Feasibility and efficacy of combination chemotherapy with S-1 and fractional Cisplatin for advanced gastric cancer

Anticancer Res. 2010 Sep;30(9):3759-62.

Abstract

Background: There is a great need for effective outpatient chemotherapy for advanced gastric cancer in patients with good performance status. The present pilot study evaluated the use of combination chemotherapy with S-1 and fractional CDDP for unresectable-recurrent gastric cancer in an outpatient setting.

Patients and methods: A total of 41 patients with unresectable or recurrent gastric cancer were treated with this combination chemotherapy. S-1 was administered orally every day on days 1-28 and CDDP was infused on days 1, 15, and 29.

Results: Thirty-six patients had measurable lesions and 19 patients had partial responses, resulting in an overall response rate of 52.8%. The median survival time was 494 days. There was no grade 4 haematological toxicity, no grade 3 or more non-haematological toxicity, and no treatment-related death.

Conclusion: This combination chemotherapy has no serious toxicities in patients with unresectable and recurrent gastric cancer and can be used effectively in an outpatient setting.

Publication types

  • Clinical Trial

MeSH terms

  • Adenocarcinoma / drug therapy*
  • Adenocarcinoma / mortality
  • Adult
  • Aged
  • Aged, 80 and over
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Cisplatin / administration & dosage
  • Cisplatin / adverse effects
  • Drug Combinations
  • Female
  • Humans
  • Male
  • Middle Aged
  • Outpatients
  • Oxonic Acid / administration & dosage
  • Oxonic Acid / adverse effects
  • Pilot Projects
  • Stomach Neoplasms / drug therapy*
  • Stomach Neoplasms / mortality
  • Tegafur / administration & dosage
  • Tegafur / adverse effects
  • Young Adult

Substances

  • Drug Combinations
  • S 1 (combination)
  • Tegafur
  • Oxonic Acid
  • Cisplatin