Kawai Yohko, Fuji Takeshi, Fujita Satoru, Kimura Tetsuya, Ibusuki Kei, Abe Kenji, Tachibana Shintaro
International University of Health and Welfare, 8-10-16 Akasaka, Minato-ku, Tokyo 107-0052 Japan.
Department of Orthopaedic Surgery, Japan Community Healthcare Organization Osaka Hospital, 4-2-78, Fukushima, Fukushima-ku, Osaka 553-0003 Japan.
Thromb J. 2016 Dec 1;14:48. doi: 10.1186/s12959-016-0121-1. eCollection 2016.
The objective of this analysis was to assess the effects of edoxaban compared with enoxaparin on key coagulation biomarkers and present pooled primary efficacy and safety results from phase 3 STARS E-3 and STARS J-V trials for prevention of venous thromboembolism (VTE) after total knee arthroplasty (TKA) or total hip arthroplasty (THA).
In the randomized, double-blind, double-dummy, multicenter, STARS E-3 and STARS J-V trials, patients received edoxaban 30 mg or enoxaparin 2000 IU (20 mg) twice daily for 11 to 14 days. The studies were conducted in Japan and Taiwan; enoxaparin dosing was based on Japanese label recommendations. The primary efficacy endpoint was incidence of VTE; the safety endpoint was major or clinically relevant nonmajor (CRNM) bleeding. Blood samples were taken at presurgical evaluation, pretreatment (postsurgery), predose on day 7, predose on completion of treatment, and at a follow-up examination 25 to 35 days after the last dose of study drug for D-dimer, prothrombin fragment 1 + 2 (F), and soluble fibrin monomer complex (SFMC) measurement.
A total of 716 patients enrolled in STARS E-3 and 610 patients enrolled in STARS J-V; 1326 patients overall. This analysis included 657 patients who received edoxaban 30 mg QD and 650 patients who received enoxaparin 20 mg BID. Incidence of VTE was 5.1 and 10.7% for edoxaban and enoxaparin, respectively ( <0.001). Incidence of combined major and CRNM bleeding was 4.6 and 3.7% for edoxaban and enoxaparin, respectively ( = 0.427). On day 7, mean D-dimer (4.4 vs 5.5 μg/mL), F (363 vs 463 pmol/L), and SFMC (5.7 vs 6.8 μg/mL) were lower in edoxaban-treated patients relative to enoxaparin-treated patients, respectively ( <0.0001 for all). At end of treatment, mean D-dimer (5.4 vs 6.2 μg/mL), F (292 vs 380 pmol/L), and SFMC (6.2 vs 7.2 μg/mL) were lower in edoxaban-treated patients relative to enoxaparin-treated patients ( <0.0001 for all).
Edoxaban was superior to enoxaparin in prevention of VTE following TKA and THA, with comparable rates of bleeding events. Relative to enoxaparin, edoxaban significantly reduced D-dimer, F, and SFMC.
Clintrials.gov NCT01181102 and NCT01181167. Both registered 8/12/2010.
本分析的目的是评估依度沙班与依诺肝素相比对关键凝血生物标志物的影响,并呈现3期STARS E-3和STARS J-V试验预防全膝关节置换术(TKA)或全髋关节置换术(THA)后静脉血栓栓塞(VTE)的汇总主要疗效和安全性结果。
在随机、双盲、双模拟、多中心的STARS E-3和STARS J-V试验中,患者每日两次接受30 mg依度沙班或2000 IU(20 mg)依诺肝素治疗,持续11至14天。研究在日本和台湾进行;依诺肝素的给药基于日本标签建议。主要疗效终点是VTE的发生率;安全终点是主要或临床相关非主要(CRNM)出血。在术前评估、预处理(术后)、第7天给药前、治疗结束时给药前以及最后一剂研究药物后25至35天的随访检查时采集血样,以测量D-二聚体、凝血酶原片段1+2(F)和可溶性纤维蛋白单体复合物(SFMC)。
STARS E-3试验共纳入716例患者,STARS J-V试验共纳入610例患者;总计1326例患者。本分析纳入了657例每日一次接受30 mg依度沙班治疗的患者和6五百例每日两次接受20 mg依诺肝素治疗的患者。依度沙班和依诺肝素的VTE发生率分别为5.1%和10.7%(P<0.001)。依度沙班和依诺肝素的主要和CRNM出血合并发生率分别为4.6%和3.7%(P=0.427)。在第7天,依度沙班治疗的患者相对于依诺肝素治疗的患者,平均D-二聚体(4.4 vs 5.5 μg/mL)、F(363 vs 463 pmol/L)和SFMC(5.7 vs 6.8 μg/mL)更低(所有P<0.0001)。在治疗结束时,依度沙班治疗的患者相对于依诺肝素治疗的患者,平均D-二聚体(5.4 vs 6.2 μg/mL)、F(292 vs 380 pmol/L)和SFMC(6.2 vs 7.2 μg/mL)更低(所有P<0.0001)。
在预防TKA和THA后的VTE方面,依度沙班优于依诺肝素,出血事件发生率相当。相对于依诺肝素,依度沙班显著降低了D-二聚体、F和SFMC。
ClinicalTrials.gov NCT01181102和NCT01181167。均于2010年8月12日注册。