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The Paclitaxel-Eluting PTCA-Balloon Catheter in Coronary Artery Disease PEPCAD II-ISR Martin Unverdorben Rotenburg/Fulda, Germany and Richmond, VA, USA Clinical Research Institute, Center for Cardiovascular Diseases On behalf of the PEPCAD II Investigators M.Unverdorben; ACC March 2008 Presenter Disclosure Information PEPCAD II 12-Month Follow-up The following relationships exist related to this presentation: M.Unverdorben Nothing to disclose B.Scheller Consulting and lecture fees from BBraun, co-patent owner of Sequent® Please M.Unverdorben; ACC March 2008 Agenda The PACCOCATH technology PEPCAD II ISR 6-month angiographic and clinical follow-up PEPCAD II ISR 12-month clinical follow-up Statistics Descriptive statistics: Mean ± SD Inferential statistics: Student’s t-test, Fisher’s exact test, Logrank test Level of significance: p < 0.05 M.Unverdorben; ACC March 2008 DES vs. DEB (PACCOCATH) DES DEB Scheller Heart 2007, 93: 539-41 Slow and continuous drug release from stent struts ~100 - 200 µg Paclitaxel ex vivo perfusion of calf carotid Sirolimus arteries,transmural distribution Polymers with associated reactions Hwang, Circulation 2001; 104: 600-5 Implies stent deployment Instant and short term drug release from balloon ~ 300 - 600 µg Paclitaxel No polymers Stenting optional Creel, Circ Res 2000; 86: 879-884 M.Unverdorben; ACC March 2008 The Matrix Coating PACCOCATH technology creates a unique matrix coating pure paclitaxel without paclitaxel + hydrophilic spacer with PACCOCATH technology huge contact surface between lipophilic drug and the vessel wall high bioavailability of paclitaxel at the target site for rapid drug absorption by the vessel wall uniform/complete application of the drug after 1st balloon expansion M.Unverdorben; ACC March 2008 SeQuent® (uncoated balloon) SeQuent® Please* (coated balloon) *SeQuent® Please (B.Braun Vascular Systems, Berlin, Germany) is manufactured based on the PACCOCATH technology with 3µg paclitaxel/mm²; CE mark filed in the EU M.Unverdorben; ACC March 2008 Objective Safety and efficacy of the Sequent® Please DEB in the treatment of ISR in native coronary arteries (reference Ø: 2.5mm, 3.5mm; lesion length: ≤22mm) for procedural success and preservation of vessel patency in comparison to the Taxus® DES Study Design Prospective, randomized, multi-center, two-arm phase-II pilot study conducted in Germany M.Unverdorben; ACC March 2008 Primary Variable 6-month late lumen loss Secondary Variables Procedural success (≤30%) 6-month binary restenosis rate 6-month MACE MACE at 1 and 3 years M.Unverdorben; ACC March 2008 Inclusion Criteria Stable or unstable angina (no MI) ISR in native coronary arteries Medication ASS ≥ 100 mg daily Clopidogrel 75 mg daily –3 months DEB –6 months DES M.Unverdorben; ACC March 2008 