Bone and Cartilage Research Unit, Arthropole Liège, Université de Liège, Institute of Pathology, CHU Sart-Tilman, 4000, Liège, Belgium.
Artialis SA, GIGA Tower, CHU Sart-Tilman, Liège, Belgium.
BMC Musculoskelet Disord. 2019 Jun 18;20(1):293. doi: 10.1186/s12891-019-2667-0.
The objective of this pilot study was to identify biological, clinical or structural biomarkers of an intra-articular hyaluronic acid injection efficacy (HYMOVIS®) for the design of a larger placebo-controlled clinical trial studying the disease-modifying activity of this treatment.
Forty six patients with symptomatic knee Osteoarthritis (OA) were enrolled in this open-label, prospective, multicenter, pilot study. Patients received two treatment cycles of intra-articular injections (3 mL) of HYMOVIS® (8 mg/mL of hyaluronic acid hexadecylamide) at 6 months interval. Each treatment cycle involved two intra-articular injections 1 week apart. All patients had Magnetic Resonance Imaging (MRI) of the target knee at baseline and 1 year, and blood samples to assess joint biomarkers. The primary outcome was the change in type II collagen-specific biomarkers (Coll2-1, Coll2-1NO2 and CTX-II) after HYMOVIS® treatment versus baseline. Secondary endpoints included levels changes in aggrecan chondroitin sulfate 846 epitope (CS-846), Cartilage Oligomeric Matrix Protein (COMP), procollagen type II N-terminal propeptide (PIIANP), Matrix Metalloprotease (MMP)-3, Myeloperoxidase (MPO) and Interleukin (IL)-6 serum biomarkers, the ratio Coll2-1/PIIANP, CTX-II/PIIANP, variation of MRI cartilage volume, and Knee injury and Osteoarthritis Outcome Score (KOOS) index.
Coll2-1 serum levels significantly increased overtime while Coll2-1NO2 levels were only increased at D360. Serum PIIANP levels also progressively and significantly enhanced with time. In contrast, other serum biomarker levels including CTX-II, CS-846, COMP, MMP-3, MPO or IL-6 did not change significantly overtime. Interestingly, the ratios Coll2-1/PIIANP and CTX-II/PIIANP decreased, indicating a decrease of cartilage catabolism. Compared to baseline value, MRI cartilage volume and thickness increased in lateral femoral and lateral trochlea compartments and not in medial compartment. These results, in addition to an improvement of T2 mapping score suggest a positive structural effect of the product. Interestingly, WORMS effusion score, an indicator of synovitis, significantly decreased. Finally, global KOOS score and subscales significantly increased overtime while pain at rest, walking pain and patients or investigators global assessment of disease activity decreased. The safety profile was favorable with a low incidence of injection-site pain.
HYMOVIS®, a well-tolerated intra-articular treatment, significantly enhanced type II collagen turnover as suggested by the increase in Coll2-1 and PIIANP levels and cartilage volume observed by MRI in lateral knee compartment. Importantly, this study provides critical information for the design of a larger phase III clinical trial investigating Disease Modifying effect of HYMOVIS®.
http://www.isrctn.com/ISRCTN12227846 11/02/2015.
本研究旨在确定透明质酸关节内注射疗效(HYMOVIS®)的生物学、临床或结构生物标志物,为设计更大规模的安慰剂对照临床试验提供依据,以研究该治疗方法的疾病修饰活性。
46 例膝关节骨关节炎(OA)患者纳入本开放性、前瞻性、多中心、初步研究。患者接受了两次 HYMOVIS®(8mg/ml 透明质酸己酰胺)关节内注射治疗周期,间隔 6 个月。每个治疗周期包括两次间隔一周的关节内注射。所有患者在基线和 1 年时均接受目标膝关节的磁共振成像(MRI)检查,并采集血液样本以评估关节生物标志物。主要终点是治疗后与基线相比 II 型胶原特异性生物标志物(Coll2-1、Coll2-1NO2 和 CTX-II)的变化。次要终点包括软骨素硫酸 846 表位(CS-846)、软骨寡聚基质蛋白(COMP)、II 型前胶原 N 端前肽(PIIANP)、基质金属蛋白酶(MMP)-3、髓过氧化物酶(MPO)和白细胞介素(IL)-6 血清生物标志物的水平变化、Coll2-1/PIIANP、CTX-II/PIIANP 比值、MRI 软骨体积变化以及膝关节损伤和骨关节炎结果评分(KOOS)指数。
Coll2-1 血清水平随时间推移而显著升高,而 Coll2-1NO2 水平仅在 D360 时升高。血清 PIIANP 水平也随时间逐渐显著升高。相比之下,CTX-II、CS-846、COMP、MMP-3、MPO 或 IL-6 的其他血清生物标志物水平在整个研究期间没有明显变化。有趣的是,Coll2-1/PIIANP 和 CTX-II/PIIANP 比值降低,表明软骨分解代谢减少。与基线值相比,外侧股骨和外侧滑车的 MRI 软骨体积和厚度增加,而内侧软骨体积和厚度没有增加。这些结果,加上 T2 映射评分的改善,提示该产品具有积极的结构效应。有趣的是,WORMS 积液评分(反映滑膜炎的指标)显著降低。最后,全球 KOOS 评分和子量表随时间推移而显著增加,而休息时疼痛、行走时疼痛以及患者或研究者对疾病活动的总体评估则下降。该治疗具有良好的耐受性,且安全性良好,注射部位疼痛发生率低。
HYMOVIS®是一种耐受性良好的关节内治疗方法,通过 MRI 观察到外侧膝关节间隙中 Coll2-1 和 PIIANP 水平的升高以及软骨体积的增加,表明 II 型胶原转化率显著增加。重要的是,这项研究为设计更大规模的 III 期临床试验提供了关键信息,以研究 HYMOVIS®的疾病修饰作用。
http://www.isrctn.com/ISRCTN12227846 11/02/2015。