Kenji Hayashihara
Hitachi
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Featured researches published by Kenji Hayashihara.
Lung Cancer | 2012
Takeshi Nawa; Tohru Nakagawa; Tetsuya Mizoue; Suzushi Kusano; Tatsuya Chonan; Kenji Hayashihara; Tetsushi Suito; Katsuyuki Endo
Recent US clinical trial demonstrated that CT screening prevents lung cancer death among high risk individuals. However, it remains unclear whether wide implementation of low-dose CT screening for lung cancer can decrease mortality in the community. Among residents in Hitachi City (Japan), where nearly 40% of inhabitants aged 50-69 years were estimated to have participated in the screening at least once from 1998 through 2009, the trend of lung cancer mortality was described in relation to the timing of implementation of the CT screening. Cancer mortality data were obtained from regional cancer registry and standardized mortality ratio (SMR) of lung cancer was calculated for each 5-year period during 1995-2009. In both men and women aged 60 years or older, age-specific lung cancer mortality rates were generally lower during 2005-2009 as compared with those during 1995-2004. For combined men and women aged 50-79 years, SMR was nearly unity prior to or during introductory phase of CT screening and during early period of implementation; however, it was significantly decreased during 2005-2009, well after the implementation of CT screening, with SMR (95% confidence interval) being 0.76 (0.67-0.86). Results suggest that wide implementation of low-dose chest CT screening may decrease lung cancer mortality in the community 4-8 years after introduction of the screening.
Oncology Letters | 2013
Takayuki Kaburagi; Hiroaki Satoh; Kenji Hayashihara; Takeshi Endo; Nobuyuki Hizawa; Koichi Kurishima; Yoshihiro Nishimura; Toshio Hashimoto; Hiroyuki Nakamura; Koji Kishi; Masaharu Inagaki; Takeshi Nawa; Hideo Ichimura; Hiroichi Ishikawa; Katsunori Kagohashi; Toshihiko Fukuoka; Yoko Shinohara; Koichi Kamiyama; Yukio Sato; Mitsuaki Sakai; Takeshi Matsumura; Keiko Uchiumi; Kinya Furukawa
To evaluate the efficacy and safety of erlotinib for non-small cell lung cancer (NSCLC), we performed a population-based observational study. The study involved 307 patients treated with erlotinib at 14 sites (17 departments) in Ibaraki (Japan) between December 2007 and December 2010. The tumor response and disease control rates were 11.1 and 46.3% in all patients, respectively. The median time to treatment failure and survival time were 1.6 months (95% confidence interval, 41–57 days) and 5.3 months (134–181 days) in all patients, respectively. Survival was significantly prolonged in EGFR mutation-positive patients compared with negative patients. EGFR mutation-negative patients who presented with a skin rash had significantly prolonged survival compared with those without a skin rash. The most common adverse event was skin disorder, followed by diarrhea. Although 45.6% of the patients in this study received erlotinib as a fourth-line or subsequent treatment, the results from this study were similar to those of clinical studies. We deduce that erlotinib is effective against NSCLC and is tolerated in clinical practice.
Molecular and Clinical Oncology | 2013
Koichi Kurishima; Hiroaki Satoh; Takayuki Kaburagi; Yoshihiro Nishimura; Yoko Shinohara; Masaharu Inagaki; Takeo Endo; Takefumi Saito; Kenji Hayashihara; Nobuyuki Hizawa; Hiroyuki Nakamura; Takeshi Nawa; Katsunori Kagohashi; Koji Kishi; Hiroichi Ishikawa; Hideo Ichimura; Toshio Hashimoto; Yukio Sato; Mitsuaki Sakai; Koichi Kamiyama; Takeshi Matsumura; Koji Unoura; Toshihiko Fukuoka; Keiko Uchiumi; Akihiro Nomura; Kinya Furukawa
The incidence and mortality of lung cancer have increased worldwide over the last decades, with an observed increased incidence particularly among elderly populations. It has not yet been determined whether erlotinib therapy exhibits the same efficacy and safety in elderly and younger patients with non-small-cell lung cancer (NSCLC). The aim of this retrospective subgroup analysis of data from a population-based observational study was to assess the efficacy and safety of erlotinib in an elderly (≥75 years, n=74) and a younger group of patients (<75 years, n=233) who received treatment for NSCLC. The time to treatment failure was similar in the elderly [median, 62 days; 95% confidence interval (95% CI): 44–80 days] compared with the younger group (median, 46 days; 95% CI: 35–53 days) (P=0.2475). The overall survival did not differ between the elderly and younger groups (median, 170 days; 95% CI: 142–239 days vs. median, 146 days; 95% CI: 114–185 days, respectively) (P=0.7642). The adverse events did not differ in incidence between the groups and were manageable, regardless of age. Among the NSCLC patients receiving erlotinib treatment, the outcomes of the elderly (≥75 years) and younger (<75 years) groups of patients were similar in our population-based observational study.
