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