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免疫治疗时代的骨肉瘤。

Bone sarcomas in the immunotherapy era.

机构信息

Université de Nantes, INSERM, CRCINA, Institut de Cancérologie de l'Ouest, Saint-Herblain, France.

"Tumor Heterogeneity and Precision Medicine", Institut de Cancérologie de l'Ouest, Saint Herblain, France.

出版信息

Br J Pharmacol. 2021 May;178(9):1955-1972. doi: 10.1111/bph.14999. Epub 2020 Feb 18.

Abstract

Bone sarcomas are primary bone tumours found mainly in children and adolescents, as osteosarcoma and Ewing's sarcoma, and in adults in their 40s as chondrosarcoma. The last four decades the development of therapeutic approaches was based on drug combinations have shown no real improvement in overall survival. Recently oncoimmunology has allowed a better understand of the crucial role played by the immune system in the oncologic process. This led to clinical trials with the aim of reprogramming the immune system to facilitate cancer cell recognition. Immune infiltrates of bone sarcomas have been characterized and their molecular profiling identified as immune therapeutic targets. Unfortunately, the clinical responses in trials remain anecdotal but highlight the necessity to improve the characterization of tumour micro-environment to unlock the immunotherapeutic response, especially in their paediatric forms. Bone sarcomas have entered the immunotherapy era and here we overview the recent developments in immunotherapies in these sarcomas. LINKED ARTICLES: This article is part of a themed issue on The molecular pharmacology of bone and cancer-related bone diseases. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v178.9/issuetoc.

摘要

骨肿瘤是主要发生在儿童和青少年的原发性骨肿瘤,如骨肉瘤和尤文肉瘤,以及 40 多岁的成年人的软骨肉瘤。在过去的四十年里,治疗方法的发展基于药物联合治疗,但在总体生存方面并没有真正的改善。最近,肿瘤免疫学使人们更好地了解了免疫系统在肿瘤发生过程中所起的关键作用。这导致了临床试验的开展,旨在重新编程免疫系统,促进癌细胞的识别。已经对骨肿瘤的免疫浸润进行了特征描述,并对其分子谱进行了鉴定,作为免疫治疗靶点。不幸的是,临床试验中的临床反应仍然是个例,但强调了必须改善肿瘤微环境的特征,以释放免疫治疗反应,特别是在其儿科形式中。骨肿瘤已经进入免疫治疗时代,在这里我们综述了这些肉瘤中免疫治疗的最新进展。相关文章:本文是关于骨和与癌症相关的骨疾病的分子药理学的专题的一部分。要查看本节中的其他文章,请访问 http://onlinelibrary.wiley.com/doi/10.1111/bph.v178.9/issuetoc/。

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