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转移性胰腺导管腺癌药物治疗进展

Advances in Drug Therapy for Metastatic Pancreatic Ductal Adenocarcinoma.

作者信息

Gao Jianjun, Wang Jiangang, Guan Canghai, Shi Wujiang, Dong Qingfu, Sheng Jialin, Zou Xinlei, Xu Zhaoqiang, Ge Yifei, Huang Ziyue, Li Jiehan, Bao Haolin, Xu Yi, Cui Yunfu, Xu Xiaoxue, Zhong Xiangyu

机构信息

Department of Hepatopancreatobiliary Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin 150086, Heilongjiang, China.

Department of General Surgery, Tangdu Hospital, Air Force Medical University, Xi'an 710032, Shanxi, China.

出版信息

J Cancer. 2024 Feb 25;15(8):2214-2228. doi: 10.7150/jca.89788. eCollection 2024.

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is an aggressive disease with a notably poor prognosis. A large number of patients with PDAC develop metastases before they are diagnosed with metastatic pancreatic cancer (mPDAC). For mPDAC, FOLFIRINOX or gemcitabine plus nab-paclitaxel are the current first-line treatments. It is important to note, however, that many patients will fail chemotherapy because of drug resistance. ​Heterogeneous tumors and complex tumor microenvironments are key factors. As a result, clinical researchers are exploring a variety of alternative treatment modalities. Current understanding of the molecular signature and immune landscape of PDAC has motivated the emergence of different targeted and immune-based therapeutic approaches, some of which have shown promising results. The purpose of this review is to discuss the new targets and new drugs for mPDAC in terms of specific pathogenic factors such as metabolic vulnerability, DNA damage repair system, tumor microenvironment and immune system, in order to identify potential vulnerabilities in mPDAC patients and hopefully improve the prognosis of mPDAC patients.

摘要

胰腺导管腺癌(PDAC)是一种侵袭性疾病,预后明显较差。大量PDAC患者在被诊断为转移性胰腺癌(mPDAC)之前就已发生转移。对于mPDAC,FOLFIRINOX方案或吉西他滨联合纳米白蛋白结合型紫杉醇是目前的一线治疗方案。然而,需要注意的是,许多患者会因耐药而化疗失败。肿瘤异质性和复杂的肿瘤微环境是关键因素。因此,临床研究人员正在探索多种替代治疗方式。目前对PDAC分子特征和免疫格局的认识推动了不同靶向治疗和免疫治疗方法的出现,其中一些已显示出有前景的结果。本综述的目的是从代谢脆弱性、DNA损伤修复系统、肿瘤微环境和免疫系统等特定致病因素方面讨论mPDAC的新靶点和新药,以识别mPDAC患者潜在的脆弱性,有望改善mPDAC患者的预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4861/10937276/887dc443e8e8/jcav15p2214g001.jpg

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