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基于证据的骨科生物制剂指南。

Evidence-based guidelines on orthobiologics.

作者信息

Winkler Tobias, Oehme Stephan, Hildebrandt Alexander, Paolucci Azzurra, Pichler Lorenz

出版信息

EFORT Open Rev. 2025 Jun 2;10(6):345-351. doi: 10.1530/EOR-2025-0069.

Abstract

Orthobiologics (OBs) have seen a constant increase in the number of available therapies and their clinical applications. Existing therapies can be categorized into blood-based (e.g., platelet-rich plasma (PRP)) and tissue/cell-based (e.g. mesenchymal stromal cells) approaches. While the popularity of OBs continues to grow, their diverse natures create unique challenges for the establishment of evidence-based guidelines. PRP has been reported by meta-analyses to increase patient-reported outcomes for conditions such as knee osteoarthritis (KOA), lateral epicondylitis and plantar fasciitis. However, the randomized controlled trials (RCTs) included often exhibit a high risk of bias due to the heterogeneity in the PRP preparation protocols and accompanying measures as well as inconsistent trial quality. The development pipeline of cell/tissue-based therapies is typically longer and more cost-intensive than that of blood-based therapies. Nevertheless, several products have demonstrated clinical safety. While some RCTs and meta-analyses on the outcome of cell/tissue-based therapies exist, their number is considerably lower than that of blood-based therapies and they focus mainly on KOA, with limited evidence on other orthopedic indications. Orthopedic societies such as ESSKA and AAOS have taken on the challenge of developing guidelines for OBs by combining high-level synthesized evidence with expert consensus. Patient stratification strategies represent a promising key to unlocking the full potential of OBs and are currently being investigated in ongoing studies. Further efforts to establish guidelines for the use of OBs should focus on developing frameworks for clinical trials and their reporting, alongside standardized protocols for the preparation, application and accompanying measures of OB therapies.

摘要

骨科生物制剂(OBs)的可用疗法及其临床应用数量一直在不断增加。现有疗法可分为基于血液的(如富血小板血浆(PRP))和基于组织/细胞的(如间充质基质细胞)方法。虽然OBs的受欢迎程度持续上升,但其多样的性质为制定循证指南带来了独特挑战。荟萃分析报告称,PRP可改善患者报告的膝关节骨关节炎(KOA)、外侧上髁炎和足底筋膜炎等疾病的预后。然而,纳入的随机对照试验(RCT)往往因PRP制备方案和伴随措施的异质性以及试验质量不一致而存在较高的偏倚风险。基于细胞/组织的疗法的研发流程通常比基于血液的疗法更长且成本更高。尽管如此,一些产品已证明具有临床安全性。虽然存在一些关于基于细胞/组织疗法结果的RCT和荟萃分析,但其数量远低于基于血液的疗法,且主要集中在KOA,其他骨科适应症的证据有限。欧洲运动创伤、关节镜与骨科协会(ESSKA)和美国骨科医师学会(AAOS)等骨科协会通过将高级综合证据与专家共识相结合,承担起了为OBs制定指南的挑战。患者分层策略是充分发挥OBs潜力的一个有前景的关键,目前正在正在进行的研究中进行调查。进一步努力制定OBs使用指南应侧重于制定临床试验及其报告的框架,以及OB疗法制备、应用和伴随措施的标准化方案。

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