• 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
Up-to-Date Tailored Systemic Treatment in Pancreatic Ductal Adenocarcinoma.胰腺癌的最新定制全身治疗
Gastroenterol Res Pract. 2019 Sep 5;2019:7135437. doi: 10.1155/2019/7135437. eCollection 2019.
2
Current and emerging therapies for patients with advanced pancreatic ductal adenocarcinoma: a bright future.目前和新兴的治疗方法为晚期胰腺导管腺癌患者带来希望。
Lancet Oncol. 2020 Mar;21(3):e135-e145. doi: 10.1016/S1470-2045(19)30795-8.
3
Tumor microenvironment in pancreatic ductal adenocarcinoma: Implications in immunotherapy.胰腺导管腺癌中的肿瘤微环境:免疫治疗的意义。
World J Gastroenterol. 2022 Jul 21;28(27):3297-3313. doi: 10.3748/wjg.v28.i27.3297.
4
Translational advances in pancreatic ductal adenocarcinoma therapy.胰腺导管腺癌治疗的转化进展。
Nat Cancer. 2022 Mar;3(3):272-286. doi: 10.1038/s43018-022-00349-2. Epub 2022 Mar 29.
5
Therapeutic options for the management of pancreatic cancer.胰腺癌治疗的选择
World J Gastroenterol. 2014 Aug 28;20(32):11142-59. doi: 10.3748/wjg.v20.i32.11142.
6
Tumor Microenvironment Features and Chemoresistance in Pancreatic Ductal Adenocarcinoma: Insights into Targeting Physicochemical Barriers and Metabolism as Therapeutic Approaches.胰腺导管腺癌的肿瘤微环境特征与化疗耐药性:针对物理化学屏障和代谢作为治疗方法的见解
Cancers (Basel). 2021 Dec 6;13(23):6135. doi: 10.3390/cancers13236135.
7
Uncovering key targets of success for immunotherapy in pancreatic cancer.揭示胰腺癌免疫治疗的关键靶点。
Expert Opin Ther Targets. 2021 Nov;25(11):987-1005. doi: 10.1080/14728222.2021.2010044. Epub 2021 Dec 13.
8
New developments in pancreatic cancer treatment.胰腺癌治疗的新进展。
Minerva Gastroenterol Dietol. 2012 Dec;58(4):427-43.
9
Future of immunotherapy in pancreas cancer and the trials, tribulations and successes thus far.胰腺癌免疫疗法的未来以及迄今为止的试验、磨难与成功。
Semin Oncol. 2021 Feb;48(1):57-68. doi: 10.1053/j.seminoncol.2021.02.007. Epub 2021 Apr 17.
10
Inflammation, Biomarkers and Immuno-Oncology Pathways in Pancreatic Cancer.胰腺癌中的炎症、生物标志物与免疫肿瘤学通路
J Pers Med. 2019 Apr 26;9(2):20. doi: 10.3390/jpm9020020.

引用本文的文献

1
Andrographis Reverses Gemcitabine Resistance through Regulation of ERBB3 and Calcium Signaling Pathway in Pancreatic Ductal Adenocarcinoma.穿心莲通过调节胰腺导管腺癌中的ERBB3和钙信号通路逆转吉西他滨耐药性。
Biomedicines. 2023 Jan 3;11(1):119. doi: 10.3390/biomedicines11010119.
2
Complement and Fungal Dysbiosis as Prognostic Markers and Potential Targets in PDAC Treatment.补体与真菌失调作为 PDAC 治疗的预后标志物和潜在靶点。
Curr Oncol. 2022 Dec 14;29(12):9833-9854. doi: 10.3390/curroncol29120773.
3
Berberine Overcomes Gemcitabine-Associated Chemoresistance through Regulation of Rap1/PI3K-Akt Signaling in Pancreatic Ductal Adenocarcinoma.黄连素通过调节胰腺导管腺癌中的Rap1/PI3K-Akt信号通路克服吉西他滨相关的化疗耐药性。
Pharmaceuticals (Basel). 2022 Sep 28;15(10):1199. doi: 10.3390/ph15101199.
4
Can Nimesulide Nanoparticles Be a Therapeutic Strategy for the Inhibition of the KRAS/PTEN Signaling Pathway in Pancreatic Cancer?尼美舒利纳米颗粒能否成为抑制胰腺癌中KRAS/PTEN信号通路的治疗策略?
Front Oncol. 2021 Jul 20;11:594917. doi: 10.3389/fonc.2021.594917. eCollection 2021.
5
Micro- and Mycobiota Dysbiosis in Pancreatic Ductal Adenocarcinoma Development.胰腺导管腺癌发生过程中的微生物群和真菌群失调
Cancers (Basel). 2021 Jul 8;13(14):3431. doi: 10.3390/cancers13143431.

