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本文引用的文献

1
Development of a multimarker assay for early detection of ovarian cancer.开发一种用于早期检测卵巢癌的多标志物检测方法。
J Clin Oncol. 2010 May 1;28(13):2159-66. doi: 10.1200/JCO.2008.19.2484. Epub 2010 Apr 5.
2
Role of eotaxin-1 signaling in ovarian cancer.嗜酸性粒细胞趋化因子-1信号通路在卵巢癌中的作用。
Clin Cancer Res. 2009 Apr 15;15(8):2647-56. doi: 10.1158/1078-0432.CCR-08-2024. Epub 2009 Apr 7.
3
Validation of serum biomarkers for detection of early-stage ovarian cancer.用于检测早期卵巢癌的血清生物标志物的验证
Am J Obstet Gynecol. 2009 Jun;200(6):639.e1-5. doi: 10.1016/j.ajog.2008.12.042. Epub 2009 Mar 14.
4
A serum based analysis of ovarian epithelial tumorigenesis.基于血清的卵巢上皮肿瘤发生分析。
Gynecol Oncol. 2009 Jan;112(1):47-54. doi: 10.1016/j.ygyno.2008.09.043. Epub 2008 Nov 12.
5
A novel multiple marker bioassay utilizing HE4 and CA125 for the prediction of ovarian cancer in patients with a pelvic mass.一种利用人附睾蛋白4(HE4)和癌抗原125(CA125)预测盆腔肿块患者卵巢癌的新型多标志物生物测定法。
Gynecol Oncol. 2009 Jan;112(1):40-6. doi: 10.1016/j.ygyno.2008.08.031. Epub 2008 Oct 12.
6
Multianalyte profiling of serum antigens and autoimmune and infectious disease molecules to identify biomarkers dysregulated in epithelial ovarian cancer.对血清抗原、自身免疫和传染病分子进行多分析物分析,以鉴定上皮性卵巢癌中失调的生物标志物。
Cancer Epidemiol Biomarkers Prev. 2008 Oct;17(10):2872-81. doi: 10.1158/1055-9965.EPI-08-0464.
7
Prediction of ovarian cancer prognosis and response to chemotherapy by a serum-based multiparametric biomarker panel.基于血清的多参数生物标志物组合对卵巢癌预后及化疗反应的预测
Br J Cancer. 2008 Oct 7;99(7):1103-13. doi: 10.1038/sj.bjc.6604630. Epub 2008 Sep 2.
8
Benign disorders of the ovary.卵巢良性疾病
Obstet Gynecol Clin North Am. 2008 Jun;35(2):271-84, ix. doi: 10.1016/j.ogc.2008.03.004.
9
Clinical implications of the ErbB/epidermal growth factor (EGF) receptor family and its ligands in ovarian cancer.表皮生长因子受体(ErbB)家族及其配体在卵巢癌中的临床意义
Biochim Biophys Acta. 2008 Apr;1785(2):232-65. doi: 10.1016/j.bbcan.2008.01.001. Epub 2008 Feb 7.
10
Diagnostic markers for early detection of ovarian cancer.用于早期检测卵巢癌的诊断标志物。
Clin Cancer Res. 2008 Feb 15;14(4):1065-72. doi: 10.1158/1078-0432.CCR-07-1569. Epub 2008 Feb 7.

用于鉴别附件包块患者良恶性病例的血清生物标志物组合。

Serum biomarker panels for the discrimination of benign from malignant cases in patients with an adnexal mass.

机构信息

University of Pittsburgh Cancer Institute, Hillman Cancer Center, 5117 Centre Avenue 1.18, Pittsburgh, PA 15213, USA.

出版信息

Gynecol Oncol. 2010 Jun;117(3):440-5. doi: 10.1016/j.ygyno.2010.02.005. Epub 2010 Mar 24.

DOI:10.1016/j.ygyno.2010.02.005
PMID:20334903
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2873171/
Abstract

OBJECTIVES

The diagnosis of an adnexal mass is a prevalent issue among women in the United States, although current methods of identifying those at high risk of malignancy remain insufficient. Ineffective triage of women with malignant masses is associated with delayed or inappropriate treatment and a negative effect on disease outcome.

METHODS

We performed an evaluation of 65 ovarian cancer-related biomarkers in the circulation of women diagnosed with an adnexal mass. Our subject group consisted of women diagnosed with benign masses and early- and late-stage ovarian cancer.

RESULTS

More than half of the biomarkers tested were found to differ significantly between benign and malignant cases. As individual markers, HE4 and CA-125 provided the greatest level of discrimination between benign and malignant cases, and the combination of these two biomarkers provided a higher level of discriminatory power than either marker considered alone. Multivariate statistical analysis identified several multimarker panels that could discriminate early-stage, late-stage, and combined ovarian cancers from benign cases with similar or slightly improved SN/SP levels to the CA-125/HE4 combination; however, these larger panels could not outperform the 2-biomarker panel in an independent validation set. We also identified a 3-biomarker panel with particular utility in premenopausal women.

CONCLUSIONS

Our findings serve to advance the development of blood-based screening methods for the discrimination of benign and malignant ovarian masses by confirming and expanding upon the superior utility of the CA-125/HE4 combination.

摘要

目的

在美国女性中,附件包块的诊断是一个常见问题,尽管目前确定那些恶性肿瘤风险高的方法仍然不够。对有恶性肿块的女性进行无效分诊与治疗延迟或不当以及对疾病结局产生负面影响有关。

方法

我们对诊断为附件包块的女性的循环中的 65 种卵巢癌相关生物标志物进行了评估。我们的研究对象组包括被诊断为良性肿块和早期及晚期卵巢癌的女性。

结果

超过一半的测试生物标志物在良性和恶性病例之间存在显著差异。作为单个标志物,HE4 和 CA-125 在良性和恶性病例之间提供了最大的区分度,这两种标志物的组合提供了比单独考虑任何一种标志物更高的区分能力。多变量统计分析确定了几个多标志物面板,可以将早期、晚期和合并的卵巢癌与良性病例区分开来,其 SN/SP 水平与 CA-125/HE4 组合相似或略有提高;然而,这些更大的面板在独立验证集中无法超过 2 个标志物面板。我们还确定了一个在绝经前妇女中具有特殊用途的 3 个标志物面板。

结论

我们的发现通过证实和扩展 CA-125/HE4 组合的优越效用,有助于推进用于区分良性和恶性卵巢肿块的基于血液的筛查方法的发展。