Efficacy of Everolimus-Eluting Versus Zotarolimus-Eluting Sten for Coronary Lesions in Acute Myocardial Infarction (EVERZOTA)

The recruitment status of this study is unknown because the information has not been verified recently.
Verified February 2011 by Yonsei University.
Recruitment status was  Active, not recruiting
Sponsor:
Information provided by:
Yonsei University
ClinicalTrials.gov Identifier:
NCT01347554
First received: April 27, 2011
Last updated: July 12, 2011
Last verified: February 2011
  Purpose

Most of the previous data regarding the efficacy of the everolimus-eluting stent (EES) was derived from studies comparing EES with bare metal stent (BMS) or EES with paclitaxel-eluting (PES). Although sirolimus-eluting stents (SES) have been shown to be the most efficacious drug regarding inhibition of neointima and late loss, there have been no previous head to head comparisons between EES and zotarolimus-eluting stent (ZES). Both everolimus and sirolimus are macrocyclic lactones that target the mTOR (mammalian target of rapamycin) to reduce vascular smooth muscle proliferation after vessel injury and therefore in principle may show similar results after stenting in humans. Data pooled from the EES arm that received follow up angiography in the SPIRIT III trial and the SES arm in the SIRIUS trial show similar rates of binary restenosis and late loss. However, the stent and polymer platform is not the same between the EES and ZES and it is reported that the EES system has the thinnest stent + polymer thickness (88.6um) of all of the previously KFDA-approved drug-eluting stent (DES). In addition, there are no data available on the efficacy of the EES and ZES in "real world" lesions other than the selected lesions studied in the previous trials, such as acute myocardial infarction.


Condition Intervention Phase
Myocardial Infarction
Device: Everolimus stent (Xience V)
Device: Zotarolimus stent (Endeavor resolute)
Phase 4

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Comparison of the Efficacy of Everolimus-Eluting Versus Zotarolimus-Eluting Stent for Coronary Lesions in Acute Myocardial Infarction

Resource links provided by NLM:


Further study details as provided by Yonsei University:

Primary Outcome Measures:
  • Major adverse cardiac events (MACE) defined as the composite of cardiac death, myocardial infarction, ischemia driven target lesion revascularization at 12 months. [ Time Frame: One year ] [ Designated as safety issue: Yes ]

Secondary Outcome Measures:
  • Individual components of safety issue [ Time Frame: Two years ] [ Designated as safety issue: Yes ]
    All Death/Cardiac death

  • Individual components of safety issue [ Time Frame: Two years ] [ Designated as safety issue: Yes ]
    Bleeding

  • Individual components of efficacy issue [ Time Frame: 12 months ] [ Designated as safety issue: Yes ]
    Myocardial infarction (Q-wave and non-Q wave)

  • Individual components of efficacy issue [ Time Frame: 12 months ] [ Designated as safety issue: Yes ]
    Target vessel revascularization (TVR)

  • Individual components of efficacy issue [ Time Frame: 12 months ] [ Designated as safety issue: Yes ]
    Target lesion revascularization (TLR)

  • Individual components of efficacy issue [ Time Frame: 12 months ] [ Designated as safety issue: Yes ]
    Stent thrombosis

  • Individual components of efficacy issue [ Time Frame: 12 months ] [ Designated as safety issue: Yes ]
    Acute success

  • Individual components of efficacy issue [ Time Frame: 12 months ] [ Designated as safety issue: Yes ]
    In-segment late luminal loss (LL) at 9~12 months

  • Individual components of efficacy issue [ Time Frame: 12 months ] [ Designated as safety issue: Yes ]
    In-stent late loss at 9~12 months

  • Individual components of efficacy issue [ Time Frame: 12 months ] [ Designated as safety issue: No ]
    Angiographic pattern of restenosis at 9~12 months angiographic follow-up

  • Individual components of efficacy issue [ Time Frame: 12 months ] [ Designated as safety issue: No ]
    In-stent and in-segment % diameter stenosis (%DS) at 9~12 months

  • Individual components of efficacy issue [ Time Frame: 24 months ] [ Designated as safety issue: Yes ]
    MACE at 24 months


Enrollment: 500
Study Start Date: January 2009
Estimated Study Completion Date: December 2012
Estimated Primary Completion Date: December 2011 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: Xience V stent group
Xience V (Everolimus eluting stent) insertion in patients with acute myocardial infarction
Device: Everolimus stent (Xience V)
Everolimus eluting stent stenting
Other Name: Xience V
Active Comparator: Endeavor resolute group
Endeavor resolute (Zotarolimus eluting stent) insertion in patients with acute myocardial infarction
Device: Zotarolimus stent (Endeavor resolute)
Zotarolimus eluting stent stenting
Other Name: Endeavor resolute

