Observational of Adjuvant Treatment of Breast Cancer With Liposomal Doxorubicin Regimen

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18-75
SponsorSecond Affiliated Hospital, School of Medicine, Zhejiang University

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 volunteers

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 population

Early breast cancer patients who required four cycles of chemotherapy after curative resection of breast cancer

Trial design

Design model

Cohort

Time perspective

Retrospective

Treatments tested in this trial

  • Liposomal doxorubicin containing regimen

    Drug

    Liposomal doxorubicin hydrochloride (PLD) 30-40mg/m2 D1 + other drugs (decided by investigators); All patients were treated with 4 cycles.

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Cardiac safety

Cardiac ejection fraction

Time frame
10 years

Secondary outcomes

1

Overall survival

Time frame
10 years

Other outcomes

Sponsors and contacts

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