Why the study?
Does early biomarker-guided detection and prophylactic treatment with ACE inhibitors prevent LVEF reduction and cardiac events in cancer patients on chemotherapy?
Does early biomarker-guided detection and prophylactic treatment with ACE inhibitors prevent LVEF reduction and cardiac events in cancer patients on chemotherapy?
Biomarker-guided early detection of cardiotoxicity and prompt initiation of ACE inhibitors may prevent irreversible left ventricular dysfunction in cancer patients undergoing chemotherapy.
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Biomarker monitoring may enable earlier prophylaxis before functional decline; leaves open optimal thresholds for routine practice.
Cardiac toxicity induced by anticancer therapy is of considerable concern for, once it develops, it may compromise the clinical effectiveness of treatment independent of the oncologic prognosis. The main strategy to minimize cardiotoxicity is to detect high-risk patients and begin prophylactic treatment as early as possible. According to the current standard for monitoring cardiac function cardiotoxicity is usually detected only once a functional impairment has already occurred, thus precluding any chance of prevention. The measurement of cardio-specifi c biomarkers can be a valid diagnostic tool for the early identifi cation, assessment and monitoring of cardiotoxicity. The role of Troponin I in identifying patients with subclinicalcardiotoxicity and their subsequent treatment with angiotensin- converting enzyme inhibitors to prevent left ventricular ejection fraction (LVEF) reduction and cardiac events, is emerging as an effective strategy against these complications. When this approach is not feasible, a complete LVEFrecovery and a reduction in cardiac events may be achieved if left ventricular dysfunction (LVD) is detected early and the patient promptly treated with angiotensin-converting enzyme inhibitors, possibly in combination with beta-blocking agents.
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Bacchiani et al. (2017) studied this question.
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