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Published on: January 22, 2013
Genetic risk assessment for hereditary renal cell carcinoma: Clinical consensus statement
Gennady Bratslavsky1, Neil Mendhiratta2, Michael Daneshvar1,3
1Department of Urology, State University of New York (SUNY, Upstate Medical University, Syracuse, New York.
This study established the first consensus on genetic risk assessment for hereditary renal cell carcinoma (RCC). Experts agreed on 30 statements guiding genetic testing and counseling for kidney cancer patients.
Area of Science:
- Oncology
- Genetics
- Urology
Background:
- Hereditary factors significantly contribute to renal cell carcinoma (RCC) development.
- Existing guidelines for genetic risk assessment in RCC are lacking.
- Clinicians face challenges in identifying patients needing genetic evaluation for hereditary kidney cancer.
Purpose of the Study:
- To gauge expert opinion on genetic risk assessment for hereditary RCC.
- To develop consensus statements guiding clinicians in evaluating patients with suspected hereditary kidney cancer.
- To address the need for standardized genetic risk assessment protocols in RCC.
Main Methods:
- A North American multidisciplinary expert panel was convened.
- Modified Delphi methodology was employed to generate and refine consensus questions.
- Uniform consensus was defined as ≥85% agreement among panelists.
Main Results:
- Thirty-three experts, including urologists, oncologists, and geneticists, participated.
- Uniform consensus was achieved on 30 statements regarding RCC genetic risk assessment.
- Key areas of agreement included family history criteria, risk assessment for specific disease presentations, multigene panel utility, and counseling acceptance.
Conclusions:
- The first consensus panel on hereditary RCC genetic risk assessment reached 30 statements.
- These statements offer guidance for clinicians evaluating patients for hereditary kidney cancer.
- Further research and discussion are needed, with a future meeting planned.
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