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. 2022 Jan 28;9:805525. doi: 10.3389/fcvm.2022.805525

Table 4.

Clinical trials evaluating personalized antiplatelet therapy based exclusively on platelet function testing.

Study Number of patients Studied population Antiplatelet therapy Platelet function test Outcome
ANTARCTIC (176) 877 Post-PCI in ACS patients (≥75 years old) ASA+prasugrel (5 mg) VerifyNowTM No improvement in clinical outcome
LTPR: ASA+clopidogrel (75 mg)
HTPR: ASA+prasugrel (10 mg)
Aradi et al. (173) 741 Post-PCI in high risk ACS patients ASA+clopidogrel (75 mg) Multiplate® Unlike high-dose clopidogrel, switching to prasugrel reduces ischemic risk in HTPR patients
HTPR: ASA+prasugrel (10 mg) or ASA+clopidogrel (150 mg or additional 600 mg LD+75 mg)
ARCTIC (179) 1,227 (control) Post-PCI in CAD/ACS patients Control: treatment choice left to physician's discretion VerifyNowTM No improvement in clinical outcome in the guided-therapy group
1,213 (guided) HTPR: ASA+prasugrel (10 mg) or ASA+clopidogrel (150 mg)
LTPR: ASA+clopidogrel (75 mg)
GRAVITAS (178) 2,214 Post-PCI in CAD/NSTE-ACS patients ASA+clopidogrel (75 mg) VerifyNowTM No reduction of the incidence of death or cardiovascular events
HTPR: ASA+clopidogrel (150 mg)
ISAR-HPR (172) 428 (control) Post-PCI in CAD/ACS patients Control: ASA+clopidogrel (75 mg) Multiplate® Significant reduction of the incidence of death from any cause in the guided-therapy group
571 (guided) Guided: ASA+clopidogrel (75 mg) vs. ASA+clopidogrel (additional 600 mg LD+75 mg) or ASA+prasugrel (10 mg) if HPR
MADONNA (171) 395 (control) Post-PCI in STEMI and NSTE-ACS patients Control: ASA+clopidogrel (75 mg) Multiplate® Reduction of the incidence of stent thrombosis and ACS in the guided-therapy group but no difference in cardiac death or bleeding
403 (guided) Guided: ASA+clopidogrel (75 mg) vs. ASA+clopidogrel (additional 600 mg LD + 75 mg) or ASA+prasugrel (60 mg LD + 10 mg) if HTPR
TRIGGER-PCI (177) 236 Post-PCI in CAD HPR patients ASA+clopidogrel (75 mg) vs. ASA+prasugrel (10 mg) VerifyNowTM Switching from clopidogrel to prasugrel afforded effective platelet inhibition.
Study stopped prematurely for futility (lower than expected incidence of adverse ischemic events)
TROPICAL-ACS (174) 1,306 (control) Post-PCI in ACS patients Control: ASA+prasugrel (10 mg) Multiplate® Non-inferiority of guided therapy in terms of cardiovascular death, myocardial infarction, stroke or bleeding complications
1,304 (guided) Guided: ASA+clopidogrel (75 mg) vs. ASA+prasugrel (10 mg) if HTPR

ACS, acute coronary syndrome; CAD, stable coronary artery disease; DES, drug-eluting stent; HTPR, high on-treatment platelet reactivity; LD, loading dose; LTPR, low on-treatment platelet reactivity; NSTE, non-ST elevation; PCI, percutaneous coronary intervention, PFT, platelet function testing; STEMI, non-ST elevation myocardial infarction.