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Feasibility study of S-1 alternate-day and Carboplatin in advanced or recurrent non- small cell lung cancer.

Not Applicable
Conditions
advanced or recurrent NSCLC
Registration Number
JPRN-UMIN000010593
Lead Sponsor
Tokushima university hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
33
Inclusion Criteria

Not provided

Exclusion Criteria

1) Patients with pleural or pericardial effusion ,or ascites. 2) Patients with active double cancer. 3)Patients with significant complications. 4)Patients with serious diarrhea. 5)Patients with active infection. 6)Patients with symptomatic brain metastasis. 7)Being treated with flucytosine, phenytoin,warfarin. 8)Uncontrolled psychiatric disease. 9) allergic more than and equal to grade3. 10)Patients with interstitial pneumonia or pulmonary fibrosis. 11)History of serious allergic reaction with S-1 or CBDCA. 12)Patients with pregnancy or lactation. 13)Patients with HIV,HBV 14)Any patients judged by the investigator to be unfit to participate in the study

Study & Design

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