Cardiovascular function in leukemia patients: an observational prospective study
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- STATUS
- Enrolling By Invitation
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- participants needed
- 133
Summary
In the last decade, both the incidence and the survival of acute leukemia has been increasing. Therefore, detection of associated illnesses is important. We have recently observed that patients with acute leukemia treated with anthracyclines develop a high rate of symptomatic heart failure. To avoid this life-threatening illness, early detection of cardiac dysfunction and implementation of cardioprotective therapies are crucial. The aims of this study are three folds: 1) to define the rate of cardiac and vascular complications in adult patients with acute leukemia 2) to follow the time course of parameters of cardiac size and function and blood pressure in these patients 3) to test whether changes in sensitive parameters of cardiac or vascular function detected using echocardiograms, tonometry and blood tests, or preexisting genetic mutations, can predict later decrease in cardiac function in these patients. We will also examine whether these sensitive parameters of cardiac function identify patients who will develop cardiovascular events. This is a prospective, observational, single-center study. Adults with recently diagnosed acute leukemia at the hospital of University of Pennsylvania or the outpatient Perleman Center for Advanced Medicine will be selected. All patients will be studied using echocardiograms and blood tests before chemotherapy, 14 days, 28 days, 45-60 days, 6 months, and 12 months after the first dose of chemotherapy, for a total of 6 studies in 1 year. Our study sample size is 100 patients.
Details
| Condition | ['Mucinous Neoplasm', 'Colorectal Tumor', 'Appendiceal Tumor'] |
|---|---|
| Age | 99years or below |
| Clinical Study Identifier | TBD |
| Last Modified on | 19 February 2024 |
Eligibility
How to participate?
Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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