Xu Zhengli, Mo Xiaodong, Kong Yuan, Wen Qi, Han Tingting, Lyu Meng, Xu Lanping, Chang Yingjun, Zhang Xiaohui, Huang Xiaojun, Wang Yu
Peking University People's Hospital, Peking University Institute of Hematology, National Clinical Research Center for Hematologic Disease, Beijing Key Laboratory of Hematopoietic Stem Cell Transplantation, Collaborative Innovation Center of Hematology, Peking University, Beijing 100044, China.
Peking-Tsinghua Center for Life Sciences, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing 100044, China.
J Transl Int Med. 2023 Sep 2;11(3):255-264. doi: 10.2478/jtim-2023-0111. eCollection 2023 Sep.
Acute graft-versus-host disease (aGvHD) remains a major complication after allogeneic hematopoietic stem cell transplantation (allo-HSCT). Methylprednisolone (MP; 1-2 mg/kg/day) remains the standard first-line therapy for aGvHD, although no response is detected in nearly one-half of the patients with aGvHD. This study aimed to investigate the feasibility of mini-dose methotrexate (MTX) combined with standard-dose MP as a front-line therapy for aGvHD.
A prospective Phase 2 clinical trial was performed to evaluate the safety and efficacy of 5 mg/m2 MTX combined with 1 mg/kg/day MP as the initial therapy in 31 patients with aGvHD. Moreover, the effects of MTX combined with MP were explored in a humanized xenogeneic murine model of aGvHD.
The overall response and complete response rate at 7 days after the initial treatment were 100% and 83%, respectively. The overall response rate on day 28 was 87%. The complete response rates for aGvHD grades I, II, and III were 100% (6/6), 82% (18/22), and 66% (2/3), respectively. Grade 3 toxicities occurred in only three patients presenting with cytopenia. Importantly, MTX and MP demonstrated synergistic effects on ameliorating aGvHD in humanized xenogeneic murine model.
The current study suggests that mini-dose MTX combined with standard-dose MP could potentially become a novel first-line therapy for patients with aGvHD.
急性移植物抗宿主病(aGvHD)仍是异基因造血干细胞移植(allo-HSCT)后的主要并发症。甲泼尼龙(MP;1-2毫克/千克/天)仍是aGvHD的标准一线治疗药物,尽管近一半的aGvHD患者未检测到反应。本研究旨在探讨小剂量甲氨蝶呤(MTX)联合标准剂量MP作为aGvHD一线治疗的可行性。
进行一项前瞻性2期临床试验,以评估5毫克/平方米MTX联合1毫克/千克/天MP作为初始治疗对31例aGvHD患者的安全性和有效性。此外,在aGvHD的人源化异种小鼠模型中探讨MTX联合MP的效果。
初始治疗7天后的总缓解率和完全缓解率分别为100%和83%。第28天的总缓解率为87%。aGvHD I、II和III级的完全缓解率分别为100%(6/6)、82%(18/22)和66%(2/3)。仅3例出现血细胞减少的患者发生3级毒性反应。重要的是,MTX和MP在人源化异种小鼠模型中对改善aGvHD表现出协同作用。
当前研究表明,小剂量MTX联合标准剂量MP可能成为aGvHD患者的新型一线治疗方法。