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成纤维细胞性骨化发育不良成人患者flare-ups 的特征及 garetosmab 的影响:LUMINA-1 试验的一项随机、双盲、安慰剂对照的事后分析。

Characterization of flare-ups and impact of garetosmab in adults with fibrodysplasia ossificans progressiva: a post hoc analysis of the randomized, double-blind, placebo-controlled LUMINA-1 trial.

机构信息

Centre for Metabolic Bone Disease, Royal National Orthopaedic Hospital NHS Trust, London, W1W 5AQ, United Kingdom.

Program for Metabolic Bone Disorders, Vanderbilt University Medical Center, Nashville, TN 37232, United States.

出版信息

J Bone Miner Res. 2024 Sep 26;39(10):1486-1492. doi: 10.1093/jbmr/zjae140.

Abstract

Fibrodysplasia ossificans progressiva (FOP) is an ultra-rare disorder, characterized by progressive heterotopic ossification (HO) and painful soft-tissue inflammatory flare-ups. This was a post hoc analysis from a phase 2 (NCT03188666) trial in which adults with FOP received intravenous anti-activin A antibody garetosmab 10 mg/kg or placebo every 4 wk over 28 wk (Period 1), followed by a 28-wk open-label treatment and extension (Periods 2 and 3). Here we describe flare-ups, their relationship to new HO lesions, and the impact of garetosmab on flare-ups. Volume of new HO lesions was measured by CT. Patient-reported flare-ups were defined by any 2 of the following: new onset of pain, swelling, joint stiffness, decrease in movement, or perceived presence of HO. Flare-ups were experienced by 71% (17/24) of placebo-treated patients, 59% (10/17) of whom developed a new HO lesion irrespective of flare-up location; 24% of flare-ups location-matched new HO lesions. Twenty-nine new HO lesions occurred in the placebo cohort by week 28, of which 12 (41%) occurred in the same location as new or ongoing flare-ups. A higher volume of newly formed heterotopic bone (week 28) occurred in placebo-treated patients who had experienced a prior flare-up vs those without (median [Q1:Q3] of 16.6 [12.0:31.1] vs 3.2 cm3). Garetosmab was previously shown to decrease patient-reported flare-up frequency in Period 1; here, garetosmab reduced the median (Q1:Q3) duration of patient-reported flares (15.0 [6.0:82.0] vs 48.0 [15.0:1.00] d) and the severity of flare-ups vs placebo. Frequency of corticosteroid use was numerically reduced in those treated with garetosmab (40.0%) vs placebo (58.3%). In this analysis, 71% of placebo-treated adults with FOP experienced flare-ups over 28 wk, which were associated with an increased volume of newly formed heterotopic bone. Garetosmab reduced the severity and duration of flare-ups, with effects sustained during the entire trial.

摘要

进行性骨化性纤维发育不良(FOP)是一种超罕见疾病,其特征为进行性异位骨化(HO)和伴有疼痛的软组织炎症发作。这是一项 2 期(NCT03188666)试验的事后分析,该试验中,FOP 成人患者接受静脉注射抗激活素 A 抗体 garetosmab 10mg/kg 或安慰剂,每 4 周一次,持续 28 周(第 1 期),随后进行 28 周的开放标签治疗和扩展(第 2 期和第 3 期)。在此,我们描述了发作情况,它们与新的 HO 病变的关系,以及 garetosmab 对发作的影响。通过 CT 测量新 HO 病变的体积。患者报告的发作定义为以下任何 2 种情况:疼痛、肿胀、关节僵硬、运动减少或感知到 HO 的出现。71%(17/24)接受安慰剂治疗的患者经历了发作,其中 59%(10/17)的患者出现了新的 HO 病变,而与发作部位无关;24%的发作与部位匹配的新 HO 病变。安慰剂组在第 28 周时发生了 29 处新的 HO 病变,其中 12 处(41%)发生在新的或持续发作的同一部位。与没有发作的患者相比,经历过发作的安慰剂治疗患者的新形成异位骨(第 28 周)体积更大(中位数[Q1:Q3]为 16.6[12.0:31.1]与 3.2cm3)。garetosmab 在第 1 期显示可降低患者报告的发作频率;在此,garetosmab 降低了患者报告的发作持续时间(15.0[6.0:82.0]与 48.0[15.0:1.00]d)和发作严重程度的中位数(Q1:Q3)与安慰剂相比。与安慰剂相比,接受 garetosmab 治疗的患者皮质类固醇的使用频率呈数值降低(40.0%)。在这项分析中,28 周内,71%接受安慰剂治疗的 FOP 成人患者经历了发作,这与新形成异位骨的体积增加有关。garetosmab 降低了发作的严重程度和持续时间,其效果在整个试验中持续存在。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3af7/11425702/febd9620d3aa/zjae140f1.jpg

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