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. Author manuscript; available in PMC: 2021 Dec 1.
Published in final edited form as: Eur J Heart Fail. 2020 Oct 2;22(12):2290–2309. doi: 10.1002/ejhf.1985

Table 4.

Summary of recommendations for baseline and long-term monitoring of cardiotoxicities in patients with cancer

Who to screen When and how
ASCO guidelines80
  • Patients with clinical signs or symptoms suggestive of cardiac dysfunction

  • Echocardiogram

  • CMR or MUGA if echocardiogram is not available or not feasible

  • Serum cardiac biomarkers (troponins, natriuretic peptides) or echocardiography-derived strain imaging plus routine diagnostic imaging

  • Asymptomatic patients at increased risk for cardiac dysfunction

  • Routine surveillance imaging

  • Echocardiogram, 6 and 12 months after completion of cancer therapy

  • CMR or MUGA if echocardiogram is not available or not technically feasible

  • No recommendations on frequency and duration of surveillance in patients who have no evidence of cardiac dysfunction on a 6–12-month post-treatment echocardiogram

ESMO guidelines24
  • Any patient on potentially cardiotoxic therapy

  • High-risk patients (pre-existing CVD) or those receiving high-dose cardiotoxic therapy (e.g. anthracycline)

  • ECG, including QTc at baseline

  • Cardiac biomarkers: hs-cardiac troponins (TnI or TnT), BNP or NT-proBNP at baseline and periodically thereafter (3–6 weeks or before each cycle)

  • Reassessment of LV function based on cumulative anthracycline dose

  • Patients scheduled to receive cancer therapy associated with HF or LV dysfunction

  • Imaging evaluation of LVEF and diastolic function at baseline

  • Baseline and serial blood pressure monitoring

  • Periodic cardiac physical examination, cardiac biomarkers and/or cardiac imaging

ESC guidance3
  • All patients receiving cancer therapy

  • Assessment of CAD based on history, age, and gender

  • 12-lead electrocardiogram and QTc interval at baseline and during treatment

  • Blood pressure at baseline and periodically during treatment

  • Frequency of surveillance depends on patient and treatment characteristics

  • Patients with a history of QT prolongation, cardiac disease, bradycardia, thyroid dysfunction, electrolyte abnormalities

  • Monitor with repeated 12-lead electrocardiogram

  • Patients with severe hypertension

  • Close monitoring and evaluation of adherence to antihypertensive drugs

  • Patients treated with pyrimidine analogues or at risk for myocardial ischaemia

  • Echocardiography (3D preferred) to monitor for myocardial ischaemia and to estimate LVEF and LV volumes before, during and after treatment

  • Exact interval is not established, but should be repeated during follow-up to confirm recovery, or detect irreversible LV dysfunction

  • Patients receiving radiotherapy

  • Adults and survivors of childhood cancers exposed to chest radiotherapy should be offered lifelong surveillance

3D, three-dimensional; ASCO, American Society of Clinical Oncology; BNP, B-type natriuretic peptide; CAD, coronary artery disease; CMR, cardiac magnetic resonance; CVD, cardiovascular disease; ECG, electrocardiography; ESC, European Society of Cardiology; ESMO, European Society for Medical Oncology; HF, heart failure; hs-TnI or TnT, high-sensitivitycardiac troponins (I or T); LV, left ventricular; LVEF, left ventricular ejection fraction; MUGA, multi-gated acquisition; NT-proBNP, N-terminal pro-B-type natriuretic peptide.