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供者源性急性髓系白血病与实体器官移植。

Donor-derived acute myeloid leukemia in solid organ transplantation.

机构信息

Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, New York, USA.

Department of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

出版信息

Am J Transplant. 2022 Dec;22(12):3111-3119. doi: 10.1111/ajt.17174. Epub 2022 Sep 8.

Abstract

We report the transmission of acute myeloid leukemia (AML) undetected at donation from a deceased organ donor to two kidneys and one liver recipients. We reviewed the medical records, and performed molecular analyses and whole exome sequencing (WES) to ascertain AML donor origin and its molecular evolution. The liver recipient was diagnosed 11 months after transplantation and died from complications 2 months later. The two kidney recipients (R1 and R2) were diagnosed 19 and 20 months after transplantation and both received treatment for leukemia. R1 died of complications 11 months after diagnosis, while R2 went into complete remission for 44 months, before relapsing. R2 died 10 months later of complications from allogenic bone marrow transplantation. Microsatellite analysis demonstrated donor chimerism in circulating cells from both kidney recipients. Targeted molecular analyses and medical records revealed NPM1 mutation present in the donor and recipients, while FLT3 was mutated only in R1. These findings were confirmed by WES, which revealed additional founder and clonal mutations, and HLA genomic loss in R2. In conclusion, we report the first in-depth genomic analysis of AML transmission following solid organ transplantation, revealing distinct clonal evolution, and providing a potential molecular explanation for tumor escape.

摘要

我们报告了一例在器官捐献者死亡时未被发现的急性髓系白血病(AML)通过器官传播给两名肾脏和一名肝脏受者的情况。我们查阅了病历,并进行了分子分析和全外显子组测序(WES),以确定 AML 供体的来源及其分子进化。肝脏受者在移植后 11 个月被诊断出患有 AML,并在 2 个月后因并发症死亡。两名肾脏受者(R1 和 R2)在移植后 19 个月和 20 个月被诊断出患有 AML,均接受了白血病治疗。R1 在诊断后 11 个月因并发症死亡,而 R2 在缓解 44 个月后复发。R2 在接受异基因骨髓移植 10 个月后因并发症死亡。微卫星分析显示两名肾脏受者的循环细胞中有供体嵌合体。靶向分子分析和病历显示供体和受者均存在 NPM1 突变,而仅在 R1 中存在 FLT3 突变。WES 证实了这些发现,WES 还揭示了 R2 中存在额外的创始和克隆突变以及 HLA 基因组缺失。总之,我们报告了首例在实体器官移植后发生的 AML 传播的深入基因组分析,揭示了独特的克隆进化,并为肿瘤逃逸提供了潜在的分子解释。

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