TY - JOUR
T1 - Increasing prevalence of human papillomavirus–positive oropharyngeal cancers among older adults
AU - Windon, Melina J.
AU - D'Souza, Gypsyamber
AU - Rettig, Eleni M.
AU - Westra, William H.
AU - van Zante, Annemieke
AU - Wang, Steven J.
AU - Ryan, William R.
AU - Mydlarz, Wojciech K.
AU - Ha, Patrick K.
AU - Miles, Brett A.
AU - Koch, Wayne
AU - Gourin, Christine
AU - Eisele, David W.
AU - Fakhry, Carole
N1 - Publisher Copyright:
© 2018 American Cancer Society
PY - 2018/7/15
Y1 - 2018/7/15
N2 - BACKGROUND: The incidence of oropharyngeal squamous cell carcinoma (OPSCC) is increasing among older adults. It is unknown whether these trends can be explained by human papillomavirus (HPV) and whether HPV-related tumors remain associated with an improved prognosis among older patients. METHODS: In a retrospective study of OPSCCs diagnosed from 1995 to 2013 at 2 National Comprehensive Cancer Network–designated cancer centers, p16 immunohistochemistry and in situ hybridization (ISH) for HPV-16, high-risk DNA, and/or E6/E7 RNA were performed. The median age at diagnosis was compared by p16 and ISH tumor status. Trends in age were analyzed with nonparametric trends. Survival was analyzed with the Kaplan-Meier method and Cox proportional hazards models. RESULTS: Among 239 patients, 144 (60%) were p16-positive. During 1998-2013, the median age increased among p16-positive patients (Ptrend =.01) but not among p16-negative patients (Ptrend =.71). The median age of p16-positive patients increased from 53 years (interquartile range [IQR] in 1995-2000, 45-65 years) to 58 years (IQR for 2001-2013, 53-64 years). Among patients ≥ 65 years old, the proportion of OPSCCs that were p16-positive increased from 41% during 1995-2000 to 75% during 2007-2013 (Ptrend =.04). Among all age groups, including older patients, a p16-positive tumor status conferred improved overall survival in comparison with a p16-negative status. CONCLUSIONS: The median age at diagnosis for HPV-related OPSCC is increasing as the proportion of OPSCCs caused by HPV rises among older adults. The favorable survival conferred by an HPV-positive tumor status persists in older adults. Cancer 2018;124:2993-9.
AB - BACKGROUND: The incidence of oropharyngeal squamous cell carcinoma (OPSCC) is increasing among older adults. It is unknown whether these trends can be explained by human papillomavirus (HPV) and whether HPV-related tumors remain associated with an improved prognosis among older patients. METHODS: In a retrospective study of OPSCCs diagnosed from 1995 to 2013 at 2 National Comprehensive Cancer Network–designated cancer centers, p16 immunohistochemistry and in situ hybridization (ISH) for HPV-16, high-risk DNA, and/or E6/E7 RNA were performed. The median age at diagnosis was compared by p16 and ISH tumor status. Trends in age were analyzed with nonparametric trends. Survival was analyzed with the Kaplan-Meier method and Cox proportional hazards models. RESULTS: Among 239 patients, 144 (60%) were p16-positive. During 1998-2013, the median age increased among p16-positive patients (Ptrend =.01) but not among p16-negative patients (Ptrend =.71). The median age of p16-positive patients increased from 53 years (interquartile range [IQR] in 1995-2000, 45-65 years) to 58 years (IQR for 2001-2013, 53-64 years). Among patients ≥ 65 years old, the proportion of OPSCCs that were p16-positive increased from 41% during 1995-2000 to 75% during 2007-2013 (Ptrend =.04). Among all age groups, including older patients, a p16-positive tumor status conferred improved overall survival in comparison with a p16-negative status. CONCLUSIONS: The median age at diagnosis for HPV-related OPSCC is increasing as the proportion of OPSCCs caused by HPV rises among older adults. The favorable survival conferred by an HPV-positive tumor status persists in older adults. Cancer 2018;124:2993-9.
KW - elderly
KW - head and neck squamous cell carcinoma (HNSCC)
KW - human papillomavirus (HPV)
KW - in situ hybridization (ISH)
KW - oropharyngeal squamous cell carcinoma (OPSCC)
KW - p16
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U2 - 10.1002/cncr.31385
DO - 10.1002/cncr.31385
M3 - Article
C2 - 29710393
AN - SCOPUS:85046096447
SN - 0008-543X
VL - 124
SP - 2993
EP - 2999
JO - Cancer
JF - Cancer
IS - 14
ER -