Kyung Yoon Soo, Hong Ki-Sung, Chung Hyung-Min, Hyun Shin Jung, Choo Myung-Soo, Kim Eun-Young, Shin Jeong Min, Kang Ah Reum, Seo Jin Won, Park Juhyun, Park Se-Pill
Department of Urology, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, Korea.
Health Screening and Promotion Center, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, Korea.
Stem Cells Transl Med. 2025 May 19;14(5). doi: 10.1093/stcltm/szaf018.
This study investigated the safety and efficacy of MR-MC-01, a mesenchymal stem cell therapy derived from human embryonic stem cells, in patients with interstitial cystitis (IC), particularly those with Hunner lesions unresponsive to pentosan polysulfate sodium (PPS). Conducted as a prospective, randomized, double-blind, placebo-controlled phase I/IIa clinical trial, it enrolled 22 patients, with six completing phase I and 16 participating in phase IIa. Phase I tested 2 doses (2.0 × 107 and 5.0 × 107 cells) to determine the maximum tolerated dose (MTD), revealing no dose-limiting toxicities and only mild adverse events such as transient hemorrhage and bladder pain. In phase IIa, 12 participants received the MTD of 5.0 × 107 cells, and 4 received placebo. Significant reductions in interstitial cystitis questionnaire (ICQ) and pain urgency frequency (PUF) scores were observed in the treatment group. Improvements were noted in nocturnal voiding frequency and Hunner lesion size, with 8 patients showing either a reduction or complete resolution of lesions after 6 months. The global response assessment (GRA) reported moderate to marked improvement in 41.67% of treated patients versus 25% in the placebo group. MR-MC-01 demonstrated no serious drug-related adverse events, highlighting its favorable safety profile. These findings suggest that MR-MC-01 not only alleviates symptoms but also promotes structural recovery in IC, making it a promising treatment option. Further large-scale, long-term studies are warranted to confirm these results and optimize therapeutic protocols. (Identifier: NCT04610359).
本研究调查了源自人胚胎干细胞的间充质干细胞疗法MR-MC-01治疗间质性膀胱炎(IC)患者的安全性和有效性,尤其是对戊聚糖多硫酸钠(PPS)无反应的Hunner病变患者。该研究作为一项前瞻性、随机、双盲、安慰剂对照的I/IIa期临床试验进行,共纳入22例患者,其中6例完成I期试验,16例参与IIa期试验。I期试验测试了2个剂量(2.0×10⁷和5.0×10⁷个细胞)以确定最大耐受剂量(MTD),结果显示无剂量限制性毒性,仅出现短暂出血和膀胱疼痛等轻度不良事件。在IIa期试验中,12名参与者接受了5.0×10⁷个细胞的MTD,4名接受安慰剂。治疗组间质性膀胱炎问卷(ICQ)和疼痛急迫频率(PUF)评分显著降低。夜间排尿频率和Hunner病变大小有所改善,6个月后有8例患者病变缩小或完全消退。整体反应评估(GRA)报告,治疗组41.67%的患者有中度至显著改善,而安慰剂组为25%。MR-MC-01未出现严重的药物相关不良事件,突出了其良好的安全性。这些发现表明,MR-MC-01不仅能缓解症状且能促进IC的结构恢复,使其成为一种有前景的治疗选择。需要进一步开展大规模、长期研究以证实这些结果并优化治疗方案。(标识符:NCT04610359)