TY - JOUR
T1 - Phase I study of stereotactic body radiation therapy for centrally located stage IA non-small cell lung cancer (JROSG10-1)
AU - Kimura, Tomoki
AU - Nagata, Yasushi
AU - Harada, Hideyuki
AU - Hayashi, Shinya
AU - Matsuo, Yukinori
AU - Takanaka, Tsuyoshi
AU - Kokubo, Masaki
AU - Takayama, Kenji
AU - Onishi, Hiroshi
AU - Hirakawa, Koichi
AU - Shioyama, Yoshiyuki
AU - Ehara, Takeshi
N1 - Publisher Copyright:
© 2017, Japan Society of Clinical Oncology.
PY - 2017/10/1
Y1 - 2017/10/1
N2 - Background: To investigate the maximum tolerated dose (MTD) and recommended dose (RD) of stereotactic body radiation therapy (SBRT) for centrally located stage IA non-small cell lung cancer (NSCLC). Methods: Five dose levels, ranging from of 52 to 68 Gy in eight fractions, were determined; the treatment protocol began at 60 Gy (level 3). Each dose level included 10 patients. Levels 1–2 were indicated if more than four patients exhibited dose-limiting toxicity (DLT), which was defined as an occurrence of a grade 3 (or worse) adverse effect within 12 months after SBRT initiation. MTD was defined as the lowest dose level at which more than four patients exhibited DLT. Results: Ten patients were enrolled in the level 3 study. One patient was considered unsuitable because of severe emphysema. Therefore, nine patients were evaluated and no patient exhibited DLT. The level 3 results indicated that we should proceed to level 4 (64 Gy). However, due to the difficulty involved in meeting the dose constraints, further dose escalation was not feasible and the MTD was found to be 60 Gy. Conclusions: The RD of SBRT for centrally located stage IA NSCLC was 60 Gy in eight fractions.
AB - Background: To investigate the maximum tolerated dose (MTD) and recommended dose (RD) of stereotactic body radiation therapy (SBRT) for centrally located stage IA non-small cell lung cancer (NSCLC). Methods: Five dose levels, ranging from of 52 to 68 Gy in eight fractions, were determined; the treatment protocol began at 60 Gy (level 3). Each dose level included 10 patients. Levels 1–2 were indicated if more than four patients exhibited dose-limiting toxicity (DLT), which was defined as an occurrence of a grade 3 (or worse) adverse effect within 12 months after SBRT initiation. MTD was defined as the lowest dose level at which more than four patients exhibited DLT. Results: Ten patients were enrolled in the level 3 study. One patient was considered unsuitable because of severe emphysema. Therefore, nine patients were evaluated and no patient exhibited DLT. The level 3 results indicated that we should proceed to level 4 (64 Gy). However, due to the difficulty involved in meeting the dose constraints, further dose escalation was not feasible and the MTD was found to be 60 Gy. Conclusions: The RD of SBRT for centrally located stage IA NSCLC was 60 Gy in eight fractions.
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U2 - 10.1007/s10147-017-1125-y
DO - 10.1007/s10147-017-1125-y
M3 - Article
C2 - 28466183
AN - SCOPUS:85018416917
SN - 1341-9625
VL - 22
SP - 849
EP - 856
JO - International Journal of Clinical Oncology
JF - International Journal of Clinical Oncology
IS - 5
ER -