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Momelotinib 的长期安全性和生存获益:3 期随机对照临床试验的综合分析。

Momelotinib long-term safety and survival in myelofibrosis: integrated analysis of phase 3 randomized controlled trials.

机构信息

The University of Texas MD Anderson Cancer Center, Houston, TX.

UT Health San Antonio Cancer Center, San Antonio, TX.

出版信息

Blood Adv. 2023 Jul 25;7(14):3582-3591. doi: 10.1182/bloodadvances.2022009311.

Abstract

Momelotinib is the first inhibitor of Janus kinase 1 (JAK1) and JAK2 shown to also inhibit activin A receptor type 1 (ACVR1), a key regulator of iron homeostasis, and has demonstrated improvements in splenomegaly, constitutional symptoms, and anemia in myelofibrosis (MF). This long-term analysis pooled data from 3 randomized phase 3 studies of momelotinib (MOMENTUM, SIMPLIFY-1, and SIMPLIFY-2), representing MF disease from early (JAK inhibitor-naive) to late (JAK inhibitor-experienced) stages. Patients in the control arms (danazol in MOMENTUM, ruxolitinib in SIMPLIFY-1, and best available therapy in SIMPLIFY-2) could cross over to receive momelotinib at the end of the 24-week randomized period, and all patients could continue momelotinib treatment after the completion of these studies via an extended access protocol (XAP). Across these studies, 725 patients with MF received momelotinib; 12% remained on therapy for ≥5 years, with a median treatment exposure of 11.3 months (range, 0.1-90.4 months). The most common nonhematologic treatment-emergent adverse event (AE) occurring in ≥20% of patients was diarrhea (any grade, 27% and grade ≥3, 3%). Any-grade thrombocytopenia, anemia, and neutropenia occurred in 25%, 23%, and 7% of patients, respectively. The most common reason for momelotinib discontinuation was thrombocytopenia (4% discontinuation rate). The incidence of AEs of clinical importance (eg, infections, malignant transformation, peripheral neuropathy, and hemorrhage) did not increase over time. This analysis of one of the largest randomized trial databases for a JAK inhibitor to date in MF demonstrated a consistent safety profile of momelotinib without long-term or cumulative toxicity. These trials were registered at www.clinicaltrials.gov as: MOMENTUM (#NCT04173494), SIMPLIFY-1 (#NCT01969838), SIMPLIFY-2 (#NCT02101268), and XAP (#NCT03441113).

摘要

莫洛替尼是首个被证实可同时抑制激活素 A 受体 1(ACVR1)的 Janus 激酶 1(JAK1)和 JAK2 抑制剂,ACVR1 是铁稳态的关键调节剂。在骨髓纤维化(MF)中,莫洛替尼可改善脾肿大、全身症状和贫血。这项长期分析汇总了来自 3 项莫洛替尼随机 3 期研究(MOMENTUM、SIMPLIFY-1 和 SIMPLIFY-2)的数据,代表了 MF 疾病从早期(JAK 抑制剂初治)到晚期(JAK 抑制剂经治)的阶段。对照组(MOMENTUM 中的达那唑、SIMPLIFY-1 中的鲁索利替尼和 SIMPLIFY-2 中的最佳可用疗法)的患者可在 24 周随机期结束时交叉接受莫洛替尼治疗,所有患者可在这些研究完成后通过扩展获得途径(XAP)继续接受莫洛替尼治疗。在这些研究中,725 名 MF 患者接受了莫洛替尼治疗;12%的患者持续治疗时间≥5 年,中位治疗暴露时间为 11.3 个月(范围:0.1-90.4 个月)。最常见的≥20%患者发生的非血液学治疗中出现的不良事件(AE)是腹泻(任何级别,27%和≥3 级,3%)。任何级别的血小板减少症、贫血和中性粒细胞减少症分别发生在 25%、23%和 7%的患者中。莫洛替尼停药的最常见原因是血小板减少症(停药率为 4%)。有临床意义的 AE(如感染、恶性转化、周围神经病和出血)的发生率并未随时间增加。这项迄今为止针对 MF 的最大规模随机试验数据库之一的分析显示,莫洛替尼具有一致的安全性,没有长期或累积毒性。这些试验在 www.clinicaltrials.gov 上注册为:MOMENTUM(#NCT04173494)、SIMPLIFY-1(#NCT01969838)、SIMPLIFY-2(#NCT02101268)和 XAP(#NCT03441113)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e39/10368854/5f9c8a266eae/BLOODA_ADV-2022-009311-fx1.jpg

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