What is the optimal duration, dose and frequency for anti-PD1 therapy of non-small cell lung cancer?

被引:2
|
作者
Kuah, Chii Yang [2 ]
Monfries, Robert [2 ]
Quartagno, Matteo [3 ]
Seckl, Michael J. [1 ]
Ghorani, Ehsan [1 ]
机构
[1] Imperial Coll London, Dept Med Oncol, Charing Cross Hosp Campus, London W6 8RF, England
[2] Imperial Coll London, Dept Med Oncol, Charing Cross Hosp Campus, London, England
[3] UCL, Inst Clin Trials & Methodol, London, England
关键词
non-small cell lung cancer; immunotherapy; overtreatment; checkpoint inhibitor; duration; dose; CD8(+) T-CELLS; PD-1; BLOCKADE; PHASE-I; PEMBROLIZUMAB; CHEMOTHERAPY; SUPERFAMILY; SENSITIVITY; LANDSCAPE; NIVOLUMAB; SAFETY;
D O I
10.1177/17588359231210271
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Over the past decade, immune checkpoint inhibitors (ICIs) have transformed the management of multiple malignancies including lung cancer. However, the optimal use of these agents in terms of duration, dose and administration frequency remains unknown. Focusing on anti-PD1 agents nivolumab and pembrolizumab in the context of non-small cell lung cancer, we argue that several lines of evidence suggest current administration regimens of these drugs may result in overtreatment with potentially important implications for cost, quality of life and toxicity. This review summarizes evidence for the scope to optimize anti-PD1 regimens, the limitations of existing data and potential approaches to solve these problems including with a novel multi-arm clinical trial design implemented in the recently opened REFINE-Lung study.
引用
收藏
页数:13
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