Superiority of MACI® Versus Microfracture Treatment in Patients With Symptomatic Articular Cartilage Defects in the Knee

Articular Cartilage Defect Clinical Trial

— SUMMIT  

Official title:

A Prospective, Randomized, Open-label, Parallel-group, Multi-center Study to Demonstrate the Superiority of MACI® Versus Arthroscopic Microfracture for the Treatment of Symptomatic Articular Cartilage Defects of the Femoral Condyle Including the Trochlea.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00719576
• Other study ID #: MACI00206
• Secondary ID: 2006-004817-16
• Status: Completed
• Phase: Phase 3
• Start date: July 2008
• Est. completion date: March 2012

Study information

• Verified date: May 2021
• Source: Vericel Corporation
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The objective of this trial is to demonstrate superior efficacy and safety of MACI compared with arthroscopic microfracture in the treatment of patients (aged 18 to 55 years) with symptomatic articular cartilage defects of the knee.

Description:

This is a prospective, randomized, open-label, parallel-group, multicenter study designed to investigate the outcome of MACI implant versus arthroscopic microfracture in the treatment of articular cartilage defects in the knee in patients between ages of 18 and 55 years.

All patients who meet the eligibility criteria and are considered suitable for inclusion will have a cartilage biopsy taken prior to randomization to study treatment. Eligible patients will then be randomized during the index arthroscopy procedure to receive either MACI implant or microfracture treatment.

Patients randomized to treatment with MACI implant will return within approximately 4 to 8 weeks of the index arthroscopy to undergo the chondrocyte implantation procedure via arthrotomy. Patients randomized to microfracture will undergo the procedure during the index arthroscopy.

Patients will be assessed post-arthroscopy and post-arthrotomy at intervals during 2 years follow-up. Evaluations include adverse events, functional and pain outcomes, arthroscopic and histologic evaluation and magnetic resonance imaging (MRI).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 144
• Est. completion date: March 2012
• Est. primary completion date: March 2012
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria:

• Symptomatic, single or multiple full-thickness cartilage defects of the knee with or without bone involvement

Exclusion Criteria:

• Known history of hypersensitivity to gentamicin, other aminoglycosides, or products of porcine or bovine origin

• Severe osteoarthritis of the knee

• Inflammatory arthritis, inflammatory joint disease, or uncorrected congenital blood coagulation disorders

• Prior knee surgery (within 6 months), excluding surgery to procure a biopsy or a concomitant procedure to prepare the knee for a MACI implant.

Related Conditions & MeSH terms

• Articular Cartilage Defect
• Cartilage Diseases
• Fractures, Stress

Intervention

Biological:
• autologous cultured chondrocytes on porcine collagen membrane
Implantation via mini-arthrotomy

Procedure:
• Microfracture
Microfracture performed by arthroscopic surgery

Locations

Country	Name	City	State
Czechia	Urazova nemocnice v Brne	Brno
Czechia	Fakultni Nemocnice Na Bulovce	Prague
Czechia	Fakultni Nemocnice v Motole	Prague
France	Hopital d'instruction des armees Robert Picque	Bordeaux
France	Centre Hospitalier Lyon Sud	Lyon
France	Polyclinique Saint-Roch	Montpellier
France	Chirurgien Orthopediste et Traumatologue du Sport, Institut de I'Appareil Locomoteur Nollet	Paris
Netherlands	Academisch Ziekenhuis Maastricht	Maastricht
Netherlands	St. Elisabeth Ziekenhuis	Tilburg
Netherlands	UMC Utrecht	Utrecht
Norway	St Olavs Hospital	Trondheim
Poland	Szpital Uniwersytecki	Bydgoszcz
Poland	Regional Hospital of Traumatologic Surgery	Piekary Slaskie
Poland	Center for Sports Medicine CMS	Warsaw
Poland	Medical Academy Warsaw	Warsaw
Sweden	Kungsbacka Hospital	Kungsbacka
Sweden	Capio Artro Clinic AB	Stockholm
United Kingdom	The South West London Elective Orthopaedic Centre (SWLEOC)	Epsom
United Kingdom	Nuffield Dept. of Orthopaedic Surgery, University of Oxford	Oxford
United Kingdom	Spire Cheshire Hospital	Warrington

