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      A Study on the Efficacy and Safety of Rivaroxaban in Urologic Cancer-Associated Venous Thromboembolism

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      https://www.riss.kr/link?id=A106488310

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      다국어 초록 (Multilingual Abstract)

      Purpose: Although direct oral anticoagulants (DOACs) are recommended as an alternative to low-molecular weighted heparin for cancer-associated venous thromboembolism (VTE), there is no firm evidence on the efficacy and safety of DOACs in patients with urologic cancer. Therefore, we compared the efficacy and safety of rivaroxaban and dalteparin for treating cancer-associated VTE in urologic cancer.
      Materials and Methods: We reviewed the medical records of 124 eligible VTE patients with urologic cancers who were treated with dalteparin or rivaroxaban. The primary outcome was the composite event of clinically relevant bleeding or VTE recurrence. The secondary outcomes were VTE recurrence, clinically relevant bleeding events, and all-cause mortality.
      Results: During anticoagulation period, there was no significant difference in primary and secondary outcomes between the groups. In Cox proportional hazards model for composite events, although there was no statistical significance, rivaroxaban presented lower hazard ratio (HR) than dalteparin (HR, 0.472; 95% confidence interval [CI], 0.210–1.060; p=0.069 in univariate analysis; HR, 0.505; 95% CI, 0.206–1.234; p=0.134 in multivariate analysis). In clinically relevant bleeding events, there was no significance difference between rivaroxaban and dalteparin (HR, 0.568; 95% CI, 0.238–1.358; p=0.203 in univariate analysis; HR, 0.617; 95% CI, 0.232–1.636; p=0.331 in multivariate analysis).
      Conclusions: Rivaroxaban can be regarded as a valuable option for VTE in urologic cancer. Further prospective studies are warranted to prove the safety or efficacy of rivaroxaban for treating VTE in patients with urologic cancer.
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      Purpose: Although direct oral anticoagulants (DOACs) are recommended as an alternative to low-molecular weighted heparin for cancer-associated venous thromboembolism (VTE), there is no firm evidence on the efficacy and safety of DOACs in patients with...

      Purpose: Although direct oral anticoagulants (DOACs) are recommended as an alternative to low-molecular weighted heparin for cancer-associated venous thromboembolism (VTE), there is no firm evidence on the efficacy and safety of DOACs in patients with urologic cancer. Therefore, we compared the efficacy and safety of rivaroxaban and dalteparin for treating cancer-associated VTE in urologic cancer.
      Materials and Methods: We reviewed the medical records of 124 eligible VTE patients with urologic cancers who were treated with dalteparin or rivaroxaban. The primary outcome was the composite event of clinically relevant bleeding or VTE recurrence. The secondary outcomes were VTE recurrence, clinically relevant bleeding events, and all-cause mortality.
      Results: During anticoagulation period, there was no significant difference in primary and secondary outcomes between the groups. In Cox proportional hazards model for composite events, although there was no statistical significance, rivaroxaban presented lower hazard ratio (HR) than dalteparin (HR, 0.472; 95% confidence interval [CI], 0.210–1.060; p=0.069 in univariate analysis; HR, 0.505; 95% CI, 0.206–1.234; p=0.134 in multivariate analysis). In clinically relevant bleeding events, there was no significance difference between rivaroxaban and dalteparin (HR, 0.568; 95% CI, 0.238–1.358; p=0.203 in univariate analysis; HR, 0.617; 95% CI, 0.232–1.636; p=0.331 in multivariate analysis).
      Conclusions: Rivaroxaban can be regarded as a valuable option for VTE in urologic cancer. Further prospective studies are warranted to prove the safety or efficacy of rivaroxaban for treating VTE in patients with urologic cancer.

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      참고문헌 (Reference)

      1 Vedovati MC, "Venous thromboembolism and cancer: Current and future role of direct- acting oral anticoagulants" 177 : 33-41, 2019

      2 Zareba P, "Thromboembolism in Patients with Bladder Cancer: Incidence, Risk Factors and Prevention" 4 : 139-147, 2018

      3 Brodie MM, "Severity of Gastrointestinal Bleeding in Patients Treated with Direct-Acting Oral Anticoagulants" 131 : 573.e9-573.e15, 2018

      4 Khorana AA, "Role of direct oral anticoagulants in the treatment of cancer-associated venous thromboembolism: guidance from the SSC of the ISTH" 16 : 1891-1894, 2018

      5 이장호, "Rivaroxaban versus Low-Molecular- Weight Heparin for Venous Thromboembolism in Gastrointestinal and Pancreatobiliary Cancer" 대한의학회 34 (34): 1-13, 2019

      6 EINSTEIN Investigators, "Oral rivaroxaban for symptomatic venous thromboembolism" 363 : 2499-2510, 2010

      7 Short NJ, "New oral anticoagulants and the cancer patient" 19 : 82-93, 2014

      8 Streiff MB, "NCCN Guidelines Insights: Cancer-Associated Venous Thromboembolic Disease, Version 2.2018" 16 : 1289-1303, 2018

      9 Weinz C, "Metabolism and excretion of rivaroxaban, an oral, direct factor Xa inhibitor, in rats, dogs, and humans" 37 : 1056-1064, 2009

      10 Frydman A, "Low-molecular-weight heparins: an overview of their pharmacodynamics, pharmacokinetics and metabolism in humans" 26 (26): 24-38, 1996

      1 Vedovati MC, "Venous thromboembolism and cancer: Current and future role of direct- acting oral anticoagulants" 177 : 33-41, 2019

