Sacubitril/valsartan for cardioprotection in breast cancer (MAINSTREAM): design and rationale of the randomized trial

Author:

Tajstra Mateusz1ORCID,Dyrbuś Maciej1ORCID,Rutkowski Tomasz2ORCID,Składowski Krzysztof2ORCID,Sosnowska‐Pasiarska Barbara3ORCID,Góźdź Stanisław4ORCID,Radecka Barbara56ORCID,Staszewski Marek7,Majsnerowska Aleksandra1,Myrda Krzysztof1ORCID,Nowowiejska‐Wiewióra Alicja1ORCID,Skoczylas Ilona1,Rymkiewicz Igor8,Niklewski Tomasz9,Nowak Jolanta1ORCID,Przybyłowski Piotr9ORCID,Gąsior Mariusz1ORCID,Jarząb Michał10ORCID

Affiliation:

1. 3rd Department of Cardiology, School of Medical Sciences in Zabrze Medical University of Silesia Katowice Poland

2. Department of Radiation and Clinical Oncology Maria Skłodowska‐Curie National Research Institute of Oncology, Gliwice Branch Gliwice Poland

3. Department of Oncocardiology Holy Cross Cancer Centre Kielce Poland

4. Holy Cross Cancer Centre Kielce Poland

5. Department of Oncology, Institute of Medical Sciences University of Opole Opole Poland

6. Department of Clinical Oncology Tadeusz Koszarowski Cancer Centre in Opole Opole Poland

7. Tadeusz Koszarowski Cancer Centre in Opole Opole Poland

8. Silesian Centre for Heart Diseases Zabrze Poland

9. Department of Cardiac, Vascular and Endovascular Surgery and Transplantology Medical University of Silesia, Silesian Centre for Heart Diseases Zabrze Poland

10. Breast Cancer Unit Maria Skłodowska‐Curie National Research Institute of Oncology, Gliwice Branch Gliwice Poland

Abstract

AbstractAimsIn recent years, survival in patients with breast cancer has increased. Despite the improvement in outcomes of those patients, the risk of treatment‐related cardiotoxicity remains high, and its presence has been associated with a higher risk of treatment termination and thus lower therapeutic efficacy. Prior trials demonstrated that a preventive initiation of heart failure drugs, including the renin–angiotensin–aldosterone inhibitors, might reduce the risk of treatment‐related cardiotoxicity. However, to date, no study investigated the efficacy of sacubitril/valsartan, a novel antineurohormonal drug shown to be superior to the previous therapies, in the prevention of cardiotoxicity in patients with early‐stage breast cancer, which is the aim of the trial.Methods and resultsMAINSTREAM is a randomized, placebo‐controlled, double‐blind, multicentre, clinical trial. After the run‐in period, a total of 480 patients with early breast cancer undergoing treatment with anthracyclines and/or anti‐human epidermal growth factor receptor 2 drugs will be randomized to the highest tolerated dose of sacubitril/valsartan, being preferably 97/103 mg twice daily or placebo in 1:1 ratio. The patients will be monitored, including routine transthoracic echocardiography (TTE) and laboratory biomarker monitoring, for 24 months. The primary endpoint of the trial will be the occurrence of a decrease in left ventricular ejection fraction by ≥5% in TTE within 24 months. The key secondary endpoints will be the composite endpoint of death from any cause or hospitalization for heart failure, as well as other imaging, laboratory, and clinical outcomes, including the occurrence of the cancer therapy‐related cardiac dysfunction resulting in the necessity to initiate treatment. The first patients are expected to be recruited in the coming months, and the estimated completion of the study and publication of the results are expected in December 2027, pending recruitment.ConclusionsThe MAINSTREAM trial will determine the efficacy and safety of treatment with sacubitril/valsartan as a prevention of cardiotoxicity in patients with early breast cancer (ClinicalTrials.gov number: NCT05465031).

Funder

Agencja Badań Medycznych

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine

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