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Study of combination chemotherapy of Albumin-bound paclitaxel / Cyclophosphamide in recurrent or metastatic breast cancer

Study of combination chemotherapy of Albumin-bound paclitaxel / Cyclophosphamide in recurrent or metastatic breast cancer - Study of combination chemotherapy of Albumin-bound paclitaxel / Cyclophosphamide in recurrent or metastatic breast cancer

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000009616
Enrollment
30
Registered
2012-12-24
Start date
2012-11-01
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

Breast cancer

Interventions

Cyclophosphamide:600mg/m2 day1 Albumin-bound paclitaxel:150mg/m2-260mg/m2 day1 every 3 weeks

Sponsors

Yokohama City University Medical Center
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1Histological confirmed primary breast cancer 2Reccurent,metastatic breast cancer 3No prior chemotherapy for metastasis, the recurrent breast cancer 4The case that passes after treatment of the adjuvant chemotherapy more than 24 weeks 5HER2 negative. 6An age of 20 years to 75 years 7ECOG Performance Status is 0 or 1 8Patient with measurable disease 9Required baseline laboratory data 10Expected survival time more than 60 days 11Written informed consent

Exclusion criteria

Exclusion criteria: 1allergy of the medication 2Serious complications 3Previous or current history of malignant neoplasm 4Clinically significant heart disease 5Peripheral neuropathy grade2 or greater 6Active infection 7Symptomatic brain metastasis 8Uncontrollable pleural effusion or ascites requiring 9During administraton of pentostatin 10With mental disorder which become problem on clinical practice 11Current pregnancy or lacation,or possibility of pregnancy 12Cases who physician judged improper to entry this trial

Design outcomes

Primary

MeasureTime frame
To determinate maximum tolerated dose and recommended dose

Countries

Japan

Outcome results

None listed

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