Katia Khoury1,2, Filipa Lynce1,3, Ana Barac4, Xue Geng5, Chau Dang6, Anthony F Yu6, Karen L Smith7, Christopher Gallagher8, Paula R Pohlmann1, Raquel Nunes7, Pia Herbolsheimer9, Robert Warren1, Monvadi B Srichai4, Mark Hofmeyer4, Federico Asch4, Ming Tan1, Claudine Isaacs1,5, Sandra M Swain10,11,12. 1. Lombardi Comprehensive Cancer Center, MedStar Georgetown University Hospital, Washington DC, USA. 2. O'Neal Comprehensive Cancer Center at UAB, The University of Alabama at Birmingham, Birmingham, AL, USA. 3. Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA. 4. MedStar Heart and Vascular Institute, Washington DC, USA. 5. Georgetown University, Washington DC, USA. 6. Memorial Sloan Kettering Cancer Center, New York, NY, USA. 7. Johns Hopkins Sidney Kimmel Comprehensive Cancer Center, Baltimore, MD, USA. 8. Washington Cancer Institute, MedStar Washington Hospital Center, Washington DC, USA. 9. AstraZeneca, Gaithersburg, MD, USA. 10. Lombardi Comprehensive Cancer Center, MedStar Georgetown University Hospital, Washington DC, USA. sandra.swain@georgetown.edu. 11. MedStar Health, Columbia, MD, USA. sandra.swain@georgetown.edu. 12. Georgetown University Medical Center, Building D Room 120, 4000 Reservoir Road NW, Washington DC, 20057, USA. sandra.swain@georgetown.edu.
Abstract
PURPOSE: HER2-targeted therapies are associated with cardiotoxicity which is usually asymptomatic and reversible. We report the updated cardiac safety assessment of patients with compromised heart function receiving HER2-targeted therapy for breast cancer, enrolled in the SAFE-HEaRt trial, at a median follow-up of 3.5 years. METHODS: Thirty patients with stage I-IV HER2-positive breast cancer receiving trastuzumab with or without pertuzumab, or ado-trastuzumab emtansine (T-DM1), with asymptomatic LVEF (left ventricular ejection fraction) 40-49%, were started on cardioprotective medications, with the primary endpoint being completion of HER2-targeted therapy without cardiac events (CE) or protocol-defined asymptomatic worsening of LVEF. IRB-approved follow-up assessment included 23 patients. RESULTS: Median follow-up as of June 2020 is 42 months. The study met its primary endpoint with 27 patients (90%) completing their HER2-targeted therapies without cardiac issues. Of the 23 evaluable patients at long-term f/u, 14 had early stage breast cancer, and 9 had metastatic disease, 8 of whom remained on HER2-targeted therapies. One patient developed symptomatic heart failure with no change in LVEF. There were no cardiac deaths. The mean LVEF improved to 52.1% from 44.9% at study baseline, including patients who remained on HER2-targeted therapy, and those who received prior anthracyclines. CONCLUSIONS: Long-term follow-up of the SAFE-HEaRt study continues to provide safety data of HER2-targeted therapy use in patients with compromised heart function. The late development of cardiac dysfunction is uncommon and continued multi-disciplinary oncologic and cardiac care of patients is vital for improved patient outcomes.
PURPOSE: HER2-targeted therapies are associated with cardiotoxicity which is usually asymptomatic and reversible. We report the updated cardiac safety assessment of patients with compromised heart function receiving HER2-targeted therapy for breast cancer, enrolled in the SAFE-HEaRt trial, at a median follow-up of 3.5 years. METHODS: Thirty patients with stage I-IV HER2-positive breast cancer receiving trastuzumab with or without pertuzumab, or ado-trastuzumab emtansine (T-DM1), with asymptomatic LVEF (left ventricular ejection fraction) 40-49%, were started on cardioprotective medications, with the primary endpoint being completion of HER2-targeted therapy without cardiac events (CE) or protocol-defined asymptomatic worsening of LVEF. IRB-approved follow-up assessment included 23 patients. RESULTS: Median follow-up as of June 2020 is 42 months. The study met its primary endpoint with 27 patients (90%) completing their HER2-targeted therapies without cardiac issues. Of the 23 evaluable patients at long-term f/u, 14 had early stage breast cancer, and 9 had metastatic disease, 8 of whom remained on HER2-targeted therapies. One patient developed symptomatic heart failure with no change in LVEF. There were no cardiac deaths. The mean LVEF improved to 52.1% from 44.9% at study baseline, including patients who remained on HER2-targeted therapy, and those who received prior anthracyclines. CONCLUSIONS: Long-term follow-up of the SAFE-HEaRt study continues to provide safety data of HER2-targeted therapy use in patients with compromised heart function. The late development of cardiac dysfunction is uncommon and continued multi-disciplinary oncologic and cardiac care of patients is vital for improved patient outcomes.
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