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2.
Am J Clin Oncol ; 45(4): 155-160, 2022 04 01.
Article in English | MEDLINE | ID: mdl-35320816

ABSTRACT

OBJECTIVES: To identify patients at high risk of developing cardiovascular disease through the identification of risk factors among a large population of breast cancer women and to assess the performance of Abdel-Qadir risk prediction model score. MATERIALS AND METHODS: The medical records and baseline characteristics of all patients/tumors diagnosed with breast cancer from 2010 to 2011 in a French comprehensive cancer center were collected. Cardiovascular events were defined as arterial and cardiac events, atrial fibrillation and venous thromboembolism occurring during the 5-year follow-up. Abdel-Qadir multivariable prediction model for major adverse cardiovascular events were used with the concordance index (c-index) score to assess calibration by comparing predicted risks to observed probabilities. RESULTS: Among the 943 breast cancer patients included, 83 patients (8.8%) presented with at least one cardiovascular event, leading to a cumulative incidence of 0.07 at 5 years (95% confidence interval [CI], 0.055-0.088). The cumulative incidence of atrial fibrillation at 5 years was 0.01 (95% CI, 0.005-0.018). Factors associated with the occurrence of cardiovascular events were pre-existing cardiovascular diseases including high blood pressure (hazard ratio [HR]=1.78, 95% CI=1.07-2.97, P=0.028), acute coronary syndrome (HR=5.28, 95% CI: 2.16-12.88, P<0.05) and grade 3 Scarff-Blool-Richardson (HR=1.95, 95% CI: 1.21-3.15, P=0.006). With a c-index inferior to 0.7, the Abdel-Qadir score was not fully validated in our population. CONCLUSION: These findings call for the assessment of the performance of risk prediction models such as Abdel-Qadir score coupled with other factors such as Scarff Bloom and Richardson grading in order to identify patients at high risk of experiencing cardiotoxicity.


Subject(s)
Atrial Fibrillation , Breast Neoplasms , Cardiovascular Diseases , Atrial Fibrillation/complications , Breast Neoplasms/pathology , Cardiovascular Diseases/epidemiology , Cardiovascular Diseases/etiology , Female , Humans , Incidence , Risk Assessment , Risk Factors
3.
Expert Opin Drug Saf ; 21(4): 453-465, 2022 Apr.
Article in English | MEDLINE | ID: mdl-34551666

ABSTRACT

INTRODUCTION: Thanks to the emergence of new therapeutics, prognosis and outcome of breast cancer patients (any subtype) have improved significantly. This raises the issue of the interactions and side effects related to the use of multiple drugs. Thus, to decide on a treatment, the optimal benefit risk-ratio should be carefully watched as toxicities such as cardiac ones effect on long-term survival. Indeed, nowadays in France, cardiovascular diseases rank first as causes of death in women. AREAS COVERED: This non-exhaustive review aims to report the currently available data on cardiac side effects caused by the use of emerging drugs in breast cancer, in localized or metastatic diseases alike. We will focus on HER2-inhibitors, cyclin-dependent-kinase 4/6 and PARP inhibitors, chemotherapy and immunotherapy, before discussing the means of prevention. EXPERT OPINION: Although this issue has largely been studied, the recent emergence of new drugs emphasizes the necessity for oncologists to adapt their practice to a multidisciplinary model that includes cardio-oncology.


Subject(s)
Breast Neoplasms , Cardiovascular Diseases , Breast Neoplasms/drug therapy , Cardiovascular Diseases/chemically induced , Cardiovascular Diseases/prevention & control , Female , France , Humans , Immunotherapy/adverse effects , Poly(ADP-ribose) Polymerase Inhibitors
4.
Anticancer Res ; 41(11): 5355-5364, 2021 Nov.
Article in English | MEDLINE | ID: mdl-34732405

ABSTRACT

Cardiotoxicity is a common side effect induced by cancer therapies, which increases the risk of long-term morbidity and mortality in cancer survivors. To date, the mechanism leading to this toxicity is still unclear, thus complicating cardiac safety assessment and predictive factor identification. The advances in technology, particularly regarding radiation therapy and constant development of novel antineoplastic agents, require urgent development of efficient preclinical models to detect drug cardiotoxicity. A myriad of empirical preclinical models have been used to investigate cardiotoxicity, though with limited success. Recently, multicellular spheroid models have gained attention by mimicking the in vivo microenvironment. The aim of this review is to focus on the most relevant preclinical models used to assess antineoplastic drug- and radiotherapy-related cardiotoxicities, with an overview on their current use. It also aims to discuss the possible directions of translational research in the cardio-oncology field.


Subject(s)
Antineoplastic Agents , Heart Diseases/chemically induced , Radiation Injuries/etiology , Translational Research, Biomedical , Animals , Biosensing Techniques , Cardiotoxicity , Cell Line , Coculture Techniques , Disease Models, Animal , Heart Diseases/metabolism , Heart Diseases/pathology , Heart Diseases/physiopathology , Humans , Myocytes, Cardiac/metabolism , Myocytes, Cardiac/pathology , Radiation Injuries/metabolism , Radiation Injuries/pathology , Radiation Injuries/physiopathology , Radiotherapy , Risk Factors , Species Specificity , Tumor Microenvironment
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