Sponsors (1)

Lead Sponsor	Collaborator
Vericel Corporation

Countries where clinical trial is conducted

Czechia,  France,  Netherlands,  Norway,  Poland,  Sweden,  United Kingdom, 

References & Publications (1)

Saris D, Price A, Widuchowski W, Bertrand-Marchand M, Caron J, Drogset JO, Emans P, Podskubka A, Tsuchida A, Kili S, Levine D, Brittberg M; SUMMIT study group. Matrix-Applied Characterized Autologous Cultured Chondrocytes Versus Microfracture: Two-Year Fo — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change From Baseline to Week 104 for the Participant's Knee Injury and Osteoarthritis Outcome Score (KOOS) Pain and Function (Sports and Recreational Activities) Scores.	The KOOS is a validated knee-specific instrument developed to assess the patients' opinion of their knee and associated problems. KOOS consists of 5 subscales: Pain, Function in sports and recreational activities, other Symptoms, Function in activities of daily living (ADL), and knee related Quality of life (QOL). A 5-point Likert scale was used to record the response to each item ranging from 0 (no problems) to 4 (extreme problems). Within each subscale, items were added up and normalized to a value between 0 (extreme problems) and 100 (no problems). Subscales are not combined to calculate a total score.	Baseline and Week 104
Secondary	Histological Evaluation of Structural Repair of Evaluable Biopsies Harvested From the Core of the Index Lesion During Arthroscopy at Week 104	The mean microscopic International Cartilage Repair Society (ICRS) II overall assessment score was used to assess the histology efficacy endpoint.; Scoring of the cartilage repair biopsies was completed using the ICRS II histology scoring system (Mainil-Varlet, 2010, Am J Sports Med) by 2 independent pathologists blinded to the patient's assigned study treatment. This scoring system includes 14 parameters, comprising an overall assessment score reported here, as well as 13 other items related to chondrocyte phenotype, tissue structure, and other factors, each scored on a scale from 0 to 100 representing poor to good quality cartilage.	Week 104
Secondary	Assessment of Defect Fill by Magnetic Resonance Imaging (MRI)	Number of participants with MRI degree of defect fill > 50%. Evaluation of MRI data was performed by independent central review blinded to the participant's treatment.; Appropriate MRI sequences were used to image cartilage repair tissue.	Week 104
Secondary	Response Rate Based on KOOS Pain and Function (Sports and Recreational Activities) Scores at Week 104.	A responder is defined as a participant with at least a 10-point improvement in both the KOOS Pain and Function (Sports and Recreational activities) scores from Baseline	Week 104
Secondary	Treatment Failure	The planned analyses concerning time to treatment failure were not conducted due to the small number of per protocol treatment failure cases. As such, the number of participants with treatment failure is being reported.; Patients were considered as a treatment failure if all of the following 5 criteria were met: Patient's global assessment of their knee joint compared to Baseline was the same or worse; Physician's global assessment of the patient's knee joint compared to Baseline was the same, worse, or significantly worse.; Percent improvement from Baseline in KOOS Pain score was less than 10%.; Physician diagnostic evaluation of failure excluded etiologies (eg, meniscal tear) other than failed treatment of the index lesion.; The physician decided that surgical re-treatment of the index lesion(s) was required that involved either extensive debridement for lesion expansion, violation of the subchondral bone, or autologous cultured chondrocyte implantation.	Week 104
Secondary	Change From Baseline at Week 104 in the Remaining 3 Subscales of the KOOS Instrument (Activities of Daily Living, Knee-related Quality of Life, and Other Symptoms)	The KOOS is a validated knee-specific instrument developed to assess the patients' opinion of their knee and associated problems. KOOS consists of 5 subscales: Pain, Function in sports and recreational activities, other Symptoms, Function in activities of daily living (ADL), and knee related Quality of life (QOL). A 5-point Likert scale was used to record the response to each item ranging from 0 (no problems) to 4 (extreme problems). Within each subscale, items were added up and normalized to a value between 0 (extreme problems) and 100 (no problems).	Baseline and Week 104
Secondary	Participants With Treatment-Emergent Adverse Events		Week 104