Phase I dose-escalation study of docetaxel, nedaplatin, and 5-fluorouracil combination chemotherapy in patients with advanced esophageal cancer
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  • 作者:Tatsuya Miyazaki (1)
    Makoto Sohda (1)
    Naritaka Tanaka (1)
    Shigemasa Suzuki (1)
    Keisuke Ieta (1)
    Makoto Sakai (1)
    Akihiko Sano (1)
    Takehiko Yokobori (1)
    Takanori Inose (1)
    Masanobu Nakajima (2)
    Minoru Fukuchi (1)
    Hitoshi Ojima (1)
    Hiroyuki Kato (2)
    Hiroyuki Kuwano (1)
  • 关键词:Docetaxel ; Nedaplatin ; 5 ; Fluorouracil ; Chemotherapy ; Esophageal cancer
  • 刊名:Cancer Chemotherapy and Pharmacology
  • 出版年:2013
  • 出版时间:April 2013
  • 年:2013
  • 卷:71
  • 期:4
  • 页码:853-857
  • 全文大小:160KB
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  • 作者单位:Tatsuya Miyazaki (1)
    Makoto Sohda (1)
    Naritaka Tanaka (1)
    Shigemasa Suzuki (1)
    Keisuke Ieta (1)
    Makoto Sakai (1)
    Akihiko Sano (1)
    Takehiko Yokobori (1)
    Takanori Inose (1)
    Masanobu Nakajima (2)
    Minoru Fukuchi (1)
    Hitoshi Ojima (1)
    Hiroyuki Kato (2)
    Hiroyuki Kuwano (1)

    1. Department of General Surgical Science (Surgery 1), Gunma University Graduate School, 3-39-22, Showa-machi, Maebashi, Gunma, 371-8511, Japan
    2. First Department of Surgery, Dokkyo Medical University, Tochigi, Japan
  • ISSN:1432-0843
文摘
More effective protocols are needed for unresectable and recurrent esophageal cancer. Therefore, we conducted a phase I trial to establish the recommended dose of docetaxel, nedaplatin, and 5-fluorouracil (DNF) as combination chemotherapy. Fourteen patients with esophageal cancer were enrolled and received DNF combination therapy at different dose levels according to the treatment and examination plan. Dose-limiting toxicities (DLTs) included febrile neutropenia. DLTs occurred in 3/5 patients at level 4. The recommended doses (level 3) of DNF were 60?mg/m2 (day 1), 70?mg/m2 (day 1), and 700?mg/m2 (days 1-), respectively, given at 3-week intervals. In conclusion, DNF combined chemotherapy for advanced esophageal cancer was associated with relatively minor adverse events and was safely administered at the recommended dose. A phase II study is now underway.
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