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An Imaging Biomarker of Tumor-Infiltrating Lymphocytes to Risk-Stratify Patients With HPV-Associated Oropharyngeal Cancer.

Authors :
Corredor, Germán
Toro, Paula
Koyuncu, Can
Lu, Cheng
Buzzy, Christina
Bera, Kaustav
Fu, Pingfu
Mehrad, Mitra
Ely, Kim A
Mokhtari, Mojgan
Yang, Kailin
Chute, Deborah
Adelstein, David J
Thompson, Lester D R
Bishop, Justin A
Faraji, Farhoud
Thorstad, Wade
Castro, Patricia
Sandulache, Vlad
Koyfman, Shlomo A
Source :
JNCI: Journal of the National Cancer Institute; Apr2022, Vol. 114 Issue 4, p609-617, 9p
Publication Year :
2022

Abstract

<bold>Background: </bold>Human papillomavirus (HPV)-associated oropharyngeal squamous cell carcinoma (OPSCC) has excellent control rates compared to nonvirally associated OPSCC. Multiple trials are actively testing whether de-escalation of treatment intensity for these patients can maintain oncologic equipoise while reducing treatment-related toxicity. We have developed OP-TIL, a biomarker that characterizes the spatial interplay between tumor-infiltrating lymphocytes (TILs) and surrounding cells in histology images. Herein, we sought to test whether OP-TIL can segregate stage I HPV-associated OPSCC patients into low-risk and high-risk groups and aid in patient selection for de-escalation clinical trials.<bold>Methods: </bold>Association between OP-TIL and patient outcome was explored on whole slide hematoxylin and eosin images from 439 stage I HPV-associated OPSCC patients across 6 institutional cohorts. One institutional cohort (n = 94) was used to identify the most prognostic features and train a Cox regression model to predict risk of recurrence and death. Survival analysis was used to validate the algorithm as a biomarker of recurrence or death in the remaining 5 cohorts (n = 345). All statistical tests were 2-sided.<bold>Results: </bold>OP-TIL separated stage I HPV-associated OPSCC patients with 30 or less pack-year smoking history into low-risk (2-year disease-free survival [DFS] = 94.2%; 5-year DFS = 88.4%) and high-risk (2-year DFS = 82.5%; 5-year DFS = 74.2%) groups (hazard ratio = 2.56, 95% confidence interval = 1.52 to 4.32; P < .001), even after adjusting for age, smoking status, T and N classification, and treatment modality on multivariate analysis for DFS (hazard ratio = 2.27, 95% confidence interval = 1.32 to 3.94; P = .003).<bold>Conclusions: </bold>OP-TIL can identify stage I HPV-associated OPSCC patients likely to be poor candidates for treatment de-escalation. Following validation on previously completed multi-institutional clinical trials, OP-TIL has the potential to be a biomarker, beyond clinical stage and HPV status, that can be used clinically to optimize patient selection for de-escalation. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00278874
Volume :
114
Issue :
4
Database :
Complementary Index
Journal :
JNCI: Journal of the National Cancer Institute
Publication Type :
Academic Journal
Accession number :
156372874
Full Text :
https://doi.org/10.1093/jnci/djab215