IFN-γ和供体白细胞输注治疗异基因造血干细胞移植后复发的髓母细胞恶性肿瘤 。

IF 6.3 1区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
JCI insight Pub Date : 2025-03-25 eCollection Date: 2025-05-08 DOI:10.1172/jci.insight.190655
Sawa Ito, Emily Geramita, Kedwin Ventura, Biswas Neupane, Shruti Bhise, Erika M Moore, Scott Furlan, Warren D Shlomchik
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引用次数: 0

摘要

背景:移植物抗白血病(GVL)效应有助于同种异体干细胞移植(alloSCT)的疗效。然而,复发,表明GVL衰竭,是治疗失败的最大单一原因。基于临床前数据显示IFN-γ对髓母细胞对同种异体反应性T细胞的敏感性很重要,我们进行了IFN-γ联合供体白细胞输注(DLI)的I期试验,用于治疗hla匹配同种异体细胞移植后复发的髓母细胞恶性肿瘤。方法:对同种异体细胞移植后复发的急性髓性白血病或骨髓增生异常综合征患者进行研究。患者自我给予IFN-γ治疗4周(队列1)或1周(队列2),随后DLI和同时给予IFN-γ治疗共12周。骨髓样本通过单细胞RNA测序(scRNAseq)进行分析,以评估恶性成髓细胞对IFN-γ的体内反应。结果:所有受试者对IFN-γ单药治疗耐受良好(n=7)。DLI后的治疗相关毒性包括:I-II级移植物抗宿主病(n=5)、免疫效应细胞相关神经毒性综合征(n=2)和特发性肺综合征(n=1),所有这些都通过皮质类固醇缓解。6名DLI受者中有4名达到了最小残留疾病阴性完全缓解和供体造血完全恢复。应答者的中位总生存期为579天(范围97-906天)。ScRNAseq证实,在分析样本中,IFN-γ作用后,造血干细胞样细胞或髓系祖细胞中的IFN-γ反应途径在体内被激活。结论:在这项I期研究中,IFN-γ治疗同种异体细胞移植后复发的AML/MDS是安全且耐受性良好的,与DLI联合使用具有良好的疗效信号。需要更大规模的研究来正式测试这种方法的有效性。RESGISTRATION审判。临床试验:gov NCT04628338。资助:该研究得到了UPMC希尔曼癌症中心癌症免疫学和免疫治疗项目(CIIP)试点奖和“触手可及的治愈:药物重新利用临床试验来影响血癌”的支持。重组ifn - γ (actitimmune®)由Horizon Therapeutics公司捐赠。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
IFN-γ and donor leukocyte infusions for relapsed myeloblastic malignancies after allogeneic hematopoietic stem cell transplantation.

BACKGROUNDThe graft-versus-leukemia (GVL) effect contributes to the efficacy of allogeneic stem cell transplantation (alloSCT). However, relapse, indicative of GVL failure, is the greatest single cause of treatment failure. Based on preclinical data showing that IFN-γ is important to sensitize myeloblasts to alloreactive T cells, we performed a phase I trial of IFN-γ combined with donor leukocyte infusions (DLIs) in myeloblastic malignancies that relapsed after HLA-matched alloSCT.METHODSPatients with relapsed acute myeloid leukemia or myelodysplastic syndrome after alloSCT were eligible. Patients self-administered IFN-γ for 4 weeks (cohort 1) or 1 week (cohort 2), followed by DLI and concurrent IFN-γ for a total of 12 weeks. Bone marrow samples were analyzed by single-cell RNA sequencing (scRNA-Seq) to assess in vivo responses to IFN-γ by malignant myeloblasts.RESULTSIFN-γ monotherapy was well tolerated by all participants (n = 7). Treatment-related toxicities after DLI included grade I-II graft-versus-host disease (n = 5), immune effector cell-associated neurotoxicity syndrome (n = 2), and idiopathic pulmonary syndrome (n = 1), all of which resolved with corticosteroids. Four of 6 DLI recipients achieved minimal residual disease-negative complete remissions and full donor hematopoietic recovery. Median overall survival was 579 days (range, 97-906) in responders. scRNA-Seq validated in vivo activation of the IFN-γ response pathway in hematopoietic stem cell-like or myeloid progenitor cells after IFN-γ in analyzed samples.CONCLUSIONIFN-γ was safe and well tolerated in this phase I study of IFN-γ for relapsed acute myeloid leukemia and myelodysplastic syndrome after alloSCT, with a promising efficacy signal when combined with DLI. Larger studies are needed to formally test the efficacy of this approach.TRIAL REGISTRATIONClinicalTrials.gov NCT04628338.FUNDINGUPMC Hillman Cancer Center Cancer Immunology and Immunotherapy Program Pilot Award and Cure Within Reach: Drug Repurposing Clinical Trials to Impact Blood Cancers.

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来源期刊
JCI insight
JCI insight Medicine-General Medicine
CiteScore
13.70
自引率
1.20%
发文量
543
审稿时长
6 weeks
期刊介绍: JCI Insight is a Gold Open Access journal with a 2022 Impact Factor of 8.0. It publishes high-quality studies in various biomedical specialties, such as autoimmunity, gastroenterology, immunology, metabolism, nephrology, neuroscience, oncology, pulmonology, and vascular biology. The journal focuses on clinically relevant basic and translational research that contributes to the understanding of disease biology and treatment. JCI Insight is self-published by the American Society for Clinical Investigation (ASCI), a nonprofit honor organization of physician-scientists founded in 1908, and it helps fulfill the ASCI's mission to advance medical science through the publication of clinically relevant research reports.
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