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Cohort study of Patients with metastatic colorectal cancer Treated by XELOX with bevacizumab

Cohort study of Patients with metastatic colorectal cancer Treated by XELOX with bevacizumab - Cohort study of Patients with metastatic colorectal cancer Treated by XELOX with bevacizumab

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000004896
Enrollment
38
Registered
2011-01-18
Start date
2011-01-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

colorectal cancer

Interventions

1)Capecitabine at a dose of 2,000mg/m2/day orally in 2 divided doses for 2weeks on and 1week rest 2) tri-Weekly oxaliplatin at a dose of 130mg/m2 intravenously 3) tri-weekly bevacizumab at a dose

Sponsors

Nagoya City University Gastrointestinal Surgery
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. 20 years or older 2.Histologically confirmed colorectal cancer 3.With target lesion by RECIST ver.1.1 4.Unrecetable recurrent or metastatic colorectal cancer.Not be administered any therapies except radio therapy when primary disease or primary recurrence and not be administered any therapy for reccurent tumor 5.Patients who can take food orally 6. Patients who will be administered the therapy of XELOX+Bevacizumab 7.Written IC

Exclusion criteria

Exclusion criteria: 1. Prior or synchronous invasive malignancy unless disease free for a minimum of 5 years 2.Previous history of severe drug-induced allergy caused by capecitabine 3.Be Administered or less than 7 days finished administration Compound Drug of tegafur,gimeracil and oteracil potassium 4.Severe kidney trouble 5.Previous history of severe drug-induced allergy caused by oxaliplatin 6. Neuropathy or sensory dysfunction 7.Previous history of severe drug-induced allergy caused by bevacizumab 8.Pregnant women who are capable of pregnancy or intend to get pregnant 9.Patients judged inappropriate for this study by the physicians

Design outcomes

Primary

MeasureTime frame
Frequency and Degree of Hand-foot symdrome(HFS),Neuropathy and Vascular disorders

Secondary

MeasureTime frame
Time To Failure, Disease Free Survival, Overall Survival, Overall Response Rate, Frequency and Degree of Adverse Events Except HFS,Neuropathy and Vascular disorders. Resection Rate of Liver Metastases, Rate of R0 Resection of Liver Metastases

Countries

Japan

Contacts

Public ContactMikinori Sato, Masayasu Hara

Nagoya City University Gastrointestinal Surgery

mshara@med.nagoya-cu.ac.jp052-853-8226

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026