Cardiotoxicity in targeted therapy for breast cancer: A study of the FDA adverse event reporting system (FAERS)

Saranrat Wittayanukorn1, Jingjing Qian1, Brandon S Johnson2,3

  • 11 Harrison School of Pharmacy, Auburn University, Auburn, AL, USA.

Insights

Chemotherapy can harm the heart, especially targeted therapies like trastuzumab. This study analyzed real-world data, finding specific drugs and combinations pose higher cardiotoxicity risks for breast cancer patients.

Area of Science:

  • Oncology
  • Cardiology
  • Pharmacovigilance

Background:

  • Chemotherapy-induced cardiotoxicity is a significant concern in cancer treatment.
  • Existing evidence on cardiotoxicity from newer targeted therapies and their combinations is limited.
  • Real-world data is crucial for understanding cardiotoxicity patterns.

Purpose of the Study:

  • To evaluate cardiotoxicity reports associated with targeted therapies and their combinations in breast cancer patients.
  • To identify specific targeted agents and combinations with higher risks of cardiotoxicity.
  • To analyze health outcomes of reported cardiotoxicity events.

Main Methods:

  • Utilized the US Food and Drug Administration Adverse Event Reporting System (FAERS) database (2004-2012).
  • Conducted disproportionality analyses using reporting odds ratios (ROR) and 95% confidence intervals (95% CI) with a case/non-case method.
  • Identified targeted therapies and their combinations as suspect drugs for cardiotoxicity.

Main Results:

  • Identified 59,739 cardiotoxicity reports; 937 implicated targeted therapies.
  • Trastuzumab, bevacizumab, and lapatinib were the most reported targeted therapies.
  • Trastuzumab showed the highest ROR, particularly in combination with cyclophosphamide or doxorubicin.
  • Lapatinib demonstrated relatively low cardiotoxicity reporting rates.

Conclusions:

  • FAERS data analysis revealed significant signals for cardiotoxicity with targeted therapies and their combinations.
  • Clinicians should assess patient-specific factors to mitigate cardiotoxicity risks.
  • Continued surveillance and comparative studies are recommended to further understand and manage cardiotoxicity.

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