Nester Carla, Decker Dima A, Meier Matthias, Aslam Shakil, Bomback Andrew S, Caravaca-Fontán Fernando, Cook Terence H, Feldman David L, Fremeaux-Bacchi Veronique, Gale Daniel P, Gooch Ann, Johnson Sally, Licht Christoph, Mathur Mohit, Pickering Matthew C, Praga Manuel, Remuzzi Giuseppe, Selvarajah Viknesh, Smith Richard J, Tabriziani Hossein, van de Kar Nicole, Wang Yaqin, Wong Edwin, Mistry Kirtida, Lim Mark, Portillo Cesia, Balogun Seyi, Trachtman Howard, Thompson Aliza
Department of Pediatrics, Division of Nephrology, Carver College of Medicine, University of Iowa, Iowa City, Iowa.
Apellis Pharmaceuticals Inc., Waltham, Massachusetts.
Clin J Am Soc Nephrol. 2024 Sep 1;19(9):1201-1208. doi: 10.2215/CJN.0000000000000505. Epub 2024 Jun 3.
Randomized clinical trials are underway to evaluate the efficacy of novel agents targeting the alternative complement pathway in patients with C3 glomerulopathy (C3G), a rare glomerular disease. The Kidney Health Initiative convened a panel of experts in C3G to ( 1 ) assess the data supporting the use of the prespecified trial end points as measures of clinical benefit and ( 2 ) opine on efficacy findings they would consider compelling as treatment(s) of C3G in native kidneys. Two subpanels of the C3G Trial Endpoints Work Group reviewed the available evidence and uncertainties for the association between the three prespecified end points-( 1 ) proteinuria, ( 2 ) eGFR, and ( 3 ) histopathology-and anticipated outcomes. The full work group provided feedback on the summaries provided by the subpanels and on what potential treatment effects on the proposed end points they would consider compelling to support evidence of an investigational product's effectiveness for treating C3G. Members of the full work group agreed with the characterization of the data, evidence, and uncertainties, supporting the end points. Given the limitations of the available data, the work group was unable to define a minimum threshold for change in any of the end points that might be considered clinically meaningful. The work group concluded that a favorable treatment effect on all three end points would provide convincing evidence of efficacy in the setting of a therapy that targeted the complement pathway. A therapy might be considered effective in the absence of complete alignment in all three end points if there was meaningful lowering of proteinuria and stabilization or improvement in eGFR. The panel unanimously supported efforts to foster data sharing between academic and industry partners to address the gaps in the current knowledge identified by the review of the end points in the aforementioned trials.
随机临床试验正在进行中,以评估新型药物靶向替代补体途径治疗C3肾小球病(C3G,一种罕见的肾小球疾病)患者的疗效。肾脏健康倡议组织召集了一个C3G专家小组,以(1)评估支持使用预先指定的试验终点作为临床获益衡量指标的数据,以及(2)对他们认为可作为C3G天然肾脏治疗令人信服的疗效结果发表意见。C3G试验终点工作组的两个小组审查了三个预先指定终点(1)蛋白尿、(2)估算肾小球滤过率(eGFR)和(3)组织病理学与预期结果之间关联的现有证据和不确定性。整个工作组就各小组提供的总结以及他们认为对拟议终点具有何种潜在治疗效果才足以支持研究产品治疗C3G有效性证据的问题提供了反馈。整个工作组的成员同意对数据、证据和不确定性的描述,支持这些终点。鉴于现有数据的局限性,工作组无法确定任何可能被视为具有临床意义的终点变化的最低阈值。工作组得出结论,对所有三个终点产生有利的治疗效果将为针对补体途径的治疗提供令人信服的疗效证据。如果蛋白尿有显著降低且eGFR稳定或改善,即使在所有三个终点未完全一致的情况下,一种治疗也可能被认为是有效的。该小组一致支持促进学术和行业合作伙伴之间数据共享的努力,以填补上述试验终点审查所发现的当前知识空白。