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Clinical and translational pharmacology of drugs for the prevention and treatment of bone metastases and cancer‐induced bone loss

机译:药物临床和翻译药理学,用于预防和治疗骨转移和癌症诱导的骨质损失

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摘要

Bone disease is a frequent event in cancer patients, both due to cancer spread to bone and to cancer therapies. Bone is the organ most frequently affected by metastatic disease when considering the two most frequent cancers in the Western world (breast and prostate cancers). Bone metastases can have a substantial detrimental effect on patients' quality of life, as well as significant morbidity due to complications collectively known as skeletal‐related events (SREs), which include hypercalcaemia, pathological fractures, spinal cord compression, and need of radiotherapy or surgery to the bone. These have been successfully mitigated with the development of bone‐targeted agents (BTAs; bisphosphonates and denosumab), focused on inhibiting osteoclast activity. The potential direct antitumour effect of bisphosphonates, as well as the impact of osteoclast inhibition with subsequent decrease in bone metabolism, have also propelled investigation on the role of BTAs in preventing cancer relapse in bone. In this review, the authors aimed to discuss the role of BTAs in the treatment and prevention of bone metastases, as well as their potential value in preventing cancer treatment‐induced bone loss (CTIBL). The review will focus on breast and prostate cancers, with the aim of providing the most relevant clinical data emerging from bench to bedside translational research in the field of cancer‐induced bone disease.
机译:骨病是癌症患者的常见事件,既由于癌症蔓延到骨骼和癌症疗法。骨骼是在审查西方世界两种最常见的癌症(乳腺癌和前列腺癌)时最常受转移性疾病影响的器官。骨转移可以对患者的生活质量有很大的不利影响,以及由于共同称为骨骼相关事件(SRES)的并发症,其具有显着的发病率,包括高钙血症,病理骨折,脊髓压缩,并且需要放射疗法或需求手术到骨骼。这些已成功地随着骨靶向剂的发展(BTA;双膦酸盐和Denosumab)的开发,重点是抑制骨质体活性。双膦酸盐的潜在直接抗肿瘤作用以及随后的骨代谢减少的破骨细胞抑制的影响,还推动了BTA在预防骨癌中癌症复发方面的作用的研究。在本文中,作者旨在讨论BTA在治疗和预防骨转移中的作用,以及它们在预防癌症治疗诱导的骨质损失(CTIBL)的潜在价值。审查将重点关注乳腺癌和前列腺癌,目的是提供从长凳上出现的最相关的临床资料,以在癌症诱导的骨病领域的床边翻译研究。

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