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胰腺癌和放疗的临床前差距。

The preclinical gap in pancreatic cancer and radiotherapy.

机构信息

Cancer Research UK Scotland Institute, Switchback Rd, Glasgow G61 1BD, UK.

School of Cancer Sciences, University of Glasgow, Glasgow G61 1QH, UK.

出版信息

Dis Model Mech. 2024 Jul 1;17(7). doi: 10.1242/dmm.050703. Epub 2024 Jul 9.

DOI:10.1242/dmm.050703
PMID:38979684
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11261628/
Abstract

Pancreatic ductal adenocarcinoma is an aggressive malignancy with limited treatment options. Chemotherapy offers little benefit and, although there is some evidence that radiotherapy may improve response, its use in the clinical management of pancreatic cancer remains controversial due to conflicting reports on its survival benefit. There has also been a lack of clinical trials that directly investigate the efficacy of radiotherapy in pancreatic cancer. The limited progress in the development of radiotherapeutic strategies in pancreatic cancer can be attributed, at least in part, to a dearth of preclinical research and our limited understanding of the effects of radiation on the pancreatic tumour microenvironment. In this Perspective, we discuss how insight into the immunosuppressive tumour microenvironment and the complex signalling between tumour and stromal cells following radiation is needed to develop effective radiosensitising strategies for pancreatic cancer. We also highlight that to have the best chance for successful clinical translation, more preclinical research is required in appropriately complex models.

摘要

胰腺导管腺癌是一种侵袭性恶性肿瘤,治疗选择有限。化疗获益甚微,虽然有证据表明放疗可能改善反应,但由于其生存获益的报告相互矛盾,其在胰腺癌临床管理中的应用仍存在争议。此外,直接研究放疗在胰腺癌中的疗效的临床试验也很少。胰腺癌中放射治疗策略的发展进展有限,这至少部分归因于临床前研究的不足以及我们对放疗对胰腺肿瘤微环境影响的了解有限。在本观点中,我们讨论了如何深入了解免疫抑制性肿瘤微环境以及放疗后肿瘤与基质细胞之间的复杂信号传导,以开发用于胰腺癌的有效放射增敏策略。我们还强调,为了有最好的机会成功进行临床转化,需要在更复杂的模型中进行更多的临床前研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1164/11261628/aa55aea517ab/dmm-17-050703-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1164/11261628/a350d899b556/dmm-17-050703-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1164/11261628/aa55aea517ab/dmm-17-050703-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1164/11261628/a350d899b556/dmm-17-050703-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1164/11261628/aa55aea517ab/dmm-17-050703-g2.jpg

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Curr Oncol. 2023 Jul 18;30(7):6820-6837. doi: 10.3390/curroncol30070499.
3
In vivo models of pancreatic ductal adenocarcinoma.
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J Immunother Cancer. 2023 May;11(5). doi: 10.1136/jitc-2023-006842.
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