Adjusted indirect comparison of intracoronary drug-eluting stents: evidence from a metaanalysis of randomized bare-metal-stent-controlled trials

Int J Cardiol. 2005 Apr 8;100(1):119-23. doi: 10.1016/j.ijcard.2004.11.001.

Abstract

Aims: Drug-eluting stents (DES) have been recently investigated, with favorable data for many devices, but comparative data are lacking. We thus performed an adjusted indirect comparison metaanalysis of DES.

Methods: Randomized trials comparing DES vs. bare-metal stents (BMS) were systematically searched, and random effect odds ratios (OR) were computed for target lesion revascularization (TLR) and binary in-stent restenosis rate (BRR) at 6-12 months. We then generated interaction OR for the comparison of different DES.

Results: We pooled data from 17 studies (allocating 3048 patients to BMS and 3392 to nine different DES). Indirect head-to-head comparison of sirolimus-eluting Cypher (N=1007) vs. polymeric paclitaxel-eluting Taxus (N=959) showed nonsignificant differences in TLR [OR=0.8 (0.5-1.4), p=0.45] but significant reductions in BRR favoring Cypher [OR=0.3 (0.1-0.6), p<0.001]. Everolimus-eluting stents appeared noninferior to Cypher or Taxus (p>0.50 for both TLR and BRR). Actinomycin-, mycophenolate-, and apolymeric paclitaxel-eluting stents (PES) all proved significantly worse than Cypher or Taxus for TLR or BRR.

Conclusion: Notwithstanding its inherent limitations, the present metaanalysis confirms the effectiveness of both Cypher and Taxus, supports the promising role of everolimus-eluting stents, and suggests the significant inferiority of most other devices. These post hoc findings, albeit intriguing, await prospective confirmation.

Publication types

  • Comparative Study
  • Meta-Analysis

MeSH terms

  • Coronary Disease / therapy*
  • Everolimus
  • Humans
  • Immunosuppressive Agents / administration & dosage*
  • Odds Ratio
  • Paclitaxel / administration & dosage
  • Prosthesis Design
  • Randomized Controlled Trials as Topic
  • Sirolimus / administration & dosage
  • Sirolimus / analogs & derivatives
  • Stents*

Substances

  • Immunosuppressive Agents
  • Everolimus
  • Paclitaxel
  • Sirolimus