Tefferi Ayalew, Thiele Juergen, Orazi Attilio, Kvasnicka Hans Michael, Barbui Tiziano, Hanson Curtis A, Barosi Giovanni, Verstovsek Srdan, Birgegard Gunnar, Mesa Ruben, Reilly John T, Gisslinger Heinz, Vannucchi Alessandro M, Cervantes Francisco, Finazzi Guido, Hoffman Ronald, Gilliland D Gary, Bloomfield Clara D, Vardiman James W
Mayo Clinic, Rochester, MN 55905, USA.
Blood. 2007 Aug 15;110(4):1092-7. doi: 10.1182/blood-2007-04-083501. Epub 2007 May 8.
The Janus kinase 2 mutation, JAK2617V>F, is myeloid neoplasm-specific; its presence excludes secondary polycythemia, thrombocytosis, or bone marrow fibrosis from other causes. Furthermore, JAK2617V>F or a JAK2 exon 12 mutation is present in virtually all patients with polycythemia vera (PV), whereas JAK2617V>F also occurs in approximately half of patients with essential thrombocythemia (ET) or primary myelofibrosis (PMF). Therefore, JAK2 mutation screening holds the promise of a decisive diagnostic test in PV while being complementary to histology for the diagnosis of ET and PMF; the combination of molecular testing and histologic review should also facilitate diagnosis of ET associated with borderline thrombocytosis. Accordingly, revision of the current World Health Organization (WHO) diagnostic criteria for PV, ET, and PMF is warranted; JAK2 mutation analysis should be listed as a major criterion for PV diagnosis, and the platelet count threshold for ET diagnosis can be lowered from 600 to 450 x 10(9)/L. The current document was prepared by an international expert panel of pathologists and clinical investigators in myeloproliferative disorders; it was subsequently presented to members of the Clinical Advisory Committee for the revision of the WHO Classification of Myeloid Neoplasms, who endorsed the document and recommended its adoption by the WHO.
Janus激酶2突变JAK2617V>F是髓系肿瘤特异性的;其存在可排除其他原因引起的继发性红细胞增多症、血小板增多症或骨髓纤维化。此外,几乎所有真性红细胞增多症(PV)患者都存在JAK2617V>F或JAK2外显子12突变,而约一半的原发性血小板增多症(ET)或原发性骨髓纤维化(PMF)患者也存在JAK2617V>F。因此,JAK2突变筛查有望成为PV的决定性诊断试验,同时对ET和PMF的诊断起到组织学诊断的补充作用;分子检测与组织学检查相结合也应有助于诊断伴有临界血小板增多症的ET。因此,有必要修订世界卫生组织(WHO)目前关于PV、ET和PMF的诊断标准;JAK2突变分析应列为PV诊断的主要标准,ET诊断的血小板计数阈值可从600降至450×10⁹/L。本文件由骨髓增殖性疾病领域的国际病理学家和临床研究专家小组编写;随后提交给了WHO髓系肿瘤分类修订临床咨询委员会成员,他们认可了该文件并建议WHO采用。