scholarly journals Prospective observational study of carbon‐ion radiotherapy for non‐squamous cell carcinoma of the head and neck

2017 ◽  
Vol 108 (10) ◽  
pp. 2039-2044 ◽  
Author(s):  
Katsuyuki Shirai ◽  
Jun‐ichi Saitoh ◽  
Atsushi Musha ◽  
Takanori Abe ◽  
Daijiro Kobayashi ◽  
...  
Toukeibu Gan ◽  
2007 ◽  
Vol 33 (3) ◽  
pp. 260-264 ◽  
Author(s):  
Azusa Hasegawa ◽  
Jun-Etsu Mizoe ◽  
Hirohiko Tsujii ◽  
Ryou Takagi

2020 ◽  
Vol 61 (5) ◽  
pp. 733-739
Author(s):  
Daiki Takahashi ◽  
Yusuke Demizu ◽  
Sung Chul Park ◽  
Yoshiro Matsuo ◽  
Nor Shazrina Sulaiman ◽  
...  

Abstract This study aimed to determine the maximum tolerance dose (MTD) and to estimate the recommended dose (RD) of concomitant S-1 with carbon-ion radiotherapy (RT) for sinonasal squamous cell carcinoma (SCC). Nine patients with sinonasal SCC received carbon-ion RT with escalating doses of S-1 according to phase I methods. Doses of 40, 60 and 80 mg/m2/day were administered twice daily in dose levels 1, 2 and 3, respectively, from days 1 to 14 and 22 to 35. Carbon-ion RT was administered at a dose of 70.4 Gy (relative biological effectiveness) in 32 fractions, 5 days a week. Two patients developed grade 3 acute dermatitis. However, none developed dose-limiting toxicities. Therefore, the MTD of S-1 could not be determined; the RD was estimated to be 80 mg/m2/day with concurrent carbon-ion RT. Partial response and stable disease were noted in 5 and 4 patients, respectively. The 2-year overall survival and local control rates were 56 and 74%, respectively. Overall, 2 patients developed ≥grade 3 late toxicities; among them, 1 patient developed grade 3 cataract and the other developed grade 4 cataract, optic nerve disorder and hearing impairment. To the best of our knowledge, this phase I study is the first clinical trial to evaluate concomitant S-1 with carbon-ion RT for sinonasal SCC. The MTD of S-1 could not be determined, and the RD was estimated to be 80 mg/m2/day. This study demonstrated a manageable safety profile for this combination. The observed outcomes may facilitate further evaluation of this novel therapy.


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