Rebecca H Maier
Preventing cardiotoxicity in patients with breast cancer and lymphoma: protocol for a multicentre randomised controlled trial (PROACT)
Maier, Rebecca H; Plummer, Chris; Kasim, Adetayo S; Akhter, Nasima; Ogundimu, Emmanuel; Maddox, Jamie; Graham, Janine; Stewart, Michael; Wardley, Andrew; Haney, Sophie; Vahabi, Sharareh; Oxenham, Helen; Humphreys, Alison; Cresti, Nicola; Verrill, Mark; Graham, Richard; Chang, Lisa; Hancock, Helen C; Austin, David
Authors
Chris Plummer
Adetayo S Kasim
Nasima Akhter
Emmanuel Ogundimu
Jamie Maddox
Janine Graham
Michael Stewart
Andrew Wardley
Sophie Haney
Sharareh Vahabi
Helen Oxenham
Alison Humphreys
Nicola Cresti
Mark Verrill
Richard Graham
Lisa Chang
Helen C Hancock
David Austin
Abstract
Introduction: Anthracyclines are included in chemotherapy regimens to treat several different types of cancer and are extremely effective. However, it is recognised that a significant side effect is cardiotoxicity; anthracyclines can cause irreversible damage to cardiac cells and ultimately impaired cardiac function and heart failure, which may only be evident years after exposure. The PROACT trial will establish the effectiveness of the ACE inhibitor enalapril maleate (enalapril) in preventing cardiotoxicity in patients with breast cancer and non-Hodgkin’s lymphoma (NHL) receiving anthracycline-based chemotherapy. Methods and analysis: PROACT is a prospective, randomised, open-label, blinded end-point, superiority trial which will recruit adult patients being treated for breast cancer and NHL at NHS hospitals throughout England. The trial aims to recruit 106 participants, who will be randomised to standard care (high-dose anthracycline-based chemotherapy) plus enalapril (intervention) or standard care alone (control). Patients randomised to the intervention arm will receive enalapril (starting at 2.5 mg two times per day and titrating up to a maximum dose of 10 mg two times per day), commencing treatment at least 2 days prior to starting chemotherapy and finishing 3 weeks after their last anthracycline dose. The primary outcome is the presence or absence of cardiac troponin T release at any time during anthracycline treatment, and 1 month after the last dose of anthracycline. Secondary outcomes will focus on cardiac function measured using echocardiogram assessment, adherence to enalapril and side effects. Ethics and dissemination: A favourable opinion was given following research ethics committee review by West Midlands—Edgbaston REC, Ref: 17/WM/0248. Trial findings will be disseminated through engagement with patients, the oncology and cardiology communities, NHS management and commissioning groups and through peer-reviewed publication.
Citation
Maier, R. H., Plummer, C., Kasim, A. S., Akhter, N., Ogundimu, E., Maddox, J., …Austin, D. (2022). Preventing cardiotoxicity in patients with breast cancer and lymphoma: protocol for a multicentre randomised controlled trial (PROACT). BMJ Open, 12(12), Article e066252. https://doi.org/10.1136/bmjopen-2022-066252
Journal Article Type | Article |
---|---|
Acceptance Date | Nov 24, 2022 |
Online Publication Date | Dec 30, 2022 |
Publication Date | 2022-12 |
Deposit Date | Jan 6, 2023 |
Publicly Available Date | Jan 6, 2023 |
Journal | BMJ Open |
Electronic ISSN | 2044-6055 |
Publisher | BMJ Publishing Group |
Peer Reviewed | Peer Reviewed |
Volume | 12 |
Issue | 12 |
Article Number | e066252 |
DOI | https://doi.org/10.1136/bmjopen-2022-066252 |
Public URL | https://durham-repository.worktribe.com/output/1184005 |
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Copyright Statement
This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/.
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