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Molecular target therapy for bone metastasis: starting a new era with denosumab, a RANKL inhibitor

机译:骨转移分子靶向疗法:RANKL抑制剂denosumab开启新时代

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摘要

INTRODUCTION:udThe skeleton is generally the primary, and sometimes the only, site of metastasis in patients with advanced solid tumors. Bone metastases are the most frequent cause of cancer-related pain and the origin of severe morbidity in patients. Among the treatment options available for the prevention of skeletal-related events (SREs) associated with bone metastasis, zoledronic acid, an antiresorptive treatment from the group of bisphosphonates, is currently the standard of care in this setting.udAREAS COVERED:udZoledronic acid, together with denosumab (a monoclonal antibody against the receptor activator of nuclear factor kappa B ligand), is the most frequent approach for the prevention of cancer-related events in skeleton. This paper reviews several trials evaluating the efficacy of denosumab in comparison with zoledronic acid in patients with solid osteotropic tumors. In this setting of skeleton-invading cancers, denosumab was demonstrated to be superior to zoledronic acid in preventing or delaying SREs. In comparison with zoledronic acid, denosumab significantly delayed the time to first SRE by 17%.udEXPERT OPINION:udCurrent research on denosumab is addressed to prove the immunomodulator effect of this agent in humans. Other avenue of research is focused on its antitumor activity observed in some Phase III trials.
机译:导言: ud骨骼通常是晚期实体瘤患者的主要转移部位,有时是唯一的转移部位。骨转移是癌症相关疼痛的最常见原因,也是患者严重发病的起源。在预防与骨转移相关的骨骼相关事件(SRE)的可用治疗方法中,唑来膦酸是双膦酸盐类的一种抗吸收性治疗,目前是这种情况下的标准治疗方法。与denosumab(针对核因子κB配体的受体激活剂的单克隆抗体)一起使用,是预防骨骼癌相关事件的最常见方法。本文综述了几项评价地诺单抗与唑来膦酸治疗实体性骨质疏松性肿瘤的疗效的试验。在这种侵犯骨骼的癌症中,狄诺塞麦在预防或延缓SRE方面优于唑来膦酸。与唑来膦酸相比,地诺单抗将首次SRE的时间显着延迟了17%。 udEXPERT观点: ud目前正在研究地诺单抗,以证明该药在人体中的免疫调节作用。其他研究途径集中在一些III期临床试验中观察到的抗肿瘤活性。

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