Faundez Antonio, Tournier Clément, Garcia Matthieu, Aunoble Stéphane, Le Huec Jean-Charles
Hôpital Universitaire de Genève, Rue Gabrielle Perret-Gentil 4, 1211, Geneva 14, Switzerland.
Université Bordeaux, Orthospine Department 2, 146 rue Leo Saignat, 33076, Bordeaux Cedex, France.
Int Orthop. 2016 Jun;40(6):1309-19. doi: 10.1007/s00264-016-3149-8. Epub 2016 Mar 10.
Because of significant complications related to the use of autologous bone grafts in spinal fusion surgery, bone substitutes and growth factors such as bone morphogenetic protein (BMP) have been developed. One of them, recombinant human (rh) BMP-2, has been approved by the Food and Drug Administration (FDA) for use under precise conditions. However, rhBMP-2-related side effects have been reported, used in FDA-approved procedures, but also in off-label use.A systematic review of clinical data was conducted to analyse the rhBMP-2-related adverse events (AEs), in order to assess their prevalence and the associated surgery practices.
Medline search with keywords "bone morphogenetic protein 2", "lumbar spine", "anterolateral interbody fusion" (ALIF) and the filter "clinical trial". FDA published reports were also included. Study assessment was made by authors (experienced spine surgeons), based on quality of study designs and level of evidence.
Extensive review of randomised controlled trials (RCTs) and controlled series published up to the present point, reveal no evidence of a significant increase of AEs related to rhBMP-2 use during ALIF surgeries, provided that it is used following FDA guidelines. Two additional RCTs performed with rhBMP-2 in combination with allogenic bone dowels reported increased bone remodelling in BMP-treated patients. This AE was transient and had no consequence on the clinical outcome of the patients. No other BMP-related AEs were reported in these studies.
This literature review confirms that the use of rhBMP-2 following FDA-approved recommendations (i.e. one-level ALIF surgery with an LT-cage) is safe. The rate of complications is low and the AEs had been identified by the FDA during the pre-marketing clinical trials. The clinical efficiency of rhBMP-2 is equal or superior to that of allogenic or autologous bone graft in respect to fusion rate, low back pain disability, patient satisfaction and rate of re-operations. For all other off-label use, the safety and effectiveness of rhBMP-2 have not been established, and further RCTs with high level of evidence are required.
由于在脊柱融合手术中使用自体骨移植存在显著并发症,因此已开发出骨替代物和生长因子,如骨形态发生蛋白(BMP)。其中之一,重组人(rh)BMP-2已获得美国食品药品监督管理局(FDA)批准,可在精确条件下使用。然而,rhBMP-2相关的副作用不仅在FDA批准的手术中被报道,在非标签使用中也有出现。本研究对临床数据进行系统回顾,以分析rhBMP-2相关的不良事件(AE),从而评估其发生率及相关手术操作。
使用关键词“骨形态发生蛋白2”、“腰椎”、“前外侧椎间融合术”(ALIF)在Medline数据库中进行检索,并使用“临床试验”过滤器。同时纳入FDA发布的报告。由作者(经验丰富的脊柱外科医生)根据研究设计质量和证据水平进行研究评估。
对截至目前发表的随机对照试验(RCT)和对照系列进行广泛回顾,结果显示,在ALIF手术中,只要按照FDA指南使用rhBMP-2,就没有证据表明与使用rhBMP-2相关的AE会显著增加。另外两项将rhBMP-2与同种异体骨栓联合使用的RCT报告称,接受BMP治疗的患者骨重塑增加。这种AE是短暂的,对患者的临床结局没有影响。这些研究中未报告其他与BMP相关的AE。
本文献综述证实,按照FDA批准的建议使用rhBMP-2(即使用LT椎间融合器进行单节段ALIF手术)是安全的。并发症发生率较低,且FDA在上市前临床试验中已识别出这些AE。就融合率、下腰痛残疾程度、患者满意度和再次手术率而言,rhBMP-2的临床疗效等同于或优于同种异体或自体骨移植。对于所有其他非标签使用情况,rhBMP-2的安全性和有效性尚未确立,需要进一步开展具有高证据水平的RCT。