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.

IF 1.3 Q4 HEMATOLOGY
Journal of hematology Pub Date : 2024-10-01 Epub Date: 2024-10-21 DOI:10.14740/jh1327
Charley Jang, Jingmei Hsu
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引用次数: 0

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.

基于环磷酰胺的移植后移植物抗宿主病预防疗法治疗血液恶性肿瘤患者的实体器官移植后异体造血干细胞移植。
接受实体器官移植的患者通常需要终生接受免疫抑制,这增加了他们罹患血液病的风险。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疗选择。然而,人们对接受造血干细胞移植的实体器官移植患者的移植物抗宿主病(GVHD)免疫抑制方案、潜在并发症和治疗效果仍缺乏了解和指导。实体器官移植的比例每年都在增加,这也是血液科医生经常遇到的临床情况。在本病例系列中,我们介绍了接受肝脏、肾脏和心脏移植的三位患者,他们都出现了血液恶性肿瘤,需要进行异基因干细胞移植。这是首次报道两名患者在移植后接受环磷酰胺联合霉酚酸酯和他克莫司预防GVHD的病例。我们还回顾了异基因造血干细胞移植和实体器官移植预防 GVHD 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在移植后使用环磷酰胺联合霉酚酸酯和他克莫司作为移植后 GVHD 预防药物,这似乎不会损害实体器官移植的功能。我们的病例系列还提供了证据,证明异基因造血干细胞移植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方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of hematology
Journal of hematology HEMATOLOGY-
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