• 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

相似文献

1
Histologic parameters predictive of disease outcome in women with advanced stage ovarian carcinoma treated with neoadjuvant chemotherapy.新辅助化疗治疗晚期卵巢癌女性患者的组织学参数与疾病结局的相关性。
Transl Oncol. 2012 Dec;5(6):469-74. doi: 10.1593/tlo.12265. Epub 2012 Dec 1.
2
[Analysis of factors related to the prognostic benefit of neoadjuvant chemotherapy followed by interval debulking surgery in patients with advanced ovarian cancer].[晚期卵巢癌患者新辅助化疗后行间隔减瘤手术的预后获益相关因素分析]
Zhonghua Fu Chan Ke Za Zhi. 2021 Jun 25;56(6):385-392. doi: 10.3760/cma.j.cn112141-20201207-00871.
3
Primary debulking surgery versus primary neoadjuvant chemotherapy for high grade advanced stage ovarian cancer: comparison of survivals.高级别晚期卵巢癌的初次肿瘤细胞减灭术与初次新辅助化疗:生存比较。
Radiol Oncol. 2018 Sep 11;52(3):307-319. doi: 10.2478/raon-2018-0030.
4
Primary debulking surgery vs. neoadjuvant chemotherapy followed by interval debulking surgery for patients with advanced ovarian cancer.初次肿瘤细胞减灭术与新辅助化疗后间隔肿瘤细胞减灭术治疗晚期卵巢癌的疗效比较。
Arch Gynecol Obstet. 2016 Jan;293(1):163-168. doi: 10.1007/s00404-015-3813-z. Epub 2015 Jul 22.
5
Histopathology predicts clinical outcome in advanced epithelial ovarian cancer patients treated with neoadjuvant chemotherapy and debulking surgery.组织病理学预测接受新辅助化疗和肿瘤细胞减灭术治疗的晚期上皮性卵巢癌患者的临床结局。
Gynecol Oncol. 2013 Dec;131(3):531-4. doi: 10.1016/j.ygyno.2013.09.030. Epub 2013 Oct 4.
6
[Re-evaluation of interval debulking surgery in advanced epithelial ovarian cancer].[晚期上皮性卵巢癌中间减瘤手术的再评估]
Zhonghua Fu Chan Ke Za Zhi. 2012 May;47(5):355-60.
7
Optimizing the treatment of ovarian cancer: Neoadjuvant chemotherapy and interval debulking versus primary debulking surgery for epithelial ovarian cancers likely to have suboptimal resection.优化卵巢癌治疗:新辅助化疗和间隔肿瘤缩小术与初始肿瘤细胞减灭术治疗可能无法实现理想切除的上皮性卵巢癌。
Gynecol Oncol. 2017 Feb;144(2):266-273. doi: 10.1016/j.ygyno.2016.11.021. Epub 2016 Dec 1.
8
CT prediction of surgical outcome in patients with advanced epithelial ovarian carcinoma undergoing neoadjuvant chemotherapy.CT 预测接受新辅助化疗的晚期上皮性卵巢癌患者的手术结果。
Gynecol Oncol. 2019 Mar;152(3):568-573. doi: 10.1016/j.ygyno.2018.12.012. Epub 2019 Jan 12.
9
A predictive score for optimal cytoreduction at interval debulking surgery in epithelial ovarian cancer: a two- centers experience.上皮性卵巢癌间隔性肿瘤细胞减灭术的最佳减瘤预测评分:两中心经验。
J Ovarian Res. 2018 May 30;11(1):42. doi: 10.1186/s13048-018-0415-y.
10
Effect of neoadjuvant chemotherapy on platinum resistance in stage IIIC and IV epithelial ovarian cancer.新辅助化疗对IIIC期和IV期上皮性卵巢癌铂耐药性的影响。
Medicine (Baltimore). 2016 Sep;95(36):e4797. doi: 10.1097/MD.0000000000004797.

