Hamostaseologie 2012; 32(03): 177-185
DOI: 10.5482/HAMO-12-05-0003
Review
Schattauer GmbH

Antiplatelet therapy – ticagrelor

Antiplättchentherapie – Ticagrelor
E. Giannitsis
1   Department of Internal Medicine III, Cardiology, University Hospital Heidelberg, Germany
,
H. A. Katus
1   Department of Internal Medicine III, Cardiology, University Hospital Heidelberg, Germany
› Author Affiliations
Further Information

Publication History

received: 18 May 2012

accepted: 19 June 2012

Publication Date:
28 December 2017 (online)

Summary

Ticagrelor, a cyclopentyltriazolopyrimidine (CPTP), is the representative of a new chemical class of P2Y12 receptor inhibitors that differ from thienopyridines (ticlopidin, clopidogrel, prasugrel) as ticagrelor is not a prodrug requiring active biotransformation by cytochromes in the liver and thus is characterized by a more rapid, more effective and more consistent platelet inhibition than ticlopidin or clopidogrel. An extensive study program for dose finding and safety for AZD6140 (DISPERSE studies) and a large-scaled phase III trial (PLATO) were undertaken on more than 18 000 patients for validation of efficacy and safety. In the PLATO trial, patients presenting with the broad spectrum of ACS, i.e. unstable angina, non-STEMI or STEMI, were randomized to ticagrelor (Brilique, Brilinta) or clopidogrel within 24 hours after onset of symptoms, regardless whether they were allocated to a planned invasive or conservative treatment. Compared to clopidogrel, ticagrelor reduced rates of the primary endpoint consisting of cardiovascular death, non-fatal MI, or stroke, without an excess of the primary safety endpoint that was PLATO-defined major bleedings. Results from the pre-specified confirmatory subgroup of patients undergoing planned invasive treatment was consistent with PLATO main trial. In addition, the primary endpoint, as well as CV death and all cause death were consistently reduced with ticagrelor in numerous exploratory subgroups including STEMI patients, those planned for non-invasive treatment, patients undergoing CABG, patients with renal failure, and those with diabetes mellitus, although patients were pretreated before coronary angiography and patients with clopidogrel pretreatment were not excluded. Conclusions: The pharmacological properties and convincing study results of the PLATO trial have stimulated a paradigm change for dual antiplatelet therapy. The new ESC guidelines on the management of ACS without ST segment elevation recommend the use of clopidogrel only when a new antiplatelet drug, e. g. ticagrelor or prasugrel is not available or contraindicated.

Zusammenfassung

Ticagrelor ist ein neuer direkter, reversibler Thrombozytenaggregationshemmer aus der neuen chemischen Klasse der Cyclopentyltria-zolopyrimidine (CPTP). Ticagrelor führt nach oraler Einnahme zu einem schnelleren Wir-kungseintritt, einer besseren und konsistenteren Hemmung des P2Y12-Rezeptors als Clopidogrel. Die optimale Dosis und Sicherheit von Ticagrelor (AZD6140, Brilique, Brilinta) wurde in einem ausführlichen Studienprogramm getestet (DISPERSE-Studien) und abschließend in einer Phase-3-Studie an über 18 000 Patienten hinsichtlich Effektivität und Sicherheit validiert. In der PLATO Studie wurden Patienten, die innerhalb von 24 Stunden mit einem akuten Koronarsyndrom aufgenommen wurden, unabhängig von einer Vorbehandlung mit Clopidogrel und unabhängig von einem primär invasiven oder konservativem Therapieansatz, zu Ticagrelor oder Clopidogrel randomisiert. Ticagrelor zeigte eine signifikante Senkung des primären Effektivitätsendpunkts, bestehend aus kardiovaskulärem Tod, nichttödlichem Myokardinfarkt oder Schlaganfall, ohne eine Erhöhung des primären Sicherheitsendpunkts, definiert als Majorblutung nach der PLATO Blutungsdefinition. Ticagrelor reduzierte die Rate kardiovaskulärer Todesfälle sowie die Rate an Todesfällen jeglicher Ursache. Die Ergebnisse der PLATO-Hauptstudie bestätigten sich konsistent an der prä-spezifizierten konfirmatorischen Subgruppe der primär invasiv behandelten Patienten. Zahlreiche weitere explorative Subgruppenanalysen an Patienten mit STEMI, Patienten mit Diabetes mellitus, Patienten mit schwerer Niereninsuffizienz, oder primär konservativ behandelten Patienten zeigten eine konsistente Überlegenheit von Ticagrelor gegenüber Clopidogrel, obwohl in der PLATO Studie die Vorbehandlung und der Einsatz einer höheren 600-mg-Aufsättigungsdosis erlaubt war. Schlussfolgerungen: Die pharmakologischen Vorteile und überzeugenden Studienergebnisse haben zu m Paradigmenwechsel in der Behandlung des akuten Koronarsyndroms geführt. In den aktuellen ESC-Leitlinien wird der Einsatz der neuen Plättchenhemmer favorisiert, während Clopidogrel dann indiziert ist, wenn die neuen Substanzen nicht gegeben werden können.

 
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