Genomic Landscape of Pleural Mesothelioma and Therapeutic Aftermaths

被引:0
|
作者
Nash, Alistair [1 ,2 ]
Creaney, Jenette [1 ,2 ,3 ,4 ,5 ]
机构
[1] Univ Western Australia, Natl Ctr Asbestos Related Dis, Perth, Australia
[2] Univ Western Australia, Med Sch, Perth, Australia
[3] Inst Resp Hlth, Perth, WA, Australia
[4] Sir Charles Gairdner Hosp, Dept Resp Med, Perth, WA, Australia
[5] Univ Western Australia, QEII Med Ctr, Level 5,Harry Perkins Bldg,QQ Block,6 Verdun St, Nedlands, WA 6009, Australia
基金
英国医学研究理事会;
关键词
Mesothelioma; Genetics; Sequencing; Oncogenesis; GERMLINE BAP1 MUTATIONS; CHROMOSOME CHANGES; GENE; CHEMOTHERAPY; MULTICENTER; DELETION; LUNG; NF2;
D O I
10.1007/s11912-023-01479-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose of ReviewIn this article, we provide a comprehensive analysis of recent progress in the genetic characterisation of pleural mesothelioma, and the translation of these findings to clinical practice.Recent FindingsAdvancements in sequencing technology have allowed the identification of driver mutations and improved our understanding of how these mutations may shape the mesothelioma tumour microenvironment. However, the identification of frequently mutated regions including CDKN2A, BAP1 and NF2 have, to date, not yet yielded targeted therapy options that outperform standard chemo- and immunotherapies. Similarly, the association between mutational profile and the immune microenvironment or immunotherapy response is not well characterised.SummaryFurther research into the link between tumour mutational profile and response to therapy is critical for identifying targetable vulnerabilities and stratifying patients for therapy.
引用
收藏
页码:1515 / 1522
页数:8
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