A Study for the Adjuvant Treatment of Breast Cancer

Studies on postoperative adjuvant albumin paclitaxel in domestic breast cancer patients are less reported, especially in large samples, and more studies focus more on the safety and tolerability of albumin paclitaxel use. Head-to-head studies of white violet and docetaxel are not supported by data at this time, but some studies have shown that docetaxel-induced long-term Other adverse effects such as myelosuppression, hepatotoxicity and hypersensitivity reactions can have a serious impact on quality of life. Therefore, this study aims to analyse the efficacy and safety of albumin paclitaxel and docetaxel in the adjuvant treatment of breast cancer in a large randomized controlled trial, and to further analyse the efficacy and safety of albumin paclitaxel in combination with chemotherapy for postoperative breast cancer in different subtypes of breast cancer patients, in order to obtain more realistic data and provide new treatment options for breast cancer patients.

NCT Number	NCT05420467
Lead Sponsor	Second Affiliated Hospital, School of Medicine, Zhejiang University
Conditions	Breast Cancer
Enrollment	2,413 participants
Start Date	2022-07-10
Primary Completion	2027-07-10 (estimated)
Study Completion	2027-12-20 (estimated)
Updated on ClinicalTrials.gov	2022-07-01