TY - JOUR
T1 - Clinical endpoint adjudication in a contemporary all-comers coronary stent investigation
T2 - Methodology and external validation
AU - Vranckx, Pascal
AU - McFadden, Eugene
AU - Cutlip, Donald E.
AU - Mehran, Roxana
AU - Swart, Michael
AU - Kint, P. P.
AU - Zijlstra, Felix
AU - Silber, Sigmund
AU - Windecker, Stephan
AU - Serruys, Patrick W.C.J.
PY - 2013/1
Y1 - 2013/1
N2 - Background: Globalisation in coronary stent research calls for harmonization of clinical endpoint definitions and event adjudication. Little has been published about the various processes used for event adjudication or their impact on outcome reporting. Methods and results: We performed a validation of the clinical event committee (CEC) adjudication process on 100 suspected events in the RESOLUTE All-comers trial (Resolute-AC). Two experienced Clinical Research Organisations (CRO) that had already extensive internal validation processes in place, participated in the study. After initial adjudication by the primary-CEC, events were cross-adjudicated by an external-CEC using the same definitions. Major discrepancies affecting the primary end point of target-lesion failure (TLF), a composite of cardiac death, target vessel myocardial infarction (TV-MI), or clinically-indicated target-lesion revascularization (CI-TLR), were analysed by an independent oversight committee who provided recommendations for harmonization. Discordant adjudications were reconsidered by the primary CEC. Subsequently, the RAC database was interrogated for cases that based on these recommendations merited re-adjudication and these cases were also re-adjudicated by the primary CEC.Final discrepancies in adjudication of individual components of TLF occurred in 7 out of 100 events in 5 patients. Discrepancies for the (hierarchical) primary endpoint occurred in 5 events (2 cardiac deaths and 3 TV-MI). After application of harmonization recommendations to the overall RAC population (n. =. 2292), the primary CEC adjudicated 3 additional clinical-TLRs and considered 1 TV-MI as no event. Conclusions: A harmonization process provided a high level of concordance for event adjudication and improved accuracy for final event reporting. These findings suggest it is feasible to pool clinical event outcome data across clinical trials even when different CECs are responsible for event adjudication.
AB - Background: Globalisation in coronary stent research calls for harmonization of clinical endpoint definitions and event adjudication. Little has been published about the various processes used for event adjudication or their impact on outcome reporting. Methods and results: We performed a validation of the clinical event committee (CEC) adjudication process on 100 suspected events in the RESOLUTE All-comers trial (Resolute-AC). Two experienced Clinical Research Organisations (CRO) that had already extensive internal validation processes in place, participated in the study. After initial adjudication by the primary-CEC, events were cross-adjudicated by an external-CEC using the same definitions. Major discrepancies affecting the primary end point of target-lesion failure (TLF), a composite of cardiac death, target vessel myocardial infarction (TV-MI), or clinically-indicated target-lesion revascularization (CI-TLR), were analysed by an independent oversight committee who provided recommendations for harmonization. Discordant adjudications were reconsidered by the primary CEC. Subsequently, the RAC database was interrogated for cases that based on these recommendations merited re-adjudication and these cases were also re-adjudicated by the primary CEC.Final discrepancies in adjudication of individual components of TLF occurred in 7 out of 100 events in 5 patients. Discrepancies for the (hierarchical) primary endpoint occurred in 5 events (2 cardiac deaths and 3 TV-MI). After application of harmonization recommendations to the overall RAC population (n. =. 2292), the primary CEC adjudicated 3 additional clinical-TLRs and considered 1 TV-MI as no event. Conclusions: A harmonization process provided a high level of concordance for event adjudication and improved accuracy for final event reporting. These findings suggest it is feasible to pool clinical event outcome data across clinical trials even when different CECs are responsible for event adjudication.
KW - Adjudication
KW - Clinical event committee
KW - Endpoints
KW - PTCA
KW - Stenting
KW - Validation
UR - http://www.scopus.com/inward/record.url?scp=84870508383&partnerID=8YFLogxK
U2 - 10.1016/j.cct.2012.08.012
DO - 10.1016/j.cct.2012.08.012
M3 - Article
C2 - 22975439
AN - SCOPUS:84870508383
VL - 34
SP - 53
EP - 59
JO - Contemporary Clinical Trials
JF - Contemporary Clinical Trials
SN - 1551-7144
IS - 1
ER -