Y. Hattori
Nagoya City University
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Featured researches published by Y. Hattori.
Journal of Thoracic Oncology | 2015
Yuta Shibamoto; Chisa Hashizume; F. Baba; Shiho Ayakawa; A. Miyakawa; T. Murai; T. Takaoka; Y. Hattori; Ryuji Asai
Introduction: Although the protocol of 48 Gy in four fractions over 4 days has been most often employed in stereotactic body radiotherapy (SBRT) for stage I non–small-cell lung cancer in Japan, higher doses are necessary to control larger tumors, and interfraction intervals should be longer than 24 hours to take advantage of reoxygenation. We report the final results of our study testing the following regimen: for tumors less than 1.5, 1.5–3, and greater than 3 cm in diameter, 44, 48, and 52 Gy, respectively, were given in four fractions with interfraction intervals of greater than or equal to 3 days. Methods: Among 180 histologically proven patients entered, 120 were medically inoperable and 60 were operable. The median patient age was 77 years (range, 29–89). SBRT was performed with 6-MV photons using four noncoplanar and three coplanar beams. Isocenter doses of 44, 48, and 52 Gy were given to four, 124, and 52 patients, respectively. Results: The 5-year overall survival rate was 52.2% for all 180 patients and 66% for 60 operable patients. The 5-year local control rate was 86% for tumors less than or equal to 3 cm (44/48 Gy) and 73% for tumors greater than 3 cm (52 Gy; p = 0.076). Grade greater than or equal to 2 radiation pneumonitis developed in 13% (10% for the 44/48-Gy group and 21% for the 52-Gy group; p = 0.056). Other grade 2 toxicities were all less than 4%. Conclusions: Our first prospective SBRT study yielded reasonable local control and overall survival rates and acceptable toxicity. Refinement of the protocol including dose escalation may lead to better outcome.
Practical radiation oncology | 2018
S. Hashimoto; Masaki Katsurada; Rie Muramatsu; Kumiko Asai; Kenichiro Tanaka; K. Hayashi; Yoshiaki Kibe; K. Nakajima; Y. Hattori; H. Iwata; Jun-etsu Mizoe; Hiroyuki Ogino; Yuta Shibamoto
PURPOSE Suppression of respiratory movement of the liver would be desirable for high-precision radiation therapy for liver tumors. We aimed to investigate the effect of our original device-free compressed shell fixation method and breathing instruction on suppression of respiratory movement. The characteristics of liver motion based on the movement of a fiducial marker were also analyzed. METHODS AND MATERIALS First, respiratory amplitudes of the liver with the device-free compressed shell were analyzed from the data of 146 patients. The effect of this shell fixing method on liver movement was evaluated. Second, as another cohort study with 166 patients, interfractional internal motion of the liver for patients fixed in the shell was calculated using the fiducial marker coordinate data of images for position setting before daily irradiation. Third, in another 12 patients, intrafractional internal motion was calculated from the fiducial marker coordinate data using x-ray images before and after irradiation. RESULTS The median respiratory movement without the shell, after fixing with the shell, and after instructing on the breathing method with the shell was 14.2 (interquartile range, 10.7-19.8), 11.5 (8.6-17.5), and 10.4 mm (7.3-15.8), respectively. Systematic and random errors of interfractional internal motion were all ≤2 mm in the left-right and anteroposterior directions and 3.7 and 3.0 mm, respectively, in the craniocaudal direction. Systematic and random errors of intrafractional internal motion were all ≤1.3 mm in the left-right and anteroposterior directions and 0.8 and 2.4 mm, respectively, in the craniocaudal direction. CONCLUSIONS The device-free compressed shell fixation method was effective in suppressing the respiratory movement of the liver. Irradiation position matching using the fiducial marker can correct the interfractional internal motion on each day, which would contribute to the reduction of the margin to be given around the target.
