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Feasibility study of Anthracycline Based Regimen followed by Nab-Paclitaxel as adjuvant chemotherapy for elderly patients with breast cancer

Feasibility study of Anthracycline Based Regimen followed by Nab-Paclitaxel as adjuvant chemotherapy for elderly patients with breast cancer - FANAC study

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000009267
Enrollment
20
Registered
2012-11-10
Start date
2012-11-10
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

Anthracycline based regimen followed by 4 cycle nab-paclitaxel Nab-paclitaxel:175mg/m2 intravenously administered on day 1 every 3 weeks

Sponsors

Shimane University Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1.Histoligically comfirmed Breast cancer 2.Age>=60 and Age<=80 3.Expeceted to radical cure by operation 4.Recieving adjuvant therapy with any anthracycline regimen 5.PS0 or 1 6.Patients who can receive nab-paclitaxel treatment within 8 weeks after anthracycline regimen 7.no adjuvant therapy except athracycline regimen 8.Patients who can correctly fill out a questionnaire 9.Required baseline laboratory parameters(within 14 days before registration): Hb more than 9.0g/dl WBC>=3000/mm3 Neu>=1500/mm3 Plt>=75000/mm3 AST,ALT<=ULNx2.5 T-Bil<1.5mg/dl Crea<1.5mg/dl 10.adequate organ function 11.Written IC

Exclusion criteria

Exclusion criteria: 1.History of severe allergy to nab-paclitaxel 2.Metachronous bilateral breast cancer 3.Active another cancer 4.History hypersensitivity reaction 5.Physician judged improper to entry this trial

Design outcomes

Primary

MeasureTime frame
feasibility

Secondary

MeasureTime frame
safety, disease free survival

Countries

Japan

Contacts

Public ContactYoshimitsu Minari

Shimane University Hospital Breast and endcrine surgery

minari@med.shimane-u.ac.jp+81-853-20-2232

Outcome results

None listed

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