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Author Spotlight: Advancing Cancer Associated Thrombosis Research in Rodent Models
Published on: January 5, 2024
Survival After Solid Cancers in Antithrombotic Trials
Victor L Serebruany1, Ales Tomek2, Moo Hyun Kim3
1HeartDrug Research Laboratories, Johns Hopkins University, Baltimore, MD.
Abstract:
The impact of antithrombotics on cancer is currently under intense investigation because of the excess of solid cancers in trials after thienopyridines such as TRITON (prasugrel), DAPT (prasugrel and clopidogrel), PAR-1 thrombin antagonist in TRACER (vorapaxar), pyrimidines in PEGASUS (ticagrelor), and in APPRAISE-2 after apixaban. However, whether patient survival after solid cancer (SASC) in antithrombotic trials may be affected is unknown. We matched the 1-year SASC rate in antithrombotic trials reported by Food and Drug Administration with the census averages in Surveillance, Epidemiology, and End Results (SEER) Program by the US National Cancer Institute and World Health Organization (WHO) surveys. The Food and Drug Administration provided the SASC data for 3 trials with similar cancer survival of about 70% for the first year of follow-up in TRITON, APPRAISE-2, and ARISTOTEL. Adjusted cancers in TRITON with SEER (odds ratio 0.92; 95% confidence interval 0.53 to 1.59, p = 0.4351) and WHO (odds ratio 0.99; 95% confidence interval 0.57 to 1.7, p = 1.00) revealed very close if not identical SASC rates in antithrombotic trials compared to epidemiologic census estimates. In conclusion, SASC rates in patients enrolled in antithrombotic trials do not differ from SEER or World Health Organization averages.
Insights
Patient survival after solid cancer (SASC) in antithrombotic trials mirrors general population rates. This study found no significant difference in SASC when comparing trial data to SEER and WHO averages, reassuring for cancer patients on antithrombotics.
Area of Science:
- Cardiology
- Oncology
- Clinical Trials
Background:
- Antithrombotic medications are under scrutiny for potential impacts on cancer incidence.
- Limited data exists on patient survival after solid cancer (SASC) within antithrombotic clinical trials.
Purpose of the Study:
- To investigate and compare 1-year SASC rates in patients from antithrombotic trials against general population cancer survival data.
- To determine if antithrombotic drug use affects outcomes for patients who develop cancer during trials.
Main Methods:
- Utilized Food and Drug Administration (FDA) data on SASC from three major antithrombotic trials (TRITON, APPRAISE-2, ARISTOTEL).
- Matched trial SASC data with cancer survival averages from the Surveillance, Epidemiology, and End Results (SEER) Program and World Health Organization (WHO) surveys.
- Performed statistical analysis, including odds ratios and confidence intervals, to compare trial SASC rates with population averages.
Main Results:
- SASC rates in the analyzed antithrombotic trials were approximately 70% for the first year of follow-up.
- Statistical comparisons showed no significant difference between SASC rates in trials and SEER (OR 0.92, CI 0.53-1.59) or WHO (OR 0.99, CI 0.57-1.7) data.
- The findings indicate that cancer survival in patients within these antithrombotic trials is consistent with general population estimates.
Conclusions:
- Patient survival after solid cancer (SASC) in antithrombotic trials is comparable to that observed in the general population.
- The use of antithrombotics in the context of these trials does not appear to negatively impact cancer survival rates.
- These findings help address concerns regarding the interplay between antithrombotic therapy and cancer outcomes.
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