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A Feasibility study of alternate-day administrations of TS-1 as previously treated advanced non-small cell lung cancer in elderly patients

Phase 2
Conditions
Previously treated non-small cell lung cancer
Registration Number
JPRN-UMIN000011795
Lead Sponsor
Hiroshima University
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) Interstitial pneumonia or pulmonary fibrosis detectable on X ray. 2) Massive pleural or pericardial effusion,ascites 3) History of active double cancer within 5 years prior to the study. 4) Patients having active other cancers. 5) Ileus, Interstitial 6) Uncontrolled diabetes mellitus 7) Cardiac infarction or unstable angina within 6 months 8) Symptomatic brain metastases 9) Concomitant therapy with flucytocine, phenytoin or Warfarin Potassium 10) Serious psychiatric illness 11) History of severe hypersensitivity(>=Grade3) 12) History of using 5-FU o 13) Patient who is not candidates for TS-1 14) HBV-positive patients 15) Evaluated to be ineligible by a physician for other reasons

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Safety
Secondary Outcome Measures
NameTimeMethod
1yr OS,PFS,DCR
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