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真性红细胞增多症中 JAK2 V617F 等位基因负担:证据负担。

JAK2 V617F allele burden in polycythemia vera: burden of proof.

机构信息

Division of Hematology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD.

Division of Hematology, Department of Medicine, Blood Research Center, Lineberger Comprehensive Cancer Center, The University of North Carolina at Chapel Hill, Chapel Hill, NC.

出版信息

Blood. 2023 Apr 20;141(16):1934-1942. doi: 10.1182/blood.2022017697.

Abstract

Polycythemia vera (PV) is a hematopoietic stem cell neoplasm defined by activating somatic mutations in the JAK2 gene and characterized clinically by overproduction of red blood cells, platelets, and neutrophils; a significant burden of disease-specific symptoms; high rates of vascular events; and evolution to a myelofibrosis phase or acute leukemia. The JAK2V617F variant allele frequency (VAF) is a key determinant of outcomes in PV, including thrombosis and myelofibrotic progression. Here, we critically review the dynamic role of JAK2V617F mutation burden in the pathogenesis and natural history of PV, the suitability of JAK2V617F VAF as a diagnostic and prognostic biomarker, and the utility of JAK2V617F VAF reduction in PV treatment.

摘要

真性红细胞增多症 (PV) 是一种造血干细胞肿瘤,其特征为 JAK2 基因的激活体细胞突变,并表现为红细胞、血小板和中性粒细胞过度生成;疾病特异性症状负担大;血管事件发生率高;并进展为骨髓纤维化期或急性白血病。JAK2V617F 变异等位基因频率 (VAF) 是 PV 预后的关键决定因素,包括血栓形成和骨髓纤维化进展。在这里,我们批判性地回顾了 JAK2V617F 突变负担在 PV 发病机制和自然史中的动态作用,JAK2V617F VAF 作为诊断和预后生物标志物的适用性,以及 JAK2V617F VAF 降低在 PV 治疗中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a61b/10163319/38f521475610/BLOOD_BLD-2022-017697-C-fx1.jpg

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