Effects of the Endpoint Adjudication Process on the Results of a Randomised Controlled Trial: The ADVANCE Trial

被引:33
作者
Hata, Jun [1 ]
Arima, Hisatomi [1 ]
Zoungas, Sophia [1 ,2 ]
Fulcher, Greg [3 ]
Pollock, Carol [3 ]
Adams, Mark [4 ]
Watson, John [5 ]
Joshi, Rohina [1 ]
Kengne, Andre Pascal [1 ]
Ninomiya, Toshiharu [1 ]
Anderson, Craig [1 ]
Woodward, Mark [1 ]
Patel, Anushka [1 ]
Mancia, Giuseppe [6 ]
Poulter, Neil [7 ]
MacMahon, Stephen [1 ]
Chalmers, John [1 ]
Neal, Bruce [1 ]
机构
[1] Univ Sydney, George Inst Global Hlth, Sydney, NSW 2006, Australia
[2] Monash Univ, Sch Publ Hlth, Clayton, Vic, Australia
[3] Royal N Shore Hosp, Sydney, NSW, Australia
[4] Royal Prince Alfred Hosp, Sydney, NSW, Australia
[5] Univ Sydney, Sydney Med Sch, Sydney Adventist Hosp Clin Sch, Sydney, NSW 2006, Australia
[6] Univ Milano Bicocca, Milan, Italy
[7] Univ London Imperial Coll Sci Technol & Med, London, England
基金
英国医学研究理事会;
关键词
CLINICAL EVENTS COMMITTEE; MYOCARDIAL-INFARCTION; OUTCOMES; DEATH; MODE;
D O I
10.1371/journal.pone.0055807
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Endpoint adjudication committees (EPAC) are widely used in clinical trials. The aim of the present analysis is to assess the effects of the endpoint adjudication process on the main findings of the ADVANCE trial (Trial registration: ClinicalTrials.gov NCT00145925). Methods and Findings: The ADVANCE trial was a multicentre, 2x2 factorial randomised controlled trial of blood pressure lowering and intensive blood glucose control in 11140 patients with type 2 diabetes. Primary outcomes were major macrovascular (nonfatal myocardial infarction, nonfatal stroke and cardiovascular death) and microvascular (new or worsening nephropathy and retinopathy) events. Suspected primary outcomes were initially reported by the investigators at the 215 sites with subsequent adjudication by the EPAC. The EPAC also adjudicated upon potential events identified directly by ongoing screening of all reported events. Over a median follow-up of 5 years, the site investigators reported one or more primary outcomes among 2443 participants. After adjudication these events were confirmed for 2077 (85%) with 48 further events added through the EPAC-led database screening process. The estimated relative risk reductions (95% confidence intervals) in the primary outcome for the blood pressure lowering comparison were 8% (-1 to 15%) based on the investigator-reported events and 9% (0 to 17%) based on the EPAC-based events (P for homogeneity = 0.70). The corresponding findings for the glucose comparison were 8% (1 to 15%) and 10% (2% to 18%) (P for homogeneity = 0.60). The effect estimates were also highly comparable when studied separately for macrovascular events and microvascular events for both comparisons (all P for homogeneity >0.6). Conclusions: The endpoint adjudication process had no discernible impact on the main findings in ADVANCE. These data highlight the need for careful consideration of the likely impact of an EPAC on the findings and conclusions of clinical trials prior to their establishment.
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