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This study is a multicenter, prospective, observational cohort study, 125 patients with early-stage high-risk breast cancer will be enrolled, perioperative surgical specimens, peripheral blood specimens before and after adjuvant therapy and follow-up will be collected, and the predictive effect of MRD of molecular residual lesions on recurrence events and drug efficacy will be evaluated through dynamic monitoring, so as to further accurately stratify the risk and guide clinical intervention.
Enrollment
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Inclusion criteria
Informed consent signed
Age ≥18 years old
Undergoing breast surgery, the surgical specimen was diagnosed as invasive breast cancer by the central laboratory and met any of the following conditions:
ECOG 0-1
Willing to cooperate in clinical research-related treatment and follow-up, with good patient compliance
Exclusion criteria
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Data sourced from clinicaltrials.gov
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