The Emerging Role of Stereotactic Radiotherapy in Primary Renal Cell Cancer: A Systematic Review of the Literature

2019 ◽  
Vol 105 (1) ◽  
pp. E255-E256
Author(s):  
A.V. Louie ◽  
R.J.M. Correa ◽  
G. Boldt ◽  
N.G. Zaorsky ◽  
S. Siva
2006 ◽  
Vol 17 (8) ◽  
pp. 1185-1196 ◽  
Author(s):  
P. Schöffski ◽  
H. Dumez ◽  
P. Clement ◽  
A. Hoeben ◽  
H. Prenen ◽  
...  

2014 ◽  
Vol 10 (14) ◽  
pp. 2177-2187 ◽  
Author(s):  
Katarzyna Kaminska ◽  
Cezary Szczylik ◽  
Fei Lian ◽  
Anna M Czarnecka

Author(s):  
Brigitte Schlehofer ◽  
Wolfgang Pommer ◽  
Anders Mellemgaard ◽  
John H. Stewart ◽  
Margaret McCredie ◽  
...  

1990 ◽  
Vol 18 (2) ◽  
pp. 42-45 ◽  
Author(s):  
Arie Belldegrun ◽  
Alec S. Kroo ◽  
Bernard Bochner ◽  
Robert Figlin ◽  
Jean B. deKernion

Kidney Cancer ◽  
2020 ◽  
Vol 4 (1) ◽  
pp. 3-13
Author(s):  
Inga Peters ◽  
Axel S. Merseburger ◽  
Hossein Tezval ◽  
Marcel Lafos ◽  
Pouriya Faraj Tabrizi ◽  
...  

Author(s):  
Tim Eisen

Renal cancer is the commonest malignancy of the kidney and worldwide, accounts for between 2% and 3% of the total cancer burden. The mainstay of curative treatment remains surgery. There have been significant advances in surgical technique, the most important ones being nephron-sparing surgery and laparoscopic nephrectomy. The medical treatment of advanced renal cell cancer has only improved markedly in the last decade with the development of antiangiogenic tyrosine-kinase inhibitors, inhibitors of mammalian target of rapamycin, and a diminished role for immunotherapy.Tyrosine-kinase inhibitor therapy results in reduction of tumour volume in around three-quarters of patients and doubles progression-free survival, but treatment is not curative. The management of side effects in patients on maintenance tyrosine-kinase inhibitors has improved in the last 3 years, although still presents difficulties which have to be actively considered.The molecular biology of renal cell carcinoma is better understood than for the majority of solid tumours. The commonest form of renal cancer, clear-cell carcinoma of the kidney, is strongly associated with mutations in the von Hippel–Lindau gene and more recently with chromatin-remodelling genes such as PBRM1. These genetic abnormalities lead to a loss of control of angiogenesis and uncontrolled proliferation of tumour cells. There is a very wide spectrum of tumour behaviour from the extremely indolent to the terribly aggressive. It is not currently known what accounts for this disparity in tumour behaviour.A number of outstanding questions are being addressed in scientific and clinical studies such as a clearer understanding of prognostic and predictive molecular biomarkers, the role of adjuvant therapy, the role of surgery in the presence of metastatic disease, how best to use our existing agents, and investigation of novel targets and therapeutic agents, especially novel immunotherapies.


2016 ◽  
Vol 20 (4) ◽  
pp. 334-336
Author(s):  
Kathryn Woolner ◽  
Ashley O’Toole ◽  
Lauren LaBerge

Background: Reed’s syndrome, also known as hereditary leiomyomatosis and renal cell cancer (HLRCC) syndrome, is an autosomal dominant condition in which affected individuals may develop cutaneous leiomyomas, uterine fibroids, and renal cell carcinoma. Objective: This report describes a unique case of HLRCC because it presented in pregnancy with development of cutaneous pilar leiomyomas. Methods: Review of the literature for previous cases of Reed’s syndrome during pregnancy including PubMed and Medline search. Results: Genetic testing of this patient demonstrated a mutation in the fumarate hydratase ( FH) gene. Review of the literature showed only 1 previous case series that described the onset of cutaneous lesions during pregnancy. Conclusion: This case serves as a reminder that there may exist a correlation between pregnancy and the first manifestation of cutaneous lesions in patients with HLRCC, and thus an increased clinical suspicion is warranted during this period.


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