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基于卡非佐米的治疗的深度应答者的疗效和安全性特征:来自 ASPIRE 和 ENDEAVOR 的亚组分析。

Efficacy and safety profile of deep responders to carfilzomib-based therapy: a subgroup analysis from ASPIRE and ENDEAVOR.

机构信息

Department of Oncology and Hematology, University Medical Center of Hamburg-Eppendorf, Hamburg, Germany.

Institute of Biomedical Research of Salamanca (IBSAL), Cancer Research Center-IBMCC (USAL-CSIC), and Hematology Department, University Hospital of Salamanca, Salamanca, Spain.

出版信息

Leukemia. 2021 Jun;35(6):1732-1744. doi: 10.1038/s41375-020-01049-5. Epub 2020 Oct 16.

Abstract

To understand the profile of best responders (complete response or better [≥CR]) to carfilzomib, we described the characteristics, progression-free survival (PFS), overall survival (OS) data, and the safety of patients who achieved ≥CR to carfilzomib-based treatment in ASPIRE and ENDEAVOR. In post hoc analyses from ASPIRE and ENDEAVOR, median PFS and OS were longer for ≥CR patients versus those who achieved a very good partial response or partial response (VGPR/PR). In the carfilzomib arm of ASPIRE, median PFS was 50.4 months for ≥CR versus 22.1 months for VGPR/PR; median OS was 67.0 versus 44.2 months, respectively. In the carfilzomib arm of ENDEAVOR, median PFS was 34.0 for ≥CR versus 20.4 months for VGPR/PR; median OS was non-estimable. Despite the longer treatment duration, fewer patients with ≥CR versus VGPR/PR experienced treatment-emergent adverse events that led to discontinuation of carfilzomib-based treatment in ASPIRE or ENDEAVOR. Low serum lactate dehydrogenase was the only factor associated with achieving ≥CR vs patients not achieving CR in ASPIRE in multivariate regression analyses. No association was found between cytogenetic risk status and reaching ≥CR. Carfilzomib treatment may lead to rapid and deep responses, irrespective of most patient characteristics.

摘要

为了了解卡非佐米最佳应答者(完全缓解或更好[≥CR])的特征,我们描述了在 ASPIRE 和 ENDEAVOR 中达到卡非佐米治疗≥CR 的患者的特征、无进展生存期(PFS)、总生存期(OS)数据和安全性。在 ASPIRE 和 ENDEAVOR 的事后分析中,与达到非常好的部分缓解或部分缓解(VGPR/PR)的患者相比,≥CR 患者的中位 PFS 和 OS 更长。在 ASPIRE 中的卡非佐米组中,≥CR 的中位 PFS 为 50.4 个月,而 VGPR/PR 为 22.1 个月;中位 OS 分别为 67.0 和 44.2 个月。在 ENDEAVOR 中的卡非佐米组中,≥CR 的中位 PFS 为 34.0 个月,而 VGPR/PR 为 20.4 个月;中位 OS 不可估计。尽管治疗时间更长,但与 VGPR/PR 相比,≥CR 的患者发生导致卡非佐米治疗停药的治疗中出现的不良事件更少,在 ASPIRE 或 ENDEAVOR 的多变量回归分析中,低血清乳酸脱氢酶是唯一与达到≥CR 相关的因素。未发现细胞遗传学风险状况与达到≥CR 之间存在相关性。卡非佐米治疗可能会导致快速而深度的反应,而与大多数患者特征无关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ccb/8179852/8107b63d67a1/41375_2020_1049_Fig1_HTML.jpg

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