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采用基于移植后环磷酰胺的移植物抗宿主病预防方案治疗血液系统恶性肿瘤的实体器官移植患者的异基因造血干细胞移植

Allogeneic Hematopoietic Stem Cell Transplantation After Solid Organ Transplantation in Patients With Hematologic Malignancies Managed With Post-Transplant Cyclophosphamide-Based Graft-Versus-Host Disease Prophylaxis.

作者信息

Jang Charley, Hsu Jingmei

机构信息

Department of Medicine, NYU Grossman School of Medicine, New York, NY, USA.

Department of Hematology and Oncology, NYU Langone Health Perlmutter Cancer Center, NYU Grossman School of Medicine, New York, NY, USA.

出版信息

J Hematol. 2024 Oct;13(5):250-258. doi: 10.14740/jh1327. Epub 2024 Oct 21.

Abstract

Patients who receive solid organ transplants often require lifelong immunosuppression, which increases their risk for hematologic disorders. Allogeneic hematopoietic stem cell transplantation (HSCT) offers a potential curative treatment option for these patients. However, there is still a lack of understanding and guidance on graft-vs-host disease (GVHD) immunosuppression regimens, potential complications, and outcomes in patients with solid organ transplants who undergo HSCT. The rate of solid organ transplantation continues to increase annually, making this a common clinical scenario that hematologists encounter. In this case series, we present three patients who underwent liver, kidney and cardiac transplants and each developed hematological malignancies requiring allogeneic stem cell transplant. This is the first case report of two patients who received post-transplant cyclophosphamide with mycophenolate mofetil and tacrolimus GVHD prophylaxis. We also review recent advances in GVHD prophylaxis in allogeneic HSCT and solid organ transplantation including immune tolerance and immunosuppression-free protocols. Our case series support the use of post-transplant cyclophosphamide with mycophenolate mofetil and tacrolimus as post-transplant GVHD prophylaxis, which does not appear to compromise solid organ graft function. Our case series also provides evidence that allogeneic HSCT is a feasible and potentially life-saving treatment option in patients who develop hematologic malignancies after solid organ transplantation.

摘要

接受实体器官移植的患者通常需要终身免疫抑制,这增加了他们患血液系统疾病的风险。异基因造血干细胞移植(HSCT)为这些患者提供了一种潜在的治愈性治疗选择。然而,对于接受HSCT的实体器官移植患者,在移植物抗宿主病(GVHD)免疫抑制方案、潜在并发症及预后方面仍缺乏了解和指导。实体器官移植的发生率每年持续上升,这使得这成为血液科医生常见的临床情况。在本病例系列中,我们介绍了3例分别接受肝、肾和心脏移植的患者,他们均发生了需要异基因干细胞移植的血液系统恶性肿瘤。这是首例关于2例接受移植后环磷酰胺联合霉酚酸酯及他克莫司预防GVHD的病例报告。我们还回顾了异基因HSCT和实体器官移植中GVHD预防的最新进展,包括免疫耐受和无免疫抑制方案。我们的病例系列支持使用移植后环磷酰胺联合霉酚酸酯及他克莫司作为移植后GVHD预防措施,这似乎不会损害实体器官移植物功能。我们的病例系列还提供了证据,表明异基因HSCT对于实体器官移植后发生血液系统恶性肿瘤的患者是一种可行且可能挽救生命的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3227/11526586/70b9c9a212c9/jh-13-250-g001.jpg

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