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Survival After Solid Cancers in Antithrombotic Trials.

Victor L Serebruany1, Ales Tomek2, Moo Hyun Kim3

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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.

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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.