引用本文的文献

1
Effect of vitamin D and location of asprosin, spexin and meteorin-like antibodies in the liver of rats with isoproterenol-induced myocardial infarction.维生素D以及抑胃肽、信号肽和类流星蛋白抗体在异丙肾上腺素诱导的大鼠心肌梗死肝脏中的定位影响。
Naunyn Schmiedebergs Arch Pharmacol. 2025 Jun 28. doi: 10.1007/s00210-025-04409-z.
2
Germline BRCA1/2 status and chemotherapy response score in high-grade serous ovarian cancer.高级别浆液性卵巢癌中的胚系BRCA1/2状态与化疗反应评分
Br J Cancer. 2024 Dec;131(12):1919-1927. doi: 10.1038/s41416-024-02874-6. Epub 2024 Nov 16.
3
Losartan rewires the tumor-immune microenvironment and suppresses IGF-1 to overcome resistance to chemo-immunotherapy in ovarian cancer.氯沙坦重塑肿瘤免疫微环境并抑制 IGF-1 以克服卵巢癌对化疗免疫治疗的耐药性。
Br J Cancer. 2024 Nov;131(10):1683-1693. doi: 10.1038/s41416-024-02863-9. Epub 2024 Oct 5.
4
Tumor-associated fibrosis: a unique mechanism promoting ovarian cancer metastasis and peritoneal dissemination.肿瘤相关纤维化:促进卵巢癌转移和腹膜扩散的独特机制。
Cancer Metastasis Rev. 2024 Sep;43(3):1037-1053. doi: 10.1007/s10555-024-10169-8. Epub 2024 Mar 28.
5
Leydig Cell Hyperplasia of Ovary - An Unusual Finding in Postneoadjuvant Chemotherapy Case of Primary Fallopian Tube Carcinoma.卵巢间质细胞增生——原发性输卵管癌新辅助化疗后病例中的罕见发现
J Midlife Health. 2022 Jul-Sep;13(3):247-250. doi: 10.4103/jmh.jmh_117_22. Epub 2023 Jan 14.
6
LINC00494 Promotes Ovarian Cancer Development and Progression by Modulating NFκB1 and FBXO32.LINC00494通过调节NFκB1和FBXO32促进卵巢癌的发展和进展。
Front Oncol. 2021 Jan 28;10:541410. doi: 10.3389/fonc.2020.541410. eCollection 2020.
7
Pathological Chemotherapy Response Score in Patients Affected by High Grade Serous Ovarian Carcinoma: The Prognostic Role of Omental and Ovarian Residual Disease.高级别浆液性卵巢癌患者的病理化疗反应评分:网膜和卵巢残留病灶的预后作用
Front Oncol. 2019 Aug 19;9:778. doi: 10.3389/fonc.2019.00778. eCollection 2019.
8
Losartan treatment enhances chemotherapy efficacy and reduces ascites in ovarian cancer models by normalizing the tumor stroma.氯沙坦治疗通过使肿瘤基质正常化来增强卵巢癌模型中的化疗疗效并减少腹水。
Proc Natl Acad Sci U S A. 2019 Feb 5;116(6):2210-2219. doi: 10.1073/pnas.1818357116. Epub 2019 Jan 18.
9
Prediction of post-TACE necrosis of hepatocellular carcinoma usingvolumetric enhancement on MRI and volumetric oil deposition on CT, with pathological correlation.基于 MRI 容积增强和 CT 容积油沉积与病理相关性预测肝癌 TACE 后坏死。
Eur Radiol. 2018 Jul;28(7):3032-3040. doi: 10.1007/s00330-017-5198-9. Epub 2018 Jan 30.
10
AID/APOBEC-network reconstruction identifies pathways associated with survival in ovarian cancer.AID/载脂蛋白B mRNA编辑酶催化多肽样家族网络重建可识别与卵巢癌生存相关的通路。
BMC Genomics. 2016 Aug 16;17(1):643. doi: 10.1186/s12864-016-3001-y.

本文引用的文献

1
Assessing treatment effect in pancreatic cancer.评估胰腺癌的治疗效果。
Arch Pathol Lab Med. 2012 Jan;136(1):100-9. doi: 10.5858/arpa.2011-0144-RA.
2
Neoadjuvant chemotherapy or primary surgery in stage IIIC or IV ovarian cancer.新辅助化疗与初始肿瘤细胞减灭术用于 IIIC 或 IV 期卵巢癌。
N Engl J Med. 2010 Sep 2;363(10):943-53. doi: 10.1056/NEJMoa0908806.
3
Prognostic significance of histopathological tumor regression after neoadjuvant chemotherapy in esophageal adenocarcinomas.新辅助化疗后食管腺癌的组织病理学肿瘤退缩的预后意义。
Mod Pathol. 2009 Dec;22(12):1555-63. doi: 10.1038/modpathol.2009.123. Epub 2009 Oct 2.
4
Histopathologic examination and reporting of esophageal carcinomas following preoperative neoadjuvant therapy: practical guidelines and current issues.
Am J Clin Pathol. 2008 Feb;129(2):252-62. doi: 10.1309/CCR3QN4874YJDJJ7.
5
Recommendations for the reporting of surgically resected specimens of colorectal carcinoma: Association of Directors of Anatomic and Surgical Pathology.结直肠癌手术切除标本报告建议:解剖与外科病理学主任协会
Am J Clin Pathol. 2008 Jan;129(1):13-23. doi: 10.1309/6UHNC7MAD8KWNAWC.
6
An immunohistochemical and morphological analysis of post-chemotherapy ovarian carcinoma.化疗后卵巢癌的免疫组织化学及形态学分析
J Clin Pathol. 2008 May;61(5):652-7. doi: 10.1136/jcp.2007.053793. Epub 2007 Nov 15.
7
Prognostic factors for stage III epithelial ovarian cancer: a Gynecologic Oncology Group Study.Ⅲ期上皮性卵巢癌的预后因素:一项妇科肿瘤学组研究
J Clin Oncol. 2007 Aug 20;25(24):3621-7. doi: 10.1200/JCO.2006.10.2517.
8
Prognostic factors for surgical outcome and survival in 447 women treated for advanced (FIGO-stages III-IV) epithelial ovarian carcinoma.447例晚期(国际妇产科联盟分期III-IV期)上皮性卵巢癌患者手术结局及生存的预后因素
Int J Oncol. 2007 Mar;30(3):727-34.
9
Excellent interobserver agreement on grading the extent of residual carcinoma after preoperative chemoradiation in esophageal and esophagogastric junction carcinoma: a reliable predictor for patient outcome.在食管及食管胃交界癌术前放化疗后对残留癌范围进行分级时,观察者间具有出色的一致性:这是患者预后的可靠预测指标。
Am J Surg Pathol. 2007 Jan;31(1):58-64. doi: 10.1097/01.pas.0000213312.36306.cc.
10
Tumor necrosis has no prognostic value in neoadjuvant chemotherapy for soft tissue sarcoma.肿瘤坏死在软组织肉瘤新辅助化疗中无预后价值。
Clin Orthop Relat Res. 2007 Feb;455:219-24. doi: 10.1097/01.blo.0000238864.69486.59.

