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Kidney Metastatic Bone Disease

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Metastatic Bone Disease

Abstract

Renal cell carcinoma (RCC) is the eighth most common type of cancer in the USA with an estimated 13,860 deaths in 2014. Renal cell carcinoma represents a spectrum of tumors that are significantly different with respect to their cell type origin and type of genetic mutations. Metastatic lesions are quite common in RCC. They are found in one third of new cases and develop in 20–40 % patients after surgical treatment for localized disease. Historically, metastatic RCC (mRCC) has had a dismal prognosis. Currently, patients benefit from a multimodal and multispecialty treatment approach. Combination of surgical management consisting of cytoreductive nephrectomy and metastasectomy in a selected patient population followed by adjuvant therapy has been reported to achieve 5-year survival rates exceeding 70 %. Research of the von Hippel–Lindau tumor suppressor gene has led to better understanding of the RCC biology and development of novel therapeutic agents targeting specific molecules in the VHL signaling pathway. Targeted therapy has now become the adjuvant treatment of choice in mRCC. Numerous new treatment options for mRCC are currently being investigated in clinical trials.

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Luzny, P., Dechet, C. (2016). Kidney Metastatic Bone Disease. In: Randall, R. (eds) Metastatic Bone Disease. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-5662-9_7

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