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Phase II Study of bevacizumab combined with chemotherapy (paclitaxel/carboplatin) as postoperative adjuvant therapy for cervical cancer

Not Applicable
Recruiting
Conditions
Cervical cancer
Registration Number
JPRN-UMIN000029306
Lead Sponsor
niversity of the Ryukyus
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
63
Inclusion Criteria

Not provided

Exclusion Criteria

1. Patients whose pathologically confirmed para aortic lymph node (PAN) metastasis. Patients who are suspected of PAN metastasis by preoperative imaging (CT with a short diameter of 10mm or more, suspicious metastasis with PET/CT, can't be registered if pathological negative is not confirmed. 2. Patients with active double cancer (synchronous double cancer and metachronous double cancer with disease-free period within 5 years). 3. Patient who have been treated with anti-VEGF and anti-VEGFR formulations. 4. Patients with symptomatic cerebrovascular disorders. 5. Patients with a high probability of bleeding due to congenital hemorrhagic diathesis, abnormal coagulation, etc. 6. Patients with severe cardiovascular disorders (such as poor control hypertension). 7. Patients with clinical symptoms of intestinal obstruction. 8. Patients with infection requiring systemic administration such as antibiotics, antivirals, antifungal drugs at registration. 9. Patients who received radiotherapy or chemotherapy before surgery.

Study & Design

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