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Brief Title: Identification and Evaluation of Patients at Risk of Developing Cardiotoxicity After Receiving Chemotherapy for Breast Cancer, Lymphoma or Leukemia
Official Title: Identification and Evaluation of Patients at Risk of Developing Cardiotoxicity After Receiving Chemotherapy for Breast Cancer, Lymphoma or Leukemia
Study ID: NCT04541212
Brief Summary: This is an observational study of the occurrence of cardiac toxicity in patients with breast cancer,lymphoma or leukemia receiving chemotherapy including an anthracycline. Patients will be identified at the oncology clinic and will be included in the study if all eligible criteria are met. The study will involve retrospective and prospective evaluations. Safety will be assessed through reporting of serious adverse events (SAEs) related to study procedures.
Detailed Description: The aim of this study is to identify and evaluate cardiotoxicity in patients with diagnosis of breast cancer, lymphoma or leukemia scheduled to receive anthracycline-based chemotherapy (Cohort A: prospective evaluation); and patients undergoing or having received within the last 5 years anthracycline-based chemotherapy (Cohort B: retrospective and prospective evaluations). Part A and B will be conducted in parallel. This study also has the objectif of identifying biomarkers of cardiotoxicity including inflammatory response proteins and clonal hematopoiesis.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
CISSSS de Lanaudière_Hôpital Pierre LeGardeur (referring site), Terrebonne, Quebec (QC), Canada
Centre Hospitalier de l'université de Montréal (CHUM), Montreal, Quebec, Canada
CIUSSS Ouest de l'ile de Montreal - St-Mary's Hospital, Montréal, Quebec, Canada
CIUSSS de l'Est-de-l'Île-de-Montréal - Hôpital Maisonneuve-Rosemont, Montréal, Quebec, Canada
Montreal Heart Institute, Montréal, Quebec, Canada
Name: Jean-Claude Tardif, MD
Affiliation: Montreal Heart Institute
Role: PRINCIPAL_INVESTIGATOR