Radiation-induced Cardiac Toxicity After Non-small Cell Lung Cancer Radiotherapy

Description

BACKGROUND Radiation-induced cardiac toxicity after RT for breast cancer or haematological malignancies is well described, with various studies linking post-RT cardiac morbidity and mortality with radiation dose. In patients treated with RT for NSCLC the associated heart exposure is higher than in breast cancer patients, and may lead to side effects possibly reducing survival. With improving prognosis for these patients after RT, the evidence began to accumulate that overall survival (OS) after RT for NSCLC is related to the heart dose. A landmark randomized trial Radiation Therapy Oncology Group (RTOG) 0617 failed to show any OS benefit with higher RT dose, and a post-hoc analysis revealed that the heart dose was a strong predictor of inferior OS. However, heart doses are higher with lower lobe tumors irradiation where irradiated volumes are larger due to respiratory tumor motion, and better blood supply of these parts of the lungs makes the lung toxicity worse, which also affects survival. Moreover, higher heart doses result from larger target volumes, which are themselves associated with worse OS. Therefore, a prospective evaluation of the cardiac toxicity after RT for NSCLC is needed to determine whether there is a correlation between the RT dose and specific types of cardiotoxicities.

Cardiac toxicity may manifest as any of a broad spectrum of diseases: as congestive heart failure, coronary ischemia, arrythmias or conduction abnormalities, and valvular and pericardial disease, therefore it is important to evaluate dosimetric parameters of the cardiac substructures, and to correlate them with potential adverse effects. Retrospective data suggests that the predictive value for cardiac events of the doses for the corresponding heart substructures outperforms the whole heart doses. STE is a valuable tool for a quantitative analysis of the changes to the cardiac substructures. Global longitudinal strain (GLS) has been regarded as a more accurate and sensitive parameter than left ventricle ejection fraction in assessing cardiac dysfunction, and its utility in the identification of subclinical myocardial changes has been demonstrated in a variety of conditions, including hypertension, diabetes mellitus, Cushing's disease, and chemotherapy- and RT-related cardiotoxicity. Recently, GLS has also been proved useful in the evaluation of the function of both atria and a right ventricle. Thus, STE is a non-invasive method allowing not only for the identification but also for the quantitative evaluation of subclinical systolic dysfunction of all the heart chambers.

In the present study, subclinical myocardial dysfunction will be evaluated using STE before and 1, 6, and 12 months after RT in consecutive NSCLC patients treated with definitive RT with or without chemotherapy (CHT) and the association between early cardiac effects and RT dose distribution in the corresponding heart substructures will be explored. Moreover, the study will show whether subclinical alterations detected by strain imaging precede the occurrence of clinical dysfunctions, possibly allowing for earlier treatment or closer monitoring of such patients.

OBJECTIVES OF THE STUDY The aim of this prospective study is to evaluate subclinical cardiac dysfunction in consecutive NSCLC patients treated with definitive RT and to investigate the predictive value of the cardiac substructures dosimetric parameters for cardiac toxicity as evaluated using STE and traditional echocardiographic parameters. The study will also investigate whether subclinical alterations detected by echocardiography with strain imaging may serve as a marker for future clinical dysfunctions.

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