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本文引用的文献

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Randomized Phase III Study of FOLFOX Alone or With Pegilodecakin as Second-Line Therapy in Patients With Metastatic Pancreatic Cancer That Progressed After Gemcitabine (SEQUOIA).PEG 化重组人粒细胞集落刺激因子在吉西他滨治疗失败后的转移性胰腺癌二线治疗随机 III 期研究(SEQUOIA)
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Upfront molecular profiling of pancreatic cancer patients - An idea whose time has come.对胰腺癌患者进行 upfront 分子谱分析——是时候了。
Pancreatology. 2020 Apr;20(3):391-393. doi: 10.1016/j.pan.2020.01.017. Epub 2020 Feb 5.
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Dendritic Cell Paucity Leads to Dysfunctional Immune Surveillance in Pancreatic Cancer.树突状细胞缺乏导致胰腺癌免疫监视功能障碍。
Cancer Cell. 2020 Mar 16;37(3):289-307.e9. doi: 10.1016/j.ccell.2020.02.008.
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Recent insights into the biology of pancreatic cancer.胰腺癌生物学的最新见解。
EBioMedicine. 2020 Mar;53:102655. doi: 10.1016/j.ebiom.2020.102655. Epub 2020 Mar 2.
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ILC2s amplify PD-1 blockade by activating tissue-specific cancer immunity.ILC2s 通过激活组织特异性癌症免疫来增强 PD-1 阻断作用。
Nature. 2020 Mar;579(7797):130-135. doi: 10.1038/s41586-020-2015-4. Epub 2020 Feb 19.
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Current advances and outlooks in immunotherapy for pancreatic ductal adenocarcinoma.免疫治疗胰腺导管腺癌的最新进展和展望。
Mol Cancer. 2020 Feb 15;19(1):32. doi: 10.1186/s12943-020-01151-3.
7
An Emerging Paradigm for Germline Testing in Pancreatic Ductal Adenocarcinoma and Immediate Implications for Clinical Practice: A Review.在胰腺导管腺癌中进行种系检测的新兴范例及其对临床实践的直接影响:综述。
JAMA Oncol. 2020 May 1;6(5):764-771. doi: 10.1001/jamaoncol.2019.5963.
8
Role of imaging biomarkers for prognostic prediction in patients with pancreatic ductal adenocarcinoma.影像生物标志物在胰腺导管腺癌患者预后预测中的作用。
Clin Radiol. 2020 Jun;75(6):478.e1-478.e11. doi: 10.1016/j.crad.2019.12.023. Epub 2020 Feb 6.
9
Fibroblast Heterogeneity in the Pancreatic Tumor Microenvironment.胰腺肿瘤微环境中的成纤维细胞异质性。
Cancer Discov. 2020 May;10(5):648-656. doi: 10.1158/2159-8290.CD-19-1353. Epub 2020 Feb 3.
10
Cancer-Specific Loss of p53 Leads to a Modulation of Myeloid and T Cell Responses.肿瘤特异性 p53 缺失导致髓系和 T 细胞反应的调节。
Cell Rep. 2020 Jan 14;30(2):481-496.e6. doi: 10.1016/j.celrep.2019.12.028.

精准医疗时代的胰腺癌免疫肿瘤学

Pancreatic Cancer Immuno-oncology in the Era of Precision Medicine.

作者信息

Hegde Samarth

机构信息

Department of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY USA.

出版信息

Indian J Surg Oncol. 2021 Apr;12(Suppl 1):118-127. doi: 10.1007/s13193-020-01192-6. Epub 2020 Aug 25.

DOI:10.1007/s13193-020-01192-6
PMID:33994737
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8119507/
Abstract

Pancreatic malignancies carry a dismal prognosis globally, with pancreatic adenocarcinomas (PDAC) being particularly aggressive and stubborn. Unfortunately, several therapeutic strategies that show promise in other cancers have failed to make sizeable impact on pancreatic tumor outcomes. Responses to immunotherapies are especially rare in pancreatic cancer, and patients are in need of innovative approaches that can result in more durable responses. Current research in preclinical models and humans has suggested this resistance is due to a uniquely inflammatory and dysfunctional tumor microenvironment; these findings lay the groundwork for targeting these barriers and improving outcomes. Clinical analyses have also revealed unprecedented heterogeneity in tumor and stromal biology of PDAC, underscoring the need for more personalized approaches and combinatorial therapies. This review will highlight the current state of translational research focusing on PDAC immunity, summarize ongoing clinical efforts to tackle PDAC vulnerabilities, and underscore some unresolved challenges in implementing therapies more broadly. A better understanding of immune contexture and tumor heterogeneity in this disease will greatly accelerate drug discovery and implementation of precision medicine for PDAC.

摘要

在全球范围内,胰腺恶性肿瘤的预后都很糟糕,其中胰腺腺癌(PDAC)尤其具有侵袭性且顽固难治。不幸的是,一些在其他癌症中显示出前景的治疗策略,对胰腺肿瘤的治疗效果却未能产生显著影响。胰腺癌对免疫疗法的反应尤其罕见,患者需要能够产生更持久反应的创新方法。目前在临床前模型和人体中的研究表明,这种耐药性是由于肿瘤微环境具有独特的炎症性和功能失调;这些发现为针对这些障碍并改善治疗结果奠定了基础。临床分析还揭示了PDAC在肿瘤和基质生物学方面前所未有的异质性,强调了需要更个性化的方法和联合疗法。本综述将重点介绍针对PDAC免疫的转化研究现状,总结应对PDAC弱点的当前临床努力,并强调在更广泛实施治疗方面一些尚未解决的挑战。更好地了解这种疾病中的免疫情况和肿瘤异质性将极大地加速PDAC的药物发现和精准医学的实施。