Cancer Res Treat.  2005 Aug;37(4):208-211.

A Phase II Trial of Haptaplatin/5-FU and Leucovorin for Advanced Stomach Cancer

Affiliations
  • 1Department of Internal Medicine, College of Medicine, Gyeong-Sang National University, Jinju, Korea. lwshmo@hanmail.net.
  • 2Department of Surgery, College of Medicine, Gyeong-Sang National University, Jinju, Korea.
  • 3Department of Pathology, College of Medicine, Gyeong-Sang National University, Jinju, Korea.
  • 4Institute of Health Science, College of Medicine, Gyeong-Sang National University, Jinju, Korea.

Abstract

PURPOSE
Heptaplatin (SKI-2053 R) is a new platinum analogue, with a better toxicity profile than cisplatin, and has antitumor activity even in cisplatin resistant cell lines. 5-fluoruracil (5-FU) has shown synergy with platinum compounds. This phase II trial was designed to determine the efficacy and toxicities of heptaplatin/ 5-FU (5-fluorouracil) for treating stomach cancer. MATERIALS AND METHODS: Thirty-two patients with advanced, measurable gastric adenocarcinomas were enrolled in this trial. The treatment consisted of heptaplatin, 400 mg/m2/day (1 hour IV infusion), on day 1 and 5-FU, 800 mg/m2/day (12 hours IV infusion), on days 1 to 5. The cycles were repeated every 3 weeks. RESULTS: Of the 26 evaluable patients, 9 had partial responses and 1a complete response (overall response rate, 38%; 95% confidence interval, 19~57%). The median response duration was 23 weeks (range: 4~60 weeks). The median time to progression was 26 weeks (range: 3~68 weeks). The grades III-IV toxicities were mostly hematological toxicities: leucopenia was observed in 11 patients (35%) and thrombocytopenia 4 (13%). No definite neuropathy was observed. Grade I-II nephropathy was also noted: grade I high BUN/creatinine levels occurred in 5 patients (16%), grade II proteinuria 2 (6%), grade I proteinuria 5 (16%). Neutropenic fever developed in 5 patients (16%) and 1 died of pneumonia in a neutropenic state. CONCLUSION: This study suggests that the regimen of Heptaplatin/5-FU should be effective and have a favorable toxicity profile for the patients suffering with advanced stomach cancer.

Keyword

Stomach neoplasms; Heptaplatin (SKI-2053 R); 5-FU; Chemotherapy

MeSH Terms

Adenocarcinoma
Cell Line
Cisplatin
Drug Therapy
Fever
Fluorouracil
Humans
Leucovorin*
Platinum
Platinum Compounds
Pneumonia
Proteinuria
Stomach Neoplasms*
Stomach*
Thrombocytopenia
Cisplatin
Fluorouracil
Leucovorin
Platinum
Platinum Compounds

Figure

  • Fig. 1 Kaplan-Meier estimates of the time to progression of the patients with advanced gastric cancer. The median time to progression was 15 weeks (range: 3~85 weeks).


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