Lee Young-Jae, Kim Yong-Man, Kang Ji-Sik, Nam So-Hyun, Kim Dae-Yeon, Kim Young-Tak
Department of Obstetrics and Gynecology, University of Ulsan College of Medicine, Asan Medical Center, Seoul 05505, Republic of Korea.
Oncol Lett. 2020 Jul;20(1):931-938. doi: 10.3892/ol.2020.11629. Epub 2020 May 14.
The present study aimed to compare the accuracy of the Risk of Ovarian Malignancy Algorithm (ROMA) and cancer antigen (CA)125 to discriminate between benign ovarian tumors and early-stage ovarian cancer according to imaging tumor subtypes associated with post-operative histopathological findings. A total of 1,207 patients who were assessed using the ROMA test due to suspected early-stage ovarian cancer and underwent surgery at Asan Medical Center (Seoul, Korea) between September 2014 and March 2018 were identified. A total of 981 patients who met the inclusion criteria were included in the retrospective analysis. Among the 981 subjects, 816 had benign tumors, 90 had malignant tumors and 75 had borderline tumors. Of the patients diagnosed with ovarian cancer or borderline tumor, 47.3% were judged as high-risk by the ROMA test and 58.2% had CA125 levels of >35 U/ml. The specificity and accuracy of ROMA were higher compared with those of CA125 in pre-menopausal females. However, the superiority of the ROMA test in the identification of malignant ovarian tumors compared with CA125 was only observed in patients with endometriotic-type tumors but not in any of the other tumor subtypes. In the endometriotic type of ovarian tumor, the superiority of the ROMA test compared to CA125 was confirmed in triage of ovarian tumor. However, the sensitivity and specificity of ROMA and CA125 were similar for the other tumor types. Therefore, future development of better tumor-specific biomarkers for triage of ovarian tumor is required.
本研究旨在根据与术后组织病理学结果相关的影像学肿瘤亚型,比较卵巢恶性肿瘤风险算法(ROMA)和癌抗原(CA)125在鉴别良性卵巢肿瘤和早期卵巢癌方面的准确性。确定了2014年9月至2018年3月期间在韩国首尔峨山医学中心因疑似早期卵巢癌接受ROMA检测并接受手术的1207例患者。共有981例符合纳入标准的患者纳入回顾性分析。在这981名受试者中,816例患有良性肿瘤,90例患有恶性肿瘤,75例患有交界性肿瘤。在被诊断为卵巢癌或交界性肿瘤的患者中,47.3%被ROMA检测判定为高危,58.2%的CA125水平>35 U/ml。在绝经前女性中,ROMA的特异性和准确性高于CA125。然而,与CA125相比,ROMA检测在识别恶性卵巢肿瘤方面的优势仅在子宫内膜样肿瘤患者中观察到,而在其他任何肿瘤亚型中均未观察到。在子宫内膜样卵巢肿瘤中,ROMA检测在卵巢肿瘤分诊方面比CA125更具优势得到了证实。然而,对于其他肿瘤类型,ROMA和CA125的敏感性和特异性相似。因此,需要开发更好的肿瘤特异性生物标志物用于卵巢肿瘤的分诊。