Real-world assessment of treatment multiple myeloma patients on the example of one hematology center

A. S. Luchinin, N. V. Minaeva
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Abstract

Relevance. Despite significant improvements in therapeutic options, patients with multiple myeloma (MM) experience a series of remissions and relapses requiring further lines of therapy, which requires the prescription of new lines of therapy. Methods. We analyzed the types and outcomes of treatment, attrition rates (AR) — the proportion of patients who dropped out of program therapy, and refractoriness to different lines of therapy (LOT) in 447 patients with MM between 2010 and 2022. Resalts. The AR was 17% between LOT-1 and LOT-2, 15% between LOT-2 and LOT-3, and 25% between LOT-3 and LOT- 4. In multivariate regression analysis, only high MM risk significantly increased AR risk. Each new progression of MM increased the number of patients with refractory to bortezomib, lenalidomide, or daratumumab. After LOT-1, LOT-2, and LOT-6%, 26%, and 53% of patients were double-refractory, respectively, and 54% were triple-refractory. Bortezomib- or lenalidomide-refractory patients had a 2.6-fold lower chance of achieving a very good partial response or better (VGPR+). From LOT-1 to LOT-4, the overall response rate and VGPR+ decreased from 74% and 53% to 25% and 15%, respectively. Overall survival (OS) in the entire population was 7.6 years, with an actuarial 5-year OS of 67% and a 10-year OS of 44%. The median of progression-free survival (PFS) was 20 months on LOT-1, 19 months on LOT-2, and 7 months on LOT-3, and the actuarial 5-year PFS was 25%, 18%, and 10%, respectively. Conclusions: In this regard, we observe a continuing trend in the use of cisplatin-containing "rescue" chemotherapy regimens, especially in patients with an aggressive course, including extramedullary forms of MM. These patients could be candidates for bispecific antibody therapy and CAR T-cell therapy, but these options are not yet available in Russia.
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以血液学中心为例,评估多发性骨髓瘤患者的实际治疗效果
的相关性。尽管治疗方案有了显著的改善,但多发性骨髓瘤(MM)患者经历了一系列的缓解和复发,需要进一步的治疗,这需要开出新的治疗方案。方法。我们分析了2010年至2022年间447名MM患者的治疗类型和结果、损失率(AR)——退出计划治疗的患者比例,以及对不同治疗方案的难治性(LOT)。Resalts。LOT-1和LOT-2的AR为17%,LOT-2和LOT-3的AR为15%,LOT-3和LOT- 4的AR为25%。在多元回归分析中,只有高MM风险显著增加AR风险。MM的每一个新进展都增加了对硼替佐米、来那度胺或达拉单抗难治的患者数量。经LOT-1、LOT-2和LOT-1治疗后,分别有6%、26%和53%的患者为双重难治性,54%的患者为三重难治性。硼替佐米或来那度胺难治性患者获得非常好的部分缓解或更好(VGPR+)的几率低2.6倍。从LOT-1到LOT-4,总有效率和VGPR+分别从74%和53%下降到25%和15%。整个人群的总生存期(OS)为7.6年,精算5年OS为67%,10年OS为44%。LOT-1的中位无进展生存期(PFS)为20个月,LOT-2为19个月,LOT-3为7个月,精算5年PFS分别为25%,18%和10%。结论:在这方面,我们观察到使用含顺铂的“拯救”化疗方案的持续趋势,特别是在侵袭性病程的患者中,包括髓外形式的MM。这些患者可能是双特异性抗体治疗和CAR - t细胞治疗的候选人,但这些选择在俄罗斯尚不可用。
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发文量
22
审稿时长
2 weeks
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