Patients (ITT: N=131) DEB (N=66) Age [years] 64.6±9.7 Male 48 (72.7%) BMI [kg/m2] 27.9 ± 4.6 Serum cholesterol [mg/dl] 172 ± 42 Serum LDL [mg/dl] 93 ± 39 Diabetes mellitus 22 (33.3%) Current/ex-smokers 44 (66.7%) Hypertension 53 (80.3%) Family history of CAD 21 (31.8%) Previous MI 37 (56.1%) PAVD 9 (13.6%) Serum crea [mg/dL] 1.1 ± 1 M.Unverdorben; ACC March 2008 DES (N=65) 65.1±8.7 50 (76.9%) 28.6±4.2 180 ± 34 98 ± 29 17 (26.2%) 36 (55.4%) 54 (83.1%) 22 (33.8%) 28 (43.1%) 7 (10.8%) 1.0 ± 0.2 p 0.7 0.7 0.4 0.3 0.4 0.4 0.3 0.8 0.9 0.2 0.8 0.4 Baseline Angiography (ITT: N=131) DEB (N=66) DES (N=65) 1-vessel disease [%] 28.8 35.4 2-vessel disease [%] 40.9 35.4 3-vessel disease [%] 30.3 29.2 Stenosis length [mm] 15.7 6.6 15.4 6.6 Mehran I 31 (47.0%) 25 (38.5%) Mehran II 20 (30.3%) 26 (40.0%) Mehran III 14 (21.2%) 12 (18.5%) Mehran IV MLD pre PCI [mm] Stenosis pre PCI [%] MLD post PCI [mm] Stenosis post PCI [%] 1 ( 1.5%) p 0.7 0.8 0.7 2 ( 3.1%) 0.74 0.27 0.77 0.30 0.6 74 9 73 9 0.5 2.30 0.40 2.56 0.41 <0.0001 20 10 11 8 <0.001 M.Unverdorben; ACC March 2008 Outcome (ITT: N=131) DEB (N=66) DES (N=65) p 6.2 ± 0.9 6.2 ± 0.9 1 Follow-up: clinical [N] 64 (97.0%) 65 (100%) 0.5 Follow-up: angiographic [N] 57 (86.4%) 59 (90.8%) 0.6 Late lumen loss [mm] 0.20 ± 0.45 0.45 ± 0.68 0.02 Binary restenosis in segment 4/57 (7.0%) 12/59(20.3%) 0.06 TLR 4/64 (6.3%) 10/65 (15.4%) 0.1 Myocardial infarction 0/64 (0.0%) f1/65 Follow-up: clinical [months] Death Total MACE *2/64 (3.1%) 5/64 (7.8%) (w/o noncardiac death) *1 each: non-cardiac & cardiac but not lesion related ** non-cardiac death M.Unverdorben; ACC March 2008 (1.5%) 1 **1/65 (1.5%) 1 11/65 (16.9%) fNSTEMI 0.2 due to side branch occlusion As-Treated Randomization N=131 Sequent Please n=66 Taxus n=65 4 protocol violators Lesion too long (41.1mm) Multilesion PCI in metal jacket Significant flap after PCI Severe renal failure 66 DEB 4 crossing failure treat/w Sequent Please 56 DEB only 6 DEB + BMS 4 DEB (cross-over) M.Unverdorben; ACC March 2008 1 crossing failure treat/w convent balloon 60 DES 2 with additional DES Outcome (AsT: N=126) DEB (N=66) DES (N=60) P= Follow-up: clinical [months] 6.2 ± 0.8 6.2 ± 0.8 0.7 Follow-up: clinical [N] 64 (97.0%) 60 (100%) 0.4 Follow-up: angiographic [N] 58 (87.9%) 54 (90.0%) 0.8 Late lumen loss [mm] 0.19 ± 0.38 0.47 ± 0.71 0.03 Binary restenosis in segment 2/58 (3.4%) 11/54 (20.4%) 0.007 TLR 2/64 (3.1%) 10/60 (16.7%) 0.02 Myocardial infarction 0/64 (0.0%) Death Total MACE *2/64 (3.1%) (w/o noncardiac death) 3/64 (4.7%) *1 cardiac, not lesion related 2 non cardiac ** non-cardiac death M.Unverdorben; ACC March f1/60 (1.7%) 1 **1/60 (1.7%) 1 11/60 (18.3%) fNSTEMI 2008 occlusion 0.02 due to side branch Event Free Survival (ITT/As-Treated) 100 Subjects [%] 95 90 *p=0.2 ITT 85 80 75 70 0 DES/ITT DEB/ITT DES/AsT DEB/AsT 2 4 *p=0.03 As-Treated 