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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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 < 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.</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 & 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/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2021 by the authors. 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c392t-35bfafd392d0621ba8a6c25d6a334aba7404841e02c92cd517147c0f9989d1c3</citedby><cites>FETCH-LOGICAL-c392t-35bfafd392d0621ba8a6c25d6a334aba7404841e02c92cd517147c0f9989d1c3</cites><orcidid>0000-0002-2994-6671 ; 0000-0002-1635-4335</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8466236/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8466236/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,886,27926,27927,53793,53795</link.rule.ids></links><search><creatorcontrib>Liu, Yen-Liang</creatorcontrib><creatorcontrib>Yen, Chun-Che</creatorcontrib><creatorcontrib>Liu, Tzu-Shang Thomas</creatorcontrib><creatorcontrib>Chang, Chih-Hung</creatorcontrib><creatorcontrib>Shih, Tiffany Ting-Fang</creatorcontrib><creatorcontrib>Wang, Jyh-Horng</creatorcontrib><creatorcontrib>Yang, Ming-Chia</creatorcontrib><creatorcontrib>Lin, Feng-Huei</creatorcontrib><creatorcontrib>Liu, Hwa-Chang</creatorcontrib><title>Safety and Efficacy of Kartigen® in Treating Cartilage Defects: A Randomized, Controlled, Phase I Trial</title><title>Polymers</title><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.</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 & 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 ; 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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c392t-35bfafd392d0621ba8a6c25d6a334aba7404841e02c92cd517147c0f9989d1c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Arthritis</topic><topic>Bone marrow</topic><topic>Cartilage</topic><topic>Collagen</topic><topic>Columnar structure</topic><topic>Defects</topic><topic>FDA approval</topic><topic>Glycosaminoglycans</topic><topic>Knee</topic><topic>Laboratory tests</topic><topic>Microfracture</topic><topic>Osteoarthritis</topic><topic>Physical examinations</topic><topic>Safety</topic><topic>Stem cells</topic><topic>Tissue engineering</topic><topic>Transplants & implants</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Yen-Liang</creatorcontrib><creatorcontrib>Yen, Chun-Che</creatorcontrib><creatorcontrib>Liu, Tzu-Shang Thomas</creatorcontrib><creatorcontrib>Chang, Chih-Hung</creatorcontrib><creatorcontrib>Shih, Tiffany Ting-Fang</creatorcontrib><creatorcontrib>Wang, Jyh-Horng</creatorcontrib><creatorcontrib>Yang, Ming-Chia</creatorcontrib><creatorcontrib>Lin, Feng-Huei</creatorcontrib><creatorcontrib>Liu, Hwa-Chang</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>SciTech Premium Collection</collection><collection>Materials Research Database</collection><collection>Materials Science Database</collection><collection>Materials Science Collection</collection><collection>Access via ProQuest (Open Access)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Polymers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Yen-Liang</au><au>Yen, Chun-Che</au><au>Liu, Tzu-Shang Thomas</au><au>Chang, Chih-Hung</au><au>Shih, Tiffany Ting-Fang</au><au>Wang, Jyh-Horng</au><au>Yang, Ming-Chia</au><au>Lin, Feng-Huei</au><au>Liu, Hwa-Chang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Safety and Efficacy of Kartigen® in Treating Cartilage Defects: A Randomized, Controlled, Phase I Trial</atitle><jtitle>Polymers</jtitle><date>2021-09-07</date><risdate>2021</risdate><volume>13</volume><issue>18</issue><spage>3029</spage><pages>3029-</pages><issn>2073-4360</issn><eissn>2073-4360</eissn><abstract>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.</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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