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Published on: July 3, 2014
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.
Abstract:
Purpose Cancer chemotherapy-induced cardiotoxicity is concerning. Certain anthracyclines and targeted therapies are known to have potential for cardiotoxicity, but existing trial evidence is inadequate to understand real-world patterns of cardiotoxicity with newer targeted therapies and their common combinations with older agents. This study evaluated chemotherapy-related cardiotoxicity reports for targeted therapies and their combinations in breast cancer patients. Methods The US Food and Drug Administration Adverse Event Reporting System (FAERS) database from January 2004 through September 2012 was used to summarize characteristics of reported cardiotoxicity events and their health outcomes. Disproportionality analyses with reporting odds ratios (ROR) and 95% confidence intervals (95% CI) were conducted to detect event signals using a case/non-case method for each targeted therapy and combination. Results A total of 59,739 cases of cardiotoxicity reports were identified; 937 cases identified targeted therapy as the suspect drug. Trastuzumab had the highest number of reports followed by bevacizumab and lapatinib. Proportions of reports of death and disability outcomes for each targeted therapy were approximately 20-25% of the total reports of serious events. Trastuzumab had the highest ROR as a single agent (ROR = 5.74; 95% CI = 5.29-6.23) or combination use of cyclophosphamide (ROR = 16.83; 95% CI = 13.32-21.26) or doxorubicin (ROR = 17.84; 95% CI = 13.77-23.11). Relatively low cardiotoxicity reporting rates were found with lapatinib, regardless of use with combination therapy. Conclusions Analysis of FAERS data identified signals for adverse cardiotoxicity events with targeted therapies and their combinations. Practitioners should consider factors that may increase the likelihood of cardiotoxicity when assessing treatment. Findings support continued surveillance, risk factor identification, and comparative studies.
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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