Journal of Radiation Research | 2017
T. Murai; Y. Hattori; Chikao Sugie; H. Iwata; M. Iwabuchi; Yuta Shibamoto
Abstract Multileaf collimator (MLC) technology has been newly introduced with the Cyberknife system. This study investigated the advantages of this system compared with the conventional circular collimator (CC) system. Dosimetric comparisons of MLC and CC plans were carried out. First, to investigate suitable target sizes for the MLC mode, MLC and CC plans were generated using computed tomography (CT) images from 5 patients for 1, 3, 5 and 7 cm diameter targets. Second, MLC and CC plans were compared in 10 patients, each with liver and prostate targets. For brain targets, doses to the brain could be spared in MLC plans better than in CC plans (P ≤ 0.02). The MLC mode also achieved more uniform dose delivery to the targets. The conformity index in MLC plans was stable, irrespective of the target size (P = 0.5). For patients with liver tumors, the MLC mode achieved higher target coverage than the CC mode (P = 0.04). For prostate tumors, doses to the rectum and the conformity index were lowered in MLC plans compared with in CC plans (P ≤ 0.04). In all target plans, treatment times in MLC plans were shorter than those in CC plans (P < 0.001). The newly introduced MLC technology can reduce treatment time and provide favorable or comparable dose distribution for 1–7 cm targets. In particular, the MLC mode has dosimetric advantage for targets near organs at risk. Therefore, the MLC mode is recommended as the first option in stereotactic body radiotherapy.
Journal of Radiation Research | 2015
A. Hayashi; Yuta Shibamoto; Y. Hattori; Takeshi Tamura; M. Iwabuchi; S. Otsuka; Chikao Sugie; T. Yanagi
Abstract We treated prostate cancer patients with static 5-field intensity-modulated radiation therapy (IMRT) using linac 18-MV X-rays or tomotherapy with 6-MV X-rays. As X-ray energies differ, we hypothesized that 18-MV photon IMRT may be better for large patients and tomotherapy may be more suitable for small patients. Thus, we compared dose–volume parameters for the planning target volume (PTV) and organs at risk (OARs) in 59 patients with T1–3 N0M0 prostate cancer who had been treated using 5-field IMRT. For these same patients, tomotherapy plans were also prepared for comparison. In addition, plans of 18 patients who were actually treated with tomotherapy were analyzed. The evaluated parameters were homogeneity indicies and a conformity index for the PTVs, and D2 (dose received by 2% of the PTV in Gy), D98, Dmean and V10–70 Gy (%) for OARs. To evaluate differences by body size, patients with a known body mass index were grouped by that index ( <21; 21–25; and >25 kg/m2). For the PTV, all parameters were higher in the tomotherapy plans compared with the 5-field IMRT plans. For the rectum, V10 Gy and V60 Gy were higher, whereas V20 Gy and V30 Gy were lower in the tomotherapy plans. For the bladder, all parameters were higher in the tomotherapy plans. However, both plans were considered clinically acceptable. Similar trends were observed in 18 patients treated with tomotherapy. Obvious trends were not observed for body size. Tomotherapy provides equivalent dose distributions for PTVs and OARs compared with 18-MV 5-field IMRT. Tomotherapy could be used as a substitute for high-energy photon IMRT for prostate cancer regardless of body size.
Japanese Journal of Radiology | 2016
Y. Hattori; T. Murai; H. Iwata; Kaoru Uchiyama; Mikio Mimura; Eriko Kato; Rumi Murata; Yuta Shibamoto
International Journal of Radiation Oncology Biology Physics | 2014
Hiroyuki Ogino; H. Iwata; S. Hashimoto; Y. Hattori; F. Baba; M. Iwana; T. Murai; Yuta Shibamoto; Jun-etsu Mizoe
Radiation Oncology | 2018
K. Nakajima; H. Iwata; Hiroyuki Ogino; Y. Hattori; S. Hashimoto; Toshiyuki Toshito; K. Hayashi; Kenji Akita; F. Baba; Katsumi Nakamae; Jun-etsu Mizoe; Yuta Shibamoto
International Journal of Radiation Oncology Biology Physics | 2018
H. Iwata; Hiroyuki Ogino; Y. Hattori; S. Hashimoto; K. Nakajima; K. Hayashi; Toshiyuki Toshito; S. Sasaki; F. Baba; Y. Kuwabara; K. Senoo; Jun-etsu Mizoe; Yuta Shibamoto
International Journal of Radiation Oncology Biology Physics | 2018
S. Hashimoto; M. Katsurada; R. Muramatsu; K. Asai; A. Shimomura; K. Ueki; H. Kino; A. Yoshida; K. Tanaka; K. Hayashi; M. Kimura; Y. Kibe; Chihiro Omachi; Toshiyuki Toshito; K. Nakajima; Y. Hattori; H. Iwata; Jun-etsu Mizoe; Hiroyuki Ogino; Yuta Shibamoto
International Journal of Clinical Oncology | 2018
K. Nakajima; H. Iwata; Hiroyuki Ogino; Y. Hattori; S. Hashimoto; Mikiko Nakanishi; Toshiyuki Toshito; Yukihiro Umemoto; Shoichiro Iwatsuki; Yuta Shibamoto; Jun-etsu Mizoe