6 Months post PCI M.Unverdorben; ACC March 2008 8 *Logrank test 10 12-Month Follow-up: As-Treated 66 DEB 56 DEB only 6 DEB + BMS 4 DEB (cross-over) Unknown today 1/66 (1.5%) Lost to FU 0/60 (0%) Deaths 2/66 (3.0%) 60 DES 2 with additional DES Unknown today 2/60 (3.3%) Lost to FU 1/60 (1.7%) Deaths 3/60 (5%) Follow-up 12.3±0.7 months 59/60 (98.3%) Follow-up 12.3±0.8 months 57/60 (95.0%) M.Unverdorben; ACC March 2008 12-Month Event Free Survival (ITT/As-Treated) 100 Subjects [%] 95 90 P*=0.09 ITT 85 80 75 70 0 DES/ITT DEB/ITT DES/AsT DEB/AsT 5 Months post PCI M.Unverdorben; ACC March 2008 P*=0.01 As-Treated 10 *Logrank test 15 Events From 6 to 12 Months DEB – 2 Px with PCI in non-target vessel – 1/66 (1.5%) Px with re-re PCI in target lesion DES – 2 Px with non-cardiac death – 3/60 (5%) Px with re-re PCI in target lesion No new patient with MACE M.Unverdorben; ACC March 2008 Summary PEPCAD II In the treatment of ISR the paclitaxeleluting balloon catheter Sequent® Please (B.Braun Melsungen AG) … –was safe and associated with a high procedural success rate, –exhibited a significant reduction in 6-month late lumen loss and 6/12-month MACE when compared to the Taxus® stent, and –was not associated with late thrombosis in 250 patient years. M.Unverdorben; ACC March 2008 The PEPCAD II Investigators F.X. Kleber, Unfallkrankenhaus Berlin H. Heuer, N. Schulze-Waltrup; St. Johannes Hospital, Dortmund C. Vallbracht; Herz- und Kreislaufzentrum, Rotenburg an der Fulda B. Scheller; Universitätsklinikum des Saarlandes, Homburg/Saar C. Hengstenberg, Universitätsklinikum, Regensburg M. Leschke; Städtische Kliniken, Esslingen C. Hamm, M. Rau; Kerckhoff Klinik, Bad Nauheim G. Werner; Städtisches Klinikum, Darmstadt D. Antoni; Krankenhaus Bogenhausen, München W. Bocksch; Charité Virchow, Berlin H.Ackermann; Department for Biostatistics, University of Frankfurt/M M.Boxberger, B.Braun, Berlin R.Degenhardt, M.Unverdorben; Clinical Research Institute, Rotenburg an der Fulda M.Unverdorben; ACC March 2008 The PEPCAD Program Paclitaxel-Eluting PTCA-Catheter in Coronary Artery Disease Title Design Status PI PEPCAD I SVD Sequent in ≤2.8mm, 6mo-FU MU, CRI 120px, multi-center, GER 12mo-FU PEPCAD II ISR Sequent vs Taxus in ISR, 6mo-FU MU, CRI 131px, multi-center, GER 12mo-FU PEPCAD III Sequent + pre-loaded Coroflex Blue vs Cypher, 600 px, Europe Sequent vs Taxus in DM, 160px, multi-center, Thailand, Malaysia Sequent, 25px, dualcenter, GER PEPCAD IV DM PEPCAD V BIF INDICOR Coroflex Blue+Sequent, Real World, 100px M.Unverdorben; ACC March 2008 Q2/07 B.Scheller recruiting C.Hamm Q2/07 recruiting D.Rosli, MU, CRI Q3/ 07 D.Mathey recruiting F.Kleber MU, CRI IRB U.Kaul, MU,CRI This is not the end. It is not even the beginning of the end. But it is, perhaps, the end of the beginning. (Sir Winston S.Churchill) M.Unverdorben; ACC March 2008