Meta-Analysis of Interleukin-2 Receptor Antagonists as the Treatment for Steroid-Refractory Acute Graft-Versus-Host Disease

被引:19
作者
Shen, Meng-Zhu [1 ]
Li, Jing-Xia [1 ,2 ]
Zhang, Xiao-Hui [1 ]
Xu, Lan-Ping [1 ,3 ]
Wang, Yu [1 ]
Liu, Kai-Yan [1 ]
Huang, Xiao-Jun [1 ,3 ,4 ]
Hong, Shen-Da [5 ]
Mo, Xiao-Dong [1 ,3 ]
机构
[1] Peking Univ Peoples Hosp, Beijing Key Lab Hematopoiet Stem Cell Transplanta, Peking Univ Inst Hematol, Natl Clin Res Ctr Hematol Dis, Beijing, Peoples R China
[2] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Hematol, Guangzhou, Peoples R China
[3] Chinese Acad Med Sci, Res Unit Key Tech Diag & Treatments Hematol Malig, Beijing, Peoples R China
[4] Peking Tsinghua Ctr Life Sci, Beijing, Peoples R China
[5] Peking Univ, Peking Univ Hlth Sci Ctr, Natl Inst Hlth Data Sci, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
acute graft-versus-host disease; interleukin-2 receptor antagonist; second-line treatment; steroid-refractory; meta-analysis; TERM-FOLLOW-UP; STEM-CELL TRANSPLANTATION; DENILEUKIN DIFTITOX; IMPROVED SURVIVAL; COMBINATION THERAPY; UPDATED EXPERIENCE; T-CELLS; DACLIZUMAB; BASILIXIMAB; INOLIMOMAB;
D O I
10.3389/fimmu.2021.749266
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Acute graft-versus-host disease (aGVHD) is a major complication after allogeneic hematopoietic stem cell transplantation (HSCT). Corticosteroid is the first-line treatment for aGVHD, but its response rate is only approximately 50%. At present, no uniformly accepted treatment for steroid-refractory aGVHD (SR-aGVHD) is available. Blocking interleukin-2 receptors (IL-2Rs) on donor T cells using pharmaceutical antagonists alleviates SR-aGVHD. This meta-analysis aimed to compare the efficacy and safety of four commercially available IL-2R antagonists (IL-2RAs) in SR-aGVHD treatment. A total of 31 studies met the following inclusion criteria (1): patients of any race, any sex, and all ages (2); those diagnosed with SR-aGVHD after HSCT; and (3) those using IL-2RA-based therapy as the treatment for SR-aGVHD. The overall response rate (ORR) at any time after treatment with basiliximab and daclizumab was 0.81 [95% confidence interval (CI): 0.74-0.87)] and 0.71 (95% CI: 0.56-0.82), respectively, which was better than that of inolimomab 0.54 (95% CI: 0.39-0.68) and denileukin diftitox 0.56 (95% CI: 0.35-0.76). The complete response rate (CRR) at any time after treatment with basiliximab and daclizumab was 0.55 (95% CI: 0.42-0.68) and 0.42 (95%CI: 0.29-0.56), respectively, which was better than that of inolimomab 0.30 (95% CI: 0.16-0.51) and denileukin diftitox 0.37 (95% CI: 0.24-0.52). The ORR and CRR were better after 1-month treatment with basiliximab and daclizumab than after treatment with inolimomab and denileukin diftitox. The incidence of the infection was higher after inolimomab treatment than after treatment with the other IL-2RAs. In conclusion, the efficacy and safety of different IL-2RAs varied. The response rate of basiliximab was the highest, followed by that of daclizumab. Prospective, randomized controlled trials are needed to compare the efficacy and safety of different IL-2RAs.</p>
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