Evaluation and Management of Cardio Toxicity in Oncologic Patients

Condition(s) studied

Investigational drug(s) / intervention(s)

ACE inhibitors: Evaluating the cardio toxicity effect of chemotherapy and radiation and estimating the effect of ACE inhibitors and beta blockers in the prevention of heart failure.

beta blockers: Evaluating the cardio toxicity effect of chemotherapy and radiation and estimating the effect of ACE inhibitors and beta blockers in the prevention of heart failure.

Study summary

The survival rate of cancer patients has greatly increased over the past decades' mainly due to early detection and the use of new medications with higher doses and combined protocols. This achievement comes with the price of cardio toxicity, leading to cardiac dysfunction ranged from transient asymptomatic left ventricular dysfunction to cardiac death. In the long term, the risk of death from cardiovascular causes exceeds that of tumor recurrence for many types of cancer. As a result of the increasing number of long-term cancer survivors the magnitude of this problem is growing. Early identification of cardio toxicity can be identified by clinical follow-up and the use of electrocardiography, cardiac biomarkers (Troponin, brain natriuretic peptide) and echocardiogram. Past studies imply that the addition of angiotensin-converting-enzyme inhibitor (ACE inhibitor) and beta blockers to the patient's treatment may prevent the development of cardiac dysfunction. However, currently there are no specific or clear guidelines for the follow-up and management of cardio-toxicity in cancer patients.

The aim of the study: To try to identify who are the patients at increased risk for developing cardio toxicity, by follow up of clinical evaluation, cardiac biomarkers and echocardiogram examination, in purpose of early diagnosis, management and prevention of cardiac events. For achieving this the investigators will build a registry which will include all the oncologic patients going an evaluation in the cardio-oncology clinic in the Tel Aviv Medical Center .

Eligibility

Primary outcome measure(s)

• ECho-global strain — 2 years
  Predictor of reduction Ejection Fraction
• Troponin (ng/ml) — 2 years
  Predictor of reduction Heart failure
• ACE inhibitor and beta blocker treatment — 2 years
  estimating the effect of ACE inhibitors and beta blockers preventive treatment for heart failure due to chemotherapy.
• BNP (PG/ML) — 2 years
  Predictor of reduction Heart failure

Trial sites (1)

More Tel-Aviv Sourasky Medical Center trials in Israel

Other trials for the same condition