Department of Gynecology and Obstetrics, Odense University Hospital, Sdr. Boulevard 29, 5000 Odense C, Denmark; Research Unit of Gynecology and Obstetrics, Department of Clinical Research, University of Southern Denmark, Odense University Hospital, Kløvervænget 10, 10(th) floor, 5000 Odense C, Denmark.
Research Unit for ORL - Head & Neck Surgery and Audiology, Odense University Hospital, J. B. Winsløws Vej 4, 5000 Odense C, Denmark.
Gynecol Oncol. 2021 Jun;161(3):884-895. doi: 10.1016/j.ygyno.2021.04.020. Epub 2021 Apr 21.
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.
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.
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.
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.
提高上皮性卵巢癌 (EOC) 患者的存活率的方法之一是确定在疾病的不同阶段和时间点都有效的有价值的生物标志物。循环肿瘤 DNA(ctDNA)是一种有潜力的生物标志物,存在于血浆或血清中。在本次系统综述中,我们概述了 ctDNA 在 EOC 中的应用,以讨论该领域未来研究的方向。
我们在 Pubmed、Embase 和 Scopus 中进行了系统检索,以确定符合纳入标准的相关临床研究。此外,还评估了确定研究中的参考文献和相关综述,以确定其他研究。采用 PRISMA 指南进行系统综述,使用预试验数据提取表提取研究数据。
共纳入 36 项观察性研究。有 19 项研究评估了肿瘤与 ctDNA 的一致性,1 项研究评估了早期诊断,23 项研究评估了诊断,7 项研究评估了治疗反应监测,3 项研究评估了反转突变检测,9 项研究评估了预后,但没有研究评估复发的早期检测。研究数据以描述性报告呈现。这些研究在 ctDNA 分析方法上存在很大差异,样本量也有限,为 10-126 例患者。总的来说,这些研究表明 ctDNA 是一种有潜力的 EOC 生物标志物,在评估和治疗这些患者时具有多种应用价值。
尽管纳入的研究数量有限,ctDNA 分析方法也存在差异,但 ctDNA 作为 EOC 的生物标志物在诊断、治疗反应监测和预后方面具有很大的应用前景。然而,还需要更多的研究来确定 ctDNA 在 EOC 临床应用中的理想方法和应用场景。