Germline and Somatic Tumor Testing in Epithelial Ovarian Cancer: ASCO Guideline
Affiliations
- PMID: 31986064
- DOI: 10.1200/JCO.19.02960
Abstract
Purpose: To provide recommendations on genetic and tumor testing for women diagnosed with epithelial ovarian cancer based on available evidence and expert consensus.
Methods: A literature search and prospectively defined study selection criteria sought systematic reviews, meta-analyses, randomized controlled trials (RCTs), and comparative observational studies published from 2007 through 2019. Guideline recommendations were based on the review of the evidence.
Results: The systematic review identified 19 eligible studies. The evidence consisted of systematic reviews of observational data, consensus guidelines, and RCTs.
Recommendations: All women diagnosed with epithelial ovarian cancer should have germline genetic testing for BRCA1/2 and other ovarian cancer susceptibility genes. In women who do not carry a germline pathogenic or likely pathogenic BRCA1/2 variant, somatic tumor testing for BRCA1/2 pathogenic or likely pathogenic variants should be performed. Women with identified germline or somatic pathogenic or likely pathogenic variants in BRCA1/2 genes should be offered treatments that are US Food and Drug Administration (FDA) approved in the upfront and the recurrent setting. Women diagnosed with clear cell, endometrioid, or mucinous ovarian cancer should be offered somatic tumor testing for mismatch repair deficiency (dMMR). Women with identified dMMR should be offered FDA-approved treatment based on these results. Genetic evaluations should be conducted in conjunction with health care providers familiar with the diagnosis and management of hereditary cancer. First- or second-degree blood relatives of a patient with ovarian cancer with a known germline pathogenic cancer susceptibility gene variant should be offered individualized genetic risk evaluation, counseling, and genetic testing. Clinical decision making should not be made based on a variant of uncertain significance. Women with epithelial ovarian cancer should have testing at the time of diagnosis.
Similar articles
- BRCA1- and BRCA2-Associated Hereditary Breast and Ovarian CancerN Petrucelli et al. PMID 20301425. - ReviewGermline pathogenic variants in BRCA1 and BRCA2 are inherited in an autosomal dominant manner. The vast majority of individuals with a BRCA1 or BR …
- Prevalence of Germline Pathogenic BRCA1/2 Variants in Sequential Epithelial Ovarian Cancer CasesRD Morgan et al. J Med Genet 56 (5), 301-307. PMID 30683677.Five hundred and fifty-seven patients were screened. Of these, 18% had inherited a pathogenic BRCA1/2 variant. The prevalence of pathogenic BRCA1/2 v …
- Prophylactic Oophorectomy: Reducing the U.S. Death Rate From Epithelial Ovarian Cancer. A Continuing DebateMS Piver. Oncologist 1 (5), 326-330. PMID 10388011.If instead of the title "Prophylactic Oophorectomy: Reducing the U.S. Death Rate from Epithelial Ovarian Cancer," the title were "Drug X Reducing the U.S. Death Rate from …
- No. 344-Opportunistic Salpingectomy and Other Methods of Risk Reduction for Ovarian/Fallopian Tube/Peritoneal Cancer in the General PopulationS Salvador et al. J Obstet Gynaecol Can 39 (6), 480-493. PMID 28527613.This guideline was developed with resources funded by the Society of Gynecologic Oncology of Canada and SOGC.
- Genetic Tests for Breast and Ovarian Cancer [Internet]LK Juvet et al. PMID 29319983. - ReviewBackground Breast cancer is the most commonly diagnosed cancer in women. In 2005, there were about 3000 incident cases of breast cancer in Norway. Ovarian canc …
No hay comentarios:
Publicar un comentario