Table III.
Adverse events | Gr2 | Gr3 | Gr4 | % |
---|---|---|---|---|
S-1 group | ||||
Leukopenia | 2 | 0 | 0 | 10.5 |
Neutropenia | 1a | 0 | 0 | 5.2 |
Fatigue | 3 | 0 | 0 | 15.7 |
Vomiting | 2 | 0 | 0 | 10.5 |
Diarrhea | 0 | 1a | 0 | 5.2 |
Stomatitis | 13 | 1 | 0 | 73.7 |
Elevation of bilirubin level | 1 | 0 | 0 | 5.2 |
AI group | ||||
Hypochromia | 2 | 0 | 0 | 14.2 |
Leukopenia | 2 | 0 | 0 | 14.2 |
Neutropenia | 1 | 1 | 0 | 14.2 |
Thrombocytopenia | 1 | 0 | 0 | 7.1 |
Fatigue | 3 | 0 | 0 | 21.4 |
Nausea | 2 | 0 | 0 | 14.2 |
Vomiting | 0 | 1 | 0 | 7.1 |
Stomatitis | 12 | 0 | 0 | 57.1 |
Soft tissue impairment | 1b | 1c | 0 | 9.5 |
Withdrawal of S-1;
pharyngeal edema;
pharyngeal necrosis.
S-1, concurrent neoadjuvant chemoradiotherapy with S-1 and a total external irradiation dose of 30 Gy; AI, concurrent neoadjuvant chemoradiotherapy using super-selective intra-arterial infusion with cisplatin or carboplatin and a total external irradiation dose of 40 Gy; NCI-CTC, National Cancer Institute’s Common Toxicity Criteria.