Department of Hematology and Rheumatology, Tohoku University Hospital, 1-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi, 980-857, Japan.
Department of Hematology, Sendai Medical Center, National Hospital Organization, Sendai, Miyagi, Japan.
Ann Hematol. 2020 Oct;99(10):2351-2356. doi: 10.1007/s00277-020-04240-x. Epub 2020 Aug 31.
Lenalidomide (Len) and dexamethasone (dex) therapy is a standard therapy in patients with multiple myeloma. Elderly or unfit patients may reduce Len or dex doses to prevent toxicities that lead to treatment discontinuation. However, there have been few studies evaluating the efficacy and safety of lower doses of Len and dex. We conducted a phase II study of 1.5-year low-dose Len and dex therapy following melphalan and prednisolone (MP), the number of which cycles was determined by a response within 9 cycles. The Len dose was 10 mg daily and the dex dose was 20 mg weekly, which were continued for 1.5 years. Twenty-one patients were enrolled. The median number of cycles of MP was 3 (range, 2-9). The overall response rate was 81% and a very good partial response or better was achieved in 33.3% of patients. The median follow-up time for survivors was 70.5 months (range, 42-83 months), the median progression-free survival (PFS) was 27 months (95% CI, 21-33 months), and the median overall survival was not reached. Grade 3 or 4 adverse events were observed in 28.6% of patients. In conclusion, the low-dose Len and dex therapy safely achieved comparable efficacies to the standard-dose regimen in elderly patients with newly diagnosed multiple myeloma. UMIN000007889.
来那度胺(Len)和地塞米松(dex)治疗是多发性骨髓瘤患者的标准治疗方法。老年或身体状况不佳的患者可能会减少 Len 或 dex 的剂量,以防止导致治疗中断的毒性。然而,很少有研究评估低剂量 Len 和 dex 的疗效和安全性。我们进行了一项为期 1.5 年的低剂量 Len 和 dex 治疗的 II 期研究,该研究在接受美法仑和泼尼松(MP)治疗后进行,其周期数取决于 9 个周期内的反应。Len 的剂量为每天 10 毫克,dex 的剂量为每周 20 毫克,持续 1.5 年。共纳入 21 例患者。MP 的中位周期数为 3(范围,2-9)。总体缓解率为 81%,33.3%的患者达到非常好的部分缓解或更好。幸存者的中位随访时间为 70.5 个月(范围,42-83 个月),中位无进展生存期(PFS)为 27 个月(95%CI,21-33 个月),中位总生存期未达到。3 级或 4 级不良事件发生率为 28.6%。总之,低剂量 Len 和 dex 治疗在新诊断的多发性骨髓瘤老年患者中安全地达到了与标准剂量方案相当的疗效。UMIN000007889。