Terufumi Sakai
Kurume University
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Featured researches published by Terufumi Sakai.
Cancer Chemotherapy and Pharmacology | 1989
Kenji Hirai; Yoshiharu Kawazoe; Ken Yamashita; Yoshinori Aoki; Takafumi Fujimoto; Terufumi Sakai; Yasuo Majima; Masahide Abe; Kyuichi Tanikawa
SummaryAn assessment was made on the therapeutic effects of arterial chemotherapy and transcatheter arterial embolization (TAE) therapy on 378 cases with non-resectable hepatocellular carcinoma (HCC). For the 191 cases who had undergone arterial chemotherapy, 22% had a 1-year survival rate, 8.9% survived for 2 years, and 4.0% for 3 years. Of these, for the 128 cases who were compatible with our criteria for patient selection, the three survival rates were 31.4%, 12.2% and 5.9% respectively. However, for the other 63 cases, who were incompatible with our criteria, the 1-year survival rate was 1.6% and it was worse for the cases who had received supportive care alone. For the cases who had undergone arterial chemotherapy, the highest survival rates were obtained by the alternate administration of different anticancer agents, and the three survival rates were 39.0%, 13.1% and 4.9% respectively. For the 187 cases who had undergone TAE therapy, the 1-year survival rate was 66.2%, the 2-year survival rate 36.5%, and the 3-year survival rate 21.9%. For the 124 cases with a tumor progression rate of less than 20% in the liver (E1), the survival rates were 77.8%, 50.1% and 30.8% respectively. The peripheral venous drug concentrations of mitomycin C and adriamycin were lower, but were maintained for a longer period in TAE therapy than in arterial chemotherapy. These results suggest that consideration of the criteria for patient selection and the alternate administration of anticancer agents are necessary in arterial chemotherapy, and that the best therapeutic effects can be obtained by TAE therapy combined with chemotherapy for cases of non-resectable HCC because of the chemotherapeutic and ischemic effects on the tumors.
Oncology | 2013
Masahito Nakano; Masatoshi Tanaka; Ryoko Kuromatsu; Hiroaki Nagamatsu; Kenji Sakata; Satoru Matsugaki; Masahiko Kajiwara; Kunitaka Fukuizumi; Nobuyoshi Tajiri; Norito Matsukuma; Terufumi Sakai; Noriyuki Ono; Yoichi Yano; Hironori Koga; Junichi Kurogi; Akio Takata; Shuji Sumie; Manabu Satani; Shingo Yamada; Takashi Niizeki; Hajime Aino; Hideki Iwamoto; Takuji Torimura; Michio Sata
Background: Sorafenib, an oral multikinase inhibitor, was approved for the treatment of advanced hepatocellular carcinoma (HCC), but has not been adequately evaluated for safety and effectiveness in Japanese patients with advanced HCC. Aims: The purpose of this study was to prospectively assess the efficacy, safety, and risk factors for survival in patients with advanced HCC treated with sorafenib. Methods: Between May 2009 and December 2010, 96 Japanese patients with advanced HCC (76 male, 20 female, mean age: 70.4 years) were treated with sorafenib. Eighty-eight patients had Child-Pugh class A, and 8 patients had Child-Pugh class B liver cirrhosis. Barcelona Clinic Liver Cancer stage B and C were found in 64 and 32 patients, respectively. Results: Twelve patients demonstrated partial response to sorafenib therapy, 43 patients had stable disease, and 33 patients had progressive disease at the first radiologic assessment. The most frequent adverse events leading to discontinuation of sorafenib treatment were liver dysfunction (n = 8), hand-foot skin reaction (n = 7), and diarrhea (n = 4). The median survival time and time to progression were 11.6 and 3.2 months, respectively. By multivariate analysis, des-γ-carboxy prothrombin serum levels and duration of treatment were identified as independent risk factors for survival. Conclusions: This study showed that sorafenib was safe and useful in Japanese patients with advanced HCC. In addition, this study demonstrated that sorafenib should be administered as a long-term treatment for advanced HCC regardless of therapeutic effect and dosage.
