Abstract
Aims Delcasertib is a selective inhibitor of delta-protein kinase C (delta-PKC), which reduced infarct size during ischaemia/ reperfusion in animal models and diminished myocardial necrosis and improved reperfusion in a pilot study during primary percutaneous coronary intervention (PCI) for ST elevation myocardial infarction (STEMI).
Methods and results A multicentre, double-blind trial was performed in patients presenting within 6 h and undergoing primary PCI for anterior (the primary analysis cohort, n = 1010 patients) or inferior (an exploratory cohort, capped at 166 patients) STEMI. Patients with anterior STEMI were randomized to placebo or one of three doses of delcasertib (50,150, or450 mg/h) by intravenous infusion initiated before PCI and continued for ∼2.5 h.There were no differences between treatment groups in the primary efficacy endpoint of infarct size measured by creatine kinaseMB fraction area under the curve (AUC) (median 5156, 5043, 4419, and 5253 ng h/mL in the placebo, delcasertib 50, 150, and 450 mg/mL groups, respectively) in the anterior STEMI cohort. No treatment-related differences were seen in secondary endpoints of infarct size, electrocardiographic STsegment recovery AUC or time to stable ST recovery, or left ventricular ejection fraction at 3 months. No differences in rates of adjudicated clinical endpoints (death, heart failure, or serious ventricular arrhythmias) were observed.
Conclusions Selective inhibition of delta-PKC with intravenous infusion of delcasertib during PCI for acute STEMI in a population of patients treated according to contemporary standard of care did not reduce biomarkers of myocardial injury. Clinical trial registration ClinicalTrials.gov Identifier: NCT00785954.
Original language | English |
---|---|
Pages (from-to) | 2516-2523 |
Number of pages | 8 |
Journal | European heart journal |
Volume | 35 |
Issue number | 37 |
DOIs | |
Publication status | Published or Issued - 1 Oct 2014 |
Keywords
- Myocardial
- Myocardial infarction
- Pharmacology
- Reperfusion
- Stents
- Stunning
ASJC Scopus subject areas
- Cardiology and Cardiovascular Medicine
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Inhibition of delta-protein kinase C by delcasertib as an adjunct to primary percutaneous coronary intervention for acute anterior ST-segment elevation myocardial infarction : Results of the PROTECTION AMI randomized controlled trial. / Lincoff, A. Michael; Roe, Matthew; Aylward, Philip et al.
In: European heart journal, Vol. 35, No. 37, 01.10.2014, p. 2516-2523.Research output: Contribution to journal › Article › peer-review
TY - JOUR
T1 - Inhibition of delta-protein kinase C by delcasertib as an adjunct to primary percutaneous coronary intervention for acute anterior ST-segment elevation myocardial infarction
T2 - Results of the PROTECTION AMI randomized controlled trial
AU - Lincoff, A. Michael
AU - Roe, Matthew
AU - Aylward, Philip
AU - Galla, John
AU - Rynkiewicz, Andrzej
AU - Guetta, Victor
AU - Zelizko, Michael
AU - Kleiman, Neal
AU - White, Harvey
AU - McErlean, Ellen
AU - Erlinge, David
AU - Laine, Mika
AU - Dos Santos Ferreira, Jorge Manuel
AU - Goodman, Shaun
AU - Mehta, Shamir
AU - Atar, Dan
AU - Suryapranata, Harry
AU - Jensen, Svend Eggert
AU - Forster, Tamas
AU - Fernandez-Ortiz, Antonio
AU - Schoors, Danny
AU - Radke, Peter
AU - Belli, Guido
AU - Brennan, Danielle
AU - Bell, Gregory
AU - Krucoff, Mitchell
N1 - Funding Information: 1Cleveland Clinic Coordinating Center for Clinical Research (C5Research), Cleveland, OH, USA; 2Duke Clinical Research Institute, Durham, NC, USA; 3Flinders University and Medical Centre, Adelaide, Australia; 4Department of Cardiology and Cardiosurgery, University of Warmia and Mazury, Olsztyn, Poland; 5Heart Institute, Sheba Medical Center, Tel Hashomer, Israel; 6Department of Cardiology, Institute for Clinical and Experimental Medicine, Prague, Czech Republic; 7Methodist DeBakey Heart & Vascular Center, Houston, TX, USA; 8Green Lane Cardiovascular Service, Auckland City Hospital, Auckland, New Zealand; 9Department of Cardiology, Lund University, Lund, Sweden; 10Division of Cardiology, Helsinki University Central Hospital, Helsinki, Finland; 11Department of Cardiology, Hospital Santa Cruz, Carnaxide, Portugal; 12Canadian Heart Research Centre and St. Michael’s HospitalUniversity of Toronto, Toronto, Ontario, Canada; 13Department of Cardiology, Hamilton General Hospital Hamilton, Ontario, Canada; 14Department of Cardiology B, Oslo University Hospital, Norway, and Institute of Clinical Sciences, University of Oslo, Oslo, Norway; 15Department of Cardiology, Radboud University Nijmegen Medical Center, The Netherlands; 16DepartmentofCardiology,ÅrhusUniversityHospital,Aalborg,Denmark;17MedicalFaculty,UniversityofSzegedandAlbertSzent-GyorgyiMedicalandPharmaceuticalCenter,Szeged, Hungary; 18Coronary Care Unit, Hospital Clinico San Carlos, Madrid, Spain; 19Interventional Department, Universitair Ziekenhuis Brussel, Belgium; 20Department of Cardiology, Angiology,IntensiveCareMedicine,UniversityofSchleswigHolstein,Lübeck,Germany;21UnitaOperativadiEmodinamicaeCardiologiaInvasivaIstitutioClinicoHumanitas,Milano,Italy; and 22KAI Phamaceuticals and Department of Medicine, University of California San Francisco, San Francisco, CA, USA Funding Information: PROTECTION AMI was phase II, multicentre, dose-ranging, placebo-controlled, double-blind randomized trial. Patients with anterior STEMI served as the primary cohort and were randomized to placebo or one of three doses of delcasertib. An exploratory cohort of patients with high-risk inferior STEMI was randomized to placebo or the highest dose of delcasertib. The trial was sponsored by KAI Pharmaceuticals (South San Francisco, CA, USA) and Bristol-Myers Squibb (New York, NY, USA) and was coordinated by the Cleveland Clinic Coordinating Center for Clinical Research (C5Research) (Cleveland, OH, USA). Medpace (Cincinnati, OH, USA) served as the contract research organization and provided data and site management. An independent Data and Safety Monitoring Board monitored the safety of the study and had access to unblinded data. The steering committee, consisting of academic members and non-voting representatives from the sponsoring companies, designed the trial and were responsible for its scientific conduct. The final study database was provided to C5Research, where the statistical analyses for this article were independently performed. The study chairman drafted this article, with input by all of the steering committee members, and had full access to the data.
