Prospective multicenter study to investigate the introduction rate of second-line S-1 in gemcitabine-refractory unresectable pancreatic cancer
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  • 作者:Hiroki Kawashima (1)
    Akihiro Itoh (1)
    Eizaburo Ohno (1)
    Masanao Nakamura (1)
    Ryoji Miyahara (2)
    Naoki Ohmiya (1)
    Kazuo Hara (3)
    Akira Kanamori (4)
    Terutomo Itoh (5)
    Tomoyuki Taki (6)
    Takanori Hirai (7)
    Senju Hashimoto (8)
    Kinichi Takeda (9)
    Hidemi Goto (1)
    Yoshiki Hirooka (2) hirooka@med.nagoya-u.ac.jp
  • 关键词:Pancreatic cancer – Second ; line therapy – Prospective study – S ; 1 – Gemcitabine
  • 刊名:Cancer Chemotherapy and Pharmacology
  • 出版年:2011
  • 出版时间:September 2011
  • 年:2011
  • 卷:68
  • 期:3
  • 页码:677-683
  • 全文大小:281.3 KB
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  • 作者单位:1. Department of Gastroenterology, Nagoya University Graduate School of Medicine, 65 Tsuruma-cho, Showa-ku, Nagoya, 466-8550 Japan2. Department of Endoscopy, Nagoya University Hospital, 65 Tsuruma-cho, Showa-ku, Nagoya, 466-8550 Japan3. Department of Gastroenterology, Aichi Cancer Center Hospital, Nagoya, Japan4. Department of Gastroenterology, Ogaki Municipal Hospital, Ogaki, Japan5. Department of Gastroenterology, Japanese Red Cross Nagoya Daiichi Hospital, Nagoya, Japan6. Department of Gastroenterology, Yamashita Hospital, Ichinomiya, Japan7. Department of Gastroenterology, Komaki City Hospital, Komaki, Japan8. Division of Liver, Biliary Tract and Pancreas Diseases, Department of Internal Medicine, Fujita Health University, Toyoake, Japan9. Department of Gastroenterology, Nagoya Kyoritsu Hospital, Nagoya, Japan
  • 刊物类别:Biomedical and Life Sciences
  • 刊物主题:Biomedicine
    Cancer Research
    Pharmacology and Toxicology
    Oncology
  • 出版者:Springer Berlin / Heidelberg
  • ISSN:1432-0843
文摘
Purpose S-1 is one of the second-line candidate agents for gemcitabine-refractory unresectable pancreatic cancer. Two phase II studies have been reported for second-line chemotherapy with S-1, but these studies did not investigate introduction rate and suitable dose of second-line S-1. Therefore, we conducted a prospective multicenter study in which chemo-na?ve patients were enrolled and had two levels of S-1 dose.
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