BPI23-012: Real-World Frequency of ECHO Monitoring and Incidence of Anti-HER2 Therapy Related Cardiac Events in HER2+ Breast Cancer Patients

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Annette Hood Smilow Cancer Hospital at Yale New Haven Hospital; New Haven, CT

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Blerina Mukallari Smilow Cancer Hospital at Yale New Haven Hospital; New Haven, CT

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Jacqueline Majeski Smilow Cancer Hospital at Yale New Haven Hospital; New Haven, CT

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Lajos Pusztai Yale Cancer Center/Yale University; New Haven, CT

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Kerin Adelson Yale Cancer Center/Yale University; New Haven, CT

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Kejal Amin Smilow Cancer Hospital at Yale New Haven Hospital; New Haven, CT

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Background: Current guidelines recommend monitoring cardiac function every 3 months in patients on anti-HER2 therapies, such as trastuzumab and pertuzumab. The purpose of this study is to assess the frequency of ECHO monitoring in the real-world setting and to identify the incidence of anti-HER2 therapy related cardiac events within 1 year of treatment in patients with breast cancer. Methods: Patients initiated on anti-HER2 therapies from December 2018 to December 2019 for Stage I-IV HER2 positive breast cancer were included in this single center, retrospective chart review. Patients were followed for 1 year. The total number of patients who had at least 1 dose held or who had treatment discontinued for the development of a cardiac event (drop in ejection fraction [EF], arrhythmia, myocardial infarction [MI], death or other [structural changes on ECHO]) was assessed. Baseline cardiovascular risk factors were collected along with frequency of ECHO monitoring. Results: Of the 153 patients, 16 (10%) had a dose held for the development of a cardiac event. At baseline, 4 (25%) had a history of prior anthracycline, none had a baseline ECHO of less than 55% and 9 (56%) had 2 or more cardiac risk factors. A cardiac event occurred within 3 months of treatment initiation in 7 (43.8%) of the patients with doses held, with 5 (71.4%) of these patients having a history of prior anthracycline or 2 or more baseline cardiac risk factors. Of the patients who had doses held, 8 (5%) continued on treatment, while 8 (5%) had treatment discontinued. Of the patients who continued on treatment, 7 had treatment held for a drop in EF (average drop 9.7%), while 1 had treatment held for a structural change on ECHO. The average onset of a cardiac event was 26.4 weeks. Of the 8 patients who had treatment discontinued, 7 had a drop in EF (average drop 15.4%) while 1 developed an arrhythmia. Average onset of a cardiac event was 24.9 weeks. Of all 153 patients, 8 (5.2%) had no baseline cardiac risk factors or history of anthracycline but developed a cardiac event. ECHOs were monitored every 1-3 months in 55.6% of patients and every 4-6 months in 40.5% of patients. Conclusion: In patients with a history of prior anthracycline, or with at least 2 or more cardiovascular risk factors, ECHO monitoring should continue every 3 months. However, in patients with no baseline cardiovascular risk factors or history of anthracycline, extending ECHO surveillance to every 6 months may be considered.

Table.

Patient Characteristics and Cardiac Events

Table.
*

Max change in EF compared to baseline

^

structural changes on ECHO

Corresponding Author: Annette Hood, PharmD

Email: annette.hood@ynhh.org
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