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Rivaroxaban vs Dalteparin in Cancer-Associated Thromboembolism: A Randomized Trial.
Planquette, Benjamin; Bertoletti, Laurent; Charles-Nelson, Anaïs; Laporte, Silvy; Grange, Claire; Mahé, Isabelle; Pernod, Gilles; Elias, Antoine; Couturaud, Francis; Falvo, Nicolas; Sevestre, Marie Antoinette; Ray, Valérie; Burnod, Alexis; Brebion, Nicolas; Roy, Pierre-Marie; Timar-David, Miruna; Aquilanti, Sandro; Constans, Joel; Bura-Rivière, Alessandra; Brisot, Dominique; Chatellier, Gilles; Sanchez, Olivier; Meyer, Guy; Girard, Philippe; Mismetti, Patrick.
Afiliación
  • Planquette B; Service de Pneumologie et Soins Intensifs, Hôpital Européen Georges Pompidou, APHP, Université de Paris, Paris, France; INSERM UMR_S1140, Innovations Thérapeutiques en Hémostase, Laboratoire de Chirurgie expérimentale, Fondation Alain Carpentier, Paris, France; F-CRIN INNOVTE Network, Saint-Etienne,
  • Bertoletti L; F-CRIN INNOVTE Network, Saint-Etienne, France; Service de Médecine Vasculaire et Thérapeutique, CHU Saint-Etienne, Hôpital Nord, Saint-Etienne, France; INSERM, CIC-1408, CHU Saint-Etienne, Hôpital Nord, Saint-Etienne, France; SAINBIOSE U1059, Université Jean Monnet, INSERM, Saint-Etienne, France.
  • Charles-Nelson A; Unité de Recherche Clinique, CIC-EC1418, Hôpital Européen Georges-Pompidou, Paris, France.
  • Laporte S; F-CRIN INNOVTE Network, Saint-Etienne, France; Unité de Recherche Clinique, Innovation, Pharmacologie, CHU Saint-Etienne, Hôpital Nord, Saint-Etienne, France; SAINBIOSE U1059, Université Jean Monnet, INSERM, Saint-Etienne, France.
  • Grange C; F-CRIN INNOVTE Network, Saint-Etienne, France; Service de Médecine Interne, CHU de Lyon, Pierre Bénite, France.
  • Mahé I; INSERM UMR_S1140, Innovations Thérapeutiques en Hémostase, Laboratoire de Chirurgie expérimentale, Fondation Alain Carpentier, Paris, France; F-CRIN INNOVTE Network, Saint-Etienne, France; Université de Paris, APHP, Hôpital Louis Mourier, Colombes, France.
  • Pernod G; F-CRIN INNOVTE Network, Saint-Etienne, France; Service de Médecine Vasculaire, Université Grenoble-Alpes, Grenoble, France.
  • Elias A; F-CRIN INNOVTE Network, Saint-Etienne, France; Médecine Vasculaire, Pôle Cardiologie-Vasculaire, Hôpital Sainte Musse, CH de Toulon La Seyne sur Mer, Toulon, France.
  • Couturaud F; F-CRIN INNOVTE Network, Saint-Etienne, France; Département de Médecine Interne et Pneumologie, CHU de Brest, Université de Bretagne Occidentale, and EA 3878, CIC INSERM 1412, Brest, France.
  • Falvo N; F-CRIN INNOVTE Network, Saint-Etienne, France; Service de Médecine Interne, CHU de Dijon, Dijon, France.
  • Sevestre MA; F-CRIN INNOVTE Network, Saint-Etienne, France; Service de Médecine Vasculaire, CHU d'Amiens, Amiens, France.
  • Ray V; F-CRIN INNOVTE Network, Saint-Etienne, France; Service de Médecine Polyvalente, CHU de Nîmes, Nîmes, France.
  • Burnod A; Département de Soins de Support, Institut Curie, PSL Research University, Paris, France; F-CRIN INNOVTE Network, Saint-Etienne, France.
  • Brebion N; F-CRIN INNOVTE Network, Saint-Etienne, France; Service de Médecine Vasculaire, CHD de Vendée, La Roche sur Yon, France.
  • Roy PM; F-CRIN INNOVTE Network, Saint-Etienne, France; Département des Urgences, CHU d'Angers, et Institut Mitovasc UMR (CNRS 6015-INSERM 1083), Université d'Angers, Angers, France.
  • Timar-David M; Service d'Oncologie Médicale, CHU de Nîmes, Nîmes, France.
  • Aquilanti S; F-CRIN INNOVTE Network, Saint-Etienne, France; Hôpital Privé Arras les Bonnettes, Arras, France.
  • Constans J; F-CRIN INNOVTE Network, Saint-Etienne, France; Service de Médecine Interne et Vasculaire, CHU de Bordeaux, Bordeaux, France.
  • Bura-Rivière A; F-CRIN INNOVTE Network, Saint-Etienne, France; Service de Médecine Vasculaire, CHU de Toulouse, Toulouse, France; Stromalab, UMR 5273 CNRS/UPS-EFS-INSERM U1031, Toulouse, France.
  • Brisot D; F-CRIN INNOVTE Network, Saint-Etienne, France; Service de Médecine Interne et Vasculaire, CHU de Montpellier, Montpellier, France.
  • Chatellier G; Unité de Recherche Clinique, CIC-EC1418, Hôpital Européen Georges-Pompidou, Paris, France.
  • Sanchez O; Service de Pneumologie et Soins Intensifs, Hôpital Européen Georges Pompidou, APHP, Université de Paris, Paris, France; INSERM UMR_S1140, Innovations Thérapeutiques en Hémostase, Laboratoire de Chirurgie expérimentale, Fondation Alain Carpentier, Paris, France; F-CRIN INNOVTE Network, Saint-Etienne,
  • Meyer G; Service de Pneumologie et Soins Intensifs, Hôpital Européen Georges Pompidou, APHP, Université de Paris, Paris, France; INSERM UMR_S1140, Innovations Thérapeutiques en Hémostase, Laboratoire de Chirurgie expérimentale, Fondation Alain Carpentier, Paris, France; F-CRIN INNOVTE Network, Saint-Etienne,
  • Girard P; Département de Pneumologie, Institut Mutualiste Montsouris, Paris, France; F-CRIN INNOVTE Network, Saint-Etienne, France. Electronic address: philippe.girard@imm.fr.
  • Mismetti P; F-CRIN INNOVTE Network, Saint-Etienne, France; Service de Médecine Vasculaire et Thérapeutique, CHU Saint-Etienne, Hôpital Nord, Saint-Etienne, France.
Chest ; 161(3): 781-790, 2022 03.
Article en En | MEDLINE | ID: mdl-34627853
ABSTRACT

