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来那度胺联合硼替佐米和地塞米松治疗复发/难治性 t(11;14)和 1q21 增益多发性骨髓瘤。

Filanesib plus bortezomib and dexamethasone in relapsed/refractory t(11;14) and 1q21 gain multiple myeloma.

机构信息

Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, New York, USA.

Winship Cancer Institute, Emory University, Atlanta, Georgia, USA.

出版信息

Cancer Med. 2022 Jan;11(2):358-370. doi: 10.1002/cam4.4451. Epub 2021 Dec 17.

Abstract

Filanesib is a first-in-class kinesin spindle protein inhibitor which demonstrated safety and encouraging activity in combination with bortezomib and dexamethasone in relapsed/refractory multiple myeloma in a preliminary analysis of dose-escalation phase results. This multicenter study included first a dose-escalation phase to determine maximum tolerated dose of two schedules of filanesib, bortezomib, and dexamethasone and a subsequent dose-expansion phase using the maximum tolerated doses. In the dose-expansion phase, 28 patients were evaluable for safety and efficacy. The most common grade ≥3 adverse events were neutropenia (21%) and anemia (18%), which were noncumulative and reversible, and hypertension (18%). The overall response rate was 43% with median duration of response not yet reached (range, 2.8-23.7+ months) with median follow-up of 6.3 months. A post hoc analysis incorporated 29 dose-escalation phase patients who received therapeutic filanesib doses, with an overall response rate of 39% and median duration of response of 18.0 months among the 57 total patients with median progression-free survival of 8.5 months. Notably, the PFS of high risk patients was comparable at 8.5 months, driven by the patients with 1q21 gain, characterized by increased MCL-1 expression, with a PFS of 9.1 months versus 3.5 months for the remainder of high risk patients. Patients with t(11;14) also had an encouraging PFS of 15.0 months. The combination of filanesib, bortezomib, and dexamethasone continues to show safety and encouraging activity in relapsed/refractory multiple myeloma, particularly in those patients with 1q21 gain and t(11;14).

摘要

非奈司他是一种首创的驱动蛋白纺锤体蛋白抑制剂,在复发/难治性多发性骨髓瘤的初步分析中,与硼替佐米和地塞米松联合使用显示出安全性和令人鼓舞的疗效。这项多中心研究首先进行了剂量递增阶段,以确定两种方案的非奈司他、硼替佐米和地塞米松的最大耐受剂量,然后使用最大耐受剂量进行后续剂量扩展阶段。在剂量扩展阶段,28 名患者可评估安全性和疗效。最常见的≥3 级不良事件是中性粒细胞减少症(21%)和贫血(18%),这些不良事件是非累积性和可逆的,还有高血压(18%)。总缓解率为 43%,中位缓解持续时间尚未达到(范围 2.8-23.7+ 个月),中位随访时间为 6.3 个月。一项事后分析纳入了 29 名接受治疗剂量非奈司他的剂量递增阶段患者,总缓解率为 39%,57 名总患者的中位缓解持续时间为 18.0 个月,中位无进展生存期为 8.5 个月。值得注意的是,高风险患者的 PFS 为 8.5 个月,与 1q21 增益患者的 PFS 为 9.1 个月,而其余高风险患者的 PFS 为 3.5 个月相当,这些患者的特征是 MCL-1 表达增加。携带 t(11;14)的患者也有令人鼓舞的 PFS 为 15.0 个月。非奈司他、硼替佐米和地塞米松的联合治疗在复发/难治性多发性骨髓瘤中继续显示出安全性和令人鼓舞的疗效,特别是在那些 1q21 增益和 t(11;14)的患者中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4aab/8729045/eecf0d4e7947/CAM4-11-358-g004.jpg

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