PY - 2014/10/1
Y1 - 2014/10/1
N2 - Aims Delcasertib is a selective inhibitor of delta-protein kinase C (delta-PKC), which reduced infarct size during ischaemia/ reperfusion in animal models and diminished myocardial necrosis and improved reperfusion in a pilot study during primary percutaneous coronary intervention (PCI) for ST elevation myocardial infarction (STEMI).Methods and results A multicentre, double-blind trial was performed in patients presenting within 6 h and undergoing primary PCI for anterior (the primary analysis cohort, n = 1010 patients) or inferior (an exploratory cohort, capped at 166 patients) STEMI. Patients with anterior STEMI were randomized to placebo or one of three doses of delcasertib (50,150, or450 mg/h) by intravenous infusion initiated before PCI and continued for ∼2.5 h.There were no differences between treatment groups in the primary efficacy endpoint of infarct size measured by creatine kinaseMB fraction area under the curve (AUC) (median 5156, 5043, 4419, and 5253 ng h/mL in the placebo, delcasertib 50, 150, and 450 mg/mL groups, respectively) in the anterior STEMI cohort. No treatment-related differences were seen in secondary endpoints of infarct size, electrocardiographic STsegment recovery AUC or time to stable ST recovery, or left ventricular ejection fraction at 3 months. No differences in rates of adjudicated clinical endpoints (death, heart failure, or serious ventricular arrhythmias) were observed.Conclusions Selective inhibition of delta-PKC with intravenous infusion of delcasertib during PCI for acute STEMI in a population of patients treated according to contemporary standard of care did not reduce biomarkers of myocardial injury. Clinical trial registration ClinicalTrials.gov Identifier: NCT00785954.
AB - Aims Delcasertib is a selective inhibitor of delta-protein kinase C (delta-PKC), which reduced infarct size during ischaemia/ reperfusion in animal models and diminished myocardial necrosis and improved reperfusion in a pilot study during primary percutaneous coronary intervention (PCI) for ST elevation myocardial infarction (STEMI).Methods and results A multicentre, double-blind trial was performed in patients presenting within 6 h and undergoing primary PCI for anterior (the primary analysis cohort, n = 1010 patients) or inferior (an exploratory cohort, capped at 166 patients) STEMI. Patients with anterior STEMI were randomized to placebo or one of three doses of delcasertib (50,150, or450 mg/h) by intravenous infusion initiated before PCI and continued for ∼2.5 h.There were no differences between treatment groups in the primary efficacy endpoint of infarct size measured by creatine kinaseMB fraction area under the curve (AUC) (median 5156, 5043, 4419, and 5253 ng h/mL in the placebo, delcasertib 50, 150, and 450 mg/mL groups, respectively) in the anterior STEMI cohort. No treatment-related differences were seen in secondary endpoints of infarct size, electrocardiographic STsegment recovery AUC or time to stable ST recovery, or left ventricular ejection fraction at 3 months. No differences in rates of adjudicated clinical endpoints (death, heart failure, or serious ventricular arrhythmias) were observed.Conclusions Selective inhibition of delta-PKC with intravenous infusion of delcasertib during PCI for acute STEMI in a population of patients treated according to contemporary standard of care did not reduce biomarkers of myocardial injury. Clinical trial registration ClinicalTrials.gov Identifier: NCT00785954.
KW - Myocardial
KW - Myocardial infarction
KW - Pharmacology
KW - Reperfusion
KW - Stents
KW - Stunning
UR - http://www.scopus.com/inward/record.url?scp=84907396129&partnerID=8YFLogxK
U2 - 10.1093/eurheartj/ehu177
DO - 10.1093/eurheartj/ehu177
M3 - Article
C2 - 24796339
AN - SCOPUS:84907396129
VL - 35
SP - 2516
EP - 2523
JO - European Heart Journal
JF - European Heart Journal
SN - 0195-668X
IS - 37
ER -