d -二聚体抗凝治疗3个月后与癌症相关的孤立远端深静脉血栓的结果

Tatsuya Nishikawa , Yugo Yamashita , Masashi Fujita , Takeshi Morimoto , Nao Muraoka , Michihisa Umetsu , Yuji Nishimoto , Takuma Takada , Yoshito Ogihara , Nobutaka Ikeda , Kazunori Otsui , Daisuke Sueta , Yukari Tsubata , Masaaki Shoji , Ayumi Shikama , Yutaka Hosoi , Yasuhiro Tanabe , Ryuki Chatani , Kengo Tsukahara , Naohiko Nakanishi , Takeshi Kimura
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引用次数: 0

摘要

摘要肿瘤相关性孤立性远端深静脉血栓形成(IDDVT)是癌症患者常见的并发症。癌症患者孤立性远端深静脉血栓的最佳抗凝治疗时间研究显示,依多沙班治疗12个月比3个月在血栓形成风险方面具有优势。然而,抗凝期间d -二聚体水平是否影响延长抗凝的疗效尚不清楚。在这项事后亚组分析中,我们根据3个月d -二聚体水平将519例患者分为低d -二聚体(1.0 μg/mL) (n = 308)和高d -二聚体(≥1.0 μg/mL) (n = 211)亚组。在低d二聚体中,12个月的依多沙班组症状性复发性静脉血栓栓塞(VTE)或VTE相关死亡的累计发生率低于3个月的依多沙班组(0.8% vs 5.6%;p = .02;优势比[OR], 0.12;95%可信区间[CI], 0.01-0.66)和高d -二聚体(0.9% vs 10.2%;p = .01;或者,0.11;95% CI, 0.01-0.62)亚组无相互作用。此外,低d -二聚体组12个月和3个月的累积大出血发生率无显著差异(3.6% vs 1.8%;p = .64;或者,1.96;95% CI, 0.47-9.67)和高d -二聚体(18.3% vs 14.6%;p = .29;或者,1.27;95% CI, 0.60-2.75),无相互作用。总之,无论抗凝治疗3个月后d -二聚体水平如何,12个月的依多沙班治疗癌症相关性IDDVT在减少血栓事件方面优于3个月的治疗。无论3个月时d -二聚体水平如何,12个月的依多沙班组与3个月的依多沙班组相比,大出血的风险没有显著增加。该试验在www.clinicaltrials.gov注册为#NCT03895502。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
D-dimer after 3 months of anticoagulation therapy and outcomes in cancer-associated isolated distal deep vein thrombosis

Abstract

Cancer-associated isolated distal deep vein thrombosis (IDDVT) is a common complication in patients with cancer. The Optimal Duration of Anticoagulation Therapy for Isolated Distal Deep Vein Thrombosis in Patients with Cancer study revealed the superiority of 12- over 3-month edoxaban treatment with respect to thrombotic risk. However, it remains unclear whether D-dimer levels during anticoagulation influence the efficacy of extended anticoagulation. In this post hoc subgroup analysis, we stratified 519 patients into the low D-dimer (<1.0 μg/mL) (n = 308) and high D-dimer (≥1.0 μg/mL) (n = 211) subgroups based on D-dimer levels at 3 months. The cumulative incidence of a composite of symptomatic recurrent venous thromboembolism (VTE) or VTE-related death was lower in the 12-month edoxaban group than in the 3-month edoxaban group in both the low D-dimer (0.8% vs 5.6%; P = .02; odds ratio [OR], 0.12; 95% confidence interval [CI], 0.01-0.66) and high D-dimer (0.9% vs 10.2%; P = .01; OR, 0.11; 95% CI, 0.01-0.62) subgroups without interaction. Furthermore, there was no significant difference in the cumulative incidence of major bleeding between the 12- and 3-month groups in both the low D-dimer (3.6% vs 1.8%; P = .64; OR, 1.96; 95% CI, 0.47-9.67) and high D-dimer (18.3% vs 14.6%; P = .29; OR, 1.27; 95% CI, 0.60-2.75) subgroups without interaction. In conclusion, a 12-month edoxaban treatment for cancer-associated IDDVT was superior to a 3-month treatment in reducing thrombotic events, irrespective of D-dimer levels after 3 months of anticoagulation therapy. There was no significant increased risk of major bleeding in the 12-month edoxaban group relative to the 3-month edoxaban group regardless of the D-dimer levels at 3 months. This trial was registered at www.clinicaltrials.gov as #NCT03895502.
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