      2 Zareba P, "Thromboembolism in Patients with Bladder Cancer: Incidence, Risk Factors and Prevention" 4 : 139-147, 2018

      3 Brodie MM, "Severity of Gastrointestinal Bleeding in Patients Treated with Direct-Acting Oral Anticoagulants" 131 : 573.e9-573.e15, 2018

      4 Khorana AA, "Role of direct oral anticoagulants in the treatment of cancer-associated venous thromboembolism: guidance from the SSC of the ISTH" 16 : 1891-1894, 2018

      5 이장호, "Rivaroxaban versus Low-Molecular- Weight Heparin for Venous Thromboembolism in Gastrointestinal and Pancreatobiliary Cancer" 대한의학회 34 (34): 1-13, 2019

      6 EINSTEIN Investigators, "Oral rivaroxaban for symptomatic venous thromboembolism" 363 : 2499-2510, 2010

      7 Short NJ, "New oral anticoagulants and the cancer patient" 19 : 82-93, 2014

      8 Streiff MB, "NCCN Guidelines Insights: Cancer-Associated Venous Thromboembolic Disease, Version 2.2018" 16 : 1289-1303, 2018

      9 Weinz C, "Metabolism and excretion of rivaroxaban, an oral, direct factor Xa inhibitor, in rats, dogs, and humans" 37 : 1056-1064, 2009

      10 Frydman A, "Low-molecular-weight heparins: an overview of their pharmacodynamics, pharmacokinetics and metabolism in humans" 26 (26): 24-38, 1996

      11 Lee AY, "Low-molecular-weight heparin versus a coumarin for the prevention of recurrent venous thromboembolism in patients with cancer" 349 : 146-153, 2003

      12 Desai J, "Gastrointestinal bleeding with the new oral anticoagulants--defining the issues and the management strategies" 110 : 205-212, 2013

      13 Cheung KS, "Gastrointestinal bleeding in patients on novel oral anticoagulants: Risk, prevention and management" 23 : 1954-1963, 2017

      14 Sherwood MW, "Gastrointestinal Bleeding in Patients With Atrial Fibrillation Treated With Rivaroxaban or Warfarin: ROCKET AF Trial" 66 : 2271-2281, 2015

      15 Chan NC, "Evolving Treatments for Arterial and Venous Thrombosis: Role of the Direct Oral Anticoagulants" 118 : 1409-1424, 2016

      16 Dong Y, "Efficacy and safety of direct oral anticoagulants versus low-molecular-weight heparin in patients with cancer: a systematic review and meta-analysis" 48 : 400-412, 2019

      17 Raskob GE, "Edoxaban for the Treatment of Cancer-Associated Venous Thromboembolism" 378 : 615-624, 2018

      18 Li A, "Direct oral anticoagulant (DOAC) versus low-molecular-weight heparin (LMWH) for treatment of cancer associated thrombosis (CAT): A systematic review and meta-analysis" 173 : 158-163, 2019

      19 김상아, "Current Management of Cancer- associated Venous Thromboembolism: Focus on Direct Oral Anticoagulants" 대한의학회 34 (34): 1-15, 2019

      20 Cohen AT, "Comparison of the Novel Oral Anticoagulants Apixaban, Dabigatran, Edoxaban, and Rivaroxaban in the Initial and Long-Term Treatment and Prevention of Venous Thromboembolism: Systematic Review and Network Meta-Analysis" 10 : e0144856-, 2015

      21 Jang Ho Lee, "Comparison of rivaroxaban and dalteparin for the long-term treatment of venous thromboembolism in patients with gynecologic cancers" 대한부인종양학회 31 (31): 1-10, 2020

      22 oung AM, "Comparison of an Oral Factor Xa Inhibitor With Low Molecular Weight Heparin in Patients With Cancer With Venous Thromboembolism: Results of a Randomized Trial (SELECT-D)." 36 : 2017-2023, 2018

      23 Scarpa RM, "Clinically overt venous thromboembolism after urologic cancer surgery: results from the @RISTOS Study" 51 : 130-135, 2007

      24 Caio J. Fernandes, "Cancer-associated thrombosis: the when, how and why" European Respiratory Society (ERS) 28 (28): 180119-, 2019

      25 Franchini M, "Cancer-associated thrombosis: investigating the role of new oral anticoagulants" 135 : 777-781, 2015

      26 Smrke A, "Cancer-Associated Venous Thromboembolism: A Practical Review Beyond Low-Molecular- Weight Heparins" 4 : 142-, 2017

      27 Wallis CJD, "Association Between Use of Antithrombotic Medication and Hematuria-Related Complications" 318 : 1260-1271, 2017

      28 Uppuluri EM, "Assessment of venous thromboembolism treatment in patients with cancer on low molecular weight heparin, warfarin, and the direct oral anticoagulants" 25 : 261-268, 2019

      29 Kearon C, "Antithrombotic Therapy for VTE Disease: CHEST Guideline and Expert Panel Report" 149 : 315-352, 2016

      30 Lee JH, "A Retrospective Study on Efficacy and Safety of Rivaroxaban and Dalteparin for Long-Term Treatment of Venous Thromboembolism in Patients with Lung Cancer" 98 : 203-211, 2019

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2026 평가예정 재인증평가 신청대상 (재인증)
      2020-01-01 평가 등재학술지 유지 (재인증) KCI등재
      2017-01-01 평가 등재학술지 선정 (계속평가) KCI등재
      2015-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.04 0.04 0
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0 0 0 0.04
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