We evaluated the efficacy of adjuvant concurrent chemoradiotherapy with a 3-weekly cycle of cisplatin (3W-CDDP/RT) for patients with post-operative high-risk squamous cell carcinoma of the head and neck. High-risk factors were a microscopically incomplete resection, extracapsular extension and two or more lymph node metastases. Patients received three cycles of cisplatin at a dose of 80mg/m
2 or 100mg/m
2 concurrent with radiation therapy.
Between April 2007 and November 2013, 52 patients were enrolled: 45 males and 7 females, with a median age of 62 years (range 22-75), Stage III/IVA/IVB/recurrent (4/35/2/11), and oral cavity/oropharynx/hypopharynx/larynx (23/4/20/5). The protocol completion rate was 84.6%. After a median follow-up of 28 months, estimated 3-year locoregional control rate and overall survival were 75.5% and 56.2%, respectively. On multivariate analysis, oral cavity cancer and a cumulative cisplatin dose below 200mg/m
2 seemed to be poor prognostic factors.
Among high-risk patients with post-operative locally advanced head and neck cancer, adjuvant concurrent chemoradiotherapy improved the rate of locoregional control.
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