Safety and Efficacy of Kartigen® in Treating Cartilage Defects: A Randomized, Controlled, Phase I Trial

Here, we aimed to investigate the safety and preliminary efficacy of Kartigen®, a matrix with autologous bone marrow mesenchymal stem cell-derived chondrocyte precursors embedded in atelocollagen. As a surgical graft, Kartigen® was implanted onto the cartilage defects at the weight-bearing site of t...

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Veröffentlicht in:Polymers 2021-09, Vol.13 (18), p.3029
Hauptverfasser: Liu, Yen-Liang, Yen, Chun-Che, Liu, Tzu-Shang Thomas, Chang, Chih-Hung, Shih, Tiffany Ting-Fang, Wang, Jyh-Horng, Yang, Ming-Chia, Lin, Feng-Huei, Liu, Hwa-Chang
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container_issue 18
container_start_page 3029
container_title Polymers
container_volume 13
creator Liu, Yen-Liang
Yen, Chun-Che
Liu, Tzu-Shang Thomas
Chang, Chih-Hung
Shih, Tiffany Ting-Fang
Wang, Jyh-Horng
Yang, Ming-Chia
Lin, Feng-Huei
Liu, Hwa-Chang
description Here, we aimed to investigate the safety and preliminary efficacy of Kartigen®, a matrix with autologous bone marrow mesenchymal stem cell-derived chondrocyte precursors embedded in atelocollagen. As a surgical graft, Kartigen® was implanted onto the cartilage defects at the weight-bearing site of the medial femoral condyle of the knee. Fifteen patients were enrolled and stratified into two groups, undergoing either Kartigen® implantation (n = 10) or microfracture (control group, n = 5). The primary endpoint was to evaluate the safety of Kartigen® by monitoring the occurrence of adverse events through physician queries, physical examinations, laboratory tests, and radiological analyses for 2 years. There were no infections, inflammations, adhesions, loose body, or tumor formations in the Kartigen®-implanted knees. The preliminary efficacy was assessed using the International Knee Documentation Committee (IKDC) score, visual analog scale, and second-look arthroscopy. The postoperative IKDC scores of the Kartigen® group significantly improved in the 16th week (IKDC = 62.1 ± 12.8, p = 0.025), kept increasing in the first year (IKDC = 78.2 ± 15.4, p < 0.005), and remained satisfactory in the second year (IKDC = 73.6 ± 13.8, p < 0.005), compared to the preoperative condition (IKDC = 47.1 ± 17.0), while the postoperative IKDC scores of the control group also achieved significant improvement in the 28th week (IKDC = 68.5 ± 6.1, p = 0.032) versus preoperative state (IKDC = 54.0 ± 9.1). However, the IKDC scores decreased in the first year (IKDC = 63.5 ± 11.6) as well as in the second year (IKDC = 52.6 ± 16.4). Thirteen patients underwent second-look arthroscopy and biopsy one year after the operation. The Kartigen® group exhibited integration between Kartigen® and host tissue with a smooth appearance at the recipient site, whereas the microfracture group showed fibrillated surfaces. The histological and immunohistochemical analyses of biopsy specimens demonstrated the columnar structure of articular cartilage and existence of collagen type II and glycosaminoglycan mimic hyaline cartilage. This study indicates that Kartigen® is safe and effective in treating cartilage defects.
doi_str_mv 10.3390/polym13183029
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As a surgical graft, Kartigen® was implanted onto the cartilage defects at the weight-bearing site of the medial femoral condyle of the knee. Fifteen patients were enrolled and stratified into two groups, undergoing either Kartigen® implantation (n = 10) or microfracture (control group, n = 5). The primary endpoint was to evaluate the safety of Kartigen® by monitoring the occurrence of adverse events through physician queries, physical examinations, laboratory tests, and radiological analyses for 2 years. There were no infections, inflammations, adhesions, loose body, or tumor formations in the Kartigen®-implanted knees. The preliminary efficacy was assessed using the International Knee Documentation Committee (IKDC) score, visual analog scale, and second-look arthroscopy. The postoperative IKDC scores of the Kartigen® group significantly improved in the 16th week (IKDC = 62.1 ± 12.8, p = 0.025), kept increasing in the first year (IKDC = 78.2 ± 15.4, p &lt; 0.005), and remained satisfactory in the second year (IKDC = 73.6 ± 13.8, p &lt; 0.005), compared to the preoperative condition (IKDC = 47.1 ± 17.0), while the postoperative IKDC scores of the control group also achieved significant improvement in the 28th week (IKDC = 68.5 ± 6.1, p = 0.032) versus preoperative state (IKDC = 54.0 ± 9.1). However, the IKDC scores decreased in the first year (IKDC = 63.5 ± 11.6) as well as in the second year (IKDC = 52.6 ± 16.4). Thirteen patients underwent second-look arthroscopy and biopsy one year after the operation. The Kartigen® group exhibited integration between Kartigen® and host tissue with a smooth appearance at the recipient site, whereas the microfracture group showed fibrillated surfaces. The histological and immunohistochemical analyses of biopsy specimens demonstrated the columnar structure of articular cartilage and existence of collagen type II and glycosaminoglycan mimic hyaline cartilage. This study indicates that Kartigen® is safe and effective in treating cartilage defects.