A Novel JAK1 Inhibitor SHR0302 Combined With Prednisone for First-Line Treatment of Chronic Graft-Versus-Host Disease: A Phase I Clinical Trial.

IF 3.2 4区 医学 Q3 CELL & TISSUE ENGINEERING
Qiaomei He, Xi Sun, Jiahua Niu, Jun Yang, Ying Wang, Chongmei Huang, Kun Zhou, Yin Tong, Yu Cai, Baoxia Dong, Liping Wan, Xianmin Song, Huiying Qiu
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Abstract

Chronic graft-versus-host disease (cGVHD) is a potentially life-threatening complication after allogeneic hematopoietic stem cell transplantation. Standard steroid first-line treatment could not satisfy therapeutic needs due to limited efficacy. As a highly selective Janus kinase (JAK) 1 inhibitor, SHR0302 exhibits a reduced inhibition effect on JAK2 and might have less effect on hematopoiesis. This phase I clinical trial investigated the tolerability and safety of SHR0302 in combination with prednisone, and its early efficacy evidence as a potential first-line treatment to moderate/severe cGVHD. The standard 3 + 3 dose escalation was implemented to find the optimal dose of SHR0302. And prednisone was concurrently administrated with a dose of 1 mg/kg/d and then gradually tapered after 2 weeks. Eighteen patients were enrolled into the study. Grade ≥ 3 treatment-related adverse events were observed in 38.9% of patients. Only one patient developed DLT (grade ≥ 3 hypercholesterolemia) in the highest dose-level group who had pre-existing hypercholesterolemia. The maximum tolerated dose was not reached. No patient discontinued treatment due to AEs. Sixteen out of 18 patients were evaluable for responses, the ORR at week 4 and week 24 were 94.4 and 87.5%, respectively. Overall, the treatment of SHR0302 combined with prednisone was safe and well-tolerated, preliminary clinical results presented a high response for previously untreated cGVHD and a significant reduction in prednisone use in this study. A phase II trial will be conducted to further investigate its therapeutic effects clinically.

新型 JAK1 抑制剂 SHR0302 联合泼尼松一线治疗慢性移植物抗宿主病:一期临床试验。
慢性移植物抗宿主疾病(cGVHD)是异基因造血干细胞移植后一种可能危及生命的并发症。由于疗效有限,标准的类固醇一线治疗无法满足治疗需求。作为一种高选择性的Janus激酶(JAK)1抑制剂,SHR0302对JAK2的抑制作用较弱,对造血的影响可能较小。这项 I 期临床试验研究了 SHR0302 与泼尼松联用的耐受性和安全性,以及其作为中度/重度 cGVHD 潜在一线治疗的早期疗效证据。为了找到 SHR0302 的最佳剂量,试验采用了标准的 3+3 剂量递增法。同时使用泼尼松,剂量为 1 mg/kg/d,2 周后逐渐减量。研究共招募了 18 名患者。38.9%的患者出现了≥3级的治疗相关不良反应。在最高剂量组中,仅有一名原有高胆固醇血症的患者出现了 DLT(≥ 3 级高胆固醇血症)。未达到最大耐受剂量。没有患者因 AEs 而中断治疗。18名患者中有16名可进行反应评估,第4周和第24周的ORR分别为94.4%和87.5%。总体而言,SHR0302联合泼尼松治疗安全且耐受性良好,初步临床结果显示,既往未治疗过的cGVHD患者应答率高,本研究中泼尼松用量显著减少。我们将开展 II 期试验,进一步研究其临床治疗效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cell Transplantation
Cell Transplantation 生物-细胞与组织工程
CiteScore
6.00
自引率
3.00%
发文量
97
审稿时长
6 months
期刊介绍: Cell Transplantation, The Regenerative Medicine Journal is an open access, peer reviewed journal that is published 12 times annually. Cell Transplantation is a multi-disciplinary forum for publication of articles on cell transplantation and its applications to human diseases. Articles focus on a myriad of topics including the physiological, medical, pre-clinical, tissue engineering, stem cell, and device-oriented aspects of the nervous, endocrine, cardiovascular, and endothelial systems, as well as genetically engineered cells. Cell Transplantation also reports on relevant technological advances, clinical studies, and regulatory considerations related to the implantation of cells into the body in order to provide complete coverage of the field.
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