Your browser doesn't support javascript.
loading
Rationale and Design of the Cessation Of Pharmacotherapy In Recovered Chemotherapy-induced cardioToxicity (COP-RCT): A Pilot Study.
Yu, Christopher; Negishi, Tomoko; Pathan, Faraz; Sverdlov, Aaron; Thomas, Liza; Shirazi, Mitra; Koo, Chieh Yang; Tan, Li Ling; Miyazaki, Sakiko; Negishi, Kazuaki.
Afiliação
  • Yu C; Sydney Medical School, Charles Perkins Centre Nepean, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia.
  • Negishi T; Sydney Medical School, Charles Perkins Centre Nepean, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia.
  • Pathan F; Sydney Medical School, Charles Perkins Centre Nepean, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia.
  • Sverdlov A; Faculty of Health and Medicine, The University of Newcastle, Newcastle, NSW, Australia; Cardio-oncology Research Group, Hunter Medical Research Institute, Newcastle, NSW, Australia; Cardiovascular Department, John Hunter Hospital, Newcastle, NSW, Australia.
  • Thomas L; Department of Cardiology, Westmead Hospital, Sydney, NSW, Australia.
  • Shirazi M; Department of Cardiology, Royal Adelaide Hospital, Adelaide, SA, Australia.
  • Koo CY; Department of Cardiology, National University Heart Centre, Singapore.
  • Tan LL; Department of Cardiology, National University Heart Centre, Singapore.
  • Miyazaki S; Juntendo University Graduate School of Medicine, Tokyo, Japan.
  • Negishi K; Sydney Medical School, Charles Perkins Centre Nepean, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia. Electronic address: kazuaki.negishi@sydney.edu.au.
Heart Lung Circ ; 2023 Nov 08.
Article em En | MEDLINE | ID: mdl-37949748
ABSTRACT

BACKGROUND:

Cancer therapeutics-related cardiac dysfunction (CTRCD) is a well-recognised complication of cancer treatment. Treatment of CTRCD involves cardioprotective therapy (CPT) which can lead to a recovery of CTRCD with normalisation of the left ventricular ejection fraction (LVEF). As a result, there are potentially millions of cancer survivors with recovered CTRCD on CPT. Cardioprotective therapy can be associated with an undesirable long-term pill burden, financial costs, and side effects. Cancer survivorship is anticipated to increase significantly by the end of this decade. To date, there is no evidence of the safety of stopping CPT in this setting. This study seeks to evaluate the hypothesis that ceasing cardioprotective medication is a feasible and safe option without significant impact on LVEF in low-risk patients who have recovered from CTRCD. METHODS AND

ANALYSIS:

We will perform a multicentre prospective open-label randomised controlled trial with blinded endpoint (PROBE) of supervised CPT cessation compared to continuing CPT (control). The primary study end point is the change in LVEF by cardiac magnetic resonance imaging at 6 months of enrolment between the two groups. Secondary end points include changes in quality-of-life questionnaires, other cardiac imaging parameters, and recurrence of heart failure.

CONCLUSION:

Cessation Of Pharmacotherapy In Recovered Chemotherapy-induced cardioToxicity (COP-RCT) is one of the first studies currently underway to evaluate the safety of ceasing CPT in recovered CTRCD. The results will inform clinical practice in this evidence-free zone.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article