</description><identifier>ISSN: 2073-4360</identifier><identifier>EISSN: 2073-4360</identifier><identifier>DOI: 10.3390/polym13183029</identifier><identifier>PMID: 34577930</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Arthritis ; Bone marrow ; Cartilage ; Collagen ; Columnar structure ; Defects ; FDA approval ; Glycosaminoglycans ; Knee ; Laboratory tests ; Microfracture ; Osteoarthritis ; Physical examinations ; Safety ; Stem cells ; Tissue engineering ; Transplants &amp; implants</subject><ispartof>Polymers, 2021-09, Vol.13 (18), p.3029</ispartof><rights>2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). 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The histological and immunohistochemical analyses of biopsy specimens demonstrated the columnar structure of articular cartilage and existence of collagen type II and glycosaminoglycan mimic hyaline cartilage. This study indicates that Kartigen® is safe and effective in treating cartilage defects.</description><subject>Arthritis</subject><subject>Bone marrow</subject><subject>Cartilage</subject><subject>Collagen</subject><subject>Columnar structure</subject><subject>Defects</subject><subject>FDA approval</subject><subject>Glycosaminoglycans</subject><subject>Knee</subject><subject>Laboratory tests</subject><subject>Microfracture</subject><subject>Osteoarthritis</subject><subject>Physical examinations</subject><subject>Safety</subject><subject>Stem cells</subject><subject>Tissue engineering</subject><subject>Transplants &amp; implants</subject><issn>2073-4360</issn><issn>2073-4360</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNpdkc1qGzEUhUVoaULqZfeCbLLoJPobzSiLQnCcHxJoab0X1xrJVtCMXGkccB6qD5Enq0xMSaqNDlffPZyri9AXSs44V-R8HcO2p5y2nDB1gI4YaXgluCQf3uhDNMn5kZQjailp8wkdclE3jeLkCK1-gbPjFsPQ4Zlz3oDZ4ujwPaTRL-3w8gf7Ac-ThdEPSzzdlQMsLb6yzpoxX-BL_LM0x94_2-4rnsZhTDGEnf6xgmzxXen2ED6jjw5CtpP9fYzm17P59LZ6-H5zN718qAxXbKx4vXDguqI7IhldQAvSsLqTwLmABTSCiFZQS5hRzHQ1bahoDHFKtaqjhh-jb6-2682it52xJQ4EvU6-h7TVEbx-_zL4lV7GJ90KKRmXxeB0b5Di743No-59NjYEGGzcZM3Kz4laKUoLevIf-hg3aSjT7SgpFGE1K1T1SpkUc07W_QtDid5tUb_bIv8Lw1yPAw</recordid><startdate>20210907</startdate><enddate>20210907</enddate><creator>Liu, Yen-Liang</creator><creator>Yen, Chun-Che</creator><creator>Liu, Tzu-Shang Thomas</creator><creator>Chang, Chih-Hung</creator><creator>Shih, Tiffany Ting-Fang</creator><creator>Wang, Jyh-Horng</creator><creator>Yang, Ming-Chia</creator><creator>Lin, Feng-Huei</creator><creator>Liu, Hwa-Chang</creator><general>MDPI AG</general><general>MDPI</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>JG9</scope><scope>KB.</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-2994-6671</orcidid><orcidid>https://orcid.org/0000-0002-1635-4335</orcidid></search><sort><creationdate>20210907</creationdate><title>Safety and Efficacy of Kartigen® in Treating Cartilage Defects: A Randomized, Controlled, Phase I Trial</title><author>Liu, Yen-Liang ; 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As a surgical graft, Kartigen® was implanted onto the cartilage defects at the weight-bearing site of the medial femoral condyle of the knee. Fifteen patients were enrolled and stratified into two groups, undergoing either Kartigen® implantation (n = 10) or microfracture (control group, n = 5). The primary endpoint was to evaluate the safety of Kartigen® by monitoring the occurrence of adverse events through physician queries, physical examinations, laboratory tests, and radiological analyses for 2 years. There were no infections, inflammations, adhesions, loose body, or tumor formations in the Kartigen®-implanted knees. The preliminary efficacy was assessed using the International Knee Documentation Committee (IKDC) score, visual analog scale, and second-look arthroscopy. The postoperative IKDC scores of the Kartigen® group significantly improved in the 16th week (IKDC = 62.1 ± 12.8, p = 0.025), kept increasing in the first year (IKDC = 78.2 ± 15.4, p &lt; 0.005), and remained satisfactory in the second year (IKDC = 73.6 ± 13.8, p &lt; 0.005), compared to the preoperative condition (IKDC = 47.1 ± 17.0), while the postoperative IKDC scores of the control group also achieved significant improvement in the 28th week (IKDC = 68.5 ± 6.1, p = 0.032) versus preoperative state (IKDC = 54.0 ± 9.1). However, the IKDC scores decreased in the first year (IKDC = 63.5 ± 11.6) as well as in the second year (IKDC = 52.6 ± 16.4). Thirteen patients underwent second-look arthroscopy and biopsy one year after the operation. The Kartigen® group exhibited integration between Kartigen® and host tissue with a smooth appearance at the recipient site, whereas the microfracture group showed fibrillated surfaces. The histological and immunohistochemical analyses of biopsy specimens demonstrated the columnar structure of articular cartilage and existence of collagen type II and glycosaminoglycan mimic hyaline cartilage. This study indicates that Kartigen® is safe and effective in treating cartilage defects.</abstract><cop>Basel</cop><pub>MDPI AG</pub><pmid>34577930</pmid><doi>10.3390/polym13183029</doi><orcidid>https://orcid.org/0000-0002-2994-6671</orcidid><orcidid>https://orcid.org/0000-0002-1635-4335</orcidid><oa>free_for_read</oa></addata></record>
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subjects Arthritis
Bone marrow
Cartilage
Collagen
Columnar structure
Defects
FDA approval
Glycosaminoglycans
Knee
Laboratory tests
Microfracture
Osteoarthritis
Physical examinations
Safety
Stem cells
Tissue engineering
Transplants & implants
title Safety and Efficacy of Kartigen® in Treating Cartilage Defects: A Randomized, Controlled, Phase I Trial
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