Recruiting
Neoadjuvant High-Intensity Focused Ultrasound (HIFU) Combined With Toripalimab and Chemotherapy for ER-Positive /HER2-Negative Breast Cancer
The purpose of this study is to evaluate the efficacy and safety of high-intensity focused ultrasound (HIFU) combined with toripalimab and chemotherapy as neoadjuvant therapy for ER+/HER2- breast cancer.
ClinicalTrials.gov IDNCT06964906
PhasePHASE2
Enrollment30
SponsorSecond Affiliated Hospital, Zhejiang University, School of Medicine
Age18 Years
SexFEMALE
Conditions studied
ER+/HER2- Breast Cancer
About this study
The purpose of this study is to evaluate the efficacy and safety of high-intensity focused ultrasound (HIFU) combined with toripalimab and chemotherapy as neoadjuvant therapy for ER+/HER2- breast cancer.
Interventions
- Procedure: HIFU — HIFU therapy is administered to the targeted breast lesion site.
- Drug: Toripalimab — 240 mg, IV infusion, Q3W
- Drug: nab-Paclitaxel (nab-P) — 125 mg/m2, IV infusion, QW
- Drug: Epirubicin (E) — 90 mg/m2, IV infusion, Q3W
- Drug: Cyclophosphamide (C) — 600 mg/m2, IV infusion, Q3W
Primary outcomes
- Total Pathological Complete Response (tpCR) Rate: ypT0/Tis, ypN0 (Up to approximately 30 weeks)
Eligibility information
Inclusion Criteria:
1. Female patients aged 18-75 years.
2. Invasive breast cancer without distant metastasis, including either T1c-T4 (≥ 2 cm), cN0-cN3.
3. Histopathologically confirmed ER-positive/HER2-negative, PR \< 20% or Ki67 ≥ 20%, Grade 3 breast cancer.
4. Eastern Cooperative Oncology Group (ECOG) performance status of 0-1.
Exclusion Criteria:
1. Female patients during pregnancy or lactation.
2. Diagnosis of bilateral breast cancer, occult breast cancer, or distant metastasis confirmed by pathology.
3. Has an active autoimmune disease that has received systemic treatment in the last 2 years.
4. Has a known history of human immunodeficiency virus (HIV), hepatitis B, or known active hepatitis C virus infection.
5. Has received prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent.
6. Has a known history of invasive malignancy that required systemic treatment in the last 5 years.
7. Uncontrolled concomitant diseases include severe infection, liver disease, cardiovascular disease, kidney disease, respiratory disease, diabetes, and others requiring systemic treatment.
Study locations
- 2nd Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang 310000 China
Before you participate: Varda Clinical is an independent discovery tool, not the study sponsor or a medical provider. Eligibility can only be determined by the official study team. Discuss potential risks and benefits with a qualified healthcare professional.
Source: ClinicalTrials.gov. Record last refreshed by Varda Clinical: 2026-09-27.