BACKGROUND:

Direct oral anticoagulants (DOACs) are an alternative to low-molecular-weight heparin for treating cancer-associated VTE. RESEARCH QUESTION Is rivaroxaban as efficient and safe as dalteparin to treat patients with cancer-associated VTE? STUDY DESIGN AND

METHODS:

In a randomized open-label noninferiority trial, patients with active cancer who had proximal DVT, pulmonary embolism (PE), or both were assigned randomly to therapeutic doses of rivaroxaban or dalteparin for 3 months. The primary outcome was the cumulative incidence of recurrent VTE, a composite of symptomatic or incidental DVT or PE, and worsening of pulmonary vascular or venous obstruction at 3 months.

RESULTS:

Of 158 randomized patients, 74 and 84 patients were assigned to receive rivaroxaban and dalteparin, respectively. Mean age was 69.4 years, and 115 patients (76.2%) had metastatic disease. The primary outcome occurred in 4 and 6 patients in the rivaroxaban and dalteparin groups, respectively (both the intention-to-treat and per-protocol populations cumulative incidence, 6.4% vs 10.1%; subdistribution hazard ratio [SHR], 0.75; 95% CI, 0.21-2.66). Major bleeding occurred in 1 and 3 patients in the rivaroxaban and dalteparin groups, respectively (cumulative incidence, 1.4% vs 3.7%; SHR, 0.36; 95% CI, 0.04-3.43). Major or clinically relevant nonmajor bleeding occurred in 9 and 8 patients in the rivaroxaban and dalteparin groups, respectively (cumulative incidence, 12.2% vs 9.8%; SHR, 1.27; 95% CI, 0.49-3.26). Overall, 19 patients (25.7%) and 20 patients (23.8%) died in the rivaroxaban and dalteparin groups, respectively (hazard ratio, 1.05; 95% CI, 0.56-1.97).

INTERPRETATION:

In this trial comparing rivaroxaban and dalteparin in the treatment of cancer-associated VTE, the number of patients was insufficient to reach the predefined criteria for noninferiority, but efficacy and safety results were consistent with those previously reported with DOACs. An updated meta-analysis of randomized trials comparing DOACs with low-molecular-weight heparin in patients with cancer-associated VTE is provided. TRIAL REGISTRY ClinicalTrials.gov; No. NCT02746185; URL www. CLINICALTRIALS gov.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Dalteparina / Tromboembolia Venosa / Rivaroxabán / Neoplasias Tipo de estudio: Clinical_trials / Etiology_studies / Guideline / Risk_factors_studies Límite: Aged / Humans Idioma: En Revista: Chest Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Dalteparina / Tromboembolia Venosa / Rivaroxabán / Neoplasias Tipo de estudio: Clinical_trials / Etiology_studies / Guideline / Risk_factors_studies Límite: Aged / Humans Idioma: En Revista: Chest Año: 2022 Tipo del documento: Article