Randomized Multicenter Controlled Phase III Study of Postoperative Adjuvant Therapy for Stage II/IIIA Gastric Cancer Using TS-1 Alone or TS-1+PSK Combined Therapy
Trial Snapshot
- Phase
- Phase 3
- Status
- Completed
- Sponsor
- Enrollment
- 255
- Locations
- 42
- Primary Endpoint
- Time of recurrence (calculation of 3-year disease-free survival and overall survival rates)
Study Overview
Brief Summary
A randomized controlled study is conducted on patients with resected gastric cancer assigned to postoperative adjuvant therapy of TS-1 alone or PSK combined with TS-1, with the objective to examine or validate the outcome, QOL and prognostic factors (host and tumor factors), and explore the factors enhancing the antitumor effect of TS-1.
Detailed Description
The 5-year survival after gastric cancer surgery remains poor as the cancer advances to stages II, IIIA, IIIB and IV. Tegafur-gimeracil-oteracil potassium (TS-1) is used as the first line treatment for advanced and recurrent gastric cancer. But TS-1 is accompanied by an adverse drug reaction of bone marrow suppression that is not readily seen in conventional oral fluoropyrimidines. Among randomized controlled trials on postoperative adjuvant chemotherapy for gastric cancer, the beneficial results of survival rates using Krestin (PSK) in combination with chemotherapy have been reported. With the objective to enhance the antitumor effect of TS-1 and to improve the QOL of patients, we have planned to validate the clinical significance of combined PSK and TS-1 therapy as postoperative adjuvant therapy for gastric cancer, using in principle the TS-1 regimen of 2-week dosing 1-week off for 6 months followed by 2-week dosing 2-week off for 6 months.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- None
Eligibility Criteria
- Ages
- 20 Years to 80 Years (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Patients with microscopic stage II or IIIA resectable gastric cancer
- •Patients who have not received preoperative cancer therapy (radiotherapy, chemotherapy or immunotherapy)
- •Patients with serum immunosuppressive acidic protein (IAP) measured within 2 weeks before surgery
- •Patients with no metachronous or synchronous multiple cancer
- •Patients without severe impairment of renal, hepatic and bone marrow functions
- •Patients who are judged to be capable of tolerating surgery
- •Patients with preoperative performance status 0 to 2
- •Patients with no serious concurrent complications (such as bone marrow suppression, diarrhea and infection)
- •Patients who are judged to be capable of tolerating this treatment, and who have given written informed consent to participate in this study
Exclusion Criteria
- •Patients with fresh hemorrhage from the gastrointestinal tract
- •Patients with retention of body fluid necessitating treatment
- •Patients with infection, intestinal palsy or intestinal occlusion
- •Patients who are pregnant or hope to become pregnant during the study period
- •Patients with diabetes treated by continuous use of insulin or showing poor glycemic control
- •Patients with a history of ischemic heart disease
- •Patients with concurrent psychiatric disease or psychotic symptoms, and judged to have difficulties participating in the study
- •Patients receiving continuous administration of steroids
- •Patients who have experienced serious drug allergy in the past
- •Others, patients judged by the investigator or subinvestigator to be inappropriate as subject
Arms & Interventions
1
TS-1 Group: The group treated with TS-1 mono-therapy
Intervention: Tegafur-gimeracil-oteracil potassium (TS-1) (Drug)
2
TS-1+PSK Group: The group treated with combination therapy using TS-1 and PSK
Intervention: Tegafur-gimeracil-oteracil potassium (TS-1) (Drug)
2
TS-1+PSK Group: The group treated with combination therapy using TS-1 and PSK
Intervention: Krestin (PSK) (Drug)
Outcomes
Primary Outcomes
Time of recurrence (calculation of 3-year disease-free survival and overall survival rates)
Time Frame: Five years after surgery
Secondary Outcomes
- Relations of survival rate with compliance, postoperative complication, QOL, adverse events, recurrence status, and expression of immune or tumor markers(Five years after surgery)
Investigators
Takashi Fujimura
Assistant Professor of Gastroenterologic Surgery, Kanazawa University Hospital
Hokuriku-Kinki Immunochemotherapy Study Group