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January 14, 2020European Heart Journal296 citationsOpen Access

Classification, prevalence, and outcomes of anticancer therapy-induced cardiotoxicity: the CARDIOTOX registry

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JLJosé López‐SendónCÁCarlos Álvarez-OrtegaPAPilar Auñón

Key Result

Cardiotoxicity was identified in 37.5% of patients, with severe cases exhibiting a mortality rate of 22.9 deaths per 100 patient-years compared to 2.3 in other groups (HR 10.2).

Structured PICO

What is the prevalence and prognostic impact of anticancer therapy-induced cardiotoxicity?

P
Population
865 patients, aged 54.7 ± 13.9; 16.3% men, scheduled for anticancer therapy related with moderate/high cardiotoxicity risk.
I
Intervention
Anticancer therapy related with moderate/high cardiotoxicity risk
O
Outcome
Cardiotoxicity (defined as new or worsening of myocardial damage/ventricular function from baseline during follow-up)composite

While mild cardiotoxicity is common during or after cancer therapy, severe cardiotoxicity is rare but strongly associated with increased mortality.

Abstract

Abstract Aim Cardiotoxicity (CTox) is a major side effect of cancer therapies, but uniform diagnostic criteria to guide clinical and research practices are lacking. Methods and results We prospectively studied 865 patients, aged 54.7 ± 13.9; 16.3% men, scheduled for anticancer therapy related with moderate/high CTox risk. Four groups of progressive myocardial damage/dysfunction were considered according to current guidelines: normal, normal biomarkers (high-sensitivity troponin T and N-terminal natriuretic pro-peptide), and left ventricular (LV) function; mild, abnormal biomarkers, and/or LV dysfunction (LVD) maintaining an LV ejection fraction (LVEF) ≥50%; moderate, LVD with LVEF 40–49%; and severe, LVD with LVEF ≤40% or symptomatic heart failure. Cardiotoxicity was defined as new or worsening of myocardial damage/ventricular function from baseline during follow-up. Patients were followed for a median of 24 months. Cardiotoxicity was identified in 37.5% patients during follow-up 95% confidence interval (CI) 34.22–40.8%, 31.6% with mild, 2.8% moderate, and 3.1% with severe myocardial damage/dysfunction. The mortality rate in the severe CTox group was 22.9 deaths per 100 patients-year vs. 2.3 deaths per 100 patients-year in the rest of groups, hazard ratio of 10.2 (95% CI 5.5–19.2) (P 0.001). Conclusions The majority of patients present objective data of myocardial injury/dysfunction during or after cancer therapy. Nevertheless, severe CTox, with a strong prognostic relationship, was comparatively rare. This should be reflected in protocols for clinical and research practices.

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Cite This Study

López‐Sendón et al. (2020) studied this question. Cardiotoxicity was identified in 37.5% of patients, with severe cases exhibiting a mortality rate of 22.9 deaths per 100 patient-years compared to 2.3 in other groups (HR 10.2).

synapsesocial.com/papers/6971366ecfea4c1fcf6a58e8https://doi.org/10.1093/eurheartj/ehaa006
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