Cancer-Associated Thrombosis on Bevacizumab: Risk of Recurrence and Bleeding When Bevacizumab Is Stopped or Continued

Author:

Mayenga Marie1ORCID,Falvo Nicolas2,Mahé Isabelle345ORCID,Jannot Anne-Sophie6,Gazeau Benoit7,Meyer Guy158,Gendron Nicolas910ORCID,Sanchez Olivier158,Djennaoui Sadji34,Planquette Benjamin158

Affiliation:

1. Department of Pulmonology and Intensive Care, Hôpital Européen Georges-Pompidou, AP-HP, 75015 Paris, France

2. Department of Vascular Pathology, Centre Hospitalier Universitaire Dijon-Bourgogne, 21000 Dijon, France

3. Université Paris Cité, Service de Médecine Interne, Hôpital Louis Mourier, AP-HP, 92700 Colombes, France

4. Innovative Therapies in Haemostasis, INSERM UMR_S1140, 75006 Paris, France

5. INNOVTE-FCRIN, 42055 Saint-Etienne, France

6. Department of Biostatistics, Medical Informatics and Public Health, Hôpital Européen Georges-Pompidou, AP-HP, 75015 Paris, France

7. Department of Respiratory Medicine, Centre Hospitalier de Bourg-en-Bresse, 01012 Bourg-en-Bresse, France

8. Université Paris Cité, Innovative Therapies in Haemostasis, INSERM, 75006 Paris, France

9. Department of Biological Hematology, Hôpital Européen Georges-Pompidou, AP-HP, 75015 Paris, France

10. Université de Paris, Innovative Therapies in Haemostasis, Laboratoire de Recherches Biochirugicales (Fondation Carpentier), 75005 Paris, France

Abstract

Cancer-associated thrombosis (CAT) is a common complication during cancer, with complex management due to an increased risk of both recurrence and bleeding. Bevacizumab is an effective anti-angiogenic treatment but increases the risk of bleeding and potentially the risk of venous thromboembolism (VTE). The aim of this study was to evaluate the efficacy and safety of anticoagulant therapy in patients with CAT receiving bevacizumab, according to the continuation or discontinuation of bevacizumab. In a retrospective multicenter study, patients receiving anticoagulant for CAT occurring under bevacizumab therapy were included. The primary endpoint combined recurrent VTE and/or major or clinically relevant non-major bleeding. Among the 162 patients included, bevacizumab was discontinued in 70 (43.2%) patients and continued in 92 (56.8%) patients. After a median follow-up of 318 days, 21 (30.0%) patients in the discontinuation group experienced VTE recurrence or major or clinically relevant non-major bleeding, compared to 27 (29.3%) in the continuation group. The analysis of survival following the first event showed no significant difference between the groups in uni- or multivariate analysis (p = 0.19). The primary endpoint was not influenced by the duration of bevacizumab exposure. These results suggest that the efficacy and safety of anticoagulant therapy in patients with CAT receiving bevacizumab is not modified regardless of whether bevacizumab is continued or discontinued.

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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