4.6 Article

ECG Scoring for the Evaluation of Therapy-Naive Cancer Patients to Predict Cardiotoxicity

期刊

CANCERS
卷 13, 期 6, 页码 -

出版社

MDPI
DOI: 10.3390/cancers13061197

关键词

ECG; cardio-oncology; cancer; score; cardiotoxicity

类别

资金

  1. German Research Foundation (Deutsche Forschungsgemeinschaft, DFG) [RA 964/12-2]
  2. IFORES research grant, Medical Faculty, University Duisburg-Essen, Essen, Germany
  3. German Centre for Cardiovascular Research (DZHK) Partner site Munich
  4. Deutsche Forschungsgemeinschaft (DFG
  5. German Research Foundation) [DO637/23-1, 394433254]
  6. German Cancer Consortium (DKTK)

向作者/读者索取更多资源

This study evaluated a new electrocardiographic (ECG) score in therapy-naive cancer patients to predict cardiotoxicity, showing that an ECG score of >= 2 points was associated with a higher risk of developing cardiotoxicity. High-risk patients did not differ in age, LV ejection fraction, cardiovascular risk factors, or cardiac biomarkers compared to those with a low-risk ECG score.
Simple Summary Due to improved survival upon effective anti-cancer therapies, the management of treatment-related side-effects is of increasing interest and importance. Cardiovascular side-effects of chemo-, targeted- and/or immunotherapies are common and can be harmful. To date, the identification of patients who could experience those cardiovascular side-effects prior to the anti-cancer therapy start is difficult. We show that the use of a simple electrocardiographic (ECG) score can help to predict the occurrence of cardiovascular toxicity of anti-cancer therapies. Objective: To evaluate a new electrocardiographic (ECG) score reflecting domains of electrical and structural alterations in therapy-naive cancer patients to assess their risk of cardiotoxicity. Methods: We performed a retrospective analysis of 134 therapy-naive consecutive cancer patients in our two university hospitals concerning four ECG score parameters: Contiguous Q-waves, markers of left ventricular (LV) hypertrophy, QRS duration and JTc prolongation. Cardiotoxicity was assessed after a short-term follow-up (up to 12 months). Results: Of all the patients (n = 25), 19% reached 0 points, 50% (n = 67) reached 1 point, 25% (n = 33) reached 2 points, 5% (n = 7) reached 3 points and 0.7% reached 4 or 5 points (n = 1 respectively). The incidence of cardiotoxicity (n = 28 [21%]) increased with the ECG score, with 0 points at 0%, 1 point 7.5%, 2 points 55%, 3 points 71% and >= 3 points 50%. In the ROC (Receiver operating curves) analysis, the best cut-off for predicting cardiotoxicity was an ECG score of >= 2 points (sensitivity 82%, specificity 82%, AUC 0.84, 95% CI 0.77-0.92, p < 0.0001) which was then defined as a high-risk score. High-risk patients did not differ concerning their age, LV ejection fraction, classical cardiovascular risk factors or cardiac biomarkers compared to those with a low-risk ECG score. Conclusion: ECG scoring prior to the start of anti-cancer therapies may help to identify therapy-naive cancer patients at a higher risk for the development of cardiotoxicity.

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