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特发性肺纤维化的衰老细胞清除剂达沙替尼和槲皮素:一项 I 期、单盲、单中心、随机、安慰剂对照的可行性和耐受性初步试验结果。

Senolytics dasatinib and quercetin in idiopathic pulmonary fibrosis: results of a phase I, single-blind, single-center, randomized, placebo-controlled pilot trial on feasibility and tolerability.

机构信息

University of Texas Health Science Center San Antonio, San Antonio, TX, USA; South Texas Veterans Health Care System, San Antonio, TX, USA.

University of Texas Health Science Center San Antonio, San Antonio, TX, USA; South Texas Veterans Health Care System, San Antonio, TX, USA.

出版信息

EBioMedicine. 2023 Apr;90:104481. doi: 10.1016/j.ebiom.2023.104481. Epub 2023 Feb 28.

Abstract

BACKGROUND

Idiopathic pulmonary fibrosis (IPF) is an age-related, chronic, irreversible fibrotic lung disease. IPF is associated with increased senescent cells burden, which may be alleviated with administration of senescent cell targeting drugs termed 'senolytics'. We previously conducted an open-label single-arm pilot study of the senolytic combination of dasatinib and quercetin (D + Q) in patients with IPF but lack of control group limited interpretation and next-stage trial planning. The primary objective of this confirmatory randomized placebo-controlled pilot trial (RCT; NCT02874989) was to report adverse events with D + Q and inform study feasibility for future efficacy trials.

METHODS

Twelve participants with IPF aged >50 years were blinded and randomized at a 1:1 ratio to either receive three weeks of D + Q (D: 100 mg/d and Q: 1250 mg/d, three consecutive days per week) or matching placebo.

FINDINGS

All participants completed the scheduled drug dosing regimen (108/108 doses) and planned assessments (60/60). While the placebo arm reported fewer overall non-serious AEs (65 vs 22), there were no serious adverse events related to D + Q. Most AEs in the D + Q arm are common in IPF patients or anticipated side effects of D. Sleep disturbances and anxiety were disproportionately represented in the D + Q arm (4/6 vs 0/6). Frailty, pulmonary, or physical function were explored before and after intermittent D + Q; though under-powered to evaluate change, these measures do not appear to differ meaningfully between groups.

INTERPRETATION

Intermittently-dosed D + Q in patients with IPF is feasible and generally well-tolerated. Further prospective studies, such as a larger RCT, are needed to confirm the safety and efficacy of D + Q in patients with IPF.

FUNDING

This work was supported by National Institutes of Health grants R33AG61456 (JLK, TT), Robert and Arlene Kogod (JLK, TT), the Connor Fund (JLK, TT), Robert J. and Theresa W. Ryan (JLK, TT), and the Noaber Foundation (JLK, TT) San Antonio Claude D. Pepper Older Americans Independence Center's (OAIC)Pilot/Exploratory Studies Core (PESC) Grant (AMN, NM); NIHK01 AG059837 (JNJ), P30 AG021332 (SBK, JNJ); NIHR37 AG013925 (JLK), the Connor Group (JLK), Glenn/AFAR BIG Award (JLK), Robert J. and Theresa W. Ryan (JLK), and the Noaber and Ted Nash Long Life Foundations (JLK).

摘要

背景

特发性肺纤维化(IPF)是一种与年龄相关的慢性、不可逆转的肺纤维化疾病。IPF 与衰老细胞负担增加有关,用称为“衰老细胞清除剂”的靶向衰老细胞的药物治疗可能会缓解这种情况。我们之前对 IPF 患者进行了一项达沙替尼和槲皮素联合治疗的开放性单臂试验研究,但缺乏对照组,限制了对研究结果的解释和下一步试验计划。本确证性随机安慰剂对照试验(RCT;NCT02874989)的主要目的是报告 D+Q 的不良事件,并为未来的疗效试验提供研究可行性信息。

方法

12 名年龄>50 岁的 IPF 患者被随机分为 1:1 比例的两组,分别接受 3 周的 D+Q(D:100mg/d,Q:1250mg/d,每周连续 3 天)或匹配的安慰剂治疗。

结果

所有参与者均完成了预定的药物剂量方案(108/108 剂)和计划评估(60/60)。虽然安慰剂组报告的非严重不良事件总数较少(65 例 vs 22 例),但没有与 D+Q 相关的严重不良事件。D+Q 组的大多数不良事件在 IPF 患者中较为常见,或为 D 的预期副作用。睡眠障碍和焦虑在 D+Q 组中比例过高(4/6 例 vs 0/6 例)。在接受间歇性 D+Q 治疗前后,对虚弱、肺部或身体功能进行了探索;尽管评估变化的能力不足,但这些措施在组间似乎没有明显差异。

解释

在 IPF 患者中使用间歇性剂量的 D+Q 是可行的,且通常耐受性良好。需要进一步的前瞻性研究,如更大规模的 RCT,以确认 D+Q 在 IPF 患者中的安全性和疗效。

资金

这项工作得到了美国国立卫生研究院 R33AG61456 项目(JLK、TT)、Robert 和 Arlene Kogod 项目(JLK、TT)、Connor 基金(JLK、TT)、Robert J. 和 Theresa W. Ryan 项目(JLK、TT)和 Noaber 基金会(JLK、TT)圣安东尼奥 Claude D. Pepper 老年美国人独立中心的 Pilot/Exploratory Studies Core (PESC)拨款(AMN、NM);NIHK01AG059837 项目(JNJ)、P30AG021332 项目(SBK、JNJ);NIHR37AG013925 项目(JLK)、Connor 集团(JLK)、Glenn/AFAR BIG 奖(JLK)、Robert J. 和 Theresa W. Ryan 项目(JLK)以及 Noaber 和 Ted Nash Long Life 基金会(JLK)的资助。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebd5/10006434/9aea3342f1f2/gr1.jpg

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