RecruitingPhase 2NCT07394387

Neoadjuvant Study of HIFU With or Without PD-1 Inhibitors Followed by Abraxane Plus Carboplatin in Triple-Negative Breast Cancer.

A Single-Center, Phase II Clinical Study of HIFU With or Without PD-1 Inhibitors Followed by Abraxane Plus Carboplatin Neoadjuvant Therapy in Triple-Negative Breast Cancer.


Sponsor

The First Affiliated Hospital with Nanjing Medical University

Enrollment

39 participants

Start Date

Jan 1, 2025

Study Type

INTERVENTIONAL

Summary

Background: Triple-negative breast cancer (TNBC) is an aggressive type of breast cancer with limited treatment options. Research suggests that using High-Intensity Focused Ultrasound (HIFU) to destroy the tumor and/or PD-1 inhibitor drugs to activate the immune system before starting chemotherapy may improve treatment effectiveness. This study aims to investigate this new approach. Objective: To evaluate the effectiveness and safety of using HIFU, with or without a PD-1 inhibitor (Sintilimab), before and during combination chemotherapy in patients with early-stage TNBC. The primary goal is to determine if this strategy can increase the rate of pathological complete response (pCR). Study Design: This is a single-center, Phase II clinical study. Approximately 40 participants with Stage II-III TNBC will be enrolled and assigned to one of two groups (cohorts) without randomization: Cohort A: Receives HIFU treatment. Two weeks later, begins standard chemotherapy (Abraxane and carboplatin) combined with the PD-1 inhibitor Sintilimab for 6 cycles. Cohort B: Receives HIFU treatment combined with a single dose of the PD-1 inhibitor Sintilimab. Two weeks later, begins the same 6 cycles of chemotherapy (Abraxane and carboplatin) combined with Sintilimab. Main Measures: The primary measure is the rate of pathological complete response (pCR), defined as the absence of invasive cancer in the breast and lymph nodes after surgery following the completion of neoadjuvant therapy. Other important measures include: The ability of the treatment to activate the immune system (measured by changes in CD8+ T cells or IFN-γ). The percentage of patients whose tumors shrink significantly (Objective Response Rate). How long patients live without their cancer getting worse (Event-Free Survival). The rate of patients who can undergo breast-conserving surgery. The frequency and severity of side effects.


Eligibility

Sex: FEMALEMin Age: 18 YearsMax Age: 70 Years

Plain Language Summary

Simplified for easier understanding

This trial is testing whether adding HIFU (high-intensity focused ultrasound, a non-invasive tumor-ablating technique) and/or a PD-1 immunotherapy drug before standard neoadjuvant chemotherapy (nab-paclitaxel plus carboplatin) improves outcomes in women with triple-negative breast cancer (TNBC) — a particularly aggressive subtype. **You may be eligible if...** - You are a woman aged 18 to 65 - You have been confirmed to have invasive triple-negative breast cancer (TNBC), stage II or III, by biopsy - You have not received any prior breast cancer treatment - Your general health is good (ECOG 0–1) and you have adequate blood counts and organ function - You have at least one measurable tumor **You may NOT be eligible if...** - You have already received chemotherapy, radiation, surgery, or immunotherapy for this cancer - Your cancer is stage I or has spread to distant organs (stage IV) - You have serious heart problems - You are pregnant or breastfeeding Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGSintilimab

200 mg, administered intravenously every 3 weeks.

DRUGAbraxane

260 mg/m², administered intravenously on Day 1 of each 21-day cycle.

DRUGCarboplatin

AUC = 6, administered intravenously on Day 1 of each 21-day cycle.

PROCEDUREHigh-intensity focused ultrasound (HIFU)

HIFU sparse scanning. Under ultrasound guidance, the tumor and a 5mm margin of surrounding normal tissue are ablated using a point-by-point protocol (150W power, 3s irradiation per point, 5mm point spacing). Performed once.


Locations(1)

The First Affiliated Hospital with Nanjing Medical University

Nanjing, Jiangsu, China

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NCT07394387