MedPath

A phase 2 study of weekly Nab-Paclitaxel followed by FEC (Fluorouracil, Epirubicin, Cyclophosphamide) as primary therapy for operable breast cancer

Phase 2
Completed
Conditions
Breast cancer
Registration Number
JPRN-UMIN000007510
Lead Sponsor
ahanishi Clinic
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
Female
Target Recruitment
30
Inclusion Criteria

Not provided

Exclusion Criteria

1. Cases with prior history of hypersensitivity reaction to the drugs or solvents (e.g. albumin, paclitaxel) used in this protocol. 2. Bilateral breast cancer cases. 3. Cases with inflammatory breast cancer. 4. Male breast cancer cases. 5. Cases with active secondary malignancy (current secondary malignancy or other malignancy within 5 years) . 6. Cases with conditions with the potential to compromise the planned treatment, such as cases with active infection, diarrhea, intestinal paralysis, intestinal obstruction, uncontrolled diabetes, uncontrolled angina and myocardial infarction within 6 months, heart failure, and other serious conditions. 7. Pregnant or breast feeding cases. 8. Cases with pulmonary fibrosis or interstitial pneumonia. 9. Cases with severe myelodepression, renal or liver dysfunction. 10. Cases in which the treating physician deems inappropriate to be entered into this study for other reasons.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath