STK11段
mTORC1型
克拉斯
肺癌
背景(考古学)
医学
埃罗替尼
内科学
PTEN公司
肿瘤科
生物
癌症
PI3K/AKT/mTOR通路
表皮生长因子受体
遗传学
古生物学
细胞凋亡
结直肠癌
作者
Gary Middleton,H.L. Robbins,Peter Fletcher,Joshua Savage,Manita Mehmi,Yvonne Summers,Alastair Greystoke,Nicola Steele,Sanjay Popat,Pooja Jain,James Spicer,Judith Cave,P. Nicholas Shaw,David Gilligan,Danielle Power,Dean A. Fennell,Maya Bajracharya,David J. McBride,Uma Maheswari,Alexander M. Frankell
标识
DOI:10.1038/s41698-025-00838-4
摘要
Abstract There are no current stratified medicine options for STK11-deficient NSCLC. STK11 loss mediates mTORC activation, GLUT1 up-regulation and increased glycolysis. This metabolic reprogramming might represent a therapeutic vulnerability targetable with mTORC1/2 inhibition. In arm B2 of the National Lung Matrix Trial 54 patients with NSCLC received vistusertib, of which 49 were STK11-deficient (30 with KRAS mutation (B2D), 19 without (B2S)). Objective response (OR) and durable clinical benefit (DCB) rates with 95% credible intervals (CrI) were estimated from posterior probability distributions generated using Bayesian beta-binomial conjugate analysis. In B2D, 2 per-protocol patients obtained OR (estimated true OR rate (95%CrI) 9.8% (2.4–24.3). Estimates of true DCB rate (95%CrI): B2D 24.4% (11.1–42.3), B2S 14.6% (3.6–34.7). Overall, vistusertib cannot be recommended in this context. Longitudinal ctDNA analysis demonstrates enrichment of SMARCA4 mutations post-treatment. In vitro studies show adaptive resistance to mTORC1/2 inhibition via AKT reactivation. (NCT02664935, ISRCTN38344105, EudraCT 2014-000814-73, 10 June 2015)
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