Belumosudil for Chronic Graft-Versus-Host Disease: Analysis of Long-Term Results from the KD025-208 and ROCKstar Studies.

IF 3.6 3区 医学 Q2 HEMATOLOGY
Stephanie J Lee, Steven Pavletic, Bruce R Blazar, Yu Yao, Ran Ji, Kathy Marshall, Corey Cutler
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Abstract

Belumosudil is an oral selective rho-associated coiled-coil-containing protein kinase-2 (ROCK2) inhibitor approved for the treatment of chronic graft-versus-host disease (cGVHD) following an allogeneic hematopoietic cell transplant in patients aged ≥12 years after failure of ≥2 prior systemic lines of therapy. The KD025-208 (NCT02841995) and KD025-213 (ROCKstar; NCT03640481) studies demonstrated that belumosudil was well tolerated, with clinically meaningful responses in patients with cGVHD. KD025-217 (NCT05305989) is a follow-up study that evaluated extended treatment with belumosudil in patients enrolled in the parent studies, KD025-208 and ROCKstar. This pooled analysis reports the long-term follow-up (overall median follow-up duration of 31.4 months) results from these studies in patients with cGVHD. The study included a total of 208 patients across 3 cohorts. Cohort 1 (n = 95) received belumosudil 200 mg once daily, cohort 2 (n = 92) received belumosudil 200 mg twice daily, and cohort 3 (n = 21) received belumosudil 400 mg once daily. The primary endpoint was best overall response rate (ORR). Duration of response (DOR), failure-free survival (FFS), and time to next treatment (TTNT) were also evaluated in this analysis. The best ORR in the modified intent-to-treat (mITT) population was 72%. The median DOR for the responder population was 62.3 weeks (range, 36.1 to 82.6 weeks). The median FFS in the mITT population was 15.1 months (range, 11.3 to 20.6 months). The 1- and 2-year FFS rates were 56% and 40%, respectively. The median TTNT was 22.1 months (range, 15.2 to 40.3 months), where 47% of patients received a new systemic therapy for cGVHD by 36 months. When compared with the published data, the long-term results from this pooled analysis of these two phase 2 studies demonstrated belumosudil was associated with durable responses, and it remained well tolerated with no new safety concerns.

白莫硫地尔治疗慢性移植物抗宿主病:KD025-208和ROCKstar研究的长期结果分析
背景:Belumosudil是一种口服选择性rho相关的含螺旋状蛋白激酶-2 (ROCK2)抑制剂,被批准用于治疗年龄≥12岁的异基因造血细胞移植(alloHCT)后慢性移植物抗宿主病(cGVHD),患者在既往≥2个系统性治疗线(LOTs)失败后。KD025-208 (NCT02841995)和KD025-213 (ROCKstar;NCT03640481)研究表明,白莫硫地尔耐受性良好,在cGVHD患者中具有临床意义的应答。KD025-217 (NCT05305989)是一项随访研究,评估了在母研究KD025-208和ROCKstar中入组的患者使用白莫硫地尔的延长治疗。目的:本汇总分析报告了这些研究对cGVHD患者的长期随访(总中位随访时间为31.4个月)结果。研究设计:本研究共纳入3个队列的208例患者。队列1 (n=95)接受白莫硫地尔200 mg每日1次,队列2 (n=92)接受白莫硫地尔200 mg每日2次,队列3 (n=21)接受白莫硫地尔400 mg每日1次。主要终点为最佳总有效率(ORR)。该分析还评估了反应持续时间(DOR)、无故障生存期(FFS)和下一次治疗时间(TTNT)。结果:改良意向治疗(mITT)人群的最佳ORR为72%。应答人群的DOR中位数为62.3周(范围36.1-82.6周)。mITT人群中位FFS为15.1个月(范围11.3-20.6个月)。1年和2年FFS率分别为56%和40%。中位TTNT为22.1个月(15.2-40.3个月),其中47%的患者在36个月前接受了新的全身治疗。结论:与已发表的数据相比,这两项2期研究的汇总分析的长期结果表明,白莫硫地尔具有持久的疗效,并且耐受性良好,没有新的安全性问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.00
自引率
15.60%
发文量
1061
审稿时长
51 days
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