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Updated: Mar 28, 2026

Therapy Testing in a Spheroid-based 3D Cell Culture Model for Head and Neck Squamous Cell Carcinoma
Published on: April 20, 2018
Recurrent/metastatic relapse after definitive treatment for HNSCC: timing, patterns, and survival
Kewen Qu1, Margaret Stalker2, Wei-Ting Hwang1
1Department of Biostatistics, Epidemiology, and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States.
Background:
Timing and outcomes of recurrence after definitive therapy for HNSCC are incompletely understood.
Methods:
This study included patients in a nationwide EHR-derived de-identified database who received systemic therapy for R/M HNSCC. Time from definitive treatment to R/M systemic therapy initiation (TTRM), and overall survival (OS) from R/M systemic therapy initiation, were estimated and compared between patients stratified by cancer site and prior definitive treatment modality.
Results:
Of 7657 patients receiving R/M therapy, the median age was 65 (IQR 58-72), 77% male, 74% white, 79% with smoking history, and 79% ECOG PS 0-1. 1684 (22%) patients had no recorded prior definitive therapy (de novo metastatic); of the remaining 5973 patients, most common definitive treatment types were radiation alone (RT only; 43%), followed by surgery plus radiation (Surg + RT; 21%), surgery alone (Surg only; 16%), chemoradiation (CRT; 14%), and surgery plus chemoradiation (Surg + CRT; 6%). Patients treated with high-risk treatment types (Surg + CRT, CRT) had higher disease stage at presentation, shorter TTRM (median 6-7 vs 17-19 months), and shorter OS from R/M treatment to death (median 8 vs 12 months) compared to patients in low-risk treatment groups (RT only, Surg + RT, Surg only). Patients with HPV+ oropharynx cancer had numerically longer TTRM (median 17 vs 13 months, p = 0.4309) and significantly longer OS (median 18 vs 10 months, p < 0.001) than HPV- cancers.
Conclusions:
Patients with locoregionally advanced HNSCC treated with CRT and surgery plus CRT represent a high-risk cohort with rapid R/M disease and poor survival, who need improved therapeutic options.
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Published on: May 11, 2016
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