Diagnostic accuracy of a three-protein signature in women with suspicious breast lesions: a multicenter prospective trial.

Eun-Shin Lee, Yumi Kim, Hee-Chul Shin, Ki-Tae Hwang, Junwon Min, Min Kyoon Kim, SooKyung Ahn, So-Youn Jung, Hyukjai Shin, MinSung Chung, Tae-Kyung Yoo, Seungpil Jung, Sang Uk Woo, Ju-Yeon Kim, Dong-Young Noh, Hyeong-Gon Moon
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Abstract

Background: Mammography screening has been proven to detect breast cancer at an early stage and reduce mortality; however, it has low accuracy in young women or women with dense breasts. Blood-based diagnostic tools may overcome the limitations of mammography. This study assessed the diagnostic performance of a three-protein signature in patients with suspicious breast lesions.

Findings: This trial (MAST; KCT0004847) was a prospective multicenter observational trial. Three-protein signature values were obtained using serum and plasma from women with suspicious lesions for breast malignancy before tumor biopsy. Additionally, blood samples from women who underwent clear or benign mammography were collected for the assays. Among 642 participants, the sensitivity, specificity, and overall accuracy values of the three-protein signature were 74.4%, 66.9%, and 70.6%, respectively, and the concordance index was 0.698 (95% CI 0.656, 0.739). The diagnostic performance was not affected by the demographic features, clinicopathologic characteristics, and co-morbidities of the participants.

Conclusions: The present trial showed an accuracy of 70.6% for the three-protein signature. Considering the value of blood-based biomarkers for the early detection of breast malignancies, further evaluation of this proteomic assay is warranted in larger, population-level trials. This Multi-protein Assessment using Serum to deTermine breast lesion malignancy (MAST) was registered at the Clinical Research Information Service of Korea with the identification number of KCT0004847 ( https://cris.nih.go.kr ).

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三蛋白标记在可疑乳腺病变女性中的诊断准确性:一项多中心前瞻性试验
背景:乳房x线摄影筛查已被证明可以在早期发现乳腺癌并降低死亡率;然而,在年轻女性或乳房致密的女性中,它的准确性很低。基于血液的诊断工具可能克服乳房x光检查的局限性。本研究评估了三蛋白标记在可疑乳腺病变患者中的诊断性能。结果:该试验(MAST;KCT0004847)是一项前瞻性多中心观察性试验。在肿瘤活检前使用可疑乳腺恶性病变妇女的血清和血浆获得三蛋白特征值。此外,从接受透明或良性乳房x光检查的妇女收集血液样本进行分析。在642名受试者中,三蛋白特征的敏感性、特异性和总体准确性分别为74.4%、66.9%和70.6%,一致性指数为0.698 (95% CI为0.656,0.739)。诊断表现不受人口统计学特征、临床病理特征和参与者的合并症的影响。结论:本试验显示三蛋白标记的准确性为70.6%。考虑到基于血液的生物标志物对乳腺恶性肿瘤早期检测的价值,需要在更大规模的人群水平试验中进一步评估这种蛋白质组学分析。该血清多蛋白鉴定乳腺病变恶性(MAST)已在韩国临床研究信息院注册,识别号为KCT0004847 (https://cris.nih.go.kr)。
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