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Clinical Trials/JPRN-UMIN000000493
JPRN-UMIN000000493
Unknown
Phase 2

A Phase II study of docetaxel (T) and cyclophosphamide(C) as adjuvant chemotherapy for patients with high risk, node negative, early stage breast cancer - JECBC04

Japan East Cancer Center Breast Cancer Consortium0 sites50 target enrollmentStarted: October 1, 2006Last updated:
ConditionsBreast cancer

Overview

Phase
Phase 2
Sponsor
Japan East Cancer Center Breast Cancer Consortium
Enrollment
50

Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
20years-old to 70years-old (—)
Sex
Female

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Male A history of other malignancies within the last 5 years except for adequately treated non\-melanoma skin cancer or carcinoma in situ of the cervix Bilateral breast cancer Inflammatory breast cancer A history of hypersensitivity reaction to drugs formulated with Polysorbate 80 Uncontrolled medical conditions (e.g., malignant hypertension, congestive heart failure, renal failure, myocardial infarction in the previous 6 months, treatment required arrhythmia, infection, hemorrhage) Grade 2\-4 peripheral neuropathy Pleural or pericardial effusion requiring treatment Severe peripheral edema. Significant interstitial pneumonia or pulmonary fibrosis by CT scan or X\-ray Patients who require concurrent treatment by corticosteroids except for premedication. Evere psychiatric disorders Pregnant or lactating women Patients judged by the investigator to be unfit to be enrolled into the study Prior chemotherapy or radiation therapy for other cancer within 3 years including neo\-adjuvant chemotherapy for locally advanced breast cancer.

Investigators

Sponsor
Japan East Cancer Center Breast Cancer Consortium

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