Clinical outcomes in elderly patients with human papillomavirus-positive squamous cell carcinoma of the oropharynx treated with definitive chemoradiation therapy

Background The benefit of combined chemoradiation in elderly patients with human papillomavirus (HPV)‐positive locally advanced oropharyngeal squamous cell carcinoma (SCC) must be balanced with the potential for higher toxicity rates. We performed a retrospective review of our institutional experien...

Full description

Saved in:
Bibliographic Details
Published inHead & neck Vol. 38; no. 6; pp. 846 - 851
Main Authors Hanasoge, Sheela, Magliocca, Kelly R., Switchenko, Jeffrey M., Saba, Nabil F., Wadsworth, J. Trad, El-Deiry, Mark W., Shin, Dong M., Khuri, Fadlo, Beitler, Jonathan J., Higgins, Kristin A.
Format Journal Article
LanguageEnglish
Published United States Blackwell Publishing Ltd 01.06.2016
Wiley Subscription Services, Inc
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Background The benefit of combined chemoradiation in elderly patients with human papillomavirus (HPV)‐positive locally advanced oropharyngeal squamous cell carcinoma (SCC) must be balanced with the potential for higher toxicity rates. We performed a retrospective review of our institutional experience. Methods Patients 70 years or older with p16‐positive oropharyngeal SCC treated with definitive chemoradiation from 2005 to 2013 were evaluated. Overall survival (OS), disease‐free survival (DFS), and locoregional failure–free survival were calculated. Results Twenty‐one eligible patients had a follow‐up of 22.4 months. Estimated 5‐year OS, DFS, and locoregional failure–free survival were 76.0%, 40%, and 95%, respectively. There was 1 death from acute toxicity, and 50% had unplanned hospitalizations. Sixty percent had late toxicity, and 6‐month feeding tube dependence was 25%. Conclusion Elderly patients with HPV‐positive locally advanced SCC of the oropharynx treated with definitive chemoradiation had good OS but high rates of acute and long‐term toxicity. © 2015 Wiley Periodicals, Inc. Head Neck 38: 846–851, 2015
Bibliography:istex:1CD47855DCD914012437B5ED20AA26D4F903F051
ark:/67375/WNG-2F7DZW02-2
ArticleID:HED24073
Research reported in this publication was supported in part by the Biostatistics and Bioinformatics Shared Resource of the Winship Cancer Institute of Emory University and National Institutes of Health/National Cancer Institute under award number P30CA138292. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1043-3074
1097-0347
DOI:10.1002/hed.24073