本文引用的文献

1
A phase II trial of GSK2256098 and trametinib in patients with advanced pancreatic ductal adenocarcinoma.一项关于GSK2256098与曲美替尼治疗晚期胰腺导管腺癌患者的II期试验。
J Gastrointest Oncol. 2022 Dec;13(6):3216-3226. doi: 10.21037/jgo-22-86.
2
Ibrutinib in combination with nab-paclitaxel and gemcitabine for first-line treatment of patients with metastatic pancreatic adenocarcinoma: phase III RESOLVE study.伊布替尼联合 nab-紫杉醇和吉西他滨一线治疗转移性胰腺导管腺癌患者的 III 期 RESOLVE 研究。
Ann Oncol. 2021 May;32(5):600-608. doi: 10.1016/j.annonc.2021.01.070. Epub 2021 Feb 1.
3
Phase Ib Study of Wnt Inhibitor Ipafricept with Gemcitabine and nab-paclitaxel in Patients with Previously Untreated Stage IV Pancreatic Cancer.Ipafricept 联合吉西他滨和 nab-紫杉醇治疗未经治疗的 IV 期胰腺癌的 Ib 期研究。
Clin Cancer Res. 2020 Oct 15;26(20):5348-5357. doi: 10.1158/1078-0432.CCR-20-0489. Epub 2020 Jul 21.
4
Maintenance Olaparib for Germline -Mutated Metastatic Pancreatic Cancer.维持奥拉帕利治疗种系突变转移性胰腺癌。
N Engl J Med. 2019 Jul 25;381(4):317-327. doi: 10.1056/NEJMoa1903387. Epub 2019 Jun 2.
5
Results from a Phase IIb, Randomized, Multicenter Study of GVAX Pancreas and CRS-207 Compared with Chemotherapy in Adults with Previously Treated Metastatic Pancreatic Adenocarcinoma (ECLIPSE Study).一项关于 GVAX 胰腺和 CRS-207 与化疗在先前治疗过的转移性胰腺腺癌成人中的 IIb 期、随机、多中心研究的结果(ECLIPSE 研究)。
Clin Cancer Res. 2019 Sep 15;25(18):5493-5502. doi: 10.1158/1078-0432.CCR-18-2992. Epub 2019 May 24.
6
Comparative Effectiveness of Gemcitabine plus Nab-Paclitaxel and FOLFIRINOX in the First-Line Setting of Metastatic Pancreatic Cancer: A Systematic Review and Meta-Analysis.吉西他滨联合纳米白蛋白紫杉醇与FOLFIRINOX用于转移性胰腺癌一线治疗的疗效比较:一项系统评价和荟萃分析
Cancers (Basel). 2019 Apr 5;11(4):484. doi: 10.3390/cancers11040484.
7
Phase IB/II Randomized Study of FOLFIRINOX Plus Pegylated Recombinant Human Hyaluronidase Versus FOLFIRINOX Alone in Patients With Metastatic Pancreatic Adenocarcinoma: SWOG S1313.FOLFIRINOX 联合聚乙二醇重组人透明质酸酶与单纯 FOLFIRINOX 治疗转移性胰腺导管腺癌的 Ib/II 期随机研究:SWOG S1313
J Clin Oncol. 2019 May 1;37(13):1062-1069. doi: 10.1200/JCO.18.01295. Epub 2019 Feb 28.
8
NAPOLI-1 phase 3 study of liposomal irinotecan in metastatic pancreatic cancer: Final overall survival analysis and characteristics of long-term survivors.NAPOLI-1 期研究:脂质体伊立替康治疗转移性胰腺癌:最终总生存分析和长期生存者特征。
Eur J Cancer. 2019 Feb;108:78-87. doi: 10.1016/j.ejca.2018.12.007. Epub 2019 Jan 14.
9
FOLFIRINOX or Gemcitabine as Adjuvant Therapy for Pancreatic Cancer.FOLFIRINOX 或吉西他滨作为胰腺癌的辅助治疗。
N Engl J Med. 2018 Dec 20;379(25):2395-2406. doi: 10.1056/NEJMoa1809775.
10
Inter- and intra-tumoural heterogeneity in cancer-associated fibroblasts of human pancreatic ductal adenocarcinoma.人胰腺导管腺癌中肿瘤相关成纤维细胞的肿瘤内和肿瘤间异质性。
J Pathol. 2019 May;248(1):51-65. doi: 10.1002/path.5224. Epub 2019 Feb 22.

胰腺癌的最新定制全身治疗

Up-to-Date Tailored Systemic Treatment in Pancreatic Ductal Adenocarcinoma.

作者信息

Fong Caroline Y K, Burke Emma, Cunningham David, Starling Naureen

机构信息

The Royal Marsden NHS Foundation Trust, Downs Road, Sutton SM2 5PT, UK.

出版信息

Gastroenterol Res Pract. 2019 Sep 5;2019:7135437. doi: 10.1155/2019/7135437. eCollection 2019.

DOI:10.1155/2019/7135437
PMID:31582971
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6748185/
Abstract

Despite intensive research efforts, pancreatic ductal adenocarcinoma is still regarded as an aggressive and life-limiting malignancy. Combination chemotherapy regimens that underpin the current treatment approach in the advanced setting have led to incremental survival gains in recent years but have failed to confer patients with a median overall survival that exceeds 12 months from diagnosis. Research has since focussed on understanding the role and interplay between various components of the desmoplastic stroma and tumour microenvironment, in addition to developing targeted therapies based on molecular features to improve the prognosis associated with this malignancy. This review will summarise the available systemic treatment options and discuss potential methods to refine the resolution of patient selection to enhance responses to currently available therapies. Furthermore, it will explore newer approaches anticipated to come to the fore of future clinical practice, such as agents targeting the DNA damage response and tumour microenvironment as well as immunotherapy-based combinations.

摘要

尽管进行了深入的研究,但胰腺导管腺癌仍被视为一种侵袭性强、危及生命的恶性肿瘤。近年来,作为晚期胰腺癌当前治疗方法基础的联合化疗方案已使患者的生存期逐步延长,但仍无法使患者的中位总生存期超过自诊断起12个月。此后,研究重点转向了解促纤维增生性基质和肿瘤微环境各成分之间的作用及相互作用,同时开发基于分子特征的靶向治疗方法,以改善这种恶性肿瘤的预后。本综述将总结现有的全身治疗选择,并讨论优化患者选择策略以提高对现有疗法反应的潜在方法。此外,还将探讨有望在未来临床实践中崭露头角的新方法,如靶向DNA损伤反应和肿瘤微环境的药物以及基于免疫疗法的联合治疗。