Ospedali Riuniti di Bergamo, Bergamo, Italy.
J Clin Oncol. 2011 Aug 10;29(23):3179-84. doi: 10.1200/JCO.2010.34.5298. Epub 2011 Jul 11.
The WHO diagnostic criteria underscore the role of bone marrow (BM) morphology in distinguishing essential thrombocythemia (ET) from early/prefibrotic primary myelofibrosis (PMF). This study examined the clinical relevance of such a distinction.
Representatives from seven international centers of excellence for myeloproliferative neoplasms convened to create a clinicopathologic database of patients previously diagnosed as having ET (N = 1,104). Study eligibility criteria included availability of treatment-naive BM specimens obtained within 1 year of diagnosis. All bone marrows subsequently underwent a central re-review.
Diagnosis was confirmed as ET in 891 patients (81%) and was revised to early/prefibrotic PMF in 180 (16%); 33 patients were not evaluable. In early/prefibrotic PMF compared with ET, the 10-year survival rates (76% and 89%, respectively) and 15-year survival rates (59% and 80%, respectively), leukemic transformation rates at 10 years (5.8% and 0.7%, respectively) and 15 years (11.7% and 2.1%, respectively), and rates of progression to overt myelofibrosis at 10 years (12.3% and 0.8%, respectively) and 15 years (16.9% and 9.3%) were significantly worse. The respective death, leukemia, and overt myelofibrosis incidence rates per 100 patient-years for early/prefibrotic PMF compared with ET were 2.7% and 1.3% (relative risk [RR], 2.1; P < .001), 0.6% and 0.1% (RR, 5.2; P = .001), and 1% and 0.5% (RR, 2.0; P = .04). Multivariable analysis confirmed these findings and also identified age older than 60 years (hazard ratio [HR], 6.7), leukocyte count greater than 11 × 10(9)/L (HR, 2.01), anemia (HR, 2.95), and thrombosis history (HR, 2.81) as additional risk factors for survival. Thrombosis and JAK2V617F incidence rates were similar between the two groups. Survival in ET was similar to the sex- and age-standardized European population.
This study validates the clinical relevance of strict adherence to WHO criteria in the diagnosis of ET and provides important information on survival, disease complication rates, and prognostic factors in strictly WHO-defined ET and early/prefibrotic PMF.
世界卫生组织(WHO)的诊断标准强调了骨髓(BM)形态学在鉴别原发性骨髓纤维化(PMF)早期/前纤维化与特发性血小板增多症(ET)中的作用。本研究探讨了这种鉴别诊断的临床相关性。
来自七个国际骨髓增殖性肿瘤卓越中心的代表齐聚一堂,创建了一个临床病理数据库,其中包括之前被诊断为 ET(N=1104)的患者。研究纳入标准包括在诊断后 1 年内可获得未经治疗的 BM 标本。所有骨髓随后均进行了中心重新评估。
891 例(81%)患者的诊断被确认为 ET,180 例(16%)患者的诊断被修订为早期/前纤维化 PMF;33 例患者无法评估。与 ET 相比,早期/前纤维化 PMF 的 10 年生存率(分别为 76%和 89%)和 15 年生存率(分别为 59%和 80%)、10 年白血病转化率(分别为 5.8%和 0.7%)和 15 年白血病转化率(分别为 11.7%和 2.1%)、10 年进展为明显骨髓纤维化的比例(分别为 12.3%和 0.8%)和 15 年进展为明显骨髓纤维化的比例(分别为 16.9%和 9.3%)均显著较差。与 ET 相比,早期/前纤维化 PMF 患者的死亡、白血病和明显骨髓纤维化发生率分别为每 100 患者年 2.7%和 1.3%(相对风险[RR],2.1;P<.001)、0.6%和 0.1%(RR,5.2;P=.001)和 1%和 0.5%(RR,2.0;P=.04)。多变量分析证实了这些发现,并确定年龄大于 60 岁(风险比[HR],6.7)、白细胞计数大于 11×10(9)/L(HR,2.01)、贫血(HR,2.95)和血栓形成史(HR,2.81)是生存的其他危险因素。两组之间的血栓形成和 JAK2V617F 发生率相似。ET 的生存情况与性别和年龄标准化的欧洲人群相似。
本研究验证了严格遵守 WHO 标准在 ET 诊断中的临床相关性,并为严格符合 WHO 标准的 ET 和早期/前纤维化 PMF 的生存、疾病并发症发生率和预后因素提供了重要信息。