Journal of Gastroenterology | 1995
Yukihiro Tsuchiya; Fumitake Ishihara; Goro Kajiyama; Saburo Nakazawa; Masao Otho; Hiroshi Tanimura; Yoshikazu Akura; Minoru Harada; Masabumi Hihara; Yukio Kawai; Yukihiro Kono; Hajime Koshiyama; Masahiro Morita; Michiko Nakajima; Kyoichiro Nishina; Sagawa H; Terufumi Sakai; Mitsuo Shoji; Kayoko Sone; Yoshihiro Sugimoto; Keiichi Sugiyama; Osamu Takahara; Tomoo Takamura; Susumu Tazuma; Hideki Wakamatsu
The use of bile acid dissolution therapy in extracorporeal shockwave lithotripsy of gallstones, remains controversial. Our study examined whether chemolitholysis after sufficient disintegration enhanced stone clearance within 6 months of the first lithotripsy. A total of 143 patients who developed one to three radiolucent stones measuring⪯30 mm in diameter were randomly separated into two treatment groups: 47% were given lithotripsy alone, and 53% lithotripsy plus ursodeoxycholic acid (UDCA). Repeated piezoelectric lithotripsy was given, with no limit on the total number of treatment sessions, to pulverize or disintegrate stones into fragments<3 mm. Stones were disintegrated in 97% of all patients, and the fragments were ⪯2 mm in 50% of these patients. According to an intention-to-treat analysis, 52% in the lithotripsy alone group and 58% in the UDCA group were free of stones 6 months after the first lithotripsy (P=0.61). Of the patients with fragments⪯2 mm, 71% in the former and 86% in the latter group were free of stones 6 months after the first lithotripsy, with no significant difference between the groups. Biliary pain occurred in 25% of all patients, including 3 with acute cholecystitis. We concluded that the sufficient disintegration of gallstones achieved with repeated lithotripsy enhanced the early clearance of fragments, regardless of whether chemolitholysis was employed.
Digestive Endoscopy | 1997
Hideo Ikeda; Makoto Kohakura; Tomoaki Minetoma; Nobuhiro Ikeda; Shinzo Kawaguchi; Yutaka Imamura; Yuji Ito; Terufumi Sakai; Koichi Ide; Michiko Tomoyose; Osamu Tsuruta; Atsushi Toyonaga; Kyuichi Tanikawa
Abstract: Churg‐Strauss syndrome (CSS), a relatively rare disorder which is associated with serious complications, has a highly variable course and several possible manifestations. We present the case of a 35‐year‐old woman with a history of bronchial asthma, admitted for evaluation of lower abdominal pain and melena, whose clinical course had certain features in common with CSS. On admission, the white blood cell count was 45,300/mm3 with 65% eosinophils, and the serum immunoglobulin E (5,300 u/ml) level was remarkably elevated. At colonoscopy, there were shallow ulcers, irregular in shape, throughout the large intestine. Abdominal pain and melena were relieved by oral administration of prednisolone. Most previously reported cases have not been recognized as having colonic involvement until surgery or autopsy. In only a few reports of CSS and related disorders were colonoscopic examination findings described.
Kanzo | 1988
Misa Ishii; Masahide Abe; Kenji Hirai; Yasuo Majima; Terufumi Sakai; Tsutomu Miura; Masatoshi Tanaka; Takefumi Kuwahara; Kyuichi Tanikawa; Shigetaka Sugihara; Masamichi Kojiro
Radiation Medicine | 1998
Kazuhiro Funatsu; Harumi Nishihara; Yoshimi Nozaki; Terufumi Sakai; Nobuyuki Tomoda; Yuji Itoh; Naofumi Hayabuchi
Kanzo | 1986
Takafumi Fujimoto; Yasuo Majima; Masatoshi Tanaka; Ichirou Iwai; Terufumi Sakai; Kenji Hirai; Masahide Abe; Kyuichi Tanikawa; Kunihiro Kenmochi
The Kurume Medical Journal | 1998
Terufumi Sakai
Internal Medicine | 1993
Hideya Noguchi; Kenji Hirai; Atushi Seo; Masao Yoshitake; Terufumi Sakai; Hirohiko Abe; Reiichiro Hidaka; Tomoki Aritaka; Kyuichi Tanikawa
Internal Medicine | 1997
Satoshi Itano; Terufumi Sakai; Hiroyasu Ijuin; Kenshi Koga; Yasutsugu Yoshiyama; Tomoyuki Yoshida; Masahiko Kajiwara; Naofumi Ono; Hideya Noguchi; Kenji Hirai; Kyuichi Tanikawa