Germline and Somatic Tumor Testing in Epithelial Ovarian Cancer: ASCO Guideline

被引:259
作者
Konstantinopoulos, Panagiotis A. [1 ]
Norquist, Barbara [2 ]
Lacchetti, Christina [3 ]
Armstrong, Deborah [4 ]
Grisham, Rachel N. [5 ]
Goodfellow, Paul J. [6 ]
Kohn, Elise C. [7 ]
Levine, Douglas A. [8 ]
Liu, Joyce F. [1 ]
Lu, Karen H. [9 ]
Sparacio, Dorinda
Annunziata, Christina M. [10 ]
机构
[1] Dana Farber Canc Inst, Boston, MA 02115 USA
[2] Univ Washington Med, Seattle, WA USA
[3] Amer Soc Clin Oncol, 2318 Mill Rd,Ste 800, Alexandria, VA 22314 USA
[4] Johns Hopkins, Baltimore, MD USA
[5] Mem Sloan Kettering Canc Ctr, 1275 York Ave, New York, NY 10021 USA
[6] Ohio State Univ, Comprehens Canc Ctr, Columbus, OH 43210 USA
[7] NCI, Gynecol Canc Therapeut, Bethesda, MD 20892 USA
[8] NYU, Langone Hlth, New York, NY USA
[9] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
[10] NCI, Womens Malignancies Branch, Bethesda, MD 20892 USA
关键词
OLAPARIB MAINTENANCE THERAPY; MICROSATELLITE INSTABILITY DETECTION; HOMOLOGOUS RECOMBINATION GENES; MISMATCH REPAIR DEFICIENCY; PARP INHIBITOR RUCAPARIB; SHARED DECISION-MAKING; AMERICAN SOCIETY; FALLOPIAN-TUBE; BRCA MUTATION; DOUBLE-BLIND;
D O I
10.1200/JCO.19.02960
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PURPOSETo provide recommendations on genetic and tumor testing for women diagnosed with epithelial ovarian cancer based on available evidence and expert consensus.METHODSA 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.RESULTSThe systematic review identified 19 eligible studies. The evidence consisted of systematic reviews of observational data, consensus guidelines, and RCTs.RECOMMENDATIONSAll 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. (c) 2020 by American Society of Clinical Oncology
引用
收藏
页码:1222 / +
页数:27
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