• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

复发性妇科癌症基因匹配疗法的临床结果:单机构经验

Clinical Outcomes of Genotype-Matched Therapy for Recurrent Gynecological Cancers: A Single Institutional Experience.

作者信息

Sawada Kiyoka, Nakayama Kentaro, Nakamura Kohei, Yoshimura Yuki, Razia Sultana, Ishikawa Masako, Yamashita Hitomi, Ishibashi Tomoka, Sato Seiya, Kyo Satoru

机构信息

Department of Obstetrics and Gynecology, Shimane University School of Medicine, Izumo 693-8501, Japan.

出版信息

Healthcare (Basel). 2021 Oct 19;9(10):1395. doi: 10.3390/healthcare9101395.

DOI:10.3390/healthcare9101395
PMID:34683075
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8535840/
Abstract

Recent advances in next-generation sequencing and genome medicine have contributed to treatment decisions in patients with cancer. Most advanced gynecological cancers develop resistance to chemotherapy and have a poor prognosis. Therefore, we conducted genomic tests in gynecological tumors to examine the efficacy and clinical feasibility of genotype-matched therapy. Target sequencing was performed in 20 cases of gynecological cancers (cervical cancer, 6; endometrial cancer, 6; and ovarian cancer, 6). Both actionable and druggable genes were identified in 95% (19/20) of the cases. Among them, seven patients (35%) received genotype-matched therapy, which was effective in three patients. Of the three patients, one patient with a mutation received everolimus, another patient with a mutation received everolimus and letrozole, and the patient with a mutation received olaparib. Subsequently, disease control in these three patients lasted for more than half a year. However, all patients relapsed between 9 and 13 months after the initiation of genotype-matched therapy. In this study, the response rate of genotype-matched therapy was 43% (3/7), which may have contributed to improved prognoses. Therefore, genotype-matched therapies may help patients with refractory gynecological cancers achieve better outcomes.

摘要

新一代测序和基因组医学的最新进展为癌症患者的治疗决策提供了帮助。大多数晚期妇科癌症会对化疗产生耐药性,预后较差。因此,我们对妇科肿瘤进行了基因组检测,以研究基因型匹配疗法的疗效和临床可行性。对20例妇科癌症(宫颈癌6例、子宫内膜癌6例、卵巢癌6例)进行了靶向测序。95%(19/20)的病例中鉴定出了可操作和可用药的基因。其中,7例患者(35%)接受了基因型匹配疗法,3例患者治疗有效。在这3例患者中,1例携带 突变的患者接受了依维莫司治疗,另1例携带 突变的患者接受了依维莫司和来曲唑治疗,携带 突变的患者接受了奥拉帕利治疗。随后,这3例患者的疾病控制持续了半年以上。然而,所有患者在基因型匹配疗法开始后的9至13个月内均复发。在本研究中,基因型匹配疗法的缓解率为43%(3/7),这可能有助于改善预后。因此,基因型匹配疗法可能有助于难治性妇科癌症患者获得更好的治疗效果。

相似文献

1
Clinical Outcomes of Genotype-Matched Therapy for Recurrent Gynecological Cancers: A Single Institutional Experience.复发性妇科癌症基因匹配疗法的临床结果:单机构经验
Healthcare (Basel). 2021 Oct 19;9(10):1395. doi: 10.3390/healthcare9101395.
2
Genotype-matched treatment for patients with advanced type I epithelial ovarian cancer (EOC).为晚期 I 型上皮性卵巢癌(EOC)患者进行基因匹配治疗。
Gynecol Oncol. 2017 Feb;144(2):250-255. doi: 10.1016/j.ygyno.2016.12.002. Epub 2017 Jan 3.
3
Impact of molecular testing in clinical practice in gynecologic cancers.妇科癌症临床实践中分子检测的影响。
Cancer Med. 2019 May;8(5):2013-2019. doi: 10.1002/cam4.2064. Epub 2019 Mar 7.
4
Feasibility of Large-Scale Genomic Testing to Facilitate Enrollment Onto Genomically Matched Clinical Trials.大规模基因组检测以促进纳入基因组匹配临床试验的可行性。
J Clin Oncol. 2015 Sep 1;33(25):2753-62. doi: 10.1200/JCO.2014.60.4165. Epub 2015 May 26.
5
Antitumor activity of everolimus in recurrent metastatic endometrial cancer with deletion: a case report.依维莫司对伴缺失的复发性转移性子宫内膜癌的抗肿瘤活性:一例报告
Gland Surg. 2021 Aug;10(8):2585-2590. doi: 10.21037/gs-21-422.
6
Impact of somatic molecular profiling on clinical trial outcomes in rare epithelial gynecologic cancer patients.体细胞分子谱分析对罕见妇科上皮性癌患者临床试验结局的影响。
Gynecol Oncol. 2019 May;153(2):304-311. doi: 10.1016/j.ygyno.2019.02.005. Epub 2019 Feb 18.
7
Changes in HER3 expression profiles between primary and recurrent gynecological cancers.原发性与复发性妇科癌症之间HER3表达谱的变化。
Cancer Cell Int. 2023 Feb 3;23(1):18. doi: 10.1186/s12935-022-02844-z.
8
Molecular profiling of advanced solid tumors and patient outcomes with genotype-matched clinical trials: the Princess Margaret IMPACT/COMPACT trial.晚期实体瘤的分子特征分析与基因匹配临床试验的患者预后:玛格丽特公主癌症中心IMPACT/COMPACT试验
Genome Med. 2016 Oct 25;8(1):109. doi: 10.1186/s13073-016-0364-2.
9
Prospective Clinical Integration of an Amplicon-Based Next-Generation Sequencing Method to Select Advanced Non-Small-Cell Lung Cancer Patients for Genotype-Tailored Treatments.前瞻性临床整合基于扩增子的下一代测序方法,以选择晚期非小细胞肺癌患者进行基于基因型的治疗。
Clin Lung Cancer. 2018 Jan;19(1):65-73.e7. doi: 10.1016/j.cllc.2017.06.008. Epub 2017 Jun 23.
10
Application of natural polysaccharides and their novel dosage forms in gynecological cancers: therapeutic implications from the diversity potential of natural compounds.天然多糖及其新型剂型在妇科癌症中的应用:天然化合物多样潜力的治疗意义
Front Pharmacol. 2023 Jun 13;14:1195104. doi: 10.3389/fphar.2023.1195104. eCollection 2023.

