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Feasibility study of alternate-day S-1 as adjuvant chemotherapy for head and neck cancer.

AbstractAIM:
This study analyzed the safety and feasibility of alternate-day S-1, a mixture of tegafur, dehydroxypyrimidine and potassium oxonate, as adjuvant chemotherapy for head and neck cancers.
PATIENTS AND METHODS:
Patients with head and neck squamous cell carcinoma (HNSCC) who underwent primary treatment received alternate-day S-1 (80 mg/day for 1 year). The primary end-point was treatment completion rate. The secondary end-point was adverse events. Three-year overall survival (OS) and disease-free survival (DFS) were calculated using the Kaplan-Meier method.
RESULTS:
One-year completion rate was 65.6%. Out of 26 patients, 19.0% had grade III adverse events. All adverse reactions were tolerable and reversible. Three-year OS and DFS were 74.8% and 57.3%, respectively.
CONCLUSION:
S-1 therapy is an effective adjuvant treatment for head and neck cancer patients with relatively mild side-effects and does not adversely affect quality of life. A phase I/II study is warranted to investigate the appropriate dose for an alternate-day S-1 regimen.
AuthorsYorihisa Moro, Yasunao Kogashiwa, Dai Sato, Yoshifumi Matsumoto, Takehiro Nakamura, Koichi Yamauchi, Hiroyuki Sakurai, Naoyuki Kohno
JournalAnticancer research (Anticancer Res) Vol. 35 Issue 2 Pg. 977-81 (Feb 2015) ISSN: 1791-7530 [Electronic] Greece
PMID25667484 (Publication Type: Journal Article)
CopyrightCopyright© 2015 International Institute of Anticancer Research (Dr. John G. Delinassios), All rights reserved.
Chemical References
  • Drug Combinations
  • S 1 (combination)
  • Tegafur
  • Oxonic Acid
Topics
  • Adult
  • Aged
  • Aged, 80 and over
  • Chemotherapy, Adjuvant
  • Drug Combinations
  • Feasibility Studies
  • Female
  • Head and Neck Neoplasms (drug therapy)
  • Humans
  • Male
  • Middle Aged
  • Oxonic Acid (therapeutic use)
  • Tegafur (therapeutic use)

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