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干扰素-γ与供体白细胞输注用于异基因造血干细胞移植后复发的髓母细胞性恶性肿瘤

IFN-γ and donor leukocyte infusions for relapsed myeloblastic malignancies after allogeneic hematopoietic stem cell transplantation.

作者信息

Ito Sawa, Geramita Emily, Ventura Kedwin, Neupane Biswas, Bhise Shruti, Moore Erika M, Furlan Scott, Shlomchik Warren D

机构信息

Division of Hematology-Oncology, Department of Medicine.

Thomas E. Starzl Transplantation Institute; and.

出版信息

JCI Insight. 2025 Mar 25;10(9). doi: 10.1172/jci.insight.190655. eCollection 2025 May 8.

Abstract

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.

摘要

背景

移植物抗白血病(GVL)效应有助于异基因干细胞移植(alloSCT)的疗效。然而,复发是治疗失败的最主要单一原因,提示GVL效应失败。基于临床前数据显示干扰素-γ(IFN-γ)对于使成髓细胞对同种异体反应性T细胞敏感很重要,我们开展了一项IFN-γ联合供者白细胞输注(DLI)用于HLA匹配的alloSCT后复发的髓细胞性恶性肿瘤的I期试验。

方法

alloSCT后复发的急性髓系白血病或骨髓增生异常综合征患者符合条件。患者自行注射IFN-γ 4周(队列1)或1周(队列2),随后进行DLI并同时注射IFN-γ,共12周。通过单细胞RNA测序(scRNA-Seq)分析骨髓样本,以评估恶性成髓细胞对IFN-γ的体内反应。

结果

所有参与者(n = 7)对IFN-γ单药治疗耐受性良好。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),所有这些均通过皮质类固醇治疗得到缓解。6名接受DLI的患者中有4名实现了微小残留病阴性的完全缓解和完全的供者造血恢复。缓解者的中位总生存期为579天(范围97 - 906天)。scRNA-Seq验证了在分析样本中IFN-γ作用后造血干细胞样或髓系祖细胞中IFN-γ反应途径的体内激活。

结论

在这项针对alloSCT后复发的急性髓系白血病和骨髓增生异常综合征的IFN-γ I期研究中,IFN-γ安全且耐受性良好,与DLI联合使用时具有有前景的疗效信号。需要更大规模的研究来正式检验这种方法的疗效。

试验注册

ClinicalTrials.gov NCT04628338。

资助

匹兹堡大学医学中心希尔曼癌症中心癌症免疫学和免疫治疗项目试点奖以及“触手可及的治愈:用于影响血液癌症的药物重新利用临床试验”。

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