Key result
High Neutrophil-to-Lymphocyte Ratio (≥ 2.58) during anthracycline therapy is associated with a 4-fold increased risk of developing left ventricular dysfunction (OR 4.63) in breast cancer patients.
Why the study?
Cardiotoxicity is a significant side effect of anthracycline therapy requiring early markers, but whether elevated neutrophil-to-lymphocyte ratio predicts its development is unknown.
Does elevated Neutrophil-to-Lymphocyte Ratio predict cardiotoxicity in breast cancer patients treated with anthracyclines?
Cohort (n=74)
No
Does elevated Neutrophil-to-Lymphocyte Ratio predict cardiotoxicity in breast cancer patients treated with anthracyclines?
Elevated neutrophil-to-lymphocyte ratio (≥2.58) during anthracycline therapy is an independent predictor of early cardiotoxicity (LV GLS reduction) in breast cancer patients.
Elevated post-anthracycline NLR may flag cardiotoxicity risk; leaves open whether it improves risk stratification beyond current tools.
Background: Cardiotoxicity, defined mainly as left ventricle (LV) dysfunction, is a significant side effect of anthracyclines (ANT) therapy. The need for an early simple marker to identify patients at risk is crucial. High Neutrophil-to-Lymphocyte Ratio (NLR) has been associated with poor prognosis in cancer patients, however, its role as a predictor for cardiotoxicity development is unknown. Objective: We aimed to evaluate whether elevated NLR, following ANT exposure, plays a predictive role in the development of cardiotoxicity as defined by LV global longitudinal strain (LV GLS) relative reduction (≥10%).Methods and results: Data were prospectively collected as part of the Israel Cardio-Oncology Registry (ICOR). A total of 74 female patients with breast cancer, scheduled for ANT therapy were included. NLR levels were assessed at baseline (T1) and during ANT therapy (T2). All patients underwent serial echocardiography at baseline (T1) and after the completion of ANT therapy (T3). NLR≥ 2.58 was found to be the optimal predictive cut-off for LV GLS deterioration. A relative LV GLS reduction ≥10% was significantly more common among patients with high NLR (50% vs. 20%, p=0.009). NLR ≥ 2.58 increases the risk for LV GLS reduction by 4-fold (OR 4.63, 95%CI 1.29-16.5, p = 0.02), with each increase of 1-point NLR adding an additional 15% risk (OR 1.15, 95%CI 1.01-1.32, p = 0.046).Conclusions: Our study provides novel data that high NLR levels, following ANT exposure, have an independent association with the development of LV dysfunction. Routine surveillance of NLR may be an effective means of risk-stratifying.
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Baruch et al. (2022) conducted a cohort in Breast cancer (n=74). High Neutrophil-to-Lymphocyte Ratio (NLR ≥ 2.58) during anthracycline therapy vs. Low Neutrophil-to-Lymphocyte Ratio (NLR < 2.58) was evaluated on Relative left ventricular global longitudinal strain (LV GLS) reduction ≥ 10% (OR 4.63, 95% CI 1.29-16.5, p=0.02). High Neutrophil-to-Lymphocyte Ratio (≥ 2.58) during anthracycline therapy is associated with a 4-fold increased risk of developing left ventricular dysfunction (OR 4.63) in breast cancer patients.
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