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异基因造血干细胞移植后复发倾向的急性白血病患者中预先使用干扰素-α单药治疗的效果:一项病例对照研究。

Effects of preemptive interferon-α monotherapy in acute leukemia patients with relapse tendency after allogeneic hematopoietic stem cell transplantation: a case-control study.

机构信息

Jiangsu Institute of Hematology, The First Affiliated Hospital of Soochow University, 188 Shizi Road, Suzhou, 215006, Jiangsu, China.

Institute of Blood and Marrow Transplantation, Suzhou, China.

出版信息

Ann Hematol. 2018 Nov;97(11):2195-2204. doi: 10.1007/s00277-018-3429-z. Epub 2018 Jul 11.

DOI:10.1007/s00277-018-3429-z
PMID:29995264
Abstract

Interferon-α (IFN-α) inhibits tumor growth and mimics graft-versus-leukemia after allogeneic hematopoietic stem cell transplantation (allo-HSCT). In the current case-control study, we compared treatment responses in acute leukemia patients with relapse tendency post-allo-HSCT receiving preemptive IFN-α after withdrawal of immunosuppressants (n = 31) vs. receiving no IFN-α (n = 67). In the IFN-α group, 25 patients responded to the treatment without progressing to hematological relapse. In the non-IFN-α group, only 22 patients responded to the treatment. The response rate differed significantly (80.6 vs. 32.8%, P < 0.001). The 2-year cumulative incidence of relapse was 31.6 and 61.2% in the IFN-α and the non-IFN groups, respectively (P = 0.006). The 2-year leukemia-free survival and overall survival rate was 57.4 vs. 28.4% (P < 0.001) and 67.6 vs. 32.9% (P = 0.001), respectively. Among the 31 patients in the IFN-α group, 18 patients (58.1%) developed graft-versus-host disease (GVHD): 6 acute and 12 limited chronic GVHD. Patients who developed GVHD had higher treatment response rate than patients without GVHD (88.9 vs. 53.8%, P = 0.022). In conclusion, preemptive IFN-α therapy is a safe and effective treatment to prevent disease progression in high-risk patients with relapse tendency post-allo-HSCT.

摘要

干扰素-α (IFN-α) 可抑制肿瘤生长,并在异基因造血干细胞移植 (allo-HSCT) 后模拟移植物抗白血病效应。在本病例对照研究中,我们比较了接受免疫抑制剂撤药后预防性 IFN-α治疗(n=31)与未接受 IFN-α治疗(n=67)的复发倾向急性白血病 allo-HSCT 后患者的治疗反应。IFN-α 组中,25 例患者在未进展为血液学复发的情况下对治疗有反应。在非 IFN-α 组中,仅有 22 例患者对治疗有反应。两组的反应率差异显著(80.6% vs. 32.8%,P<0.001)。IFN-α 组和非 IFN-α 组 2 年累积复发率分别为 31.6%和 61.2%(P=0.006)。IFN-α 组和非 IFN-α 组 2 年无白血病生存率和总生存率分别为 57.4%和 28.4%(P<0.001)和 67.6%和 32.9%(P=0.001)。在 IFN-α 组的 31 例患者中,18 例(58.1%)发生移植物抗宿主病(GVHD):6 例急性和 12 例慢性局限型 GVHD。发生 GVHD 的患者治疗反应率高于未发生 GVHD 的患者(88.9% vs. 53.8%,P=0.022)。总之,预防性 IFN-α 治疗是一种安全有效的治疗方法,可预防 allo-HSCT 后复发倾向高危患者疾病进展。

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引用本文的文献

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The Effects of Interferons on Allogeneic T Cell Response in GVHD: The Multifaced Biology and Epigenetic Regulations.干扰素对移植物抗宿主病中同种异体 T 细胞反应的影响:多方面的生物学和表观遗传学调控。
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Sci Rep. 2020 Nov 19;10(1):20148. doi: 10.1038/s41598-020-77186-9.
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