Phase II Study of TS-1 Therapy and TS-1+PSK Therapy Against Advanced Gastric Carcinoma

NCT ID: NCT00503321

Last Updated: 2009-01-23

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE2/PHASE3
• Total Enrollment: 13 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2006-10-31
• Study Completion Date: 2011-08-31

Brief Summary

A randomized controlled study is conducted on unresectable advanced gastric carcinoma and recurrent gastric carcinoma to compare TS-1 therapy with TS-1 + PSK therapy. The primary endpoint of this study is progression-free survival (PFS), with secondary endpoints of anticancer effect, time to treatment failure (TTF), QOL (FACT-BRM), compliance, adverse drug reactions and immunological factors.

Detailed Description

Tegafur / gimeracil / oteracil potassium (TS-1) is widely used as a first-line drug for unresectable advanced gastric carcinoma and recurrent gastric carcinoma in Japan and the response rate of TS-1 against gastric carcinoma was reported to be excellent at 46.5% in a phase II study. However, since adverse drug reactions tend to occur in patients treated with standard regimen of TS-1, drug reduction or discontinuation is often required, which is one drawback of this drug. On the other hand, although Krestin (PSK) has been reported to show survival effects in postoperative immunochemotherapy against gastric carcinoma, the efficacy of PSK has not been established in patients with unresectable advanced gastric carcinoma and recurrent gastric carcinoma. Since the main effect of PSK was to recover physiological functions, including immune function of the host, it was expected that PSK would improve the compliance of TS-1 by alleviating adverse drug reactions of TS-1 therapy and the concomitant use of TS-1 with PSK would result in the improvement of treatment results. Therefore, we decided to conduct a randomized phase II study on patients with unresectable advanced gastric carcinoma and recurrent gastric carcinoma to compare TS-1 therapy with TS-1+PSK therapy.

Conditions

Gastric Cancer

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Arm B

S-1 plus PSK group

Group Type: EXPERIMENTAL

Tegafur/gimeracil/oteracil potassium (S-1), Krestin (PSK)

Intervention Type: DRUG

S-1 80mg/m2 4weeks on 2 weeks off, PSK 3g/day

Arm A

S-1 alone

Group Type: ACTIVE_COMPARATOR

Tegafur/gimeracil/oteracil potassium (S-1)

Intervention Type: DRUG

S-1 80mg/m2, 4weeks on followed by 2 weks off

Interventions

Tegafur/gimeracil/oteracil potassium (S-1), Krestin (PSK)

S-1 80mg/m2 4weeks on 2 weeks off, PSK 3g/day

Intervention Type: DRUG

Tegafur/gimeracil/oteracil potassium (S-1)

S-1 80mg/m2, 4weeks on followed by 2 weks off

Intervention Type: DRUG

Other Intervention Names

S-1 plus PSK; S-1 alone

Eligibility Criteria

Inclusion Criteria

• Patients with unresectable advanced gastric carcinoma and recurrent gastric carcinoma.
• Patients who are 20 years old or older at the time of obtaining consent.
• Patients who have not received prior treatment, including radiotherapy, chemotherapy and immunotherapy, before the start of treatment (however, patients are excluded when six months or more have passed since they received postoperative adjuvant chemotherapy.)
• Patients who do not develop metachronous or simultaneous multi cancer.
• Patients who do not show severe impairments in renal function, liver function and bone marrow function and who maintain the major organ functions which meet all requirements as described below (laboratory values are values measured before the start of protocol treatment and should be updated ones which are measured within two weeks before protocol treatment is started.) WBC counts: >= 3,000 /mm3 and < 12,000 /mm3 Neutrophil counts (ANC): >= 1,500 /mm3 Platelet counts: >= 100,000 /mm3 Amount of hemoglobin: >= 8.0 g/dL Serum GOT and GPT: Less than 100 IU/L Serum total bilirubin: Less than 1.5 mg/dL Serum creatinine: Less than 1.5 mg/dL
• Patients whose performance status scores are 0 to 2.
• Patients who are judged that they can endure this treatment in a comprehensive manner and who have provided written informed consent to participate in this research.
• Presence or absence of measurable lesion does not matter, but if there are measurable lesions in patients, the lesions should be confirmed within 28 days before the enrollment.

Exclusion Criteria

• Patients with fresh blood in the digestive tract.
• Patients with body fluids which require treatment.
• Patients with infectious disease, intestinal paresis and ileus.
• Patients with diarrhea (watery stool).
• Female patients who are pregnant or want to become pregnant during this study or male patients who intend to make someone pregnant during this study.
• Diabetic patients who are being treated with insulin or are poorly controlled.
• Patients with ischemic heart disease which require treatment
• Patients who are complicated with psychosis and judged that it is difficult for them to participate in this study.
• Patients who continue to receive steroids.
• Patients who have experienced serious drug allergy in the past.
• Patients who are taking health foods including agaricus which are considered to have immunostimulating effects.
• Patients judged to be inappropriate for this study by investigators and sub-investigators.

• Minimum Eligible Age: 20 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Eastern Network of Cancer Immunological Therapy, Japan

OTHER

Sponsor Role: lead

Responsible Party

Shizuoka Cancer Center

Principal Investigators

Hideaki Tahara, MD

Role: STUDY_CHAIR

Eastern Network of Cancer Immunological Therapy, Japan

Locations

Shizuoka Cancer Center

Shizuoka, Shizuoka, Japan

Countries

Japan

References

Nakazato H, Koike A, Saji S, Ogawa N, Sakamoto J. Efficacy of immunochemotherapy as adjuvant treatment after curative resection of gastric cancer. Study Group of Immunochemotherapy with PSK for Gastric Cancer. Lancet. 1994 May 7;343(8906):1122-6. doi: 10.1016/s0140-6736(94)90233-x.

Reference Type: BACKGROUND

PMID: 7910230 (View on PubMed)

Other Identifiers

ENCITJ-GC01

Identifier Type: -

Identifier Source: org_study_id