Kinoshita Yuka, Fukumoto Seiji
Division of Nephrology & Endocrinology, Department of Medicine, The University of Tokyo Hospital, Japan.
Clin Calcium. 2014 Aug;24(8):1217-22.
Tumor-induced osteomalacia (TIO) is a disease caused by fibroblast growth factor 23 (FGF23) secreted from the causative tumor. This disease is cured by complete surgical removal of the tumor. However, there are several difficult cases in which the responsible tumors cannot be found, are incompletely removed, or relapse after the surgery. Anti-FGF23 antibody is being studied as a novel therapy for FGF23-related hypophosphatemic diseases. The efficacy of anti-FGF23 antibodies were confirmed using a murine model of X-linked hypophosphatemic rickets (XLHR) , which is the most common heritable form of FGF23-related hypophosphatemic disease. In addition, results of phase I study of single injection of humanized anti-FGF23 antibody for adult patients with XLHR were recently published and the safety and effectiveness of this antibody was shown. This antibody therapy may be useful for patients with TIO with similar pathogenesis to that of XLHR.
肿瘤诱导的骨软化症(TIO)是一种由致病肿瘤分泌的成纤维细胞生长因子23(FGF23)引起的疾病。这种疾病通过手术完全切除肿瘤得以治愈。然而,存在一些困难病例,其中责任肿瘤无法找到、切除不完全或术后复发。抗FGF23抗体正作为FGF23相关低磷血症疾病的一种新疗法进行研究。使用X连锁低磷血症佝偻病(XLHR)小鼠模型证实了抗FGF23抗体的疗效,XLHR是FGF23相关低磷血症疾病最常见的遗传性形式。此外,最近公布了成人XLHR患者单次注射人源化抗FGF23抗体的I期研究结果,并显示了该抗体的安全性和有效性。这种抗体疗法可能对具有与XLHR相似发病机制的TIO患者有用。