Department of Vascular Medicine, Klinikum Darmstadt GmbH, Darmstadt, Germany.
Center for Thrombosis and Hemostasis, University Medical Center Mainz, Mainz, Germany.
Thromb Haemost. 2018 May;118(5):914-921. doi: 10.1055/s-0038-1641150. Epub 2018 Apr 4.
This article assesses the impact of renal impairment (RI) on the efficacy and safety of anticoagulation in patients with cancer-associated thrombosis from the Comparison of Acute Treatments in Cancer Hemostasis (CATCH) study (NCT01130025).
Renal function was assessed using the Modification of Diet in Renal Disease equation in patients with cancer-associated thrombosis who received either tinzaparin (175 IU/kg) once daily or warfarin for 6 months, in an open-label, randomized, multi-centre trial with blinded adjudication of outcomes. Associations between baseline RI (glomerular filtration rate [GFR] <60 mL/min/1.73m) and recurrent symptomatic or incidental venous thromboembolism (VTE), clinically relevant bleeding (CRB), major bleeding and death were assessed using Fisher's exact test.
Baseline-centralized GFR data were available for 864 patients (96% of study population). RI was found in 131 patients (15%; = 69 tinzaparin). Recurrent VTE occurred in 14% of patients with and 8% of patients without RI (relative risk [RR] 1.74; 95% confidence interval [CI] 1.06, 2.85), CRB in 19% and 14%, respectively (RR 1.33; 95% CI 0.90, 1.98), major bleeding in 6.1% and 2.0%, respectively (RR 2.98; 95% CI 1.29, 6.90) and mortality rate was 40% and 34%, respectively (RR 1.20; 95% CI 0.94, 1.53). Patients with RI on tinzaparin showed no difference in recurrent VTE, CRB, major bleeding or mortality rates versus those on warfarin.
RI in patients with cancer-associated thrombosis on anticoagulation was associated with a statistically significant increase in recurrent VTE and major bleeding, but no significant increase in CRB or mortality. No differences were observed between long-term tinzaparin therapy and warfarin.
本文评估了肾功能损害(RI)对癌症相关血栓形成患者抗凝治疗疗效和安全性的影响,研究数据来自癌症止血中的急性治疗比较(CATCH)研究(NCT01130025)。
在这项开放标签、随机、多中心试验中,接受每日 175IU/kg 达肝素或华法林治疗 6 个月的癌症相关血栓形成患者,使用改良肾脏病饮食公式(Modification of Diet in Renal Disease equation)评估肾功能。采用 Fisher 确切检验评估基线 RI(肾小球滤过率 [GFR]<60mL/min/1.73m)与复发性有症状或偶发性静脉血栓栓塞症(VTE)、临床相关出血(CRB)、大出血和死亡之间的相关性。
864 例患者(研究人群的 96%)有基线中心化 GFR 数据。131 例患者(15%;达肝素组 69 例)存在 RI。RI 患者的复发性 VTE 发生率为 14%,无 RI 患者为 8%(相对风险 [RR] 1.74;95%置信区间 [CI] 1.06,2.85);CRB 发生率分别为 19%和 14%(RR 1.33;95%CI 0.90,1.98);大出血发生率分别为 6.1%和 2.0%(RR 2.98;95%CI 1.29,6.90);死亡率分别为 40%和 34%(RR 1.20;95%CI 0.94,1.53)。达肝素组 RI 患者的复发性 VTE、CRB、大出血或死亡率与华法林组无差异。
癌症相关血栓形成患者抗凝治疗时存在 RI,与复发性 VTE 和大出血显著增加相关,但 CRB 或死亡率无显著增加。达肝素长期治疗与华法林相比无差异。