[Cancer and venous thromboembolism recurrence: The keys for an optimal management].

Bull Cancer

AP-HP, université Paris 7, hôpital Louis-Mourier, service de médecine interne, 178, rue des Renouillers, 92700 Colombes, France.

Published: May 2018

AI Article Synopsis

  • Low-molecular-weight heparins (LMWH) are the recommended treatment for cancer-associated thrombosis (CAT) for 3 to 6 months, as outlined by international clinical guidelines.
  • Only about 50% of patients with CAT receive treatment in accordance with these guidelines, highlighting a gap between recommendations and actual clinical practice.
  • Addressing this issue requires understanding the factors influencing both physicians and patients, suggesting a need for a comprehensive approach to improve adherence to treatment protocols for CAT.

Article Abstract

Low-molecular-weight heparins (LMWH) are to date the standard for 3-to-6-month treatment of cancer-associated thrombosis (CAT) as they are consistently recommended by international clinical practice guidelines. Despite the high risk of VTE recurrence and death in patients with cancer and the favorable benefit-risk profile of LMWH demonstrated in randomized-control studies, the implementation of treatment guidelines remains insufficient in the clinical practice. A systematic review of observational studies, registries and surveys reveals that approximately only 50% of patients with CAT are treated according to practice guidelines while both physicians and patients may be accountable for this situation. Based on the few available published data, we have observed differences between guidelines and clinical practice and we have identified factors influencing patient's management with the perspective to improve adherence to clinical practice guidelines in patients with CAT. Improving the implementation of clinical practice guidelines requires a better knowledge of physician and patient-related factors that influence therapeutic decisions. A global approach of patients with CAT is warranted to optimize the therapeutic management of cancer-associated VTE.

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Source
http://dx.doi.org/10.1016/j.bulcan.2017.12.006DOI Listing

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