Lee Bumsup, Parvizi Javad, Bramlet Dale, Romness David W, Guermazi Ali, Noh Moon, Sodhi Nipun, Khlopas Anton, Mont Michael A
Kolon Life Science, Inc., Gwacheon, Gyeonggi, Republic of Korea.
Rothman Institute Philadelphia, Pennsylvania.
J Knee Surg. 2020 Feb;33(2):167-172. doi: 10.1055/s-0038-1676803. Epub 2019 Jan 4.
Genetically engineered chondrocytes virally transduced with a transforming growth factor (TGF)-1 (TG-C [TissueGene-C]) expression vector have been shown to have potential benefits in the nonoperative management of knee osteoarthritis. Previous literature has reported on safe dosages of TG-C. Therefore, the purpose of this study was to evaluate the Phase II results and a 24-month efficacy of this injectable mixture compared with placebo in patients with Kellgren-Lawrence (K-L) grade III knee osteoarthritis. Specifically, we assessed (1) functional outcomes, (2) pain scores, (3) adverse events (AEs), and (4) magnetic resonance imaging (MRIs) findings. We performed a multicenter, double-blinded, placebo-controlled, and randomized study of adults who had K-L grade III knee osteoarthritis. A total of 102 patients were 2:1 randomized to TG-C at a dose of 3.0 × 10 cells, or placebo injections between May 1, 2011 and October 31, 2012. Outcomes analyzed were knee joint function, pain, quality of life, adverse events, and MRI findings using the whole-organ magnetic resonance imaging score (WORMS) system. There were significant improvements in the International Knee Documentation Committee (IKDC) and visual analogue scale (VAS) scores in the TG-C cohort, when compared with the placebo cohort at weeks 12, 52, 72, and 104 ( < 0.05). No severe AEs were observed. Common AEs were arthralgia, joint inflammation, and joint effusion which were similar between both cohorts. Whole-knee MRIs at 12 months showed less progression of cartilage damage, infrapatellar fat pad-synovitis, and effusion-synovitis in the TG-C cohort. Patients who received TG-C had significant improvements in IKDC and VAS scores. These patients also reported less severe and frequent pain. Additionally, fewer patients treated with TG-C showed progression of cartilage damage, as well as less progression of infrapatellar fat pad synovitis and effusion-synovitis. Furthermore, treatment with TG-C was generally well tolerated with minor AEs. Therefore, based on these results, TG-C appears to be a safe and effective modality for the management of K-L grade III osteoarthritis.
用转化生长因子(TGF)-1(TG-C [组织基因-C])表达载体进行病毒转导的基因工程软骨细胞已被证明在膝关节骨关节炎的非手术治疗中具有潜在益处。既往文献报道了TG-C的安全剂量。因此,本研究的目的是评估这种注射混合物与安慰剂相比,在凯尔格伦-劳伦斯(K-L)III级膝关节骨关节炎患者中的II期结果和24个月疗效。具体而言,我们评估了(1)功能结果,(2)疼痛评分,(3)不良事件(AE),以及(4)磁共振成像(MRI)结果。我们对患有K-L III级膝关节骨关节炎的成年人进行了一项多中心、双盲、安慰剂对照和随机研究。2011年5月1日至2012年10月31日期间,共有102例患者按2:1随机分为接受3.0×10个细胞剂量的TG-C组或安慰剂注射组。使用全器官磁共振成像评分(WORMS)系统分析的结果包括膝关节功能、疼痛、生活质量、不良事件和MRI结果。与安慰剂组相比,在第12、52、72和104周时,TG-C组的国际膝关节文献委员会(IKDC)和视觉模拟量表(VAS)评分有显著改善(P<0.05)。未观察到严重不良事件。常见不良事件为关节痛、关节炎症和关节积液,两组相似。12个月时的全膝关节MRI显示,TG-C组软骨损伤、髌下脂肪垫滑膜炎和积液性滑膜炎的进展较少。接受TG-C治疗的患者IKDC和VAS评分有显著改善。这些患者还报告疼痛较轻且频率较低。此外,接受TG-C治疗的患者软骨损伤进展较少,髌下脂肪垫滑膜炎和积液性滑膜炎的进展也较少。此外,TG-C治疗一般耐受性良好,不良事件轻微。因此,基于这些结果,TG-C似乎是治疗K-L III级骨关节炎的一种安全有效的方法。