Especificaciones
El test Multi-Cancer Detect es un examen genético que analiza 84 genes que tienen relación con el riesgo de padecer cáncer hereditario de los 8 principales sistemas del organismo, que incluyen:
Estadística
SENSIBILIDAD Y ESPECIFICIDAD
Todos estos exámenes alcanzan una sensibilidad y especificidad de >99% para variaciones de nucleótidos simples, para inserciones y eliminaciones de <15bp de longitud y eliminaciones y duplicaciones de niveles de exones.
Referencias
- Cancer Research UK, cancerresearchuk.org. Accessed September 2019.
- National Cancer Institute, Cancer.gov, Accessed September 2019.
- American Society of Clinical Oncology, Cancer. Net Accessed September 2019.
- Desmond, A, et al. Clinical Actionability of Multigene Panel Testing for Hereditary Breast and Ovarian Cancer Risk Assessment. JAMA Oncol. 2015; :None. PMID: 26270727
- Hall, MJ, et al. Gene panel testing for inherited cancer risk. J Natl Compr Canc Netw. 2014; 12(9):1339-46. PMID: 25190699
- LaDuca, H, et al. Utilization of multigene panels in hereditary cancer predisposition testing: analysis of more than 2,000 patients. Genet. Med. 2014; 16(11):830-7. PMID: 24763289
- Kurian, AW, et al. Clinical evaluation of a multiple-gene sequencing panel for hereditary cancer risk assessment. J. Clin. Oncol. 2014; 32(19):2001-9. PMID: 24733792
- Malkin, D, et al. Predisposition to pediatric and hematologic cancers: a moving target. Am Soc Clin Oncol Educ Book. 2014; :e44-55. PMID: 24857136
- Robson, ME, et al. American Society of Clinical Oncology Policy Statement Update: Genetic and Genomic Testing for Cancer Susceptibility. J. Clin. Oncol. 2015; 33(31):3660-7. PMID: 26324357
- Garber, JE, Offit, K. Hereditary cancer predisposition syndromes. J. Clin. Oncol. 2005; 23(2):276-92. doi: 10.1200/JCO.2005.10.042. PMID: 15637391
- Hampel, H, et al. A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment. Genet. Med. 2015; 17(1):70-87. doi: 10.1038/gim.2014.147. PMID: 25394175