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肿瘤标志物在制定晚期卵巢癌治疗策略中的作用。

The Role of Tumor Biomarkers in Tailoring the Approach to Advanced Ovarian Cancer.

机构信息

Department of Maternal and Child Health and Urological Sciences, Policlinico Umberto I, Sapienza University of Rome, 00161 Rome, Italy.

Obstetrics and Gynecological Unit, Department of Woman's and Child's Health, San Camillo-Forlanini Hospital, 00152 Rome, Italy.

出版信息

Int J Mol Sci. 2024 Oct 19;25(20):11239. doi: 10.3390/ijms252011239.

Abstract

Growing evidence has demonstrated the role of mutations of tumor biomarkers in diagnosing and treating epithelial ovarian cancer. This review aims to analyze recent literature on the correlation between tumor biomarkers and chemotherapy in nonmucinous ovarian cancer, providing suggestions for personalized treatment approaches. An extensive literature search was conducted to identify relevant studies and trials. mutations are central in homologous recombination repair deficiency (HRD) in ovarian cancer, but several other genetic mutations also contribute to varying cancer risks. While the role of MMR testing in ovarian cancer is debated, it is more commonly linked to non-serous ovarian cancer, often associated with Lynch syndrome. A significant proportion of ovarian cancer patients have HRD, affecting treatment decisions in both first-line (especially in advanced stages) and second-line therapy due to HRD's connection with platinum-based therapy and PARP inhibitors' response. However, validated genetic tests to identify HRD have not yet been universally implemented. There is no definitive therapeutic algorithm for advanced ovarian cancer, despite ongoing efforts and multiple proposed tools. Future research should focus on expanding the utility of biomarkers, reducing resistance, and increasing the actionable biomarker pool.

摘要

越来越多的证据表明肿瘤标志物的突变在诊断和治疗上皮性卵巢癌中起着重要作用。本综述旨在分析非黏液性卵巢癌中肿瘤标志物与化疗之间的相关性的最新文献,为个体化治疗方法提供建议。进行了广泛的文献检索以确定相关的研究和试验。突变是卵巢癌同源重组修复缺陷(HRD)的核心,但其他几种遗传突变也与不同的癌症风险有关。虽然 MMR 检测在卵巢癌中的作用存在争议,但它更常与非浆液性卵巢癌相关,通常与林奇综合征相关。相当一部分卵巢癌患者存在 HRD,这影响了一线治疗(尤其是晚期)和二线治疗的决策,因为 HRD 与铂类治疗和 PARP 抑制剂反应有关。然而,尚未普遍实施用于识别 HRD 的经过验证的遗传检测。尽管正在进行努力并提出了多种工具,但仍没有针对晚期卵巢癌的明确治疗算法。未来的研究应侧重于扩大生物标志物的应用,降低耐药性,并增加可操作的生物标志物库。

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