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
This trial does not accept healthy volunteersQualifiers
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 population
Early breast cancer patients who required four cycles of chemotherapy after curative resection of breast cancer
Trial design
Cohort
Retrospective
Treatments tested in this trial
Liposomal doxorubicin containing regimen
DrugLiposomal doxorubicin hydrochloride (PLD) 30-40mg/m2 D1 + other drugs (decided by investigators); All patients were treated with 4 cycles.
Treatment groups
Trial outcomes
Primary outcomes
Cardiac safety
Cardiac ejection fraction
Secondary outcomes
Overall survival
Sponsors and contacts
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