Premium
Nasopharyngeal squamous cell carcinoma: a comparative analysis of keratinizing and nonkeratinizing subtypes
Author(s) -
Vazquez Alejandro,
Khan Mohemmed N.,
Govindaraj Satish,
Baredes Soly,
Eloy Jean Anderson
Publication year - 2014
Publication title -
international forum of allergy and rhinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.503
H-Index - 46
eISSN - 2042-6984
pISSN - 2042-6976
DOI - 10.1002/alr.21332
Subject(s) - medicine , malignancy , hazard ratio , epidemiology , proportional hazards model , nasopharyngeal carcinoma , oncology , incidence (geometry) , stage (stratigraphy) , cohort , cancer , retrospective cohort study , confidence interval , radiation therapy , paleontology , physics , optics , biology
Background Nasopharyngeal squamous cell carcinoma (NPSCC) is uncommon in non‐endemic regions. Two major histologic subtypes are recognized: keratinizing (K‐NPSCC) and nonkeratinizing (NK‐NPSCC). We hypothesize that significant differences exist between the 2 in terms of demographic, clinicopathologic, survival, and prognostic features. We aim to show that differentiating between the 2 subtypes is perhaps the most important first step at the time of diagnosis. Methods Using a retrospective cohort design, the U.S. National Cancer Institute's Surveillance, Epidemiology, and End Results (SEER) registry was used to extract data on the 2 major subtypes of NPSCC. Frequency, incidence, and relative survival (RS) were analyzed comparatively. Regression analysis was conducted and hazard ratios (HRs) calculated. Results A total of 1624 cases were identified: 1234 (76.0%) cases of NK‐NPSCC and 390 (24.0%) cases of K‐NPSCC. Five‐year RS was 60.6% for NK‐NPSCC and 40.5% for K‐NPSCC. Regression analysis revealed K‐NPSCC to be a poor prognostic factor (HR 2.1; 95% confidence interval, 1.8–2.6; p < 0.0001). Other factors associated with a poor prognosis included female gender in K‐NPSCC, age greater than 44 years in both groups, and advanced‐stage disease at diagnosis. Favorable prognostic factors included Asian/Pacific Islander race, and treatment with radiation therapy. Higher histologic grade did not portend a worse prognosis for either group. Conclusion NPSCC remains an uncommon malignancy in the United States. K‐NPSCC and NK‐NPSCC represent 2 different histologic entities with important clinical differences. K‐NPSCC carries a worse overall prognosis when compared to NK‐NPSCC.