Long-term survival of kidney-transplant recipient with donor-transmitted malignant melanoma after provoked rejection

IF 1.6 4区 医学 Q4 IMMUNOLOGY Transplant immunology Pub Date : 2024-09-02 DOI:10.1016/j.trim.2024.102117
Andreas Kommer , Stefan Holtz , Daniel Kraus , Simone Cosima Boedecker-Lips , Martina Koch , Julia Weinmann-Menke
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Abstract

Donor-transmitted malignancy is a rare and often fatal complication of organ transplantation. We report a case of a 55-year old male kidney transplant recipient who was diagnosed with stage-IV donor-transmitted melanoma 5 months after transplantation with metastases in the liver, spleen, lung, and brain. Immunosuppression was discontinued, and encorafenib and binimetinib, inhibitors of a serine/threonine B-Raf proto-oncogene (BRAF) and mitogen-activated protein kinase kinase (MEK) respectively, were started. Severe rejection ensued and necessitated the start of hemodialysis as well as urgent graft nephrectomy. However, the tumor progressed and BRAF/MEK inhibition was replaced by immune-checkpoint inhibition with ipilimumab and nivolumab. When this also failed to slow disease progression and seizures occurred, therapy with encorafenib and binimetinib was reinstated. Afterwards, most of the metastases remained stable. The patient has now survived for more than 4 years in good general health, which is an exceptionally long survival with donor-transmitted, metastasized melanoma.

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肾移植受者在诱发排斥反应后长期存活,并患有供体传播的恶性黑色素瘤。
供体转移性恶性肿瘤是器官移植中一种罕见且往往致命的并发症。我们报告了一例 55 岁男性肾移植受者的病例,他在移植后 5 个月被诊断出患有 IV 期供体转移性黑色素瘤,肝、脾、肺和脑均有转移。他停止了免疫抑制,开始服用安戈非尼和宾美替尼,这两种药物分别是丝氨酸/苏氨酸B-Raf原癌基因(BRAF)和丝裂原活化蛋白激酶激酶(MEK)的抑制剂。随后出现了严重的排斥反应,不得不开始进行血液透析和紧急移植肾切除术。然而,肿瘤仍在发展,BRAF/MEK抑制剂被ipilimumab和nivolumab的免疫检查点抑制剂所取代。当这一疗法也未能延缓疾病进展并出现癫痫发作时,又重新使用了安戈非尼和宾美替尼疗法。之后,大部分转移灶保持稳定。目前,该患者已存活了 4 年多,总体健康状况良好,这对于供体传播的转移性黑色素瘤患者来说是一个特别长的存活期。
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来源期刊
Transplant immunology
Transplant immunology 医学-免疫学
CiteScore
2.10
自引率
13.30%
发文量
198
审稿时长
48 days
期刊介绍: Transplant Immunology will publish up-to-date information on all aspects of the broad field it encompasses. The journal will be directed at (basic) scientists, tissue typers, transplant physicians and surgeons, and research and data on all immunological aspects of organ-, tissue- and (haematopoietic) stem cell transplantation are of potential interest to the readers of Transplant Immunology. Original papers, Review articles and Hypotheses will be considered for publication and submitted manuscripts will be rapidly peer-reviewed and published. They will be judged on the basis of scientific merit, originality, timeliness and quality.
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