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A phase I/II study of preoperative TS-1 combined chemoradiation therapy for patients with large type 3 or type 4 gastric cancer (OGSG 1303)

Not Applicable
Conditions
gastric cancer
Registration Number
JPRN-UMIN000013821
Lead Sponsor
Osaka Gastrointestinal cancer chemotherapy Study Group (OGSG)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
10
Inclusion Criteria

Not provided

Exclusion Criteria

1) with active double cancers excluding carcinoma in situ and/or prior cancer cured with longer than 5 year interval period 2) with a history of severe allergy against medicine 3) with infectious disease and febrile condition (over 38 centigrade) 4) pregnant or nursing female 5) male expecting pregnancy of partner 6) with a history of cardiac infarction within 6 months 7) under continuous steroids medication 8) Patients who are received systemic continuous administration of flucytosine, phenytoin or warfarin 9) bleeding from gastrointestinal tract 10) with uncontrollable diarrhea (watery stool and/or frequent diarrhea) 11) with HBs antigen+, and/or HCV-antibody+ 12) with severe diseases: autoimmune diseases, intestinal paralysis, interstitial pneumonitis/pulmonary fibrosis, ischemic cardiac diseases 13) Any other patients whom the physician in charge of the study judges to be unsuitable

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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