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The clininal significance of identification technique of trifluridine incorporated into DNA in colorectal cancer patients treated with trifluridine / tipiracil.( KSCC 1602-A)

Not Applicable
Conditions
Colorectal Cancer
Registration Number
JPRN-UMIN000025552
Lead Sponsor
Kyushu Study group of Clinical Cancer
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
39
Inclusion Criteria

Not provided

Exclusion Criteria

1) Serious drug-induced hypersensitivity (especially, platinum formulation, 5-FU, TFTD) 2) Patients received palliative operation (it is eligible at 28 days after the operation with the intestinal anastomosis, at 14 days after colostomy) 3) Patients with active infectious disorder 4) Patients with uncontrollable hypertension. 5) Patients with under treatment by continuous use of insulin or with complication of uncontrollable diabetes mellitus 6) Patients with cardiac disorder such as congestive heart failure, angina to need medication, transmural myocardial infarction definitely observed in ECG, clinically apparent valvular disease, symptomatic coronary disease, uncontrollable arrhythmia, anamnesis of myocardial infarction that developed within the past 12 months. 7) Patients with severe pulmonary disorder such as interstitial pneumonia, pulmonary fibrosis, severe emphysema. 8) Patients with mental disorder or with anamnesis of central nervous system disorder. 9) Patients who have the fresh bleeding from gastrointestinal tract needing a transfusion repeatedly. 10) Patients who are receiving anticoagulant. 11) Patients with watery stool (>=Grade2) 12) Active double cancer. Synchronous double cancer and metachronous double cancer within a disease-free interval of 5 years. Lesions consistent with carcinoma in situ or intramucosal carcinoma that have been cured by local treatment are not classified as active multiple cancers. 13) Male patients with hope of pregnancy of his partner. 14) Patients with cirrhosis or active hepatitis. 15) Any other patients who are regarded as unsuitable for this study by the investigators

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The association between the proportion of FTD positive cells and the response rate, overall survival or the frequency of the adverse effect of TFTD.
Secondary Outcome Measures
NameTimeMethod
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