  Hide Detailed Description

Detailed Description:

Previous randomized trials have shown the efficacy of a slow-release polymeric sirolimus-eluting stent (CYPHER, Cordis, Warren, NJ, USA), paclitaxel-eluting stent (TAXUS, Boston Scientific, Natick, MA, USA), and zotarolimus-eluting stent (Endeavor, Medtronic, Minneapolis, MN, USA) over bare metal stents in reducing neointimal hyperplasia, late luminal loss, and angiographic restenosis leading to decreased target lesion revascularization. The everolimus-eluting stent (XIENCE V, Abott Vascular, Santa Clara, CA, USA, PROMUS, Boston Scientific, Natick, MA, USA) is a newly developed drug eluting stent using the MULTILINK VISION® stent platform combined with the drug everolimus contained in a polymer coating.

In the first-in-man SPIRIT First clinical trial, XIENCE V showed a significant benefit over the bare metal VISION stent. Compared with late loss of 0.85 ± 0.36mm in the VISION arm, XIENCE V reduced late loss by 88% (0.10 ± 0.23mm). Also the clinical safety of XIENCE V was confirmed with a 6-month MACE rate of 7.7%. In the SPIRIT II clinical trial, which compared the efficacy and safety of the XIENCE V stent versus the TAXUS PECSS stent, the primary endpoint was met showing a non-inferiority of the XIENCE V compared with the TAXUS regarding in-stent late loss at 180 days. Actually, XIENCE V was superior to TAXUS and reduced in-stent late loss by 72% from a mean of 0.36 mm to 0.11 mm. In addition, analysis of other key clinical endpoints showed a lower rate of ischemia driven MACE (2.7% vs. 6.5% for XIENCE V vs. TAXUS) and protocol-defined stent thrombosis (0.5% vs. 1.3% for XIENCE V vs. TAXUS). The lower rate of ischemia driven MACE at 180 days was sustained through 1 year and there were no new instances of late stent thrombosis in either group up to 1 year.

The SPIRIT III RCT was a prospective, 2:1 randomized, active-controlled, single blinded, parallel, multi-center clinical evaluation of the XIENCE V Everolimus Eluting Coronary Stent System (XIENCE V EECSS) compared to TAXUS Paclitaxel Eluting Coronary Stent System (TAXUS PECSS) in the treatment of up to two de novo lesions. This pivotal clinical trial was designed to demonstrate the non-inferiority of the XIENCE V EECSS to the TAXUS PECSS. Patients were randomized 2:1 to XIENCE V or TAXUS and the primary endpoint was in-segment late loss at 240 days. The results showed a mean in-segment late loss of 0.14mm for XIENCE V and 0.28 mm for TAXUS (p<0.001 for non-inferiority, p=0.0037 for superiority). The secondary endpoint, which was ischemia-driven target vessel failure (TVF), was 7.6% for XIENCE V and 9.7% for TAXUS, confirming the non-inferiority of XIENCE V. Furthermore, the rate of definite and probable stent thrombosis was 1.1% and 0.6% for XIENCE V and TAXUS, respectively.

With a recent approval of new DES, zotarolimus-eluting stent (Endeavor, Medtronic, Minneapolis, MN), other comparison studies have been conducted to compare Endeavor zotarolimus-eluting stent with the sirolimus-eluting stent and paclitaxel-eluting stent. zotarolimus and sirolimus share some common structural and biological properties. In vitro data suggest that sirolimus and tetrazole containing rapamycin analogs have similar inhibitory effects in a mixed lymphocyte reaction assay. The ENDEAVOR clinical trials are currently in progress to evaluate a phosphoryl choline (PC)-coated zotarolimus-eluting stent(ZES) for the prevention of restenosis. The Endeavor zotarolimus-eluting stent utilizes a cobalt alloy balloon-expandable stent (Driver; Medtronic) with a geometry similar to the stainless steel stent used in this preliminary study (S7; Medtronic). The Endeavor ZES also employees a PC strut surface coating as the drug delivery reservoir with a dose of 10 g/mm of ABT-578. The Endeavor (ZES), however, differs from the stent used in this experimental study by the addition of a drug-free PC topcoat to serve as a diffusion barrier to retard drug release from the polymer reservoir. Angiographic analysis at 4 months in the 100-patient focal de novo lesion ENDEAVOR I feasibility study demonstrated a mean in-stent percent diameter stenosis of approximately 14% and a late lumen loss of 0.3 mm with a low frequency of target lesion revascularization (1%). The clinical outcomes from the ENDEAVOR II (1,500 patients randomized to ABT-578 or bare metal stent) and the ENDEAVOR III (436 patients randomized 3:1 to ABT-578 or Cypher) trials as well as other ongoing studies showed efficacy of the PC-coated ABT-578-eluting stent. In ENDEAVOR III study, the Endeavor stent had larger late loss and higher binary restenosis in both the analysis segment and stented segment.

