异基因造血干细胞移植后17年npm1突变AML伴髓外表现复发

IF 0.7 Q4 HEMATOLOGY
Jan Braune, Kathrin Rieger, Olga Blau, Ulrich Keller, Lars Bullinger, Jan Krönke
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引用次数: 0

摘要

大多数具有NPM1突变的急性髓性白血病(AML)患者通过强化化疗获得缓解。然而,许多患者随后复发,通常发生在治疗后的前2-3年内,而10年以上的晚期复发是罕见的,也可能代表继发性/治疗相关的AML,没有NPM1突变。在这里,我们报告了一例NPM1突变的AML,在同种异体干细胞移植后17年发生髓质和髓外复发,维持了NPM1突变和首次诊断时检测到的所有其他遗传改变。在诊断和遗传高度相关的白血病克隆复发之间的异常长潜伏期表明,在NPM1突变型AML中存在治疗耐药、持续休眠的白血病干细胞。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Relapse of <i>NPM1</i>-Mutated AML with Extramedullary Manifestation 17 Years after Allogeneic Hematopoietic Stem Cell Transplantation.

Relapse of NPM1-Mutated AML with Extramedullary Manifestation 17 Years after Allogeneic Hematopoietic Stem Cell Transplantation.

The majority of patients with acute myeloid leukemia (AML) with the NPM1 mutation achieve remission with intensive chemotherapy. However, many patients subsequently relapse, which occurs frequently within the first 2-3 years after therapy, while late relapse after more than 10 years is rare and can also represent secondary/therapy-associated AML without the NPM1 mutation. Here, we present a case of NPM1-mutated AML that developed medullary and extramedullary relapse 17 years after allogeneic stem cell transplantation, maintaining the NPM1 mutation and all other genetic alterations detected at first diagnosis. This exceptionally long latency between diagnosis and relapse of a genetically highly related leukemic clone implies the existence of therapy-resistant, persisting dormant leukemic stem cells in NPM1 mutant AML.

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