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临床及急诊生物标志物及其与卵巢癌预后的关系

Clinical and Emergent Biomarkers and Their Relationship to the Prognosis of Ovarian Cancer.

作者信息

Jatoi Aminah, Vierkant Robert A, Hawthorne Kieran M, Block Matthew S, Ramus Susan J, Larson Nicholas B, Fridley Brooke L, Goode Ellen L

机构信息

Department of Oncology, Mayo Clinic, Rochester, Minn., USA.

出版信息

Oncology. 2016;90(2):59-68. doi: 10.1159/000442710. Epub 2016 Jan 19.

Abstract

OBJECTIVE

Ovarian cancer is the most lethal gynecological malignancy, but information relevant to prognosis and outcomes remain unknown. Here, we used statistical methods to focus specifically on interactions between candidate prognostic variables.

METHODS AND RESULTS

Univariate, multivariate, and elastic net modeling of 42 variables were applied to a cohort of 542 ovarian cancer patients with 393 episodes of cancer recurrence/death. In univariate analyses, overexpression of TFF3, MDM2, and p53 were associated with improved recurrence-free survival. In multivariate analyses adjusted for age, histology, stage, grade, ascites, and residual disease, overexpression of PR appeared to provide a protective effect [hazard ratio for >50% of cells positive, 0.64 (95% confidence interval 0.44-0.94) compared to <1%], and TFF3 showed a nonlinear association. Importantly, we observed no interactions among variables. However, patients with tumors with moderate TFF3 expression were at a marginally increased risk of recurrence, and patients with tumors with high expression were at a similar to slightly lower risk, compared to those with tumors with no TFF3 expression.

CONCLUSIONS

Although no interactions among variables were observed, this study provides important precedent for seeking interactions between clinical and tumor variables in future studies.

摘要

目的

卵巢癌是最致命的妇科恶性肿瘤,但与预后和结局相关的信息仍不明确。在此,我们运用统计方法专门聚焦于候选预后变量之间的相互作用。

方法与结果

对42个变量进行单变量、多变量和弹性网络建模,并应用于542例卵巢癌患者队列,其中有393例癌症复发/死亡事件。在单变量分析中,TFF3、MDM2和p53的过表达与无复发生存期的改善相关。在针对年龄、组织学、分期、分级、腹水和残留病灶进行校正的多变量分析中,PR的过表达似乎具有保护作用[细胞阳性率>50%的风险比为0.64(95%置信区间0.44 - 0.94),相比之下<1%],且TFF3呈现非线性关联。重要的是,我们未观察到变量之间的相互作用。然而,与无TFF3表达的肿瘤患者相比,TFF3表达中等的肿瘤患者复发风险略有增加,而TFF3高表达的肿瘤患者复发风险与之相似或略低。

结论

尽管未观察到变量之间的相互作用,但本研究为未来研究探索临床和肿瘤变量之间的相互作用提供了重要先例。

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