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XELOX(+bevacizumab), efficacy, safety, QOL Study:FOLFOX(+bevacizumab) after starting therapy, for patients can't continue continuous infusion therapy

Phase 2
Conditions
advanced and recurrent colorectal cancer
Registration Number
JPRN-UMIN000003961
Lead Sponsor
Kochi Health Sciences Center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
20
Inclusion Criteria

Not provided

Exclusion Criteria

1)severe renal failure 2)severe hypersensitivity to have a history fluorouracil,lebohorinatokarushiumu, platinum, bevacizumab 3)activity with multiple cancers(After which no more than five years of activity) 4)brain metastases(only when using bevacizumab) 5)FOLFOX(+bevacizumab)treatment for 3 or more months after 6)In addition, if deemed unsuitable to participate in this study is the responsible physician

Study & Design

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