Use of Rosiglitazone in the BARI 2D Trial David Gordon, M.D., Ph.D. Division of Cardiovascular Diseases National Heart, Lung, and Blood Institute Executive.

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Use of Rosiglitazone in the BARI 2D Trial David Gordon, M.D., Ph.D. Division of Cardiovascular Diseases National Heart, Lung, and Blood Institute Executive Secretary and ex-Project Officer, BARI 2D DSMB

BARI 2D Trial PI: Sheryl Kelsey, University of Pittsburgh Study Chair: Robert Frye, Mayo Clinic Study Co-Chair: Saul Genuth, Case Western Reserve Support: –NHLBI –NIDDK –GlaxoSmithKline –Many in-kind contributors

BARI 2D Trial Bypass Angioplasty Revascularization Investigations 2 - Diabetes Multi-center 2x2 factorial RCT –Elective Revascularization + Medical Rx versus Medical Rx only –Insulin Sensitization versus Insulin Provision 2368 patients with type 2 diabetes and stable CAD (high risk) 5 years mean follow-up HbA1c goal < 7.0% End Points: –Primary: All-cause mortality (300 expected) –Secondary: All-cause mortality + nonfatal MI and stroke

Glycemia Management Strategy Drugs Used in BARI 2D at Year 1 Drug ClassISIP TZD (mainly rosiglitazone)69%3% Metformin79%7% Sulfonylureas14%57% Insulin24%53%

Glycemia Management Strategy Risk Factor Control in BARI 2D at Year 1 HbA1c: 7.1% LDL-C: 83 mg/dL (93% on statins) TG: 151 mg/dL BP: 127/72 mm Hg Current Smokers: 10.1% BMI: 32 kg/m/m

BARI 2D DSMB Appointed by and advisory to Director NHLBI –NHLBI-appointed Executive Secretary (separate from project officer) Meets at least twice per year Monitors –Safety of participants –Integrity of data collection –Evidence for differential efficacy From trial – O’Brien-Fleming stopping rule (annual “looks”) From external data –Futility – No formal stopping rule

BARI 2D DSMB Expertise Cardiology Diabetes Cardiothoracic Surgery Biostatistics Clinical Trials Bioethics

Rosigliazone - Past DSMB Recommendations (1) January : Ad hoc conference call to review preliminary GSK trial data analysis (provided unsolicited to Executive Secretary) –Letter to BARI 2D investigators alerting them to HF risk of rosiglitazone (even without insulin) –Improve monitoring for HF in BARI 2D –Additional analyses of existing BARI 2D data March 24, 2006: Regularly scheduled DSMB meeting –Disclosure statement of HF risk of rosiglitazone to be presented to and signed by participants at their next BARI 2D visit

Rosigliazone - Past DSMB Recommendations (2) October 23, 2006: Regularly scheduled DSMB conference call –Encourage BARI 2D patients should to have an ophthalmologic examination (with dilation) yearly. –Add a question to data form to ascertain whether macular edema was identified. January 29, 2007: Ad hoc conference call to discuss ADOPT fracture data –Additional prospective and retrospective data collection on fractures in BARI 2D

BARI 2D DSMB Review IS versus IP (intention-to-treat) Does being on rosiglitazone at Year 1 predict CV events, death? (Cox model) Does recent rosiglitazone use predict CV events, death? (time-dependent Cox model) –Control for baseline CV risk factor levels –Control for baseline insulin use –Control for use of other diabetes drugs during trial –Control for HbA1c, CV risk factor levels during trial

Expanded Meta-Analysis CV Death CV DeathNEvents Odds Ratio 95% CI Nissen-Wolski to2.82 RECORD to1.24 Total to1.53 BARI 2D * * Expected by the end of the BARI 2D trial, based on BARI 1 experience. Approximately 60% of follow-up completed as of 12/31/06.

Expanded Meta-Analysis Myocardial Infarction MINEvents Odds Ratio 95% CI Nissen-Wolski to2.11 RECORD to1.88 Total to1.83 BARI 2D * * Expected by the end of the BARI 2D trial.* Expected by the end of the BARI 2D trial, based on the BARI 1 experience. Approximately 60% of follow-up completed as of 12/31/06.

DSMB Statement (1) The members of the BARI 2D Data and Safety Monitoring Board (DSMB), who have extensive expertise in patient care, safety, and ethics, met on May 30, 2007, to review the safety information from the trial. The Board thoroughly reviewed the recently published data on heart attacks and deaths in patients receiving rosiglitazone (Avandia®).

DSMB Statement (2) In the research setting of BARI 2D, the Board made no observations that would justify a recommendation to terminate treatment with rosiglitazone. The Board was very satisfied with the coordinated care of BARI 2D patients. The trial participants are strongly encouraged to adhere to their recommended treatments for diabetes, hypertension, and dyslipidemia. The Board is not in a position to comment on the use of rosiglitazone in routine clinical practice.

BARI 2D and ACCORD Trials NHLBI Public Statement (6/15/07) NHLBI Statement on Use of Rosiglitazone in Two NHLBI- Funded Clinical Trials Questions and Answers: Use of Rosiglitazone (Avandia) in the National Heart, Lung, and Blood Institute's Bypass Angioplasty Revascularization Investigation 2 Diabetes (BARI 2D) and Action to Control Cardiovascular Risk in Diabetes (ACCORD) Trials