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异基因造血干细胞移植后复发性皮肤T细胞淋巴瘤的管理:附代表性患者病例回顾

Management of relapsed cutaneous T-Cell lymphoma following allogeneic hematopoietic stem cell transplantation: Review with representative patient case.

作者信息

Weiner David M, Lewis Daniel J, Spaccarelli Natalie G, Clark Rachael A, Nasta Sunita D, Loren Alison W, Rook Alain H, Kim Ellen J

机构信息

Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.

Department of Dermatology, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, USA.

出版信息

Dermatol Ther. 2022 Jul;35(7):e15538. doi: 10.1111/dth.15538. Epub 2022 May 9.

DOI:10.1111/dth.15538
PMID:35477952
Abstract

Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is a potentially curative treatment option for patients with refractory cutaneous T-cell lymphoma (CTCL) through replacement of the bone marrow responsible for lymphoma cells and possibly induction of a graft-versus-lymphoma effect. However, allo-HSCT is not always curative; relapse of CTCL occurs in about half of patients post-transplant. Treatment of relapsed CTCL after allo-HSCT is challenging because post-transplant patients are at high risk of graft-versus-host disease, and this condition may be precipitated or exacerbated by standard CTCL therapies. The benefit of each potential therapy must therefore be weighed against its risk of graft versus host disease (GVHD). In this article, we review the management of relapsed CTCL after allo-HSCT. We begin with an exemplative patient whose relapsed Sezary syndrome was successfully treated without development of GVHD. We also report high-throughput T-cell receptor sequencing data obtained during the patient's disease relapse and remission. We then review general guidelines for management of relapsed CTCL and summarize all reported cases and outcomes of relapsed CTCL after transplant. We conclude by reviewing the current CTCL therapies and their risk of GVHD.

摘要

异基因造血干细胞移植(allo-HSCT)是难治性皮肤T细胞淋巴瘤(CTCL)患者一种潜在的治愈性治疗选择,通过替换产生淋巴瘤细胞的骨髓,并可能诱导移植物抗淋巴瘤效应。然而,allo-HSCT并非总能治愈;约一半的移植后患者会出现CTCL复发。allo-HSCT后复发CTCL的治疗具有挑战性,因为移植后患者发生移植物抗宿主病的风险很高,而标准的CTCL治疗可能会引发或加重这种情况。因此,必须权衡每种潜在治疗的益处与其发生移植物抗宿主病(GVHD)的风险。在本文中,我们回顾了allo-HSCT后复发CTCL的管理。我们首先介绍一位复发性Sezary综合征患者,其在未发生GVHD的情况下成功得到治疗。我们还报告了该患者疾病复发和缓解期间获得的高通量T细胞受体测序数据。然后,我们回顾了复发CTCL管理的一般指南,并总结了移植后复发CTCL的所有报告病例和结果。我们通过回顾当前的CTCL治疗方法及其GVHD风险来得出结论。

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