Risk of bleeding in patients with essential thrombocythemia and extreme thrombocytosis.

IF 7.4 1区 医学 Q1 HEMATOLOGY
Rathnam K Venkat, Robert A Redd, Amyah C Harris, Martin J Aryee, Anna E Marneth, Baransel Kamaz, Chulwoo J Kim, Mohammed Wazir, Lachelle D Weeks, Maximilian Stahl, Daniel J DeAngelo, R Coleman Lindsley, Marlise R Luskin, Gabriela S Hobbs, Joan How
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Abstract

Abstract: Approximately 25% of patients with essential thrombocythemia (ET) present with extreme thrombocytosis (ExT), defined as having a platelet count ≥1000 × 109/L. ExT patients may have an increased bleeding risk associated with acquired von Willebrand syndrome. We retrospectively analyzed the risk of bleeding and thrombosis in ExT vs non-ExT patients with ET at Dana-Farber Cancer Institute and Massachusetts General Hospital from 2014 to 2022 to inform treatment decisions. We abstracted the first major bleed, clinically relevant nonmajor bleed (CRNMB), and thrombotic events from medical records. We identified 128 ExT patients (28%) and 323 non-ExT patients (72%). Cumulative incidence of bleeding was not different in ExT vs non-ExT patients (21% vs 13% [P = .28] for major bleed; 16% vs 15% [P = .50] for CRNMB). Very low and low thrombotic risk ExT patients were more likely to be cytoreduced than very low- and low-risk non-ExT patients (69% vs 50% [P = .060] for very low risk; 83% vs 53% [P = .0059] for low risk). However, we found no differences in bleeding between ExT and non-ExT patients when restricting the risk of bleed from diagnosis to cytoreduction start date (28% vs 19% [P = .29] for major bleed; 24% vs 22% [P = .75] for CRNMB). Cumulative incidence of thrombosis was also not different between ExT and non-ExT patients (28% vs 25%; P = .98). This suggests that cytoreduction may not be necessary to reduce bleeding risk based only on a platelet count of 1 million. We identified novel risk factors for bleeding in patients with ET including diabetes mellitus and the DNMT3A mutation.

血小板极度增多的 Essential Thrombocythemia 患者的出血风险。
约 25% 的原发性血小板增多症(ET)患者会出现极度血小板增多症(ExT),即血小板计数≥1000 x 10^9/L。ExT 患者可能会因获得性冯-威廉综合征而增加出血风险。我们回顾性分析了 2014-2022 年间丹娜法伯癌症研究所和马萨诸塞州总医院 ExT 与非 ExT ET 患者的出血和血栓形成风险,为治疗决策提供参考。我们从医疗记录中抽取了首次大出血、临床相关非大出血(CRNMB)和血栓事件。我们确定了 128 例(28%)ExT 患者和 323 例(72%)非 ExT 患者。ExT患者与非ExT患者的出血累积发生率没有差异(大出血为21%对13%,P=0.28;CRNMB为16%对15%,P=0.50)。与极低和低风险的非 ExT 患者相比,极低和低血栓风险的 ExT 患者更有可能接受细胞减灭术(极低风险为 69% 对 50%,P=0.060;低风险为 83% 对 53%,P=0.0059)。然而,如果限制从诊断到细胞减灭术开始日期的出血风险,我们发现 ExT 和非 ExT 患者的出血情况没有差异(大出血为 28% 对 19%,P=0.29;CRNMB 为 24% 对 22%,P=0.75)。血栓形成的累积发生率在 ExT 和非 ExT 患者之间也没有差异(28% 对 25%,P=0.98)。这表明,仅根据 100 万的血小板计数来降低出血风险可能并不需要进行细胞减灭术。我们发现了 ET 患者出血的新风险因素,包括糖尿病和 DNMT3A 突变。
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来源期刊
Blood advances
Blood advances Medicine-Hematology
CiteScore
12.70
自引率
2.70%
发文量
840
期刊介绍: Blood Advances, a semimonthly medical journal published by the American Society of Hematology, marks the first addition to the Blood family in 70 years. This peer-reviewed, online-only, open-access journal was launched under the leadership of founding editor-in-chief Robert Negrin, MD, from Stanford University Medical Center in Stanford, CA, with its inaugural issue released on November 29, 2016. Blood Advances serves as an international platform for original articles detailing basic laboratory, translational, and clinical investigations in hematology. The journal comprehensively covers all aspects of hematology, including disorders of leukocytes (both benign and malignant), erythrocytes, platelets, hemostatic mechanisms, vascular biology, immunology, and hematologic oncology. Each article undergoes a rigorous peer-review process, with selection based on the originality of the findings, the high quality of the work presented, and the clarity of the presentation.
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