Division of Hematologic Malignancies and Cellular Therapeutics, University of Kansas Medical Center, Westwood, KS.
University of Kansas Medical Center, Westwood, KS.
Clin Lymphoma Myeloma Leuk. 2021 Feb;21(2):e220-e226. doi: 10.1016/j.clml.2020.09.002. Epub 2020 Sep 30.
Aggressive relapsed/refractory multiple myeloma (RRMM) often requires salvage cytotoxic chemotherapy. We evaluated the efficacy and toxicity of VD-PACE (bortezomib, dexamethasone, cisplatin, doxorubicin, cyclophosphamide, etoposide) with an immunomodulatory agent (IMiD) in RRMM.
We retrospectively reviewed the effectiveness and tolerability among 30 patients with RRMM receiving ≥ 1 cycle of VD-PACE + IMiD between January 2012 to April 2019.
Of 30 patients, 26 (86%) had myeloma double refractory to protease inhibitors and IMiDs, and had received a median of 3 lines prior of therapy. The overall response rate was 67.7%, 13% patients experienced complete remission or better, and 13% experienced very good partial response. Median progression-free and median overall survival were 11 and 26 months, respectively. The most common grade 3 or higher adverse events were hematologic events, which were manageable.
VD-PACE + IMiD is an effective and tolerable salvage treatment for RRMM, with an impressive response rate in pretreated RRMM.
侵袭性复发/难治性多发性骨髓瘤(RRMM)常需要挽救性细胞毒化疗。我们评估了 VD-PACE(硼替佐米、地塞米松、顺铂、多柔比星、环磷酰胺、依托泊苷)联合免疫调节剂(IMiD)在 RRMM 中的疗效和毒性。
我们回顾性分析了 2012 年 1 月至 2019 年 4 月期间 30 例接受 VD-PACE+IMiD 治疗≥1 个周期的 RRMM 患者的有效性和耐受性。
30 例患者中,26 例(86%)对蛋白酶抑制剂和 IMiD 双重耐药,治疗前中位数接受了 3 线治疗。总体缓解率为 67.7%,13%的患者达到完全缓解或更好,13%的患者达到非常好的部分缓解。中位无进展生存期和中位总生存期分别为 11 个月和 26 个月。最常见的 3 级或以上不良事件为血液学事件,可控制。
VD-PACE+IMiD 是 RRMM 有效且耐受良好的挽救性治疗方法,在预处理 RRMM 中具有令人印象深刻的缓解率。