卵巢早衰患者经卵巢动脉移植异基因人羊膜上皮细胞的安全性和有效性:单臂一期临床试验。

IF 9.6 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL
EClinicalMedicine Pub Date : 2024-07-30 eCollection Date: 2024-08-01 DOI:10.1016/j.eclinm.2024.102744
Lichun Weng, Liutong Wei, Qiuwan Zhang, Taotao Sun, Xiaojun Kuang, Qin Huang, Yunyun Cao, Xiaoyi Liu, Qian Wang, Ying Guo, Junyan Sun, Lulu Wang, Haihong Tang, Haiou Yang, Qian Chen, Jian Zhang, Bingshun Wang, Zhaoxia Qian, Dongmei Lai
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引用次数: 0

摘要

背景:卵巢早衰(POF)是一种普遍存在的严重疾病,会损害女性健康,但目前还没有有效的治疗方法来恢复卵巢功能。人羊膜上皮细胞(hAECs)在临床前模型中表现出卵巢保护作用。因此,我们开展了一项单臂一期临床试验,以评估异基因 hAECs 治疗 POF 的安全性和有效性:共有 35 名患者通过卵巢动脉接受了 6 × 107 hAECs,并在 2020 年 12 月 30 日至 2022 年 1 月 31 日期间完成了为期 5 个月的随访。随访评估在hAECs治疗后的不同时间段进行,包括治疗后一个月(访问-1,V-1)、三个月(访问-2,V-2)和五个月(访问-3,V-3)。主要终点是不良事件(AEs)的发生率和具有临床意义的实验室异常。次要终点包括评估经阴道超声结果、性激素水平、更年期生活质量(MENQOL)问卷以及生殖指标。该试验在 www.clinicaltrials.gov 登记为 NCT02912104:在五个月的随访期间未发现严重的不良反应。最常见的AE是血肿(7/35,20.00%),其他AE包括盆腔疼痛(4/35,11.43%)、发热(2/35,5.71%)、过敏性休克(2/35,5.71%)和肝毒性(1/35,2.86%)。移植hAECs(hAECT)后,所有患者的子宫内膜厚度、左侧卵巢体积、性激素(卵泡刺激素(FSH)和雌二醇(E2))水平以及MENQOL评分在5个月的随访期间均有显著改善。其中,13 名参与者(37.14%)出现自发性月经出血,20.00% 的参与者(7/35)在接受 HAECT 治疗后报告有一次以上的定期月经出血。解读:通过卵巢动脉进行 hAECT 安全、耐受性良好,可暂时改善 POF 患者的子宫内膜厚度、卵巢大小、激素水平和更年期症状。有必要进一步开展随访时间更长、样本量更大的 hAECs 随机对照试验:国家自然科学基金(编号:82271664)、上海交通大学交叉学科项目(YG2022ZD028)、上海市卫生健康委员会(202240345)、上海市胚胎原发疾病重点实验室(编号:Shelab2022ZD01)、上海市教育委员会(编号:20152236)、国家重点研发计划(编号:2018YFC1004802)、上海市细胞治疗临床研究中心(编号:23J41900100)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Safety and efficacy of allogenic human amniotic epithelial cells transplantation via ovarian artery in patients with premature ovarian failure: a single-arm, phase 1 clinical trial.

Background: Premature ovarian failure (POF) is a prevalent and severe condition that impairs female health but there is currently no effective treatment available to restore ovarian function. Human amniotic epithelial cells (hAECs) exhibit ovarian protection in pre-clinical models. Thus, we conducted a single-arm, phase 1 clinical trial to assess the safety and efficacy of allogenic hAECs in treating POF.

Methods: A total of 35 patients received 6 × 107 hAECs via ovarian artery and completed a five-month follow-up from December 30, 2020 to January 31, 2022. The follow-up assessments were conducted at various intervals after hAECs treatment, including one month (Visit-1, V-1), three months (Visit-2, V-2), and five months (Visit-3, V-3) post-treatment. The primary endpoints were incidence of adverse events (AEs), and clinically significant laboratory abnormalities. Secondary endpoints included evaluation of transvaginal ultrasound results, sex hormone levels, Menopausal Quality of Life (MENQOL) questionnaire, as well as reproductive indicators. This trial was registered at www.clinicaltrials.gov as NCT02912104.

Findings: No serious AEs were observed throughout the five-month follow-up period. The most common AE was hematoma (7/35, 20.00%), and other AEs include pelvic pain (4/35, 11.43%), fever (2/35, 5.71%), anaphylaxis (2/35, 5.71%), and hepatotoxicity (1/35, 2.86%). After hAECs transplantation (hAECT), significant improvements were observed in the levels of endometrial thickness, left ovarian volume, sex hormones (follicle-stimulating hormone (FSH) and estradiol (E2)), and MENQOL scores in all patients during the five-month follow-up period. Among them, 13 participants (37.14%) experienced spontaneous menstrual bleeding, and 20.00% (7/35) reported more than one regular menstrual bleeding post-hAECT. In this response group, significant improvements were observed in endometrial thickness, left ovarian volume, levels of FSH, E2, anti-Müllerian hormone (AMH), and MENQOL scores one month after hAECT in comparison to pre-hAECT.

Interpretation: hAECT via ovarian artery is safe, well-tolerated and temporarily ameliorates endometrial thickness, ovarian size, hormone levels, and menopausal symptoms in POF patients. Further randomized controlled trial of hAECs with longer follow-up period and a larger sample size is warranted.

Funding: National Natural Science Foundation of China (No. 82271664), the Interdisciplinary Program of Shanghai Jiao Tong University (YG2022ZD028), the Shanghai Municipal Health Committee (202240345), Shanghai Key Laboratory of Embryo Original Diseases (No. Shelab2022ZD01), Shanghai Municipal Education Commission (No. 20152236), and National Key Research and Development Program of China (No. 2018YFC1004802), Shanghai Clinical Research Center for Cell Therapy, China (No. 23J41900100).

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来源期刊
EClinicalMedicine
EClinicalMedicine Medicine-Medicine (all)
CiteScore
18.90
自引率
1.30%
发文量
506
审稿时长
22 days
期刊介绍: eClinicalMedicine is a gold open-access clinical journal designed to support frontline health professionals in addressing the complex and rapid health transitions affecting societies globally. The journal aims to assist practitioners in overcoming healthcare challenges across diverse communities, spanning diagnosis, treatment, prevention, and health promotion. Integrating disciplines from various specialties and life stages, it seeks to enhance health systems as fundamental institutions within societies. With a forward-thinking approach, eClinicalMedicine aims to redefine the future of healthcare.
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