristine, doxorubicin, and dexamethasone(VAD)induction followed by ASCT(VAD arm)retrospectively. Thirty-three patients were treated with the BD arm, and 92 patients with the VAD arm. Thirty-one patients in the BD arm proceeded to ASCT. Thereafter, 23 and 17 patients received VRD consolidation and IMIDs maintenance therapy, respectively. The rates of complete response/Bvery good partial response after ASCT, consolidation, and maintenance therapy were 43%/61%, 76%/90% and 87%/93%, respectively. The response rates after ASCT did not differ between BD and VAD arms. The median PFS was 46.2 months(BD arm)and 30.6 months(VAD arm)(HR 0.48[0.27-0.85], p=0.0106). The median OS was not-reached(BD arm)and 90.6 months(VAD arm)(HR 0.21[0.05-0.87], p=0.0172). VRD consolidation and IMIDs maintenance therapies improved disease status after ASCT and prolonged PFS and OS.
新诊断多发性骨髓瘤(NDMM)的自体干细胞移植(ASCT)在与含新型药物的诱导及ASCT后治疗联合应用方面取得了近期进展。自硼替佐米在日本获批用于NDMM以来,我们对符合移植条件的NDMM患者采用了以下方案(BD组):BD(硼替佐米和地塞米松)诱导、ASCT、VRD巩固以及使用免疫调节剂(IMIDs)进行维持治疗。将BD组的疗效和安全性与接受长春新碱、阿霉素和地塞米松(VAD)诱导后行ASCT的患者(VAD组)进行回顾性比较。33例患者接受BD组治疗,92例患者接受VAD组治疗。BD组31例患者进行了ASCT。此后,分别有23例和17例患者接受了VRD巩固和IMIDs维持治疗。ASCT、巩固和维持治疗后的完全缓解/非常好的部分缓解率分别为43%/61%、76%/90%和87%/93%。ASCT后的缓解率在BD组和VAD组之间无差异。中位无进展生存期(PFS)在BD组为46.2个月,在VAD组为30.6个月(风险比[HR]0.48[0.27 - 0.85],p = 0.0106)。中位总生存期(OS)在BD组未达到,在VAD组为90.6个月(HR 0.21[0.05 - 0.87],p = 0.0172)。VRD巩固和IMIDs维持治疗改善了ASCT后的疾病状态,并延长了PFS和OS。