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Intratumoral Escherichia Is Associated With Improved Survival to Single-Agent Immune Checkpoint Inhibition in Patients With Advanced Non–Small-Cell Lung Cancer

医学 化学免疫疗法 癌症 癌症研究 危险系数 肺癌 大肠杆菌 队列 H&E染色 肿瘤科 免疫疗法 内科学 免疫组织化学 置信区间 生物 基因 生物化学
作者
Arielle Elkrief,Meagan Montesion,Smruthy Sivakumar,Caryn Hale,Anita S. Bowman,Ayyüce Begüm Bektaş,Martina Bradić,Wenfei Kang,Eric Chan,Pooja Gogia,Katia Manova–Todorova,Douglas A. Mata,Jacklynn V. Egger,Hira Rizvi,Nicholas D. Socci,Daniel W. Kelly,Eric Rosiek,Fanli Meng,Grittney Tam,Ning Fan,Alexander Drilon,Helena A. Yu,Gregory J. Riely,Natasha Rekhtman,Àlvaro Quintanal-Villalonga,Snjezana Doğan,Umesh Bhanot,Mithat Gönen,Brian Houck‐Loomis,Matthew D. Hellmann,Adam J. Schoenfeld,Marc Ladanyi,Charles M. Rudin,Chad Vanderbilt
出处
期刊:Journal of Clinical Oncology [American Society of Clinical Oncology]
标识
DOI:10.1200/jco.23.01488
摘要

PURPOSE The impact of the intratumoral microbiome on immune checkpoint inhibitor (ICI) efficacy in patients with non–small-cell lung cancer (NSCLC) is unknown. Preclinically, intratumoral Escherichia is associated with a proinflammatory tumor microenvironment and decreased metastases. We sought to determine whether intratumoral Escherichia is associated with outcome to ICI in patients with NSCLC. PATIENTS AND METHODS We examined the intratumoral microbiome in 958 patients with advanced NSCLC treated with ICI by querying unmapped next-generation sequencing reads against a bacterial genome database. Putative environmental contaminants were filtered using no-template controls (n = 2,378). The impact of intratumoral Escherichia detection on overall survival (OS) was assessed using univariable and multivariable analyses. The findings were further validated in an external independent cohort of 772 patients. Escherichia fluorescence in situ hybridization (FISH) and transcriptomic profiling were performed. RESULTS In the discovery cohort, read mapping to intratumoral Escherichia was associated with significantly longer OS (16 v 11 months; hazard ratio, 0.73 [95% CI, 0.59 to 0.92]; P = .0065) in patients treated with single-agent ICI, but not combination chemoimmunotherapy. The association with OS in the single-agent ICI cohort remained statistically significant in multivariable analysis adjusting for prognostic features including PD-L1 expression ( P = .023). Analysis of an external validation cohort confirmed the association with improved OS in univariable and multivariable analyses of patients treated with single-agent ICI, and not in patients treated with chemoimmunotherapy. Escherichia localization within tumor cells was supported by coregistration of FISH staining and serial hematoxylin and eosin sections. Transcriptomic analysis correlated Escherichia-positive samples with expression signatures of immune cell infiltration. CONCLUSION Read mapping to potential intratumoral Escherichia was associated with survival to single-agent ICI in two independent cohorts of patients with NSCLC.
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