Key result
Extended rivaroxaban cuts VTE risk ~74% vs placebo following laparoscopic colorectal cancer surgery.
Why the study?
The clinical benefit of extended VTE prophylaxis after laparoscopic surgery for cancer is unclear, and the efficacy and safety of direct oral anticoagulants for this indication remain unexplored.
Does extended prophylaxis with rivaroxaban reduce the composite of symptomatic VTE, asymptomatic DVT, or VTE-related death in patients after laparoscopic surgery for colorectal cancer?
RCT (n=582)
Double-blind
randomized
Does extended prophylaxis with rivaroxaban reduce the composite of symptomatic VTE, asymptomatic DVT, or VTE-related death in patients after laparoscopic surgery for colorectal cancer?
Extended prophylaxis with oral rivaroxaban after laparoscopic surgery for colorectal cancer is more effective than placebo for preventing VTE without increasing major bleeding.
Answers are grounded in this paper and cite their sources.
Supports extended rivaroxaban prophylaxis after laparoscopic colorectal cancer surgery; extends RCT evidence to minimally invasive procedures.
The clinical benefit of extended prophylaxis for venous thromboembolism (VTE) after laparoscopic surgery for cancer is unclear. The efficacy and safety of direct oral anticoagulants for this indication are unexplored. PROphylaxis of venous thromboembolism after LAParoscopic Surgery for colorectal cancer Study II (PROLAPS II) was a randomized, double-blind, placebo-controlled, investigator-initiated, superiority study aimed at assessing the efficacy and safety of extended prophylaxis with rivaroxaban after laparoscopic surgery for colorectal cancer. Consecutive patients who had laparoscopic surgery for colorectal cancer were randomized to receive rivaroxaban (10 mg once daily) or a placebo to be started at 7 ± 2 days after surgery and given for the subsequent 3 weeks. All patients received antithrombotic prophylaxis with low-molecular-weight heparin from surgery to randomization. The primary study outcome was the composite of symptomatic objectively confirmed VTE, asymptomatic ultrasonography-detected deep vein thrombosis (DVT), or VTE-related death at 28 ± 2 days after surgery. The primary safety outcome was major bleeding. Patient recruitment was prematurely closed due to study drug expiry after the inclusion of 582 of the 646 planned patients. A primary study outcome event occurred in 11 of 282 patients in the placebo group compared with 3 of 287 in the rivaroxaban group (3.9 vs 1.0%; odds ratio, 0.26; 95% confidence interval [CI], 0.07-0.94; log-rank P = .032). Major bleeding occurred in none of the patients in the placebo group and 2 patients in the rivaroxaban group (incidence rate 0.7%; 95% CI, 0-1.0). Oral rivaroxaban was more effective than placebo for extended prevention of VTE after laparoscopic surgery for colorectal cancer without an increase in major bleeding. This trial was registered at www.clinicaltrials.gov as #NCT03055026.
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Becattini et al. (2022) conducted an RCT in Colorectal cancer (n=582). Rivaroxaban vs. Placebo was evaluated on Composite of symptomatic objectively confirmed VTE, asymptomatic ultrasonography-detected deep vein thrombosis (DVT), or VTE-related death at 28 ± 2 days after surgery (OR 0.26, 95% CI 0.07-0.94, p=0.032). Extended prophylaxis with rivaroxaban after laparoscopic surgery for colorectal cancer reduced VTE or VTE-related death compared with placebo (1.0% vs 3.9%; OR 0.26; 95% CI 0.07-0.94; P=0.032).
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