A Randomized Trial of Autologous Chondrocyte Implantation Versus Alternative Forms of Surgical Cartilage Management in Patients With a Failed Primary Treatment for Chondral or Osteochondral Defects in the Knee.
Author
Snow MMiddleton L
Mehta S
Roberts A
Gray R
Richardson J
Kuiper JH
Smith A
White S
Roberts S
Griffiths D
Mohammed A
Moholkar K
Ashraf T
Green M
Hutchinson J
Bhullar T
Chitnis S
Shaw A
van Niekerk L
Hui A
Drogset JO
Knutsen G
McNicholas M
Bowditch M
Johnson D
Turner P
Chugh S
Hunt N
Ali S
Palmer S
Perry A
Davidson A
Hill P
Deo S
Satish V
Radford M
Langstaff R
Houlihan-Burne D
Spicer D
Phaltankar P
Hegab A
Marsh D
Cannon S
Briggs T
Pollock R
Carrington R
Skinner J
Bentley G
Price A
Schranz P
Mandalia V
O'Brien S
Affiliation
Robert Jones and Agnes Hunt Orthopaedic Hospital; Keele University; Birmingham University; The Dudley Group NHS Foundation Trust et alPublication date
01/02/2023Subject
Orthopaedics
Metadata
Show full item recordAbstract
There are limited randomized controlled trials with long-term outcomes comparing autologous chondrocyte implantation (ACI) versus alternative forms of surgical cartilage management within the knee. Purpose: To determine at 5 years after surgery whether ACI was superior to alternative forms of cartilage management in patients after a failed previous treatment for chondral or osteochondral defects in the knee. Study Design: Randomized controlled trial Level of evidence, 1. Methods: In total, 390 participants were randomly assigned to receive either ACI or alternative management. Patients aged 18 to 55 years with one or two symptomatic cartilage defects who had failed 1 previous therapeutic surgical procedure in excess of 6 months prior were included. Dual primary outcome measures were used: (1) patient-completed Lysholm knee score and (2) time from surgery to cessation of treatment benefit. Secondary outcome measures included International Knee Documentation Committee and Cincinnati Knee Rating System scores, as well as number of serious adverse events. Analysis was performed on an intention-to-treat basis. Results: Lysholm scores were improved by 1 year in both groups (15.4 points [95% CI, 11.9 to 18.8] and 15.2 points [95% CI, 11.6 to 18.9]) for ACI and alternative, with this improvement sustained over the duration of the trial. However, no evidence of a difference was found between the groups at 5 years (2.9 points 95% CI, -1.8 to 7.5 P = .46). Approximately half of the participants (55% 95% CI, 47% to 64% with ACI) were still experiencing benefit at 5 years, with time to cessation of treatment benefit similar in both groups (hazard ratio, 0.97 95% CI, 0.72 to 1.32 P > .99). There was a differential effect on Lysholm scores in patients without previous marrow stimulation compared with those with marrow stimulation ( P = .03 6.4 points in favor of ACI 95% CI, -0.4 to 13.1). More participants experienced a serious adverse event with ACI ( P = .02). Conclusion: Over 5 years, there was no evidence of a difference in Lysholm scores between ACI and alternative management in patients who had previously failed treatment. Previous marrow stimulation had a detrimental effect on the outcome of ACI. Registration: International Standard Randomised Controlled Trial Number: 48911177.Citation
Snow M, Middleton L, Mehta S, Roberts A, Gray R, Richardson J, Kuiper JH; ACTIVE Consortium; Smith A, White S, Roberts S, Griffiths D, Mohammed A, Moholkar K, Ashraf T, Green M, Hutchinson J, Bhullar T, Chitnis S, Shaw A, van Niekerk L, Hui A, Drogset JO, Knutsen G, McNicholas M, Bowditch M, Johnson D, Turner P, Chugh S, Hunt N, Ali S, Palmer S, Perry A, Davidson A, Hill P, Deo S, Satish V, Radford M, Langstaff R, Houlihan-Burne D, Spicer D, Phaltankar P, Hegab A, Marsh D, Cannon S, Briggs T, Pollock R, Carrington R, Skinner J, Bentley G, Price A, Schranz P, Mandalia V, O'Brien S. A Randomized Trial of Autologous Chondrocyte Implantation Versus Alternative Forms of Surgical Cartilage Management in Patients With a Failed Primary Treatment for Chondral or Osteochondral Defects in the Knee. Am J Sports Med. 2023 Feb;51(2):367-378. doi: 10.1177/03635465221141907. Epub 2023 Jan 20. PMID: 36661257.Type
ArticlePMID
36661257Publisher
Sageae974a485f413a2113503eed53cd6c53
10.1177/03635465221141907