Management of Focal Cartilage Lesions of the Knee: The Benefits of an Autograft Procedure

Objective : Primary objective: To demonstrate the benefit of the MCI approach in terms of lesion filling at 24 months post-surgery.

Secondary objectives:

• To demonstrate the clinical benefit (based on functional scores and the need for re-intervention) of the MCI approach at different follow-up visits.
• To describe all post-operative complications.
• To demonstrate the benefit of the MCI approach in terms of lesion filling at 24 months post-surgery in patients with lesions larger than 2 cm².

Outcome Measures :

Primary endpoint: Bone grafting will be measured by magnetic resonance imaging at 24 months using the MOCART score (Magnetic Resonance Observation of Cartilage Repair Tissue 2.0 Knee Score), which assesses the rate and quality of grafting. The evaluator will be blinded to the randomization arm.

Secondary endpoints:

• Functional scores at baseline, at 3, 9, and 24 months:
• Visual Analog Scale (VAS)
• Self Knee Value (SKV)
• Knee Injury and Osteoarthritis Outcome Score (KOOS score)
• and Tegner-Lysholm activity score
• Postoperative complications from all causes at each visit
• Need for reoperation at 3, 9, and 24 months post-surgery.

Single-center, controlled, randomized, blinded (patient and MRI assessor blinded), two parallel arms with a 1:1 ratio:

• Arm 1: Microfractures
• Arm 2: Minced Cartilage Implantation (MCI)

Randomization will be stratified by:

• Age (< 30 years vs ≥ 30 years)
• Lesion size (< 2 cm² vs ≥ 2 cm²)

Inclusion criteria

• Male or female, aged over 18 years.
• Patient who has signed an informed consent form.
• Patient with focal cartilage lesions of the knee, classified as grade 4 on MRI according to the International Cartilage Repair Society classification (exposure of subchondral bone), regardless of their size, and for which surgery is indicated.
• Be affiliated with a social security scheme or a beneficiary of such a scheme

Exclusion criteria

• Revision knee surgery
• Body Mass Index (BMI) > 27 kg/m2
• Joint space narrowing on standard radiographic examination
• Refusal of consent
• Patient unable to read, write, or understand French
• Vulnerable patient according to Article L1121-6 of the French Public Health Code (CSP)
• Adult patient under guardianship, curatorship, or legal protection
• Patient unable to personally give consent according to Article L.1121-8 of the French Public Health Code (CSP) or an adult protected by law
• Pregnant or breastfeeding woman according to Article L1121-5 of the French Public Health Code (CSP)
• Patient who has already participated in a study within the last 12 months
• Patient already enrolled in another ongoing clinical trial

For patients randomized to the Microfracture arm, the procedure will be as follows: under arthroscopy, the lesion is prepared by debriding it.

Using a specific punch, perforations are made perpendicular to the exposed bone surface.

The technical principles are as follows:

• Perforation depth: approximately 3 to 4 mm, allowing access to the bone marrow,
• Regular spacing between perforations: 3 to 4 mm,
• Preservation of the integrity of the interfracture bone bridges to avoid excessive weakening of the bone endplate.

For patients randomized to the MCI arm, the procedure will be as follows: during surgery, after visualization and debridement of the lesion, cartilage tissue is harvested from a low-weight, and therefore low-stress, area. This cartilage tissue is then fragmented and mixed with PRP (Platelet-Rich Plasma), collected from the patient's blood. Platelets are unique in that they have a high concentration of universal growth factors, enabling them to heal virtually all organic tissues. Adding PRP to the fragmented cartilage tissue promotes cartilage regeneration and the incorporation of the graft into the lesion. To ensure the graft adheres to the bone tissue, it is secured biologically (with thrombin). Post-operative recovery is typical, with a gradual return to walking and other activities.

The participant participation scheme is as follows:

• Baseline: clinical examination + MRI + self-administered questionnaires
• Inclusion and randomization after eligibility verification
• Day 0: surgical intervention according to randomization (MCI vs. microfractures)
• Discharge from hospital: clinical examination + complications
• Post-surgery visit (M3 +/- 1 month): clinical examination + self-administered questionnaires + complications + need for re-surgery
• Post-surgery visit (M9 +/- 1 month): clinical examination + self-administered questionnaires + complications + need for re-surgery
• Post-surgery visit (M24 +/- 1 month): clinical examination + MRI with MOCART score calculation + self-administered questionnaires + complications + need for re-surgery

To demonstrate a difference in filling rate of 30 points (90% in the MCI arm versus 60% in the Microfractures arm) with a standard deviation of 40%, a type I error rate of 5%, and a power of 80%, 28 evaluable subjects per arm are required. To account for unanalyzable data and the potential for patients lost to follow-up, we propose including a total of 80 subjects (40 per arm) in this study.

Inclusion criteria

• Male or female, aged over 18 years.
• Patient who has signed an informed consent form.
• Patient with focal cartilage lesions of the knee, classified as grade 4 on MRI according to the International Cartilage Repair Society classification (exposure of subchondral bone), regardless of size, and for which surgery is indicated.
• Be affiliated with or a beneficiary of a social security scheme.

Exclusion criteria

• Revision knee surgery
• Body Mass Index (BMI) > 27 kg/m²
• Joint space narrowing on standard radiographic examination
• Refusal of consent
• Patient unable to read, write, or understand French
• Vulnerable patient according to Article L1121-6 of the French Public Health Code (CSP)
• Adult patient under guardianship, curatorship, or legal protection
• Patient unable to give Personally, their consent according to Article L.1121-8 of the French Public Health Code (CSP) or an adult protected by law
• Pregnant or breastfeeding woman according to Article L1121-5 of the French Public Health Code (CSP)
• Patient who has already participated in a study within the last 12 months
• Patient already enrolled in another ongoing clinical trial