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Advanced Angioplasty 2008 BCIS 23rd Jan 2008 Drug Eluting Stents overhyped, overused and overpriced? William Wijns MD, PhD Cardiovascular Center Aalst http://www.cardio-aalst.be [email protected] What did we expect from DES ? • Eliminate restenosis, at last . . . • Improve durability of the results of PCI thereby justifying expanding indications • Allow vessel healing and endothelialisation, without interfering with normal vessel biology • Avoid any systemic side effects • Be affordable . . . Expected Gradient in Clinical Outcome as a function of Lesion / Patient Complexity Clinical Failure rate [%] FIM Randomized Clinical Trials Registries Real Life 40 BMS 1 30 20 DES 2 DES 1 10 Lesion / Patient complexity Adapted from E.R. Edelman, C. Rogers, Circ. 1999; 100:896-8 Efficacy of Sirolimus- and Paclitaxel-Eluting Coronary Stents SES PES Gradient = 15.8% Gradient = 9.9% Stone GW et al, NEJM 2007;356:998-1008 Long-Term Outcomes with Drug-Eluting Stents vs Bare-Metal Stents in Sweden Lagerqvist et al, NEJM 2007;356:1009-1019 The Rotterdam experience with 100% DES use - Sequential monocentric registry - Systematic use of one DES brand - Comparison with historical* controls ► Revascularisation GRADIENT BMS vs Cypher 6.7 % at 1 year 8.3 % at 2 years BMS vs Taxus 5.0 % at 1 year * Worse patient / lesion characteristics in DES era Why did the Edelman-Rogers model not work? • • • Randomised clinical trials were designed to maximise the outcome gradient between DES and BMS, in order to provide the evidence that DES should replace BMS and be used in all cases The performance of BMS used in DES trials is perceived by many as exceedingly poor compared to their experience (EU > US) Per protocol angiography results in ± doubling of TLR rates, even after adjustement for clinically-driven TLR (“oculo-stenotic reflex”) Clinical restenosis Cumulative probability of restenosis 0,10 Less well studied BMS SCAAR UCR SWEDEN 2007 0,08 Work horse BMS 0,06 0,04 DES 0,02 0,00 0 1 2 Years after PCI 3 What did we expect from DES ? • Eliminate restenosis, at last . . . • Improve durability of the results of PCI thereby justifying expanding indications • Allow vessel healing and endothelialisation, without interfering with normal vessel biology • Avoid any systemic side effects • Be affordable . . . LAD 6 months following SES Hofma et al. Eur Heart J 2006;27:166-170 Ach response 6 m following SES Hofma et al. Eur Heart J 2006;27:166-170 After intracoronary nitrates Hofma et al. Eur Heart J 2006;27:166-170 Flow-Mediated, Endothelium-Dependent Epicardial Vasomotor Changes Pacing Protocol* Coronary Angiography min Baseline Pacing 1 2 3 4 ISDN IC Nitrates QCA reference vessel, stented vessel (proximal, distal) * Stop vasoactive drugs ≥ 24 hours Change in Vessel Diameter (% from Baseline) BMS DES A DES B n=8 n = 17 n=9 30 30 30 20 20 20 10 10 10 0 0 0 -10 -10 -10 Pacing ISDN Pacing ISDN Reference Vessel Distal segment stented vessel Pacing ISDN Change in Vessel Diameter (% from Baseline) BMS DES C DES D n=8 n=5 n = 23 30 30 30 20 20 20 10 10 10 0 0 0 -10 -10 -10 Pacing ISDN Pacing ISDN Reference Vessel Distal segment stented vessel Pacing ISDN Summary of findings • Flow-mediated vasodilation is observed 6-9 months after bare metal stenting in segments proximal and distal to the stent • Vasomotor responses to increased flow vary from vasoconstriction to vasodilatation with different DES brands while non-endothelial dependent dilation to nitrates is maintained • Some drug-polymer-device combinations exert durable “toxic” effects on the endothelium at a distance from the implant Thienopyridines for ever ? • Maintaining patients at higher risk of thrombosis on dual antiplatelet therapy (DAPT) forever has no scientific foundation yet • There is some benefit associated with the extension of DAPT from 6 months up to 1 year (Eisenstein et al. JAMA 2007;297:159-68), a practice now endorsed by FDA and by the ESC PCI Guidelines (in the absence of increased risk for bleeding) • Outcomes may improve with better patient compliance, from a better understanding and identification of non-responders and with the availability of more potent antiplatelet agents. However, at the expense of excess bleeding (Triton) • Maintaining patients on long term DAPT is disruptive of other medical and surgical practices, as readily apparent in elderly patients with multiple co-morbidities • Solving the late thrombosis issue will be mandatory because trying to mask it will not be sustainable for the long term What did we expect from DES ? • Eliminate restenosis, at last . . . • Improve durability of the results of PCI thereby justifying expanding indications • Allow vessel healing and endothelialisation, without interfering with vessel biology • Avoid any systemic side effects • Be affordable . . . Overall mortality Cardiac death Health Technology Assessment I. II. III. HTA analyses are necessarily unfavorable given the lack of mortality reduction, as opposed to drugs or other devices All HTA analyses (NICE, Ontario, Belgian KCE) indicate exceedingly high incremental costs to avoid one TLR event NNT to avoid restenosis events depend on the background risk of recurrence with BMS. Absolute risk reduction is what matters ... Drug Eluting Stents overhyped, overused and overpriced? Are these the real issues ? Drug Eluting Stents