新辅助化疗治疗晚期卵巢癌女性患者的组织学参数与疾病结局的相关性。

Histologic parameters predictive of disease outcome in women with advanced stage ovarian carcinoma treated with neoadjuvant chemotherapy.

机构信息

Department of Pathology, University of Southern California, Los Angeles, CA.

出版信息

Transl Oncol. 2012 Dec;5(6):469-74. doi: 10.1593/tlo.12265. Epub 2012 Dec 1.

DOI:10.1593/tlo.12265
PMID:23397476
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3567723/
Abstract

The use of neoadjuvant chemotherapy followed by tumor reduction surgery, also called interval debulking surgery (IDS), is considered an alternative therapeutic regimen for selected patients with advanced stage epithelial ovarian cancer (EOC). Although minimal residual disease has been proven to be a prognostic factor in traditional cytoreduction for advanced stage EOC, predictive factors after IDS still remain unexplored. The aim of this study was to determine the prognostic value of post-neoadjuvant histologic changes with clinical outcome. Three pathologists evaluated 67 cases for the following parameters: fibrosis, necrosis, residual tumor, and inflammation. The Cohen's kappa statistic was used to measure agreement among pathologists. Univariate and multivariate Cox proportional hazards models were used to determine the association between histologic parameters and recurrence-free survival (RFS) and overall survival (OS). There was substantial to almost perfect agreement among the three pathologists in all four histologic parameters (k ranged from 0.65 to 0.97). Fibrosis was associated with longer RFS (P = 0.0257) with a median of 20 months for tumors with fibrosis (3+) versus 12 months for tumors with fibrosis (1+, 2+) and longer OS (P = 0.0249) with a median of 51 months for tumors with fibrosis (3+) versus 32 months for tumors with fibrosis (1+, 2+). Our results revealed that patients with tumors exhibiting fibrosis (1+, 2+), as well as necrosis (0, 1+), had significant shorter RFS and OS (P = 0.059 and P = 0.0234, respectively). We suggest that the assessment of fibrosis and necrosis should be implemented in pathologic evaluation and prospectively validated in future studies.

摘要

新辅助化疗后肿瘤缩小手术(也称为间隔减瘤术,IDS),被认为是一种选择治疗方案,适用于特定的晚期上皮性卵巢癌(EOC)患者。虽然在传统的晚期 EOC 肿瘤细胞减灭术中,微小残留病灶已被证明是预后因素,但 IDS 后的预测因素仍有待探索。本研究旨在确定新辅助化疗后组织学变化与临床结果之间的预后价值。三位病理学家评估了 67 例患者的以下参数:纤维化、坏死、残留肿瘤和炎症。采用 Cohen's kappa 统计量来衡量病理学家之间的一致性。采用单因素和多因素 Cox 比例风险模型来确定组织学参数与无复发生存(RFS)和总生存(OS)之间的关联。在所有四个组织学参数中,三位病理学家之间的一致性很高,达到几乎完全一致(κ值范围为 0.65 至 0.97)。纤维化与 RFS 延长相关(P = 0.0257),纤维化(3+)肿瘤的中位 RFS 为 20 个月,而纤维化(1+、2+)肿瘤的中位 RFS 为 12 个月;纤维化与 OS 延长相关(P = 0.0249),纤维化(3+)肿瘤的中位 OS 为 51 个月,而纤维化(1+、2+)肿瘤的中位 OS 为 32 个月。我们的结果表明,纤维化(1+、2+)和坏死(0、1+)的肿瘤患者的 RFS 和 OS 显著缩短(P = 0.059 和 P = 0.0234)。我们建议在病理评估中实施纤维化和坏死的评估,并在未来的研究中进行前瞻性验证。