Challenges in evaluating thromboembolic risk in acute leukemia: clinical profiling and limitations of current scoring systems

评估急性白血病血栓栓塞风险的挑战:临床特征分析和现有评分系统的局限性

阅读:2

Abstract

BACKGROUND: Limited evidence is available on risk factors for thrombotic events in newly diagnosed acute leukemia (AL) patients, and predictive tools in this population need further validation. OBJECTIVES: To evaluate the incidence of thrombosis in newly diagnosed AL patients and to validate known predictive scores. METHODS: We retrospectively included 421 patients between 2009 and 2022. Data on thrombotic events (venous and arterial) were collected from admission to 60 days of follow-up. The Khorana, International Society on Thrombosis and Haemostasis (ISTH) disseminated intravascular coagulation, and Siriraj Acute Myeloid/Lymphoblastic Leukemia scores were applied to the cohort. RESULTS: The cumulative incidence of thrombotic events within 60 days was 15.8%, being higher in the acute lymphoblastic leukemia subgroup (21%). Seventy-two percent of the events occurred within the first 30 days of diagnosis. Superficial vein thrombosis and catheter-related thrombosis comprised most events (38.2% and 19.1%, respectively), while arterial thrombosis represented 11.8%. Obesity and platelet count > 20 × 10(9)/L were associated with an overall risk of thrombosis in this cohort. In the acute myeloid leukemia subset, thrombotic event occurrence was associated with a higher peripheral blast percentage and elevated C-reactive protein levels. The Khorana, ISTH-disseminated intravascular coagulation, and Siriraj Acute Myeloid/Lymphoblastic Leukemia scores were not associated with thrombotic events in AL patients. CONCLUSION: The incidence of thrombotic events is not negligible, being higher in the induction phase. Further studies and better tools to improve event prediction in this population, such as biomarker development, are needed.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。