The purpose of this study is to evaluate the efficacy and safety of high-intensity focused ultrasound (HIFU) combined with toripalimab plus chemotherapy versus chemotherapy as neoadjuvant therapy for ER+/HER2- breast cancer.
Study participants will be randomly allocated to either the experimental group or the control group and receive the following treatments. Experimental group: HIFU therapy followed by 8 cycles of neoadjuvant immunotherapy and chemotherapy; Control group: 8 cycles of neoadjuvant chemotherapy alone. Each cycle lasts 21 days. Subsequently, all participants will undergo surgery within 6 weeks after completion of neoadjuvant therapy.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
140
HIFU therapy is administered to the targeted breast lesion site.
240 mg, IV infusion, Q3W
125 mg/m2, IV infusion, QW
90 mg/m2, IV infusion, Q3W
600 mg/m2, IV infusion, Q3W
2nd Affiliated Hospital, School of Medicine, Zhejiang University
Hangzhou, Zhejiang, China
RECRUITINGTotal Pathological Complete Response (tpCR) Rate: ypT0/Tis, ypN0
The tpCR rate is defined as the proportion of participants with no residual invasive cancer cells in both the breast primary tumor site (residual in situ cancer cells are permitted) and all sampled axillary lymph nodes.
Time frame: Up to approximately 30 weeks
Breast Pathological Complete Response (bpCR) Rate: ypT0/Tis
The bpCR rate is defined as the proportion of participants with no residual invasive cancer cells in the breast primary tumor site (residual in situ cancer cells are permitted).
Time frame: Up to approximately 30 weeks
Objective Response Rate (ORR)
ORR is defined as the proportion of participants with a complete or partial response.
Time frame: Up to approximately 30 weeks
Event-Free Survival (EFS)
EFS is defined as the time from randomization to any of the following events: precludes surgery, local or distant recurrence, second primary malignancy, or death due to any cause.
Time frame: Approximately five years
Adverse Event (AE)
An AE is defined as any untoward medical occurrence in a study participant administered a medicinal product, temporally associated with study intervention, without presumption of causality.
Time frame: Approximately three years
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