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Completed

NCT Number: NCT00296335

Trial of Adjuvant Chemotherapy for Gastric Cancer

This is a phase III randomized study designed to evaluate the efficacy of mitomycin, doxifluridine, and cisplatin compared to mitomycin and doxifluridine.

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Key information

Age range

18 year–69 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Asan Medical Center

Seoul, 138-736, South Korea

About this study

Stomach cancer is the most common cancer in Korea and one of the major health problems worldwide. The most effective treatment for gastric cancer is curative surgical resection of primary tumor. However, a substantial number of patients eventually die of recurrences after curative resection. A number of randomized trials investigating the role of adjuvant chemotherapy have been conducted. However, the efficacy of adjuvant chemotherapy is still controversial and varied between Western and Asian trials. Meta-analysis of Western trials didn't demonstrate the benefit of adjuvant chemotherapy after curative resection. Conversely, some Asian studies have demonstrated the efficacy of adjuvant chemotherapy after curative resection. In a previous study, mitomycin plus tegafur prolonged the survival in resected gastric cancer compared to no treatment.

This study is designed to evaluate the efficacy of mitomycin, cisplatin and prolonged treatment with doxifluridine compared to mitomycin plus doxifluridine.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Pathologically proven gastric adenocarcinoma
  • Curative resection was done
  • stage II, IIIA, IIIB, IV (including T4, lesions or N3, but excluding M1 lymph node metastasis)
  • age: 18-69 years old
  • Performance status: ECOG 0-2
  • Adequate bone marrow function (WBC ≥ 4,000/ul, platelet count ≥ 100,000/ul, hemoglobin ≥ 10 g/dl)
  • Adequate renal function (serum creatinine≤ 1.5)
  • Adequate liver function (serum bilirubin ≤1.5 mg/dl, AST/ALT ≤ 3 x normal upper limit)
  • Written informed consent was signed by the patient

Exclusion criteria

  • Previous chemotherapy or radiotherapy
  • Active ongoing infection which antibiotic treatment is needed
  • Pregnant or lactating women
  • Psychosis or convulsion disorder
  • Ascites in preoperative abdomen CT
  • Systemic disease which interfere the administration of chemotherapy
  • Previous history of other malignancy except cured non-malignant skin cancer and uterine cervical cancer in situ

Treatment and study plan

Mitomycin, doxifluridine and cisplatin

Drug

Mitomycin-C 20mg/m2 intravenously (day 1), Doxifluridine 460-600mg/m2/day per oral (day 28- day 336), Cisplatin 60mg/m2 intravenously (day 28, day 56, day 84, day 112, day 140, and day 168)

Mitomycin and doxifluridine

Drug

Mitomycin-C 20mg/m2 intravenously (day 1), Doxifluridine 460-600mg/m2/day per oral (day 28-day 84)

Primary outcomes

  1. Relapse-free Survival Rate

    Time frame: 3 years

    Relapse-free survival at 3 years was defined as the proportion of patients who did not show an evidence of disease recurrence after 3 years of surgery.

    Relapse was defined as any new tumor lesion.

Secondary outcomes

  1. Overall Survival Rate

    Time frame: 3 years

    Overall survival rate at 3 years was defined as the proportion of patients who were alive at 3 years after surgery.

  2. Number of Patients With Adverse Events

    Time frame: Up to 3 years

    Per National Cancer Institute Common Toxicity Criteria version 2.0, up to 3 years

Sponsors and collaborators

Lead sponsor

Asan Medical Center

Other

Collaborators

  • Hallym University Medical Center
  • Ulsan University Hospital

Registry information

Official study title

A Phase III Randomized Controlled Trial of Adjuvant Chemotherapy for Advanced Gastric Adenocarcinoma

Important dates

Study start
2002
Primary completion
2007
Study completion
2009
First posted
Feb 27, 2006
Registry last updated
Feb 27, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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