Next Generation Sequencing and Molecular Biomarkers in Ovarian Cancer-An Opportunity for Targeted Therapy

被引:24
作者
Harbin, Laura M. [1 ]
Gallion, Holly H. [1 ]
Allison, Derek B. [2 ]
Kolesar, Jill M. [1 ,3 ]
机构
[1] Univ Kentucky, Markey Canc Ctr, Dept Obstet & Gynecol, Div Gynecol Oncol, Lexington, KY 40536 USA
[2] Univ Kentucky, Coll Med, Dept Pathol & Lab Med, Lexington, KY 40536 USA
[3] Univ Kentucky, Coll Pharm, Dept Pharm Practice & Sci, 760 Press Ave, Lexington, KY 40536 USA
关键词
next generation sequencing; precision medicine; ovarian cancer; targeted therapy; PARP inhibitors; immunotherapy; NTRK inhibitors; HOMOLOGOUS RECOMBINATION DEFICIENCY; MISMATCH-REPAIR DEFICIENCY; ANTITUMOR-ACTIVITY; ESMO RECOMMENDATIONS; MAINTENANCE THERAPY; CLINICAL ASSAYS; DOUBLE-BLIND; SAFETY; LAROTRECTINIB; INHIBITORS;
D O I
10.3390/diagnostics12040842
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Ovarian cancer is the deadliest of all gynecologic malignancies claiming the lives of nearly 14,000 women in the United States annually. Despite therapeutic advances, the ovarian cancer mortality rate has remained stagnant since the 1980's. The molecular heterogeneity of ovarian cancers suggest they may be more effectively treated via precision medicine. Current guidelines recommend germline and somatic testing for all new epithelial ovarian cancer diagnoses to assist providers in identifying candidates for targeted therapies. Next generation sequencing (NGS) identifies targetable, driver, and novel mutations used to guide treatment decisions. Performing NGS is standard of care in many other malignancies, but for ovarian cancer the use of NGS in daily practice is still emerging. This review discusses the targetable genetic mutations and role of NGS and molecular biomarker testing in the treatment of ovarian cancer.
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页数:17
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