Hematology Department, Hospital Clínic, IDIBAPS, University of Barcelona, Villarroel 170, Barcelona, Spain.
Curr Hematol Malig Rep. 2012 Mar;7(1):43-9. doi: 10.1007/s11899-011-0102-1.
Primary myelofibrosis (PMF) is a Philadelphia chromosome-negative chronic myeloproliferative neoplasm usually affecting elderly people. Median survival currently approaches 6 years, with a few patients surviving more than 20 years but others dying soon after diagnosis. In 10% to 20% of patients, PMF evolves into acute leukemia. Conventional treatment is merely palliative and does not prolong survival. The only chance for cure is allogeneic hemopoietic stem-cell transplantation (allo-HSCT), which is associated with high morbidity and mortality. Introduction of less aggressive forms of allo-HSCT and the prospect of molecular-targeted therapies has renewed interest in prognostication in PMF. The most important prognostic factors are anemia, age over 65 years, constitutional symptoms, leukocytosis, blood blasts, and some cytogenetic abnormalities. These factors have recently been systematized into an International Prognostic Scoring System (IPSS) and further refined in a dynamic IPSS (DIPSS), useful at any time over the disease course, as well as a DIPSS-plus model including karyotypic information.
原发性骨髓纤维化(PMF)是一种费城染色体阴性的慢性骨髓增生性肿瘤,通常影响老年人。目前中位生存期接近 6 年,少数患者存活超过 20 年,但也有一些患者在诊断后很快死亡。在 10%到 20%的患者中,PMF 会发展为急性白血病。常规治疗仅仅是姑息性的,并不能延长生存期。治愈的唯一机会是异基因造血干细胞移植(allo-HSCT),但这种治疗方法与高发病率和死亡率相关。较不激进的 allo-HSCT 形式的引入和分子靶向治疗的前景,重新激发了人们对 PMF 预后的兴趣。最重要的预后因素包括贫血、年龄大于 65 岁、全身症状、白细胞增多、血液原始细胞增多和一些细胞遗传学异常。这些因素最近被系统地纳入国际预后评分系统(IPSS),并在疾病过程中的任何时间进一步细化为动态 IPSS(DIPSS),以及包括核型信息的 DIPSS-plus 模型。