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血清钙网织蛋白作为预测卵巢癌铂类耐药及预后的独立标志物。

Serum calretinin as an independent predictor for platinum resistance and prognosis in ovarian cancer.

机构信息

Department of Gynecology and Obstetrics, Medical Faculty and University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.

National Center for Tumor Diseases (NCT), Dresden, Germany: German Cancer Research Center (DKFZ), Heidelberg, Germany; Faculty of Medicine and University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany, Helmholtz-Zentrum Dresden-Rossendorf (HZDR), Dresden, Germany.

出版信息

Int J Cancer. 2020 May 1;146(9):2608-2618. doi: 10.1002/ijc.32676. Epub 2019 Nov 6.

Abstract

Calretinin (CRT) is a calcium-binding protein that controls intracellular calcium signaling. Besides its prominent expression in neurons, serum CRT (sCRT) has recently been suggested as blood-based biomarker for prediagnostic mesothelioma detection. CRT is expressed in ovarian cancer tissues in up to 40% of cases; however, its clinical relevance as blood-based biomarker for ovarian cancer is unknown. sCRT was determined by calretinin enzyme-linked immunoabsorbent assay (Calretinin-ELISA, DLD Diagnostika GmbH, Hamburg, Germany) in a total of 515 serum samples from 116 healthy controls and 134 ovarian cancer patients (thereof 86% with Fédération Internationale de Gynécologie et d'Obstétrique [FIGO] III/IV), including samples at primary diagnosis and at four longitudinal follow-up time points in the course of treatment and at recurrence. sCRT level was significantly increased in ovarian cancer patients compared to healthy controls (estimated difference = 0.3 ng/ml, p < 0.001), was mostly independent from CA125 (r ≤ 0.388) and enabled accurate discrimination between cases and controls (area under the curve = 0.85). Higher sCRT level at primary diagnosis predicted suboptimal debulking (p < 0.001) and was associated with advanced FIGO-stage (p < 0.001) and increased amount of ascites (p < 0.001). sCRT levels at primary diagnosis and its dynamics in the course of chemotherapy were independent predictors for poor progression-free survival (hazard ratio [HR] = 1.99, confidence interval [CI] = [1.13-3.52], p = 0.0181) and overall survival (HR = 15.4, CI = [1.92-124], p = 0.0099). Furthermore, sCRT at primary diagnosis or a relative sCRT increase in the time interval between surgery and the onset of chemotherapy were both independent predictors of platinum resistance (OR = 4.99, CI = [3.50-16,001], p = 0.0016; OR = 2.41, CI = [1.37-6,026], p = 0.0271, respectively). This is the first study that suggests sCRT as liquid biopsy marker for independent prediction of platinum resistance and prognosis.

摘要

钙结合蛋白 CRT 可控制细胞内钙信号转导。除了在神经元中有明显表达外,血清 CRT(sCRT)最近也被提出作为间皮瘤早期诊断的血液生物标志物。在高达 40%的卵巢癌组织中表达 CRT;然而,其作为卵巢癌血液生物标志物的临床相关性尚不清楚。在总共 515 份血清样本中,通过 calretinin 酶联免疫吸附测定(Calretinin-ELISA,DLD Diagnostika GmbH,汉堡,德国)检测了 116 名健康对照者和 134 名卵巢癌患者(其中 86%为国际妇产科联合会[FIGO] III/IV)的 sCRT,包括初诊时和治疗过程中四个纵向随访时间点以及复发时的样本。与健康对照组相比,卵巢癌患者的 sCRT 水平显著升高(估计差值=0.3ng/ml,p<0.001),与 CA125 大多独立(r≤0.388),能够准确区分病例和对照组(曲线下面积=0.85)。初诊时 sCRT 水平较高预示着减瘤效果不佳(p<0.001),与 FIGO 晚期(p<0.001)和腹水增多(p<0.001)有关。初诊时 sCRT 水平及其在化疗过程中的动态变化是无进展生存期(风险比[HR]=1.99,置信区间[CI] = [1.13-3.52],p=0.0181)和总生存期(HR=15.4,CI=[1.92-124],p=0.0099)不良的独立预测因子。此外,初诊时 sCRT 或手术与化疗开始之间时间间隔内 sCRT 的相对增加均是铂类耐药的独立预测因子(OR=4.99,CI=[3.50-16001],p=0.0016;OR=2.41,CI=[1.37-6026],p=0.0271)。这是第一项表明 sCRT 可作为独立预测铂类耐药和预后的液体活检标志物的研究。

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