Rivaroxaban for extended antithrombotic prophylaxis after laparoscopic surgery for colorectal cancer. Design of the PRO-LAPS II STUDY
| Autor: | Giancarlo Agnelli, Andrea Fares Bucci, Cecilia Becattini, Fabio Rondelli, Stefania Frasson, Giuseppe Camporese, Luigina Graziosi, Gualberto Gussoni, Annibale Donini, Alessia Biancafarina, Giampiero Avruscio, Michela Boncompagni, Paolo Delrio, Graziano Ceccarelli, Damiano Chiari, Adriana Visonà, Ugo Pace |
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| Jazyk: | angličtina |
| Rok vydání: | 2020 |
| Předmět: |
Laparoscopic surgery
medicine.medical_specialty medicine.medical_treatment 030204 cardiovascular system & hematology Placebo Asymptomatic 03 medical and health sciences 0302 clinical medicine Fibrinolytic Agents Rivaroxaban Antithrombotic Internal Medicine medicine Humans 030212 general & internal medicine Cancer business.industry Prevention Pulmonary embolism Anticoagulants Venous thromboembolism medicine.disease Surgery Orthopedic surgery Laparoscopy medicine.symptom Colorectal Neoplasms business medicine.drug |
| Popis: | Background The clinical benefit of extending prophylaxis for venous thromboembolism (VTE) beyond hospital discharge after laparoscopic surgery for cancer is undefined. Extended prophylaxis with rivaroxaban is effective in reducing post-operative VTE after major orthopedic surgery without safety concern. Methods PROLAPS II is an investigator-initiated, randomized, double-blind study aimed at assessing the efficacy and safety of extended antithrombotic prophylaxis with rivaroxaban compared with placebo after laparoscopic surgery for colorectal cancer in patients who had received antithrombotic prophylaxis with low molecular-weight heparin for 7 ± 2 days (NCT03055026). Patients are randomized to receive rivaroxaban (10 mg once daily) or placebo for 3 weeks (up to day 28 ± 2 from surgery). The primary study outcome is a composite of symptomatic objectively confirmed VTE, asymptomatic ultrasonography-detected DVT or VTE-related death at 28 ± 2 days from laparoscopic surgery. The primary safety outcome is major bleeding defined according to the International Society of Thrombosis and Haemostasis. Symptomatic objectively confirmed VTE, asymptomatic ultrasonography-detected DVT, major bleeding or death by day 28 ± 2 and by day 90 from surgery are secondary outcomes. Assuming an 8% event rate with placebo and 60% reduction in the primary study outcome with rivaroxaban, 323 patients per group are necessary to show a statistically significant difference between the study groups. Discussion The PROLAPS II is the first study with an oral anti-Xa agent in cancer surgery. The study has the potential to improve clinical practice by answering the question on the clinical benefit of extending prophylaxis after laparoscopic surgery for colorectal cancer. |
| Databáze: | OpenAIRE |
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