引用本文的文献

1
Molecular Analysis of High-Grade Serous Ovarian Carcinoma Exhibiting Low-Grade Serous Carcinoma and Serous Borderline Tumor.表现为低级别浆液性癌和浆液性交界性肿瘤的高级别浆液性卵巢癌的分子分析
Curr Issues Mol Biol. 2024 Aug 25;46(9):9376-9385. doi: 10.3390/cimb46090555.

本文引用的文献

1
Implementation of Precision Oncology for Patients with Metastatic Breast Cancer in an Interdisciplinary MTB Setting.在跨学科多学科团队(MTB)环境中为转移性乳腺癌患者实施精准肿瘤学
Diagnostics (Basel). 2021 Apr 20;11(4):733. doi: 10.3390/diagnostics11040733.
2
Next-Generation Sequencing of Advanced GI Tumors Reveals Individual Treatment Options.晚期胃肠道肿瘤的下一代测序揭示个体化治疗方案。
JCO Precis Oncol. 2020 Mar 30;4. doi: 10.1200/PO.19.00359. eCollection 2020.
3
Olaparib Monotherapy for -Mutated High-Grade Serous Endometrial Cancer.
奥拉帕利单药治疗BRCA突变的高级别浆液性子宫内膜癌。
JCO Precis Oncol. 2020 Apr 9;4. doi: 10.1200/PO.19.00368. eCollection 2020.
4
Clinical impact of a cancer genomic profiling test using an in-house comprehensive targeted sequencing system.使用内部综合靶向测序系统的癌症基因组分析测试的临床影响。
Cancer Sci. 2020 Oct;111(10):3926-3937. doi: 10.1111/cas.14608. Epub 2020 Sep 6.
5
Identification and clinical impact of potentially actionable somatic oncogenic mutations in solid tumor samples.实体瘤样本中潜在可操作的体细胞致癌突变的鉴定及其临床影响
J Transl Med. 2020 Feb 22;18(1):99. doi: 10.1186/s12967-020-02273-4.
6
Efficacy of Pembrolizumab in Patients With Noncolorectal High Microsatellite Instability/Mismatch Repair-Deficient Cancer: Results From the Phase II KEYNOTE-158 Study.帕博利珠单抗治疗非结直肠癌高度微卫星不稳定/错配修复缺陷型癌症患者的疗效:来自 II 期 KEYNOTE-158 研究的结果。
J Clin Oncol. 2020 Jan 1;38(1):1-10. doi: 10.1200/JCO.19.02105. Epub 2019 Nov 4.
7
Genomic heterogeneity and efficacy of PI3K pathway inhibitors in patients with gynaecological cancer.妇科癌症患者中PI3K通路抑制剂的基因组异质性与疗效
ESMO Open. 2019 Mar 8;4(2):e000444. doi: 10.1136/esmoopen-2018-000444. eCollection 2019.
8
Feasibility and utility of a panel testing for 114 cancer-associated genes in a clinical setting: A hospital-based study.在临床环境中检测 114 个癌症相关基因的面板的可行性和实用性:一项基于医院的研究。
Cancer Sci. 2019 Apr;110(4):1480-1490. doi: 10.1111/cas.13969. Epub 2019 Apr 2.
9
A Pilot Prospective Study of Refractory Solid Tumor Patients for NGS-Based Targeted Anticancer Therapy.一项针对难治性实体瘤患者基于二代测序的靶向抗癌治疗的前瞻性试点研究。
Transl Oncol. 2019 Feb;12(2):301-307. doi: 10.1016/j.tranon.2018.10.011. Epub 2018 Nov 16.
10
Mutational landscape of metastatic cancer revealed from prospective clinical sequencing of 10,000 patients.从10000例患者的前瞻性临床测序中揭示的转移性癌症的突变图谱。
Nat Med. 2017 Jun;23(6):703-713. doi: 10.1038/nm.4333. Epub 2017 May 8.