What is the Purpose of this Study?
Incidence of CTRCD in Cardio-Oncology services in all participating centers.
2. Identify risk factors resulting in increased CTRCD, and validate risk score models.
3. Evaluate geographic and regional differences in use of biomarkers and imaging modalities, and its impact of management of CTRCD.
4. Evaluate impact of socioeconomic and demographic variables in access to care, utilized surveillance strategies, treatments and outcomes.
5. Describe outcomes of cancer survivors treated with different potential cardio-toxic modalities in different geographic locations.
6. Provide a platform for multiple collaborations, sub-studies and prospective clinical studies.
Eligibility
- * New cardio-oncology consultation for breast cancer patients, or
- * New cardio-oncology consultation for Hodgkin's or non-Hodgkin's lymphoma patients, or
- * New cardio-oncology consultation for acute or chronic leukemia patients, or
- * New cardio-oncology consultation for multiple myeloma or AL amyloidosis, or
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Inclusion Criteria:
- * New cardio-oncology consultation for breast cancer patients, or
- * New cardio-oncology consultation for Hodgkin's or non-Hodgkin's lymphoma patients, or
- * New cardio-oncology consultation for acute or chronic leukemia patients, or
- * New cardio-oncology consultation for multiple myeloma or AL amyloidosis, or
- * New cardio-oncology consultations for immune check-point inhibitors cardiac evaluation.
- * All patients have to be 18 years old or older
Exclusion Criteria:
- * Cardio-oncology patients who have previously had cardio-oncology evaluation and follow up by the investigators.
- * Minors less than 18 years old.
- * Inability or unwillingness to consent to participate
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Where can I participate?
Torrance Memorial Medical Center (CSMC Affiliate)
More about this Clinical Trial
What is the full name of this clinical trial?
Global Cardio Oncology Registry Protocol