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
Language English Country Great Britain, England Media print-electronic
Document type Clinical Trial, Phase II, Journal Article, Multicenter Study, Randomized Controlled Trial, Research Support, Non-U.S. Gov't
PubMed
24796339
DOI
10.1093/eurheartj/ehu177
PII: ehu177
Knihovny.cz E-resources
- Keywords
- Myocardial, Myocardial infarction, Pharmacology, Reperfusion, Stents, Stunning,
- MeSH
- Chemotherapy, Adjuvant MeSH
- Biomarkers metabolism MeSH
- Double-Blind Method MeSH
- Myocardial Infarction therapy MeSH
- Protein Kinase Inhibitors administration & dosage MeSH
- Infusions, Intravenous MeSH
- Percutaneous Coronary Intervention methods MeSH
- Creatine Kinase, MB Form metabolism MeSH
- Middle Aged MeSH
- Humans MeSH
- Peptides administration & dosage MeSH
- Pilot Projects MeSH
- Area Under Curve MeSH
- Drug Administration Schedule MeSH
- Aged MeSH
- Troponin I metabolism MeSH
- Treatment Outcome MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Clinical Trial, Phase II MeSH
- Multicenter Study MeSH
- Research Support, Non-U.S. Gov't MeSH
- Randomized Controlled Trial MeSH
- Names of Substances
- Biomarkers MeSH
- Protein Kinase Inhibitors MeSH
- KAI 9803 MeSH Browser
- Creatine Kinase, MB Form MeSH
- Peptides MeSH
- Troponin I MeSH
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, or 450 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 kinase MB 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 ST-segment 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.
Canadian Heart Research Centre and St Michael's HospitalUniversity of Toronto Toronto Ontario Canada
Cleveland Clinic Coordinating Center for Clinical Research Cleveland OH USA
Coronary Care Unit Hospital Clinico San Carlos Madrid Spain
Department of Cardiology and Cardiosurgery University of Warmia and Mazury Olsztyn Poland
Department of Cardiology Århus University Hospital Aalborg Denmark
Department of Cardiology Hamilton General Hospital Hamilton Ontario Canada
Department of Cardiology Hospital Santa Cruz Carnaxide Portugal
Department of Cardiology Institute for Clinical and Experimental Medicine Prague Czech Republic
Department of Cardiology Lund University Lund Sweden
Department of Cardiology Radboud University Nijmegen Medical Center The Netherlands
Division of Cardiology Helsinki University Central Hospital Helsinki Finland
Duke Clinical Research Institute Durham NC USA
Flinders University and Medical Centre Adelaide Australia
Green Lane Cardiovascular Service Auckland City Hospital Auckland New Zealand
Heart Institute Sheba Medical Center Tel Hashomer Israel
Interventional Department Universitair Ziekenhuis Brussel Belgium
Methodist DeBakey Heart and Vascular Center Houston TX USA
Unita Operativa di Emodinamica e Cardiologia Invasiva Istitutio Clinico Humanitas Milano Italy
References provided by Crossref.org
Adjuvant cardioprotection in cardiac surgery: update
ClinicalTrials.gov
NCT00785954