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Computerized tumor multinucleation index (MuNI) is prognostic in [p16.sup.+] oropharyngeal carcinoma

Authors :
Koyuncu, Can F.
Lu, Cheng
Bera, Kaustav
Zhang, Zelin
Xu, Jun
Toro, Paula
Corredor, German
Chute, Deborah
Fu, Pingfu
Thorstad, Wade L.
Faraji, F.
Bishop, Justin A.
Mehrad, Mitra
Castro, Patricia D.
Sikora, Andrew G.
Thompson, Lester D.R.
Chernock, R.D.
Kuhs, Krystle A. Lang
Luo, Jingqin
Sandulache, Vlad
Adelstein, David J.
Koyfman, Shlomo
Lewis, James S., Jr.
Madabhushi, Anant
Source :
Journal of Clinical Investigation. April 15, 2021, Vol. 131 Issue 8
Publication Year :
2021

Abstract

BACKGROUND. Patients with [p16.sup.+] oropharyngeal squamous cell carcinoma (OPSCC) are potentially cured with definitive treatment. However, there are currently no reliable biomarkers of treatment failure for [p16.sup.+] OPSCC. Pathologist-based visual assessment of tumor cell multinucleation (MN) has been shown to be independently prognostic of disease-free survival (DFS) in [p16.sup.+] OPSCC. However, its quantification is time intensive, subjective, and at risk of interobserver variability. METHODS. We present a deep-learning-based metric, the multinucleation index (MuNI), for prognostication in [p16.sup.+] OPSCC. This approach quantifies tumor MN from digitally scanned H&E-stained slides. Representative H&E-stained whole-slide images from 1094 patients with previously untreated [p16.sup.+] OPSCC were acquired from 6 institutions for optimization and validation of the MuNI. RESULTS. The MuNI was prognostic for DFS, overall survival (OS), or distant metastasis-free survival (DMFS) in [p16.sup.+] OPSCC, with HRs of 1.78 (95% CI: 1.37-2.30), 1.94 (1.44-2.60), and 1.88 (1.43-2.47), respectively, independent of age, smoking status, treatment type, or tumor and lymph node (T/N) categories in multivariable analyses. The MuNI was also prognostic for DFS, OS, and DMFS in patients with stage I and stage III OPSCC, separately. CONCLUSION. MuNI holds promise as a low-cost, tissue-nondestructive, H&E stain-based digital biomarker test for counseling, treatment, and surveillance of patients with [p16.sup.+] OPSCC. These data support further confirmation of the MuNI in prospective trials. FUNDING. National Cancer Institute (NCI), NIH; National Institute for Biomedical Imaging and Bioengineering, NIH; National Center for Research Resources, NIH; VA Merit Review Award from the US Department of VA Biomedical Laboratory Research and Development Service; US Department of Defense (DOD) Breast Cancer Research Program Breakthrough Level 1 Award; DOD Prostate Cancer Idea Development Award; DOD Lung Cancer Investigator-Initiated Translational Research Award; DOD Peer-Reviewed Cancer Research Program; Ohio Third Frontier Technology Validation Fund; Wallace H. Coulter Foundation Program in the Department of Biomedical Engineering; Clinical and Translational Science Award (CTSA) program, Case Western Reserve University; NCI Cancer Center Support Grant, NIH; Career Development Award from the US Department of VA Clinical Sciences Research and Development Program; Dan L. Duncan Comprehensive Cancer Center Support Grant, NIH; and Computational Genomic Epidemiology of Cancer Program, Case Comprehensive Cancer Center. The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH, the US Department of VA, the DOD, or the US Government.<br />Introduction The continued increase in the incidence of oropharyngeal squamous cell carcinoma (OPSCC) in the setting of declining rates of tobacco use has been attributed to HPV, with almost 70% [...]

Details

Language :
English
ISSN :
00219738
Volume :
131
Issue :
8
Database :
Gale General OneFile
Journal :
Journal of Clinical Investigation
Publication Type :
Academic Journal
Accession number :
edsgcl.659258529
Full Text :
https://doi.org/10.1172/JCI145488.