Suggested objective performance goals and clinical trial design for evaluating catheter-based treatment of critical limb ischemia

被引:332
作者
Conte, Michael S. [1 ]
Geraghty, Patrick J. [2 ]
Bradbury, Andrew W. [3 ]
Hevelone, Nathanael D.
Lipsitz, Stuart R. [4 ]
Moneta, Gregory L. [5 ]
Nehler, Mark R. [6 ]
Powell, Richard J. [7 ]
Sidawy, Anton N. [8 ]
机构
[1] Univ Calif San Francisco, Div Vasc & Endovasc Surg, San Francisco, CA 94143 USA
[2] Washington Univ, Sch Med, Dept Surg, St Louis, MO 63130 USA
[3] Univ Birmingham, Dept Vasc Surg, Heart England NHS Trust, Birmingham B15 2TT, W Midlands, England
[4] Brigham & Womens Hosp, Div Surg, Boston, MA 02115 USA
[5] Oregon Hlth & Sci Univ, Dept Surg, Div Vasc Surg, Portland, OR 97201 USA
[6] Univ Colorado Denver, Div Vasc Surg, Denver, CO USA
[7] Dartmouth Med Sch, Dept Surg Vasc Surg, Dartmouth, NS, Canada
[8] Washington VA Med Ctr, Dept Surg, Washington, DC USA
关键词
VEIN GRAFT FAILURE; DISTAL EMBOLIZATION; PARENTERAL THERAPY; FDA PERSPECTIVE; LIPO-ECRAPROST; ANGIOPLASTY; MULTICENTER; STANDARDS; BYPASS; ANALOG;
D O I
10.1016/j.jvs.2009.09.044
中图分类号
R61 [外科手术学];
学科分类号
摘要
Objective: To develop a set of suggested objective performance goals (OPG) for evaluating new catheter-based treatments in critical limb ischemia (CLI), based on evidence from historical controls. Methods: Randomized, controlled trials of surgical, endovascular, and pharmacologic/biologic treatments for CLI were reviewed according to specified criteria regarding study population and data quality. Line-item data were obtained for selected studies from the sponsor/funding agency. A set of specific outcome measures was defined in accordance with the treatment goals for the CLI population. Risk factors were examined for their influence on key endpoints, and models of stratification based on specific clinical and anatomic variables developed. Sample size estimates were made for single-arm trial designs based on comparison to the suggested OPG. Results: Bypass with autogenous vein was considered the established standard, and data compiled from three individual randomized, controlled trials (N = 838) was analyzed. The primary efficacy endpoint was defined as perioperative (30-day) death or any major adverse limb event (amputation or major reintervention) occurring within one year. Results of open surgery controls demonstrated freedom from the primary endpoint in 76.9% (95% confidence interval [CI] 74.0%-79.9%) of patients at one year, with amputation-free survival (AFS) of 76.5% (95% CI 73.7%-79.5). An additional 3% non-inferiority margin was suggested in generating OPG for catheter-based therapies. Defined clinical (age > 80 years and tissue loss) and anatomic (infra-popliteal anatomy or lack of good quality saphenous vein) risk subgroups provided significantly different point estimates and OPG threshold values. Conclusion;: For new catheter-based therapies in CLI, OPGs offer a feasible approach for pre-market evaluation using non-randomized trial designs. Such studies should incorporate risk stratification in design and reporting as the CLI population is heterogeneous with respect to baseline variables and expected outcomes. Guidelines for CLI trial design to address consistency in study cohorts, methods of assessment, and endpoint definitions are provided. (J Vase Surg 2009;50:1462-73.)
引用
收藏
页码:1462 / 1473
页数:12
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