Clinical Respiratory Journal | 2017
Akimasa Sekine; Takefumi Saito; Hiroaki Satoh; Yukio Morishita; Yoshiya Tsunoda; Toru Tanaka; Yohei Yatagai; Shih-Yuen Lin; Kunihiko Miyazaki; Yukiko Miura; Kenji Hayashihara
It remains unclear whether transbronchial lung biopsy (TBLB) is useful for diagnosing Mycobacterium avium complex (MAC) lung disease.
Clinical Lung Cancer | 2018
Shinko Sadoyama; Akimasa Sekine; Hiroaki Satoh; Tae Iwasawa; Terufumi Kato; Satoshi Ikeda; Masafumi Sata; Tomohisa Baba; Erina Tabata; Yuko Minami; Kenji Nemoto; Kenji Hayashihara; Takefumi Saito; Koji Okudela; Kenichi Ohashi; Michihiko Tajiri; Takashi Ogura
Introduction The aim of this study was to clarify the incidence and disease behavior of brain metastases (BM) without extracranial disease (ie, isolated BM) as the first relapse after curative surgery in non–small‐cell lung cancer (NSCLC) patients, analyzed according to epidermal growth factor receptor (EGFR) mutation status. Patients and Methods A review of the medical charts of consecutive NSCLC patients diagnosed between 2005 and 2016 with BM as the first relapse after curative surgery was performed. Results Among 1191 patients evaluated for EGFR mutation status, 28 patients who met the inclusion criteria were divided into 2 groups: EGFR mutation group (16 patients) and wild type group (12 patients). At BM diagnosis, the EGFR‐mutation group tended to have more commonly isolated BM compared with that in the wild type group (11 of 16 vs. 3 of 12; P = .054). In the EGFR mutation group, the patients with isolated BM showed longer overall survival than those with non‐isolated BM (39.6 vs. 18.7 months; P = .038). Notably, isolated BM in the EGFR mutation group was neurologically asymptomatic in 10 of the 11 patients. With regard to upfront treatment for isolated BM in the EGFR mutation group, 10 of 11 patients were treated with only cranial radiotherapy without EGFR tyrosine kinase inhibitors, but two‐thirds of the patients (7 of 11; 64%) developed extracranial disease during the study period. Conclusion In curatively resected NSCLC patients with EGFR mutation, isolated BM would be correlated with better prognosis, but regarded as a precursor to systemic disease. Because isolated BM can be neurologically asymptomatic, it would be important to periodically perform cranial evaluation to detect isolated BM. Micro‐Abstract Isolated brain metastases (BM) tended to be more common as the first relapse in curatively resected non–small‐cell lung cancer patients with epidermal growth factor receptor mutation. Because isolated BM in those patients was mostly neurologically asymptomatic and would be regarded as a precursor to systemic disease, it would be preferable to periodically perform appropriate cranial evaluation.
Medical Oncology | 2014
Akimasa Sekine; Hiroaki Satoh; Tae Iwasawa; Katsumi Tamura; Kenji Hayashihara; Takefumi Saito; Terufumi Kato; Mito Arai; Koji Okudela; Kenichi Ohashi; Takashi Ogura
Medical Oncology | 2012
Hiroyuki Nakamura; Hiroaki Satoh; Takayuki Kaburagi; Yoshihiro Nishimura; Yoko Shinohara; Masaharu Inagaki; Takeo Endo; Takefumi Saito; Kenji Hayashihara; Nobuyuki Hizawa; Koichi Kurishima; Takeshi Nawa; Katsunori Kagohashi; Koji Kishi; Hiroichi Ishikawa; Hideo Ichimura; Toshio Hashimoto; Yukio Sato; Mitsuaki Sakai; Koichi Kamiyama; Takeshi Matsumura; Koji Unoura; Kinya Furukawa
Internal Medicine | 2009
Masashi Matsuyama; Kensuke Nakazawa; Minoru Katou; Kyoko Ota; Hironori Masuko; Takashi Iizuka; Takeru Mori; Hiroki Hayashi; Kenji Hayashihara; Takefumi Saito; Makoto Satoh; Nobuyuki Hizawa
Internal Medicine | 2014
Akimasa Sekine; Yukio Morishita; Koji Okudela; Yoshiya Tsunoda; Yuki Sumazaki; Toru Tanaka; Hiroyuki Takoi; Shih-Yuan Lin; Yohei Yatagai; Masaoki Shimanouchi; Toshinori Hashizume; Kenji Hayashihara; Takefumi Saito
Kekkaku(Tuberculosis) | 2008
Junichi Fujita; Kouichi Sunada; Hiroki Hayashi; Kenji Hayashihara; Takefumi Saito