Most of the previous data regarding the efficacy of the EES was derived from studies comparing EES with BMS or EES with PES. Although sirolimus eluting stents (SES) have been shown to be the most efficacious drug eluting stent regarding inhibition of neointima and late loss, there have been no previous head to head comparisons between EES and ZES. Both everolimus and sirolimus are macrocyclic lactones that target the mTOR (mammalian target of rapamycin) to reduce vascular smooth muscle proliferation after vessel injury and therefore in principle may show similar results after stenting in humans. Data pooled from the EES arm that received follow up angiography in the SPIRIT III trial and the SES arm in the SIRIUS trial show similar rates of binary restenosis and late loss. However, the stent and polymer platform is not the same between the EES and ZES and it is reported that the EES system has the thinnest stent + polymer thickness (88.6um) of all of the previously KFDA-approved DES. In addition, there are no data available on the efficacy of the EES and ZES in "real world" lesions other than the selected lesions studied in the previous trials, such as acute myocardial infarction.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Age > 18 years
  • Chest pain duration more than 10 minutes
  • At least on of the following criteria
  • A. ECG change (T inversion, ST depression and ST elevation)
  • B. Cardiac enzyme elevation more than upper normal limit
  • Significant coronary artery stenosis (>50% by visual estimate)
  • The patient or guardian agrees to the study

Exclusion Criteria:

  • Stent thrombosis
  • History of bleeding diathesis or known coagulopathy (including heparin-induced thrombocytopenia), or will refuse blood transfusions
  • Gastrointestinal or genitourinary bleeding within the prior 3 months, or major surgery within 2 months
  • An elective surgical procedure is planned that would necessitate interruption of thienopyridines during the first 12 months post enrollment
  • Non-cardiac co-morbid conditions are present with life expectancy <1 year or that may result in protocol non-compliance (per site investigator's medical judgment)
  • Severe infective state
  • Patients with LVEF <25% or those with cardiogenic shock
  • Lt. main MI
  • Creatinine level more than 3.0mg/dL or dependence on dialysis
  • Severe hepatic dysfunction (AST and ALT 3 times upper normal limit)
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01347554

Locations
Korea, Republic of
Yonsei University Wonju College of Medicine; Wonju Christian Hospital
Wonju, Korea, Republic of
Sponsors and Collaborators
Yonsei University
Investigators
Principal Investigator: Seung-Hwan Lee, MD, PhD Division of cardiology, Department of internal medicine, Wonju christian hospital, Yonsei University Wonju College of Medicine
  More Information

No publications provided

Responsible Party: Seung-Hwan Lee/Professor, Divison of cardiology, Department of internal medicine, Wonju Chrirstian Hospital
ClinicalTrials.gov Identifier: NCT01347554     History of Changes
Other Study ID Numbers: EVZT_1.0
Study First Received: April 27, 2011
Last Updated: July 12, 2011
Health Authority: Korea: Institutional Review Board

Keywords provided by Yonsei University:
drug-eluting stent
everolimus
zotarolimus
myocardial ischemia
cardiovascular diseases
MACE
safety

Additional relevant MeSH terms:
Infarction
Myocardial Infarction
Ischemia
Pathologic Processes
Necrosis
Myocardial Ischemia
Heart Diseases
Cardiovascular Diseases
Vascular Diseases
Everolimus
Sirolimus
Immunosuppressive Agents
Immunologic Factors
Physiological Effects of Drugs
Pharmacologic Actions
Antibiotics, Antineoplastic
Antineoplastic Agents
Therapeutic Uses
Antifungal Agents
Anti-Infective Agents
Anti-Bacterial Agents

ClinicalTrials.gov processed this record on July 26, 2014