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SCHOLARLY PUBLICATION ✓ Open Access

Expert consensus for multimodality imaging evaluation of adult patients during and after cancer therapy: a report from the American Society of Echocardiography and the European Association of Cardiovascular Imaging

Juan Carlos Plana, Maurizio Galderisi, Ana Barac, Michael S. Ewer, Bonnie Ky, Marielle Scherrer‐Crosbie, Javier Gáname, Igal A. Sebag, Deborah A. Agler, Luigi Paolo Badano, José Banchs, Daniela Maria Cardinale, Joseph R. Carver, M. Cerqueira, Jeanne M. DeCara, Thor Edvardsen, Scott D. Flamm, Thomas L. Force, Brian P. Griffin, Guy Jérusalem, Jennifer E. Liu, Andreia Magalhães, Thomas Hugh Marwick, Liza Y. Sanchez, Rosa Sicari, Hector R. Villarraga, Patrizio Lancellotti

📄 Abstract

Cardiac dysfunction resulting from exposure to cancer therapeutics was first recognized in the 1960s, with the widespread introduction of anthracyclines into the oncologic therapeutic armamentarium. Heart failure (HF) associated with anthracyclines was then recognized as an important side effect. As a result, physicians learned to limit their doses to avoid cardiac dysfunction. Several strategies have been used over the past decades to detect it. Two of them evolved over time to be very useful: endomyocardial biopsies and monitoring of left ven- tricular (LV) ejection fraction (LVEF) by cardiac imaging. Examination of endomyocardial biopsies proved to be the most sensitive and spe- cific parameter for the identification of anthracycline-induced LV dysfunction and became the gold standard in the 1970s. However, the interest in endomyocardial biopsy has diminished over time because of the reduction in the cumulative dosages used to treat ma- lignancies, the invasive nature of the procedure, and the remarkable progress made in noninvasive cardiac imaging. The noninvasive evaluation of LVEF has gained importance, and notwithstanding the limitations of the techniques used for its calculation, has emerged as the most widely used strategy for monitoring the changes in cardiac function, both during and after the administration of potentially car- diotoxic cancer treatment.

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