Bleeding events in patients with cancer: incidence, risk factors, and impact on prognosis in a prospective cohort study.

IF 21 1区 医学 Q1 HEMATOLOGY Blood Pub Date : 2024-11-28 DOI:10.1182/blood.2024025362
Cornelia Englisch, Florian Moik, Daniel Steiner, Angelika M Starzer, Anna S Berghoff, Matthias Preusser, Ingrid Pabinger, Cihan Ay
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Abstract

Abstract: Hemostatic imbalances are frequent in patients with cancer. Although cancer-associated thrombotic complications have been well characterized, data on bleeding events in patients with cancer are sparse. Therefore, we aimed to investigate the incidence, risk factors, and impact on prognosis of bleeding events in patients with cancer initiating systemic anticancer therapies in a prospective cohort study, the Vienna Cancer, Thrombosis, and Bleeding Study. The primary study outcome was defined as clinically relevant bleeding (CRB), comprising major bleeding (MB) and clinically relevant nonmajor bleeding. In total, 791 patients (48% female), with median age of 63 years (interquartile range [IQR], 54-70), with various cancer types, 65.5% stage IV, were included. Over a median follow-up of 19 months (IQR, 8.7-24.0), we observed 194 CRB events in 139 (17.6%) patients, of which 42 (30.0%) were tumor related, 64 (46.0%) gastrointestinal, and 7 (5.0%) intracerebral. The 12-month cumulative incidence of first CRB and MB was 16.6% (95% confidence interval [CI], 13.7-19.6) and 9.1% (95% CI, 6.8-11.3), respectively, in the whole cohort, and 14.4% (95% CI, 11.2-17.5) and 7.0% (95% CI, 4.7-9.2), respectively, in those without anticoagulation. Patients with head and neck cancer had the highest risk of CRB. Lower baseline hemoglobin and albumin were associated with bleeding in patients without anticoagulation. Seven (5.0%) bleeding events were fatal, of which 6 occurred in patients without anticoagulation. Patients with CRB were at an increased risk of all-cause mortality (multivariable transition hazard ratio, 5.80; 95% CI, 4.53-7.43). In patients with cancer, bleeding events represent a frequent complication and are associated with increased mortality.

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癌症患者的出血事件:一项前瞻性队列研究的发病率、风险因素及其对预后的影响。
癌症患者经常会出现止血失衡。虽然癌症相关的血栓并发症已经得到了很好的描述,但有关癌症患者出血事件的数据却很少。因此,我们旨在通过一项前瞻性队列研究--维也纳癌症、血栓与出血研究(CAT-BLED)--调查开始接受全身性抗癌疗法的癌症患者出血事件的发生率、风险因素及其对预后的影响。主要研究结果定义为临床相关出血(CRB),包括大出血(MB)和临床相关非大出血(CRNMB)。研究共纳入了 791 名不同癌症类型的患者(48% 为女性,中位年龄[四分位数间距,IQR]:63 [54-70] 岁),其中 65.5% 为 IV 期患者。在中位随访 19 个月(IQR:8.7-24.0)期间,我们观察到 139 名患者(17.6%)发生了 194 起 CRB 事件,其中 42 起(30%)与肿瘤相关,64 起(46.0%)与胃肠道相关,7 起(5.0%)与脑内相关。在整个队列中,首次CRB和MB的12个月累计发生率分别为16.6%(95%置信区间[CI]:13.7-19.6)和9.1%(95% CI:6.8-11.3),而在未接受抗凝治疗的患者中,首次CRB和MB的12个月累计发生率分别为14.4%(95%置信区间[CI]:11.2-17.5)和7.0%(95% CI:4.7-9.2)。头颈部癌症患者发生 CRB 的风险最高。在未接受抗凝治疗的患者中,较低的基线血红蛋白和白蛋白与出血有关。7例(5.0%)出血事件是致命的,其中6例发生在未接受抗凝治疗的患者中。CRB 患者全因死亡风险增加(多变量转换危险比 [95%CI]:5.80 [4.53-7.43])。在癌症患者中,出血事件是一种常见的并发症,与死亡率的增加有关。
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来源期刊
Blood
Blood 医学-血液学
CiteScore
23.60
自引率
3.90%
发文量
955
审稿时长
1 months
期刊介绍: Blood, the official journal of the American Society of Hematology, published online and in print, provides an international forum for the publication of original articles describing basic laboratory, translational, and clinical investigations in hematology. Primary research articles will be published under the following scientific categories: Clinical Trials and Observations; Gene Therapy; Hematopoiesis and Stem Cells; Immunobiology and Immunotherapy scope; Myeloid Neoplasia; Lymphoid Neoplasia; Phagocytes, Granulocytes and Myelopoiesis; Platelets and Thrombopoiesis; Red Cells, Iron and Erythropoiesis; Thrombosis and Hemostasis; Transfusion Medicine; Transplantation; and Vascular Biology. Papers can be listed under more than one category as appropriate.
期刊最新文献
Diagnostic guidelines for familial hemophagocytic lymphohistiocytosis revisited. JAK2/mTOR inhibition fails to prevent acute GVHD despite reduced Th1/Th17 cells: final phase 2 trial results. Antimetabolite dose intensity and adverse outcomes in children with acute lymphoblastic leukemia: a COG-AALL03N1 report. Bleeding events in patients with cancer: incidence, risk factors, and impact on prognosis in a prospective cohort study. Focal deletions of a promoter tether activate the IRX3 oncogene in T-cell acute lymphoblastic leukemia.
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