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African Americans With p161 and p162 Oropharyngeal Squamous Cell Carcinomas Have Distinctly Poor Treatment Outcomes Independent of Medical Care Access.

Authors :
Quinn O’Neill, W.
Wasman, Jay
Thuener, Jason
Chatfield-Reed, Kate
Lukesic, Lizabeth
Kyasram, Ravi
Shanahan, John
Szelesety, Blake
Vu, Brandon
Lavertu, Pierre
Rezaee, Rod
Li, Shawn
Fowler, Nicole
Teknos, Theodoros N.
Pan, Quintin
Source :
JCO Oncology Practice; May2021, Vol. 17 Issue 5, pe695-e701, 7p
Publication Year :
2021

Abstract

PURPOSE Human papilloma virus–positive (HPV+) oropharyngeal squamous cell carcinoma (OPSCC), diagnosed with p16 immunohistochemistry, is associated with favorable prognosis; however, this connection was established using European American (EA)–skewed populations. The impact of p16/human papillomavirus status on outcomes in African American (AA) OPSCC patients remains to be settled. In this study, we determine the association between cancer disparity and p16 status in an OPSCC cohort controlling for time to treatment initiation (TTI), a surrogate for medical care access. MATERIALS AND METHODS We analyzed data from all patients diagnosed with OPSCC (N = 440) between 2010 and 2017, who received treatment at our academic medical center. Associations between age, disease stage, sex, p16 status, race, TTI, and overall survival (OS) were investigated. RESULTS TTI was similar between AA and EA OPSCC patients in our p161 (P= .291) or p162 (P = .715) cohorts. Among p16+ OPSCC patients, the median OS was . 8.65 years for EA patients compared with 5.038 years (95% CI, 2.019 to 5.30; P = .003, log-rank) for AA patients. For p162 patients, the median OS was >.74 years (95% CI, 3.32 to 6.99) for EA patients and 1.85 years (95% CI, 0.978 to 4.50; P= .03, log-rank) for AA patients. Multivariate Cox regression analysis showed that race was an independent prognostic biomarker and the most impactful co-variate for OS (hazard ratio, 0.40; 95% CI, 0.00 to 0.69; P = .001). CONCLUSION Our work showed that AAs with p16+OPSCC have surprisingly poor clinical outcomes and are thus poor candidates for treatment de-escalation regimens. Caution should be exercised when extending clinical guidelines based on EA-majority studies to non-EA populations. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
26881527
Volume :
17
Issue :
5
Database :
Complementary Index
Journal :
JCO Oncology Practice
Publication Type :
Academic Journal
Accession number :
150263584
Full Text :
https://doi.org/10.1200/OP.20.01105