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Updated: Apr 23, 2026

Next Generation Sequencing for the Detection of Actionable Mutations in Solid and Liquid Tumors
Published on: September 20, 2016
The evolution of multigene panel testing for hereditary cancers.
Richard E Frieder1, Shari Goldman Snow2, Marra S Francis3
1Department of Obstetrics and Gynecology, David Geffen School of Medicine, UCLA, University of California, Los Angeles, CA.
A thorough family history evaluation is crucial for identifying hereditary cancer risk. Updated evaluations and multigene panel testing can guide management options for at-risk patients.
Area of Science:
- Oncology
- Genetics
- Preventive Medicine
Background:
- Family history evaluation is essential for identifying hereditary cancer risk.
- The American College of Obstetricians and Gynecologists (ACOG) recommends regular family history updates for all women.
- Abnormal findings necessitate further evaluation, including hereditary cancer testing.
Purpose of the Study:
- To emphasize the importance of family history in hereditary cancer risk assessment.
- To highlight the role of multigene panel testing in comprehensive genetic profiling.
- To discuss management strategies for patients with established hereditary cancer.
Main Methods:
- Review of current recommendations for family history evaluation.
- Discussion of multigene panel testing as a diagnostic tool.
- Outline of management options following hereditary cancer diagnosis.
Main Results:
- Family history evaluation is a critical first step in risk identification.
- Multigene panel testing offers broader risk assessment than single gene tests.
- Management includes surveillance, chemoprevention, and surgical options.
Conclusions:
- Integrating hereditary cancer risk assessment into clinical practice is vital.
- Workflow protocols can facilitate the implementation of risk assessment.
- Personalized management strategies improve outcomes for hereditary cancer patients.
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