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自发性红细胞集落形成和 JAK2 突变分析对原发性血小板增多症血栓事件的预后价值。

Prognostic utility of spontaneous erythroid colony formation and JAK2 mutational analysis for thrombotic events in essential thrombocythaemia.

机构信息

Haematology Department, Princess Alexandra Hospital, Brisbane, Queensland, Australia.

出版信息

Intern Med J. 2011 May;41(5):408-15. doi: 10.1111/j.1445-5994.2010.02334.x. Epub 2010 Jul 30.

Abstract

BACKGROUND

Thrombotic events in essential thrombocythaemia (ET) are difficult to predict with current risk stratification based on age and prior history of thrombosis.

AIMS

We aimed to assess the predictive value of the JAK2 V617F mutation (JAK2) and spontaneous erythroid colony (SEC) growth for the development of thrombotic events post diagnosis in patients with ET.

METHODS

Consecutive patients with ET were retrospectively identified, and clinical and laboratory correlates were evaluated. Thrombotic events were categorized according to their occurrence at or prior to diagnosis (prior thrombosis), and any time post diagnosis of ET (subsequent thrombosis). JAK2 analysis was performed by allele-specific PCR on whole blood or bone marrow.

RESULTS

A total of 62 patients was identified, median age 63 years; 67% (41/61) JAK2-positive and 47% (25/53) SEC-positive. Median follow-up was 33 months (range, 1 to 137). JAK2-positive patients showed a trend to increased prior thrombosis (27% vs 5%, P= 0.08), and a significant increase in the development of subsequent thrombosis (5-year event rate 31% vs 6%, P= 0.04), which persisted when stratified for a history of prior thrombosis (P= 0.04). Survival was not affected by JAK2 status. The SEC assay predicted an increased rate of baseline thrombosis (16% vs 0%, P= 0.04), but was not found to be predictive of any subsequent thrombotic events.

CONCLUSIONS

Patients with ET who are JAK2-positive by whole blood allele-specific PCR appear to be at increased risk of thrombotic complications, which is independent of a prior history of thrombosis.

摘要

背景

目前基于年龄和既往血栓史的危险分层方法难以预测原发性血小板增多症(ET)中的血栓事件。

目的

我们旨在评估 JAK2 V617F 突变(JAK2)和自发性红细胞集落(SEC)生长对 ET 患者诊断后血栓事件发生的预测价值。

方法

回顾性鉴定连续 ET 患者,并评估临床和实验室相关性。根据血栓事件发生于诊断前(既往血栓)或 ET 诊断后任何时间(继发血栓)进行分类。通过等位基因特异性 PCR 在全血或骨髓中进行 JAK2 分析。

结果

共鉴定出 62 例患者,中位年龄 63 岁;67%(41/61)JAK2 阳性,47%(25/53)SEC 阳性。中位随访时间为 33 个月(范围 1 至 137)。JAK2 阳性患者既往血栓的发生率增加(27%比 5%,P=0.08),且继发血栓的发生率显著增加(5 年事件率 31%比 6%,P=0.04),这种差异在既往血栓史分层时仍然存在(P=0.04)。JAK2 状态不影响生存。SEC 检测预测基线血栓的发生率增加(16%比 0%,P=0.04),但与任何继发血栓事件无关。

结论

通过全血等位基因特异性 PCR 呈 JAK2 阳性的 ET 患者似乎血栓并发症风险增加,这与既往血栓史无关。

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