Abstract
Renal cell cancer (RCC) has an incidence similar to differentiated thyroid cancer or Hodgkin’s disease and comprises approx. 2% of all cancers. More than 90% of these tumors are found in adults with a preference for the 7th and 8th decade of life. The male gender displays an increased incidence of about twice that of females. Over the last 40 years, mortality due to renal cell cancer has been rising at a rate of 2% per year in the developed countries in Europe and North America. This rise and the sex predilection are attributed to the use of tobacco products, the packaging (cardboard) industry, other environmental factors in petroleum and leather industries and exposure to cadmium, asbestos and trichlorethylene [3]. Obesity and chronic kidney failure are other contributing factors which are frequently observed in female renal cell cancer patients. The pathogenesis of renal cell cancer is still largely unclear. The prognosis of this tumor type in adults is rather poor with 5 year survival rates between 36 and 54%. If widespread tumor manifestations are present at admission, the 5-year survival rate decreases to virtually zero. All renal cell cancers are insensitive to chemotherapy with conventional cytostatic drugs and are primarily radiation resistant. Therefore, radical surgical removal of the tumor and solitary metastases are the only ways to achieve full remission. In particular, with lymph node and lung metastases, the eventual prognosis is critically dependent on the radicality of the primary surgical intervention. Additional determinants of prognosis are the size and number of metastases. Current therapeutic options for bone and liver metastases are limited and usually consist of palliation.
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Börner, A.R., Hofmann, M., Müller-Mattheis, V. (2000). Renal cell and urothelial cancer. In: Wieler, H.J., Coleman, R.E. (eds) PET in Clinical Oncology. Steinkopff, Heidelberg. https://doi.org/10.1007/978-3-642-57703-1_26
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DOI: https://doi.org/10.1007/978-3-642-57703-1_26
Publisher Name: Steinkopff, Heidelberg
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