Key result
A cardiac risk prediction model for women with HER-2 positive breast cancer on trastuzumab therapy demonstrated a negative predictive value of 94% for predicting cardiotoxicity within one year.
Why the study?
Trastuzumab is known to decrease LVEF, prompting the need for a cardiac risk prediction tool to identify HER-2 positive breast cancer patients at risk of cardiotoxicity.
Cohort (n=415)
Yes
A clinical risk prediction model can identify HER-2 positive breast cancer patients at low risk for trastuzumab-induced cardiotoxicity, potentially allowing for less frequent echocardiographic screening.
May support risk-stratified echocardiographic surveillance in trastuzumab-treated patients; hypothesis-generating and requires prospective validation.
BACKGROUND: 25% of all breast cancer patients have HER-2 overexpression. Breast Cancer patients with HER-2 overexpression are typically treated with HER-2 inhibitors such as Trastuzumab. Trastuzumab is known to cause a decrease in left ventricular ejection fraction. The aim of this study is to create a cardiac risk prediction tool among women with Her-2 positive breast cancer to predict cardiotoxicity. METHOD: Using a split sample design, we created a risk prediction tool using patient level data from electronic medical records. The study included women 18 years of age and older diagnosed with HER-2 positive breast cancer who received Trastuzumab. Outcome measure was defined as a drop in LVEF by more than 10% to less than 53% at any time in the 1-year study period. Logistic regression was used to test predictors. RESULTS: The cumulative incidence of cardiac dysfunction in our study was 9.4%. The sensitivity and specificity of the model are 46% and 84%, respectively. Given a cumulative incidence of cardiotoxicity of 9%, the negative predictive value of the test was 94%. This suggests that in a low-risk population, the interval of screening for cardiotoxicity may be performed less frequently. CONCLUSION: Cardiac risk prediction tool can be used to identify Her-2 positive breast cancer patients at risk of developing cardiac dysfunction. Also, test characteristics in addition to disease prevalence may inform a rational strategy in performing cardiac ultrasound in Her-2 breast cancer patients. We have developed a cardiac risk prediction model with high NPV in a low-risk population which has an appealing cost-effectiveness profile.
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Otchere et al. (2023) conducted a cohort in HER-2 positive breast cancer (n=415). Trastuzumab therapy was evaluated on Drop in LVEF by more than 10% to less than 53% at any time in the first year following trastuzumab therapy. A cardiac risk prediction model for women with HER-2 positive breast cancer on trastuzumab therapy demonstrated a negative predictive value of 94% for predicting cardiotoxicity within one year.
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