Peking University People's Hospital, Peking University Institute of Hematology, National Clinical Research Center for Hematologic Disease, Research Unit of Key Technique for Diagnosis and Treatments of Hematologic Malignancies, Chinese Academy of Medical Sciences, 2019RU029, Beijing Key Laboratory of Hematopoietic Stem Cell Transplantation, No. 11 Xizhimen South Street, Xicheng District, Beijing, 100044, China.
Peking-Tsinghua Center for Life Sciences, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing, China.
Sci Rep. 2020 Nov 19;10(1):20148. doi: 10.1038/s41598-020-77186-9.
Relapse was the major cause of treatment failure in patients with acute lymphoblastic leukemia (ALL) after allogeneic hematopoietic stem cell transplantation (allo-HSCT). We aimed to identify the efficacy and safety of preemptive interferon-α (IFN-α) treatment in ALL patients who had minimal residual disease (MRD) after allo-HSCT. Multiparameter flow cytometry and polymerase chain reaction assays were applied for MRD monitoring. Recombinant human IFN-α-2b injections were administered subcutaneously twice weekly in every 4 weeks cycle. Twenty-four (35.3%), 5 (7.4%), 6 (8.8%), and 13 (19.1%) patients achieved MRD negativity at 1, 2, 3, and > 3 months, respectively, after treatment. Seven patients showed grade ≥ 3 toxicities after IFN-α treatment. The 4-year cumulative incidence of total acute graft-versus-host disease (aGVHD), severe aGVHD, total chronic GVHD (cGVHD), and severe cGVHD after treatment was 14.7%, 2.9%, 40.0%, and 7.5%, respectively. The 4-year cumulative incidences of relapse and non-relapse mortality after treatment was 31.9% and 6.0%, respectively. The 4-year probabilities of disease-free survival and overall survival after IFN-α treatment were 62.1% and 71.1%, respectively. Thus, preemptive IFN-α treatment could protect against relapse and improve long-term survival for ALL patients who had MRD after allo-HSCT. The study was registered at https://clinicaltrials.gov as #NCT02185261 (09/07/2014).
复发是异基因造血干细胞移植(allo-HSCT)后急性淋巴细胞白血病(ALL)患者治疗失败的主要原因。我们旨在确定在 allo-HSCT 后存在微小残留病(MRD)的 ALL 患者中,预防性干扰素-α(IFN-α)治疗的疗效和安全性。多参数流式细胞术和聚合酶链反应检测用于 MRD 监测。每周皮下注射重组人干扰素-α-2b,每 4 周一个周期,共 2 次。治疗后 1、2、3 和 >3 个月时,分别有 24 例(35.3%)、5 例(7.4%)、6 例(8.8%)和 13 例(19.1%)患者达到 MRD 阴性。7 例患者在 IFN-α治疗后出现≥3 级毒性。治疗后 4 年总急性移植物抗宿主病(aGVHD)、严重 aGVHD、总慢性移植物抗宿主病(cGVHD)和严重 cGVHD 的累积发生率分别为 14.7%、2.9%、40.0%和 7.5%。治疗后 4 年复发和非复发死亡率的累积发生率分别为 31.9%和 6.0%。治疗后 4 年无病生存率和总生存率的概率分别为 62.1%和 71.1%。因此,预防性 IFN-α治疗可预防复发,并改善 allo-HSCT 后存在 MRD 的 ALL 患者的长期生存。该研究在 https://clinicaltrials.gov 注册为 #NCT02185261(2014 年 9 月 7 日)。