Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Department of Haematology, Rigshospitalet, Copenhagen, Denmark.
Blood. 2020 Sep 24;136(13):1499-1506. doi: 10.1182/blood.2020005338.
This trial aimed to evaluate the efficacy of sirolimus in addition to cyclosporine (CSP) and mycophenolate mofetil (MMF) for graft-versus-host disease (GVHD) prophylaxis after nonmyeloablative conditioning for HLA class I or II mismatched hematopoietic cell transplantation (HCT). Eligible patients had hematologic malignancies treatable by allogeneic HCT. Conditioning consisted of fludarabine (90 mg/m2) and 2 to 3 Gy total body irradiation. GVHD prophylaxis comprised cyclosporine, mycophenolate mofetil, and sirolimus. The primary objective was to determine whether the cumulative incidence of grade 2 to 4 acute GVHD could be reduced to <70% in HLA class I or II mismatched HCT. The study was closed on December 20, 2018. Seventy-seven participants were recruited between April 14, 2011, and December 12, 2018, of whom 76 completed the study intervention. Median follow-up was 47 months (range, 4-94 months). The cumulative incidence of grade 2 to 4 acute GVHD at day 100 was 36% (95% confidence interval [CI], 25-46), meeting the primary end point. The cumulative incidence of nonrelapse morality, relapse/progression, and overall survival was 18% (95% CI, 9-27), 30% (interquartile range, 19-40), and 62% (95% CI, 50-73) after 4 years. In conclusion, the addition of sirolimus to cyclosporine and mycophenolate mofetil resulted in a lower incidence of acute GVHD, thus translating into superior overall survival compared with historical results. This trial was registered at www.clinicaltrials.gov as #NCT01251575.
本试验旨在评估西罗莫司在非清髓性条件下与环孢素(CSP)和吗替麦考酚酯(MMF)联合应用于 HLA Ⅰ类或Ⅱ类错配造血细胞移植(HCT)后预防移植物抗宿主病(GVHD)的疗效。符合条件的患者患有可通过异基因 HCT 治疗的血液系统恶性肿瘤。预处理方案包括氟达拉滨(90mg/m2)和 2 至 3Gy 全身照射。GVHD 预防方案包括环孢素、吗替麦考酚酯和西罗莫司。主要目标是确定 HLA Ⅰ类或Ⅱ类错配 HCT 中 2 至 4 级急性 GVHD 的累积发生率是否可降低至<70%。该研究于 2018 年 12 月 20 日结束。2011 年 4 月 14 日至 2018 年 12 月 12 日期间,共招募了 77 名参与者,其中 76 名完成了研究干预。中位随访时间为 47 个月(范围:4-94 个月)。第 100 天 2 至 4 级急性 GVHD 的累积发生率为 36%(95%可信区间[CI],25-46),达到了主要终点。4 年后,非复发死亡率、复发/进展和总生存率分别为 18%(95%CI,9-27)、30%(四分位间距,19-40)和 62%(95%CI,50-73)。总之,与环孢素和吗替麦考酚酯相比,西罗莫司的加入降低了急性 GVHD 的发生率,从而转化为优于历史结果的总体生存率。该试验在 www.clinicaltrials.gov 上注册为#NCT01251575。