Epithelial ovarian cancer and the use of circulating tumor DNA: A systematic review

被引:14
|
作者
Thusgaard, Christine Fribert [1 ,2 ]
Korsholm, Malene [3 ]
Koldby, Kristina Magaard [4 ,5 ]
Kruse, Torben A. [4 ,5 ]
Thomassen, Mads [4 ,5 ]
Jochumsen, Kirsten Marie [1 ,2 ]
机构
[1] Odense Univ Hosp, Dept Gynecol & Obstet, Sdr Blvd 29, DK-5000 Odense C, Denmark
[2] Univ Southern Denmark, Odense Univ Hosp, Dept Clin Res, Res Unit Gynecol & Obstet, Klovervaenget 20,20th Floor, DK-5000 Odense C, Denmark
[3] Odense Univ Hosp, Res Unit ORL Head & Neck Surg & Audiol, JB Winslows Vej 4, DK-5000 Odense C, Denmark
[4] Odense Univ Hosp, Dept Clin Genet, JB Winslows Vej 4, DK-5000 Odense C, Denmark
[5] Univ Southern Denmark, Odense Univ Hosp, Dept Clin Res, Clin Genome Ctr, Winslows Vej 4, DK-5000 Odense C, Denmark
关键词
Epithelial ovarian cancer; Circulating tumor DNA; Biomarker; MUTATIONS; BRCA1; SERUM;
D O I
10.1016/j.ygyno.2021.04.020
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective. One way to improve the survival rate of epithelial Ovarian Cancer (EOC) is by identifying effective biomarkers useful at different stages and time points of the disease. A potential biomarker is circulating tumor DNA (ctDNA) in plasma or serum. In this systematic review, we provide an overview of applications of ctDNA in EOC to discuss the direction of future research in this field. Methods. We performed a systematic search in Pubmed, Embase, and Scopus to identify relevant clinical studies eligible for inclusion. Furthermore, the references in the identified studies and relevant reviews were assessed to identify additional studies. The PRISMA guideline was employed to perform the systematic review, and data from the studies were extracted using piloted data extraction forms. Results. A total of 36 observational studies were included. The concordance between tumor and ctDNA was assessed in 19 studies, early diagnosis in 1, diagnosis in 23, monitoring of treatment response in 7, detection of reversion mutations in 3, prognosis in 9, but no studies assessed early detection of recurrence. Data from the studies were reported descriptively. The studies had a large variation in the methods used for ctDNA analysis and limited sample sizes of 10-126 patients. Overall, the studies show that ctDNA is a potential biomarker for EOC useful in several settings during assessment and treatment of these patients. Conclusions. Although the identified studies are limited in number and their methods for ctDNA analysis vary, it is clear that ctDNA as a biomarker for EOC is promising for several applications in diagnostics, monitoring of treatment response, and prognostics. However, more studies are needed to establish the ideal methods and settings for the clinical use of ctDNA in EOC. (C) 2021 Elsevier Inc. All rights reserved.
引用
收藏
页码:884 / 895
页数:12
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