overhyped, overused and overpriced? The real challenges are … • to recover our credibiliy • to restore professional leadership • to protect our freedom to operate The SCAAR registry or the Swedish yo-yo PW Serruys, J Daemen, EuroIntervention 2007;3:297 … The impact of the NEJM on the Swedish medical practice resulted in a drop of the DES use to less than 20%,a phenomenon which has been sarcastically coined the Swedish yo-yo. It is a heavy responsability for our Swedish colleagues to assess the result of this drop in DES-use. … The SCAAR registry or the Swedish yo-yo PW Serruys, J Daemen, EuroIntervention 2007;3:297 • What about the data yo-yo ? - September 2006, Barcelona: safety concern ? - New analyses up to Stettler, 2007: no fire, neutral effect of DES on death and infarction rates up to 4 years, even in highrisk such as diabetes (!) and off label indications - September 2007, Vienna: 6-fold increase in adjusted OR for out of hospital mortality in STEMI patients treated with DES - October 2007, TCT: DES are saving lives … The SCAAR registry or the Swedish yo-yo PW Serruys, J Daemen, EuroIntervention 2007;3:297 • What about the data yo-yo ? • Why do we seem to care more about devices and technicalities than about patients ? The SCAAR registry or the Swedish yo-yo PW Serruys, J Daemen, EuroIntervention 2007;3:297 • What about the data yo-yo ? • Why do we seem to care more about devices and technicalities than about patients ? • Despite the plethora of trials and registries, essential patient-oriented questions remain unanswered. Why so few patient-oriented trials ? The SCAAR registry or the Swedish yo-yo PW Serruys, J Daemen, EuroIntervention 2007;3:297 • • • • What about the data yo-yo ? Why do we seem to care more about devices and technicalities than about patients ? Despite the plethora of trials and registries, essential patient-oriented questions remain unanswered. Why so few patient-oriented trials ? Why do we not focus on the life-saving indications of PCI that represent most of our activity ? Clinical Indications for PCI Euro Heart Survey STABLE Class I A If large ischemic area 48 % 22 % STEMI Class I A 30 % 6789 Patients across Europe NSTEMI – ACS Class I A Drug Eluting Stents overhyped, overused and overpriced? The real challenges are … • to recover our credibiliy • to restore professional leadership • to protect our freedom to operate Disclosures for W. Wijns Cardiovascular Center Aalst (B) Grants/Research: Investigator, co-PI or PI in trials for several device (Abbott, Biosensors, Biotronik, Boston Scientific, Cappella, Conor, Cordis J&J, Devax, Medtronic, Orbus Neich, Sorin, Terumo, Topspin, Volcano) and pharmaceutical (BMS, GSK, Therabel) companies All Consulting Fees, Honoraria and Research Grants go to the “Cardiovascular Research Aalst Foundation” (non profit organisation) Speaker’s Bureau: NONE Equity Interests/Stock Options/Major-Minor Stock Shareholder: NONE Royalty Income: NONE Ownership/Founder/Co-Founder: “Cardiovascular Research Aalst Foundation” co-founder of Cardio3, biotechnology start-up on Cell Therapy Which DES should be recommended ? STENT DRUG STUDY High Level of Evidence, Efficacy proven in a randomized trial with an adequate primary clinical endpoint: Cypher Sirolimus Taxus Paclitaxel Endeavor Zotarolimus SIRIUS TAXUS-IV, TAXUS-V, (TAXUS-VI) ENDEAVOR-II Medium Level of Evidence, Efficacy proven in a randomized trial with a primary surrogate endpoint: Xience-V / Promus Everolimus SPIRIT-I, -II, -III Yukon Sirolimus ISAR-Test EVALUATION PATHWAYS FOR DES 1ST GENERATION 2ND GENERATION • Preclinical • Preclinical • FIM • FIM • (Dose-response & kinetics) • (Dose-response & kinetics) • Pivotal RCT • Pivotal RCT Superiority vs BMS Non inferiority vs 1st DES Powered for combined clinical / angio endpoint Powered for angiographic efficacy endpoints • (Lesion / patient subsets) • (Lesion / patient subsets) • Real life registry • Real life registry All-cause survival On- vs. Off-label BMS/DES use 100 Overall survival, (%) 95 93.3% 92.3% 90 85 84.8% 84.6% Log rank p-values On-label use DES vs. BMS: 0.71 80 Off-label use DES vs. BMS: 0.69 75 70 0 On-label DES use On-label BMS use Off-label DES use Off-label BMS use 365 730 Days 1095 1460 Target Lesion Revascularization Non-Diabetic Patients BMS BMS PES PES SES SES SES vs BMS: 0.31 (0.21,0.41) PES vs BMS: 0.42 (0.25,0.54) SES vs PES: 0.74 (0.51,1.19) SES vs BMS: 0.29 (0.21,0.38) PES vs BMS: 0.47 (0.34,0.61) SES vs PES: 0.62 (0.46,0.83) 0 5 10 15 20 25 30 Diabetic Patients 0 BMS 1228 PES 1161 SES 1373 1 2 Years 3 4 0 1 1228 1161 1373 667 942 947 451 486 606 348 146 219 3384 3466 3505 3384 3466 3505 2 Years 2128 2776 2614 3 4 1420 1477 1512 1195 660 753 Target lesion revascularisation Myocardial infarction Death or myocardial infarction Definite stent thrombosis Advantages of Atrial Pacing as a means to induce flowmediated vasomotor changes • Mimics physiological changes that occur during exercise or tachycardia • Technically easier to obtain and to analyze than coronary angiography during physical exercise • Reference segment available in all cases and obtained with the same, simultaneously applied stimulus • Dilation is the unequivocal normal response • Patients in whom the reference segment does not dilate have a diffuse endothelial disorder and should be excluded • No need for “baseline” measurements prior to stent implantation