About this trial

The goal of this observational study aims to observe and evaluate the efficacy and safety of a liposomal doxorubicin containing regimen in the postoperative adjuvant treatment of breast cancer patients.

Eligibility criteria

Qualifiers

Female, aged 18-75 years;

Primary breast cancer diagnosed histopathologically;

Adjuvant chemotherapy regimens include liposomal doxorubicin;

ECoG PS score: 0-1 points;

Disqualifiers

Pregnant, lactating patients;

Breast cancer has been found to have distant metastasis;

Those with peripheral nervous system disorders caused by the disease or with a history of significant mental disorders and central nervous system disorders;

Those with severe infection or active peptic ulcer requiring treatment;

Trial design

Treatments tested in this trial

  • Liposomal doxorubicin containing regimen

Treatment groups

No treatment groups listed

Locations

1
Second Affiliate Hospital of Zhejiang University310009, HangzhouZhejiang, China

Sponsors and collaborators

Second Affiliated Hospital, School of Medicine, Zhejiang University

Lead sponsor