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Clinical Trial Summary

The goal of this clinical trial is to learn about the efficacy and safety of short-term sintilimab in combination with taxane and carboplatin for neoadjuvant therapy in female early-stage triple-negative breast caner patients aging from 18 to 70 years with unilateral and invasive primary lesions above 1cm. The main questions it aims to answer are: 1. Does short-term sintilimab in combination with taxane and carboplatin lead to acceptible pathological complete response (pCR) rates, objective response rates (ORR), event-free survival (EFS) and overall survival (OS)? 2. Does short-term sintilimab in combination with taxane and carboplatin lead to less adverse events than regular-term ICIs reported in literature? Participants will be given 2 cycles of sintilimab, in combination with 4 cycles of taxane and carboplatin before surgery. An optional core-needle biopsy is performed after completing 2 cycles of sintilimab. All participants will be given regular follow-up post surgery according to ASCO guidelines.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05843292
Study type Interventional
Source Shanghai Jiao Tong University School of Medicine
Contact Jiayi Wu
Phone 0086-021-64370045
Email pinkscorpio@163.com
Status Not yet recruiting
Phase Phase 4
Start date July 1, 2023
Completion date December 31, 2034

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