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Randomized phase II study of gemcitabine plus S-1 combination therapy vs. S-1 in advanced biliary tract cancer: Japan Clinical Oncology Group Study (JCOG0805).

Abstract
A randomized Phase II selection design trial comparing gemcitabine plus S-1 combination therapy with S-1 monotherapy for chemo-naïve unresectable or recurrent biliary tract cancer patients was started in Japan. The aim of this trial is to evaluate the efficacy and safety of the two regimens and to determine which is more promising as a test arm regimen to be compared with the current standard regimen, gemcitabine plus cisplatin, in a subsequent Phase III trial. Patients with unresectable or recurrent biliary tract cancer are randomized to either gemcitabine plus S-1 combination therapy arm or S-1 monotherapy arm. A total of 100 patients will be accrued for this study from 18 institutions over 1 year. The primary endpoint is the proportion of 1-year overall survival, and the secondary endpoints are progression-free survival, response rate and adverse events.
AuthorsAtsuo Takashima, Chigusa Morizane, Hiroshi Ishii, Kenichi Nakamura, Haruhiko Fukuda, Takuji Okusaka, Junji Furuse
JournalJapanese journal of clinical oncology (Jpn J Clin Oncol) Vol. 40 Issue 12 Pg. 1189-91 (Dec 2010) ISSN: 1465-3621 [Electronic] England
PMID20630899 (Publication Type: Clinical Trial, Phase II, Comparative Study, Journal Article, Multicenter Study, Randomized Controlled Trial)
Chemical References
  • Antimetabolites, Antineoplastic
  • Drug Combinations
  • Deoxycytidine
  • S 1 (combination)
  • Tegafur
  • Oxonic Acid
  • Gemcitabine
Topics
  • Administration, Oral
  • Adult
  • Aged
  • Antimetabolites, Antineoplastic (administration & dosage, adverse effects, therapeutic use)
  • Antineoplastic Combined Chemotherapy Protocols (adverse effects, therapeutic use)
  • Biliary Tract Neoplasms (drug therapy)
  • Deoxycytidine (administration & dosage, adverse effects, analogs & derivatives, therapeutic use)
  • Disease-Free Survival
  • Drug Administration Schedule
  • Drug Combinations
  • Female
  • Humans
  • Infusions, Intravenous
  • Japan
  • Male
  • Middle Aged
  • Oxonic Acid (administration & dosage, adverse effects, therapeutic use)
  • Patient Selection
  • Sample Size
  • Survival Analysis
  • Tegafur (administration & dosage, adverse effects, therapeutic use)
  • Treatment Outcome
  • Gemcitabine

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