Li Zhichao, Zhang Wenhao, Huang Fang, Hao Siguo
Department of Hematology, Xin Hua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, PR China.
Department of Lymphoma, Fudan University Shanghai Cancer Center, Shanghai, PR China.
Clinics (Sao Paulo). 2025 Jan 25;80:100575. doi: 10.1016/j.clinsp.2025.100575. eCollection 2025.
The common drugs used for the treatment of Newly Diagnosed Multiple Myeloma (NDMM) include bortezomib and lenalidomide, but the adverse effects of lenalidomide cannot be ignored, especially when it is used in the initial therapy.
This retrospective study evaluated the efficacy and safety of a modified DVD regimen (pegylated liposomal doxorubicin, bortezomib, and dexamethasone) followed by lenalidomide in the treatment of NDMM. A total of 40 NDMM patients were treated with a reduced dose of pegylated liposomal doxorubicin (20 mg/m) on day 1, subcutaneous bortezomib (1.3 mg/m) on days 1, 4, 8, and 11, and dexamethasone (20 mg) on days 1, 2, 3, 4, 8, 9, 11, and 12 (20 days for each course). When patients failed to achieve partial or better response after 2 courses of treatment, a regimen containing lenalidomide was administered. After the induction therapy, 15 eligible patients received Peripheral Blood Stem Cells (PBSC) mobilization and transplantation followed by maintenance therapy with lenalidomide.
The response rate (≥ very good partial response) was 55% and 80% after 2 and 4 courses, respectively. The 18-month Progression Free Survival (PFS) and Overall Survival (OS) were 78.6% and 83.4%, respectively. Grade 3 or 4 hematologic toxicity occurred in less than 10% of patients. In addition, all 15 transplant-eligible patients successfully mobilized PBSC (median CD34cells = 4.59 × 10/kg) and underwent autologous PSBC transplantation.
This study suggests that the modified DVD regimen followed by lenalidomide is an effective and well-tolerated regimen, and has little influence on the PBSC collection and transplantation for patients with NDMM.
用于治疗新诊断多发性骨髓瘤(NDMM)的常用药物包括硼替佐米和来那度胺,但来那度胺的不良反应不容忽视,尤其是在初始治疗中使用时。
这项回顾性研究评估了改良DVD方案(聚乙二醇化脂质体阿霉素、硼替佐米和地塞米松)序贯来那度胺治疗NDMM的疗效和安全性。共40例NDMM患者在第1天接受降低剂量的聚乙二醇化脂质体阿霉素(20mg/m),在第1、4、8和11天接受皮下注射硼替佐米(1.3mg/m),在第1、2、3、4、8、9、11和12天接受地塞米松(20mg)(每个疗程20天)。当患者在2个疗程治疗后未达到部分缓解或更好的缓解时,给予包含来那度胺的方案。诱导治疗后,15例符合条件的患者接受外周血干细胞(PBSC)动员和移植,随后接受来那度胺维持治疗。
2个疗程和4个疗程后的缓解率(≥非常好的部分缓解)分别为55%和80%。18个月的无进展生存期(PFS)和总生存期(OS)分别为78.6%和83.4%。不到10%的患者发生3级或4级血液学毒性。此外,所有15例符合移植条件的患者均成功动员PBSC(中位CD34细胞=4.59×10/kg)并接受自体PBSC移植。
本研究表明,改良DVD方案序贯来那度胺是一种有效且耐受性良好的方案,对NDMM患者采集和移植PBSC影响较小。