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加拿大来那度胺治疗多发性骨髓瘤后的治疗模式和结局的回顾性研究。

Retrospective study of treatment patterns and outcomes post-lenalidomide for multiple myeloma in Canada.

机构信息

Department of Medical Oncology and Hematology, Princess Margaret Cancer Centre, Toronto, ON, Canada.

Canadian Myeloma Research Group, Toronto, ON, Canada.

出版信息

Eur J Haematol. 2021 Oct;107(4):416-427. doi: 10.1111/ejh.13678. Epub 2021 Jun 27.

Abstract

Lenalidomide is an important component of initial therapy in newly diagnosed multiple myeloma, either as maintenance therapy post-autologous stem cell transplantation (ASCT) or as first-line therapy with dexamethasone for patients' ineligible for ASCT (non-ASCT). This retrospective study investigated treatment patterns and outcomes for ASCT-eligible and -ineligible patients who relapsed after lenalidomide as part of first-line therapy, based on data from the Canadian Myeloma Research Group Database for patients treated between January 2007 and April 2019. Among 256 patients who progressed on lenalidomide maintenance therapy, 28.5% received further immunomodulatory derivative-based (IMiD-based) therapy (lenalidomide/pomalidomide) without a proteasome inhibitor (PI) (bortezomib/carfilzomib/ixazomib), 26.2% received PI-based therapy without an IMiD, 19.5% received both an IMiD plus PI, 13.5% received daratumumab-based regimens, and 12.1% underwent salvage ASCT. Median progression-free survival (PFS) was longest for daratumumab-based therapy (22.7 months) and salvage ASCT (23.4 months) and ranged from 6.6 to 7.3 months for the other treatments (P < .0001). Median overall survival (OS) was also longest for daratumumab and salvage ASCT. A total of 87 non-ASCT patients received subsequent therapy, with 66.7% receiving bortezomib-based therapy and 13.8% receiving other PI-based therapy. Median PFS was 15.4 and 24.8 months for bortezomib-based and other PI-based therapy, respectively (P = .404). During most of the study period, daratumumab was not funded; in this setting, switching to a different therapeutic class following relapse on lenalidomide produced the longest remissions for non-ASCT patients. Further prospective studies are warranted to determine optimum treatment following relapse on lenalidomide, especially in the light of increased access to daratumumab.

摘要

来那度胺是新诊断多发性骨髓瘤初始治疗的重要组成部分,无论是自体干细胞移植 (ASCT) 后作为维持治疗,还是对于不适合 ASCT(非 ASCT)的患者,联合地塞米松作为一线治疗。这项回顾性研究基于加拿大骨髓瘤研究组数据库中 2007 年 1 月至 2019 年 4 月期间接受治疗的患者数据,调查了来那度胺作为一线治疗时复发的 ASCT 患者和非 ASCT 患者的治疗模式和结局。在 256 名接受来那度胺维持治疗后进展的患者中,28.5%的患者未接受蛋白酶体抑制剂(硼替佐米/卡非佐米/伊沙佐米)的进一步免疫调节衍生物(IMiD)治疗(来那度胺/泊马度胺),26.2%的患者接受了无 IMiD 的蛋白酶体抑制剂治疗,19.5%的患者接受了 IMiD 和蛋白酶体抑制剂联合治疗,13.5%的患者接受了达雷妥尤单抗为基础的治疗方案,12.1%的患者接受了挽救性 ASCT。达雷妥尤单抗为基础的治疗(22.7 个月)和挽救性 ASCT(23.4 个月)的中位无进展生存期(PFS)最长,而其他治疗的中位 PFS 范围为 6.6 至 7.3 个月(P<0.0001)。达雷妥尤单抗和挽救性 ASCT 的中位总生存期(OS)也最长。共有 87 名非 ASCT 患者接受了后续治疗,其中 66.7%接受了硼替佐米为基础的治疗,13.8%接受了其他蛋白酶体抑制剂为基础的治疗。硼替佐米为基础的治疗的中位 PFS 为 15.4 个月,其他蛋白酶体抑制剂为基础的治疗的中位 PFS 为 24.8 个月(P=0.404)。在研究期间的大部分时间里,达雷妥尤单抗都没有得到资助;在这种情况下,非 ASCT 患者在来那度胺治疗后复发时,切换到不同的治疗类别会产生最长的缓解期。需要进一步的前瞻性研究来确定来那度胺治疗后复发的最佳治疗方法,特别是考虑到达雷妥尤单抗的应用机会增加。

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