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[胰腺导管腺癌免疫治疗的进展]

[Advances in immunotherapy of pancreatic ductal adenocarcinoma].

作者信息

Yang J Q, Wei T, Chen Y W, Bai X L, Liang T B

机构信息

Department of Hepatopancreatobiliary Surgery, the Second Affiliated Hospital of Zhejiang University School of Medicine, Key Laboratory of Pancreatic Disease of Zhejiang Province, Hangzhou 310009, China.

出版信息

Zhonghua Wai Ke Za Zhi. 2017 May 1;55(5):396-400. doi: 10.3760/cma.j.issn.0529-5815.2017.05.018.

DOI:10.3760/cma.j.issn.0529-5815.2017.05.018
PMID:28464583
Abstract

The morbidity of pancreatic ductal adenocarcinoma (PDAC) has been increasing over years, while the treatment efficacy and prognosis of PDAC remain far from satisfying. The newly-ermerged tumor immunotherapy has not only made lots of breakthroughs in various malignancies, but also brought an opportunity to the treatment of pancreatic cancer.PDAC immunotherapies, mainly including vaccine therapy, adoptive T cell thanfer therapy, checkpoint blockade therapy, have achieved a certain effect, however, the clinical outcomes have not been satisfactory. Therefore, the combination of immunotherapies based on different theoretical views is important and is likely to be the trend in the future. Carcinoma associated fibroblast (CAF) is the most common cell in pancreatic cancer stromal component. It will be helpful to develop more potential therapeutic targets by further exploring CAF and the mechanism of fibrosis mediated immunosuppression.

摘要

近年来,胰腺导管腺癌(PDAC)的发病率一直在上升,而PDAC的治疗效果和预后仍远不尽人意。新出现的肿瘤免疫疗法不仅在各种恶性肿瘤中取得了许多突破,也为胰腺癌的治疗带来了契机。PDAC免疫疗法主要包括疫苗疗法、过继性T细胞转移疗法、检查点阻断疗法,已取得了一定效果,然而,临床结果并不令人满意。因此,基于不同理论观点的免疫疗法联合应用很重要,且可能是未来的发展趋势。癌相关成纤维细胞(CAF)是胰腺癌基质成分中最常见的细胞。进一步探索CAF及其介导免疫抑制的纤维化机制,将有助于开发更多潜在的治疗靶点。

相似文献

1
[Advances in immunotherapy of pancreatic ductal adenocarcinoma].[胰腺导管腺癌免疫治疗的进展]
Zhonghua Wai Ke Za Zhi. 2017 May 1;55(5):396-400. doi: 10.3760/cma.j.issn.0529-5815.2017.05.018.
2
Rational combinations of immunotherapy for pancreatic ductal adenocarcinoma.胰腺导管腺癌免疫治疗的合理联合方案
Chin Clin Oncol. 2017 Jun;6(3):31. doi: 10.21037/cco.2017.06.04.
3
[Pancreatic ductal adenocarcinoma immune microenvironment and immunotherapy prospects].[胰腺导管腺癌免疫微环境与免疫治疗前景]
Zhonghua Wai Ke Za Zhi. 2019 Jan 1;57(1):10-15. doi: 10.3760/cma.j.issn.0529-5815.2019.01.003.
4
Immunotherapeutic strategies in pancreatic ductal adenocarcinoma (PDAC): current perspectives and future prospects.胰腺导管腺癌 (PDAC) 的免疫治疗策略:当前的观点和未来的前景。
Mol Biol Rep. 2020 Aug;47(8):6269-6280. doi: 10.1007/s11033-020-05648-4. Epub 2020 Jul 13.
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Advances in immunotherapy for pancreatic ductal adenocarcinoma.免疫治疗在胰腺导管腺癌中的进展。
J Hepatobiliary Pancreat Sci. 2021 May;28(5):419-430. doi: 10.1002/jhbp.944. Epub 2021 Apr 3.
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Role of targeted immunotherapy for pancreatic ductal adenocarcinoma (PDAC) treatment: An overview.靶向免疫疗法在胰腺导管腺癌 (PDAC) 治疗中的作用:概述。
Int Immunopharmacol. 2021 Jun;95:107508. doi: 10.1016/j.intimp.2021.107508. Epub 2021 Mar 13.
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Pancreas adenocarcinoma: novel therapeutics.胰腺腺癌:新型疗法
Chin Clin Oncol. 2017 Jun;6(3):30. doi: 10.21037/cco.2017.06.14.
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Trials and tribulations of pancreatic cancer immunotherapy.胰腺癌免疫治疗的困境与挑战。
Cancer Lett. 2021 Apr 28;504:1-14. doi: 10.1016/j.canlet.2021.01.031. Epub 2021 Feb 4.
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The reciprocal regulation between host tissue and immune cells in pancreatic ductal adenocarcinoma: new insights and therapeutic implications.胰腺导管腺癌中宿主组织与免疫细胞的相互调控:新的见解和治疗意义。
Mol Cancer. 2019 Dec 13;18(1):184. doi: 10.1186/s12943-019-1117-9.
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Immunosuppression, immune escape, and immunotherapy in pancreatic cancer: focused on the tumor microenvironment.胰腺癌中的免疫抑制、免疫逃逸和免疫治疗:聚焦于肿瘤微环境
Cell Oncol (Dordr). 2023 Feb;46(1):17-48. doi: 10.1007/s13402-022-00741-1. Epub 2022 Nov 11.

引用本文的文献

1
Prediction of anti-CD25 and 5-FU treatments efficacy for pancreatic cancer using a mathematical model.使用数学模型预测抗 CD25 和 5-FU 治疗胰腺癌的疗效。
BMC Cancer. 2021 Nov 15;21(1):1226. doi: 10.1186/s12885-021-08770-z.
2
CD25 and TGF-β blockade based on predictive integrated immune ratio inhibits tumor growth in pancreatic cancer.基于预测性综合免疫比值的 CD25 和 TGF-β 阻断抑制胰腺癌肿瘤生长。
J Transl Med. 2018 Oct 25;16(1):294. doi: 10.1186/s12967-018-1673-6.