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静脉输注脐带间充质基质细胞疗法可能改善日本造血干细胞移植后特发性肺炎综合征患者的总生存率:一项多中心、单臂、II期试验。

Intravenous umbilical cord-derived mesenchymal stromal cell therapy may improve overall survival in Japanese patients with idiopathic pneumonia syndrome after hematopoietic stem cell transplantation: a multicenter, single-arm, phase II trial.

作者信息

Doki Noriko, Fujii Nobuharu, Kako Shinichi, Sakaida Emiko, Kanda Yoshinobu

机构信息

Hematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital, Bunkyo-Ku, Tokyo, Japan.

Department of Hematology and Oncology, Okayama University Hospital, Kita-Ku, Okayama, Okayama, Japan.

出版信息

Int J Hematol. 2025 Jul 15. doi: 10.1007/s12185-025-04024-x.

Abstract

Idiopathic pneumonia syndrome (IPS) is a serious complication of allogeneic hematopoietic stem cell transplantation (HSCT) and has a poor prognosis. Although IPS is often treated with steroids, the disease can become resistant to or dependent on steroid treatment, and there is no effective cure for patients with refractory or steroid-dependent IPS. This multicenter, open-label, single-arm, phase II clinical trial investigated the efficacy and safety of HLC-001 (allogeneic umbilical cord-derived mesenchymal stromal cells) in patients with progressive steroid-dependent or refractory IPS after HSCT. Seven male patients (all male; mean age: 43.3 years) received HLC-001 and three completed the trial. The survival rate at day 56 (primary endpoint) was 71.4% (5/7 patients; 95% confidence interval: 29.0%-96.3%) and was sustained at day 100, suggesting that HLC-001 was more effective than previously reported treatment. Three of the five patients with ≥ 100 days of follow-up died. Five patients experienced at least one adverse drug reaction, none of which were serious. These findings indicate that HLC-001 was potentially effective and generally well tolerated in Japanese patients with steroid-dependent or refractory IPS after HSCT. Given there is no effective cure for steroid-dependent or refractory IPS, HLC-001 may be a promising treatment option and further clinical evaluation is warranted.Trial registration: Japan Registry of Clinical Trials identifier: jRCT2063220014.

摘要

特发性肺炎综合征(IPS)是异基因造血干细胞移植(HSCT)的一种严重并发症,预后较差。尽管IPS通常采用类固醇治疗,但该疾病可能会对类固醇治疗产生耐药性或依赖性,对于难治性或类固醇依赖性IPS患者尚无有效的治愈方法。这项多中心、开放标签、单臂、II期临床试验研究了HLC-001(同种异体脐带间充质基质细胞)对HSCT后进展性类固醇依赖性或难治性IPS患者的疗效和安全性。7名男性患者(均为男性;平均年龄:43.3岁)接受了HLC-001治疗,其中3名完成了试验。第56天(主要终点)的生存率为71.4%(5/7例患者;95%置信区间:29.0%-96.3%),并在第100天保持,这表明HLC-001比先前报道的治疗方法更有效。5例随访时间≥100天的患者中有3例死亡。5例患者至少经历了1次药物不良反应,均不严重。这些发现表明,HLC-001对日本HSCT后类固醇依赖性或难治性IPS患者可能有效,且总体耐受性良好。鉴于类固醇依赖性或难治性IPS尚无有效的治愈方法,HLC-001可能是一种有前景的治疗选择,值得进一步进行临床评估。试验注册号:日本临床试验注册中心标识符:jRCT2063220014。

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