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Spots Global Cancer Trial Database for S-1 and Irinotecan in Treating Patients Who Are Undergoing Surgery for Locally Advanced Stomach Cancer

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Trial Identification

Brief Title: S-1 and Irinotecan in Treating Patients Who Are Undergoing Surgery for Locally Advanced Stomach Cancer

Official Title: Phase II Clinical Study of Preoperative S-1/CPT-11 Combination Chemotherapy in Patients With Locally Advanced Gastric Cancer

Study ID: NCT00134095

Conditions

Gastric Cancer

Study Description

Brief Summary: RATIONALE: Drugs used in chemotherapy, such as S-1 and irinotecan, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving more than one drug (combination chemotherapy) may kill more tumor cells. Giving chemotherapy before surgery may shrink the tumor so that it can be completely removed. PURPOSE: This phase II trial is studying how well giving S-1 together with irinotecan works in treating patients who are undergoing surgery for locally advanced stomach cancer.

Detailed Description: OBJECTIVES: Primary * Determine the efficacy of neoadjuvant S-1 and irinotecan in patients with locally advanced gastric cancer. Secondary * Determine the histological response in patients treated with this regimen. * Determine the overall survival of patients treated with this regimen. * Determine the progression-free survival of patients treated with this regimen. * Determine the toxicity of this regimen in these patients. * Determine postoperative morbidity in patients treated with this regimen. * Determine the rate of potentially curative surgery in patients treated with this regimen. OUTLINE: This is a multicenter study. Patients receive oral S-1 on days 1-21 and irinotecan IV over 90 minutes on days 1 and 15. Treatment repeats every 28 days for 2 courses in the absence of disease progression or unacceptable toxicity. Patients then undergo gastrectomy with lymphadenectomy. After surgery, patients resume treatment with S-1 alone as before for 1 year. PROJECTED ACCRUAL: A total of 70 patients will be accrued for this study.

Eligibility

Minimum Age: 20 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Yamamoto Kumiai General Hospital, Noshiro, Akita, Japan

Asahikawa Kosei General Hospital, Asahikawa, Hokkaido, Japan

Kobe City General Hospital, Kobe, Hyogo, Japan

Iwate Medical University Hospital, Morioka, Iwate, Japan

Tsuruoka Municipal Shonai Hospital, Tsuruoka, Yamagata, Japan

Fukushima Medical University Hospital, Fukushima, , Japan

Yamagata Prefectural Central Hospital, Yamagata, , Japan

Contact Details

Name: Mitsukazu Gotoh, MD

Affiliation: Fukushima Medical University Hospital

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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