TY - JOUR
T1 - Assessing the Impact of Colchicine on Coronary Plaque Phenotype After Myocardial Infarction with Optical Coherence Tomography
T2 - Rationale and Design of the COCOMO-ACS Study
AU - Montarello, Nicholas J.
AU - Singh, Kuljit
AU - Sinhal, Ajay
AU - Wong, Dennis T.L.
AU - Alcock, Richard
AU - Rajendran, Sharmalar
AU - Dautov, Rustem
AU - Barlis, Peter
AU - Patel, Sanjay
AU - Nidorf, Stefan M.
AU - Thompson, Peter L.
AU - Salagaras, Thalia
AU - Butters, Julie
AU - Nerlekar, Nitesh
AU - Di Giovanni, Giuseppe
AU - Ottaway, Juanita L.
AU - Nicholls, Stephen J.
AU - Psaltis, Peter J.
N1 - Funding Information:
This is an investigator-initiated study with funding provided by project grants from the National Health and Medical Research Council of Australia (NHMRC ID 1127159), National Heart Foundation of Australia (NHF Vanguard Grant ID 10137) and the Sylvia and Charles Viertel Charitable Foundation (VIERCI 2017016). The study protocol was developed by an academic group led by P.J.P., who will oversee the operational conduct of the study together with SAHMRI Clinical Research. D.T.L.W. receives a Level 1 Future Leader Fellowship from the National Heart Foundation of Australia (FLF 102535). S.J.N. receives a Principal Research Fellowship from the NHMRC (ID 1111630). P.J.P. receives a Level 2 Future Leader Fellowship from the National Heart Foundation of Australia (FLF 102056) and Level 2 Career Development Fellowship from the NHMRC (CDF 1161506).
Funding Information:
K.S. has received research support and consultant fees from Abbott Vascular and Bayer. A.S. has received consultant fees and speaker honoraria from Edwards Lifesciences, Medtronic, Boston Scientific, AstraZeneca and Abbott Vascular. D.T.L.W. has received speaker honoraria from AstraZeneca, Pfizer, Bayer and Boehringer Ingelheim. P.L.T. has received research grants or honoraria from Amarin, Amgen, Aspen, AstraZeneca, Boehringer Ingelheim, Bristol-Myers Squibb, DalCor, Merck and Pfizer. S.J.N. has received research support from AstraZeneca, Amgen, Anthera, Eli Lilly, Esperion, Novartis, Cerenis, The Medicines Company, Resverlogix, InfraReDx, Roche, Sanofi-Regeneron and Liposcience and is a consultant for AstraZeneca, Akcea, Eli Lilly, Anthera, Kowa, Omthera, Merck, Takeda, Resverlogix, Sanofi-Regeneron, CSL Behring, Esperion and Boehringer Ingelheim. P.J.P. has received research support from Abbott Vascular, consulting fees from Amgen and Esperion and speaker honoraria from AstraZeneca, Bayer, Boehringer Ingelheim, Merck Schering-Plough and Pfizer.
Publisher Copyright:
© 2021, Springer Science+Business Media, LLC, part of Springer Nature.
Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.
PY - 2022/12
Y1 - 2022/12
N2 - Introduction: Recurrent event rates after myocardial infarction (MI) remain unacceptably high, in part because of the continued growth and destabilization of residual coronary atherosclerotic plaques, which may occur despite lipid-lowering therapy. Inflammation is an important contributor to this ongoing risk. Recent studies have shown that the broad-acting anti-inflammatory agent, colchicine, may reduce adverse cardiovascular events in patients post-MI, although the mechanistic basis for this remains unclear. Advances in endovascular arterial wall imaging have allowed detailed characterization of the burden and compositional phenotype of coronary plaque, along with its natural history and responsiveness to treatment. One such example has been the use of optical coherence tomography (OCT) to demonstrate the plaque-stabilizing effects of statins on both fibrous cap thickness and the size of lipid pools within plaque. Methods: The Phase 2, multi-centre, double-blind colchicine for coronary plaque modification in acute coronary syndrome (COCOMO-ACS) study will evaluate the effect of colchicine 0.5 mg daily on coronary plaque features using serial OCT imaging in patients following MI. Recruitment for the trial has been completed with 64 participants with non-ST elevation MI randomized 1:1 to colchicine or placebo in addition to guideline recommended therapies, including high-intensity statins. The primary endpoint is the effect of colchicine on the minimal fibrous cap thickness of non-culprit plaque over an 18-month period. Summary: The COCOMO-ACS study will determine whether addition of colchicine 0.5 mg daily to standard post-MI treatment has incremental benefits on high-risk features of coronary artery plaques. If confirmed, this will provide new mechanistic insights into how colchicine may confer clinical benefits in patients with atherosclerotic cardiovascular disease. Trial Registration: ANZCTR trial registration number: ACTRN12618000809235. Date of trial registration: 11th of May 2018.
AB - Introduction: Recurrent event rates after myocardial infarction (MI) remain unacceptably high, in part because of the continued growth and destabilization of residual coronary atherosclerotic plaques, which may occur despite lipid-lowering therapy. Inflammation is an important contributor to this ongoing risk. Recent studies have shown that the broad-acting anti-inflammatory agent, colchicine, may reduce adverse cardiovascular events in patients post-MI, although the mechanistic basis for this remains unclear. Advances in endovascular arterial wall imaging have allowed detailed characterization of the burden and compositional phenotype of coronary plaque, along with its natural history and responsiveness to treatment. One such example has been the use of optical coherence tomography (OCT) to demonstrate the plaque-stabilizing effects of statins on both fibrous cap thickness and the size of lipid pools within plaque. Methods: The Phase 2, multi-centre, double-blind colchicine for coronary plaque modification in acute coronary syndrome (COCOMO-ACS) study will evaluate the effect of colchicine 0.5 mg daily on coronary plaque features using serial OCT imaging in patients following MI. Recruitment for the trial has been completed with 64 participants with non-ST elevation MI randomized 1:1 to colchicine or placebo in addition to guideline recommended therapies, including high-intensity statins. The primary endpoint is the effect of colchicine on the minimal fibrous cap thickness of non-culprit plaque over an 18-month period. Summary: The COCOMO-ACS study will determine whether addition of colchicine 0.5 mg daily to standard post-MI treatment has incremental benefits on high-risk features of coronary artery plaques. If confirmed, this will provide new mechanistic insights into how colchicine may confer clinical benefits in patients with atherosclerotic cardiovascular disease. Trial Registration: ANZCTR trial registration number: ACTRN12618000809235. Date of trial registration: 11th of May 2018.
KW - Colchicine
KW - Coronary plaque
KW - Fibrous cap
KW - Inflammation
KW - Optical coherence tomography
UR - http://www.scopus.com/inward/record.url?scp=85113462414&partnerID=8YFLogxK
U2 - 10.1007/s10557-021-07240-9
DO - 10.1007/s10557-021-07240-9
M3 - Article
C2 - 34432196
AN - SCOPUS:85113462414
SN - 0920-3206
VL - 36
SP - 1175
EP - 1186
JO - Cardiovascular Drugs and Therapy
JF - Cardiovascular Drugs and Therapy
IS - 6
ER -