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本文引用的文献

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Reproductive outcomes in women with BRCA 1/2 germline mutations: A retrospective observational study and literature review.携带BRCA 1/2种系突变女性的生殖结局:一项回顾性观察研究及文献综述。
Open Med (Wars). 2024 Aug 20;19(1):20249999. doi: 10.1515/med-2024-9999. eCollection 2024.
2
ESGO-ESMO-ESP consensus conference recommendations on ovarian cancer: pathology and molecular biology and early, advanced and recurrent disease.ESGO-ESMO-ESP 共识会议关于卵巢癌的建议:病理学和分子生物学以及早期、晚期和复发性疾病。
Ann Oncol. 2024 Mar;35(3):248-266. doi: 10.1016/j.annonc.2023.11.015. Epub 2024 Feb 1.
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Circulating Tumor DNA from Ascites as an alternative to tumor sampling for genomic profiling in ovarian cancer patients.腹水循环肿瘤DNA作为卵巢癌患者基因组分析肿瘤取样的替代方法。
Biomark Res. 2023 Oct 20;11(1):93. doi: 10.1186/s40364-023-00533-1.
4
Maintenance olaparib rechallenge in patients with platinum-sensitive relapsed ovarian cancer previously treated with a PARP inhibitor (OReO/ENGOT-ov38): a phase IIIb trial.奥拉帕利维持治疗在既往接受 PARP 抑制剂治疗的铂敏感复发性卵巢癌患者中的疗效(OReO/ENGOT-ov38):一项 IIIb 期试验。
Ann Oncol. 2023 Dec;34(12):1152-1164. doi: 10.1016/j.annonc.2023.09.3110. Epub 2023 Oct 4.
5
Evaluation of Borderline Ovarian Tumor Recurrence Rate after Surgery with or without Fertility-Sparing Approach: Results of a Retrospective Analysis.保留生育功能手术与非保留生育功能手术治疗交界性卵巢肿瘤术后复发率的评估:一项回顾性分析结果
Healthcare (Basel). 2023 Jul 3;11(13):1922. doi: 10.3390/healthcare11131922.
6
PARP Inhibitors in Newly Diagnosed and Recurrent Ovarian Cancer.聚腺苷二磷酸核糖聚合酶抑制剂在新发和复发性卵巢癌中的应用。
Am J Clin Oncol. 2023 Sep 1;46(9):414-419. doi: 10.1097/COC.0000000000001024. Epub 2023 Jun 12.
7
Olaparib plus bevacizumab first-line maintenance in ovarian cancer: final overall survival results from the PAOLA-1/ENGOT-ov25 trial.奥拉帕利联合贝伐珠单抗一线维持治疗卵巢癌:PAOLA-1/ENGOT-ov25 试验的最终总生存结果。
Ann Oncol. 2023 Aug;34(8):681-692. doi: 10.1016/j.annonc.2023.05.005. Epub 2023 May 19.
8
In-house homologous recombination deficiency testing in ovarian cancer: a multi-institutional Italian pilot study.卵巢癌的同源重组缺陷内检测:一项多机构的意大利用户研究。
J Clin Pathol. 2024 Jun 19;77(7):478-485. doi: 10.1136/jcp-2023-208852.
9
Overall Survival With Maintenance Olaparib at a 7-Year Follow-Up in Patients With Newly Diagnosed Advanced Ovarian Cancer and a BRCA Mutation: The SOLO1/GOG 3004 Trial.在 BRCA 突变的新诊断晚期卵巢癌患者中,7 年随访期间维持奥拉帕利的总生存期:SOLO1/GOG 3004 试验。
J Clin Oncol. 2023 Jan 20;41(3):609-617. doi: 10.1200/JCO.22.01549. Epub 2022 Sep 9.
10
NCCN Guidelines® Insights: Ovarian Cancer, Version 3.2022.NCCN 指南®洞察:卵巢癌,第 3.2022 版。
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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.

DOI:10.3390/ijms252011239
PMID:39457020
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11508316/
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。