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胰腺癌的精准治疗:从实验室到临床

Precision Therapy of Pancreatic Cancer: From Bench to Bedside.

作者信息

Ciecielski Katrin Jana, Berninger Alexandra, Algül Hana

机构信息

Comprehensive Cancer Center Munich (CCCM), Klinikum rechts der Isar, Technische Universität München, Munich, Germany.

出版信息

Visc Med. 2020 Oct;36(5):373-380. doi: 10.1159/000509232. Epub 2020 Oct 6.

DOI:10.1159/000509232
PMID:33178734
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7590788/
Abstract

BACKGROUND

Pancreatic ductal adenocarcinoma (PDAC), with a mortality rate of 94% and a 5-year-survival rate of only 8%, is one of the deadliest cancer entities worldwide, and early diagnostic methods as well as effective therapies are urgently needed.

SUMMARY

This review summarizes current clinical procedure and recent developments of oncological therapy in the palliative setting of metastatic PDAC. It further gives examples of successful, as well as failed, targeted therapy approaches and finally discusses promising ongoing research into the decade-old question of the "undruggability" of KRAS.

KEY MESSAGES

Bench-driven concepts change the clinical landscape from "one size fits all" towards precision medicine. With growing insight into the molecular mechanisms of pancreatic cancer the era of targeted therapy in PDAC is gaining a new momentum.

摘要

背景

胰腺导管腺癌(PDAC)的死亡率为94%,5年生存率仅为8%,是全球最致命的癌症类型之一,迫切需要早期诊断方法和有效的治疗方法。

总结

本综述总结了转移性PDAC姑息治疗中的当前临床程序和肿瘤治疗的最新进展。它还给出了成功和失败的靶向治疗方法的例子,最后讨论了针对KRAS“不可成药”这一由来已久问题的正在进行的有前景的研究。

关键信息

基于实验室研究的概念正在将临床格局从“一刀切”转变为精准医学。随着对胰腺癌分子机制的深入了解,PDAC的靶向治疗时代正获得新的动力。

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Precision Medicine in Pancreatitis: The Future of Acute Pancreatitis Care.精准医学在胰腺炎中的应用:急性胰腺炎治疗的未来。
Function (Oxf). 2023 Apr 5;4(3):zqad015. doi: 10.1093/function/zqad015. eCollection 2023.

本文引用的文献

1
A bright future for KRAS inhibitors.KRAS抑制剂的光明未来。
Nat Cancer. 2020 Jan;1(1):25-27. doi: 10.1038/s43018-019-0016-8.
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Overall survival in patients with pancreatic cancer receiving matched therapies following molecular profiling: a retrospective analysis of the Know Your Tumor registry trial.接受分子谱分析后接受匹配治疗的胰腺癌患者的总生存期:Know Your Tumor 登记试验的回顾性分析。
Lancet Oncol. 2020 Apr;21(4):508-518. doi: 10.1016/S1470-2045(20)30074-7. Epub 2020 Mar 2.
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Why HALO 301 Failed and Implications for Treatment of Pancreatic Cancer.为何HALO 301试验失败及其对胰腺癌治疗的启示
Pancreas (Fairfax). 2019;3(1):e1-e4. doi: 10.17140/POJ-3-e010. Epub 2019 Dec 20.
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Resistance looms for KRAS inhibitors.KRAS抑制剂面临耐药问题。
Nat Med. 2020 Feb;26(2):169-170. doi: 10.1038/s41591-020-0765-z.
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Rapid non-uniform adaptation to conformation-specific KRAS(G12C) inhibition.快速非均匀适应构象特异性 KRAS(G12C)抑制。
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The clinical KRAS(G12C) inhibitor AMG 510 drives anti-tumour immunity.临床 KRAS(G12C) 抑制剂 AMG 510 可引发抗肿瘤免疫。
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The KRAS Inhibitor MRTX849 Provides Insight toward Therapeutic Susceptibility of KRAS-Mutant Cancers in Mouse Models and Patients.KRAS 抑制剂 MRTX849 为 KRAS 突变型癌症在小鼠模型和患者中的治疗敏感性提供了新的见解。
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Palliative chemotherapy in pancreatic cancer-treatment sequences.胰腺癌治疗序列中的姑息化疗。
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Chemotherapy of pancreatic cancer in patients with poor performance.
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