Immune checkpoint inhibition for the treatment of mesothelioma

被引:19
|
作者
Nowak, Anna K. [1 ,2 ,3 ]
McDonnell, Alison [1 ,2 ,3 ]
Cook, Alistair [1 ,2 ,3 ]
机构
[1] Univ Western Australia, Natl Ctr Asbestos Related Dis, M503,35 Stirling Highway, Crawley 6009, Australia
[2] Univ Western Australia, Inst Resp Hlth, Nedlands, WA, Australia
[3] Univ Western Australia, Sch Med, Crawley, Australia
基金
英国医学研究理事会;
关键词
Antineoplastic therapy; biomarkers; checkpoint blockade; immunotherapy; mesothelioma; MALIGNANT PLEURAL MESOTHELIOMA; OPEN-LABEL; SINGLE-ARM; CHEMOTHERAPY; DIAGNOSIS; CANCER; CELLS; DNA; TREMELIMUMAB; COMBINATION;
D O I
10.1080/14712598.2019.1606209
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Introduction: Combination chemotherapy is currently standard care for advanced mesothelioma. Checkpoint blockade is a promising new treatment. Areas covered: This review covers clinical use and biomarkers of checkpoint blockade. Medline search used keywords 'mesothelioma' combined with 'checkpoint blockade' OR 'PD-L1MODIFIER LETTER PRIME OR 'PD1MODIFIER LETTER PRIME OR 'anti-CTLA4MODIFIER LETTER PRIME; the search terms AND 'clinical trial' or AND 'biomarker*' were added. Handsearching covered abstracts from relevant meetings from 2016 to 2018 and reference lists. Data informed a narrative review. Expert Opinion: Single agent anti-CTLA4 blockade is inactive in mesothelioma. Single agent PD-1 blockade as second or subsequent treatment gives 20-29% partial responses; no randomized comparisons against placebo or chemotherapy are available. Biomarkers of response have been difficult to identify. There is no consensus as to whether tumor PD-L1 expression predicts outcomes. Combination checkpoint inhibitors (CTLA4 and PD1 blockade) provide a small incremental increase in response rates and progression-free survival. Chemoimmunotherapy is the next frontier.
引用
收藏
页码:697 / 706
页数:10
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