Department of Internal Medicine, Chonbuk National University Medical School, Jeonju, Korea.
Research Institute of Clinical Medicine of Chonbuk National University-Biomedical Research Institute of Chonbuk National University Hospital, Jeonju, Korea.
Korean J Intern Med. 2019 Sep;34(5):1125-1135. doi: 10.3904/kjim.2018.097. Epub 2018 May 23.
BACKGROUND/AIMS: Limited data are available regarding the efficacy of rivaroxaban for the treatment of cancer-associated venous thromboembolism (VTE). The aim of this study was to evaluate the effectiveness and safety of rivaroxaban for the treatment of VTE in active cancer patients.
In this prospective, multicenter, open-label trial (NCT01989845), we enrolled patients with active cancer and objectively diagnosed lower-extremity deep vein thrombosis, pulmonary embolism (PE), or both from November 2013 to June 2016. Active cancer was defined as a histologically confirmed malignancy, which was diagnosed or treated within the previous 6 months, or as a recurrent/ metastatic cancer. Patients received oral rivaroxaban 15 mg twice daily for first 3 weeks, followed by 20 mg once daily for 6 months. The primary outcome was the symptomatic recurrent VTE and the secondary outcomes included any recurrent VTE, major or clinically relevant non-major (CRNM) bleeding events, and overall mortality. All study outcomes were validated by blinded central adjudication.
Of 124 patients enrolled, 110 (88.7%) had solid cancer, 93 (75.0%) had metastatic disease, and 110 (88.7%) were receiving chemotherapy or radiotherapy. During the 6-month study period, seven patients experienced symptomatic recurrent VTE (cumulative incidence, 5.9%), and two patients experienced incidental recurrent PE (cumulative incidence of any recurrent VTE, 7.6%). Major bleeding events occurred in six patients (cumulative incidence, 5.3%) and CRNM bleeding events in 11 patients (cumulative incidence, 10.2%). Twenty-eight patients (overall mortality, 24.0%) died.
Rivaroxaban is effective and safe for the treatment of VTE in patients with active cancer.
背景/目的:关于利伐沙班治疗癌症相关静脉血栓栓塞症(VTE)的疗效,相关数据有限。本研究旨在评估利伐沙班治疗活动性癌症患者 VTE 的有效性和安全性。
在这项前瞻性、多中心、开放标签试验(NCT01989845)中,我们招募了 2013 年 11 月至 2016 年 6 月期间患有活动性癌症且经客观诊断的下肢深静脉血栓形成、肺栓塞(PE)或两者均有的患者。活动性癌症定义为组织学证实的恶性肿瘤,在过去 6 个月内确诊或治疗,或为复发性/转移性癌症。患者接受口服利伐沙班 15mg,每日 2 次,治疗 3 周,随后改为 20mg,每日 1 次,治疗 6 个月。主要结局是有症状的复发性 VTE,次要结局包括任何复发性 VTE、主要或临床相关非重大(CRNM)出血事件和总死亡率。所有研究结局均通过盲法中心裁定进行验证。
在纳入的 124 例患者中,110 例(88.7%)患有实体瘤,93 例(75.0%)患有转移性疾病,110 例(88.7%)正在接受化疗或放疗。在 6 个月的研究期间,7 例患者出现有症状的复发性 VTE(累积发生率 5.9%),2 例患者出现偶发性复发性 PE(任何复发性 VTE 的累积发生率为 7.6%)。6 例患者发生大出血事件(累积发生率 5.3%),11 例患者发生 CRNM 出血事件(累积发生率 10.2%)。28 例患者(总死亡率 24.0%)死亡。
利伐沙班治疗活动性癌症患者 VTE 有效且安全。