NCT06704945招募中3 期
No Axillary Surgical Treatment in Clinically Lymph Node Negative Patients on Ultrasonography After Neoadjuvant Chemotherapy: A Prospective, Phase III Clinical Trial
适应症
干预措施
试验速览
- 阶段
- 3 期
- 状态
- 招募中
- 入组人数
- 464
- 试验地点
- 1
- 主要终点
- Invasive Disease Free Survival (iDFS)
研究概览
简要总结
NEO-NAUTILUS is a prospective, multicenter, randomized phase III clinical trial to evaluate whether omitting axillary lymph node surgery (ALND or SLNB) in clinically lymph node-negative breast cancer patients after neoadjuvant chemotherapy is non-inferior to performing SLNB in terms of 5-year disease-free survival.
详细描述
Background:
- No prospective studies have proven that axillary lymph node surgery improves survival in breast cancer patients.
- The ACOSOG Z0011 trial showed that additional axillary dissection did not improve recurrence or survival, even with a 23.7% incidence of non-sentinel node metastases.
- NSABP B-32 established the oncologic safety of SLNB, significantly reducing complications like lymphedema compared to axillary dissection. However, SLNB still carries risks of lymphedema, sensory changes, seromas, and infections.
- The trend has now shifted toward identifying candidates for omitting axillary surgery to minimize unnecessary complications.
- The SOUND trial demonstrated non-inferiority of omitting SLNB in early-stage breast cancer patients with negative axillary ultrasound. Five-year distant metastasis-free survival was comparable between SLNB and no-SLNB groups (97.7% vs. 98.0%).
- Improved ultrasound accuracy (e.g., FNR: 13.7% in SOUND; 11.3% in NAUTILUS) and the therapeutic contribution of whole-breast radiation likely support these findings.
- Patients with a complete pathological response (pCR) in the breast post-NAC rarely have residual lymph node metastases, reducing the need for axillary surgery.
- Single-arm studies (e.g., EUBREAST-01, ASICS, ASLAN) have explored omitting axillary surgery in patients with confirmed breast pCR. However, these studies face limitations due to small sample sizes, single-arm design, and the necessity of axillary surgery if pCR is not achieved.
- To address these limitations, the NEO-NAUTILUS trial proposes the first randomized trial to compare disease-free survival and local recurrence rates between patients who omit SLNB (experimental group) and those who undergo SLNB (control group) after NAC, focusing on patients deemed axillary node-negative by ultrasound.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Single (Outcomes Assessor)
入排标准
- 年龄范围
- 19 Years 至 —(Adult, Older Adult)
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Women aged ≥19 years.
- •Histologically confirmed invasive breast carcinoma treated with neoadjuvant chemotherapy.
- •Clinical staging prior to NAC: cT1-3, cN0, M0 (AJCC 8th Edition).
- •If pre-NAC staging is cT1-3, cN1, M0, must meet the following criteria:
- •HER2-positive or triple-negative breast cancer (TNBC).
- •At least 30% reduction in tumor size on MRI after NAC (comparing pre- and post-NAC MRI).
- •Negative axillary lymph node status on ultrasound after NAC.
- •Planned for breast-conserving surgery with completed neoadjuvant chemotherapy (at least half the planned regimen must be completed).
- •ECOG performance status of 0-
- •Signed written informed consent before enrollment.
排除标准
- •History of any cancer within the past 5 years.
- •Bilateral breast cancer.
- •Patients requiring mastectomy.
- •Tumor size >5 cm after NAC.
- •Male breast cancer.
- •Pregnant or breastfeeding women.
- •Inability to understand and complete questionnaires.
研究组 & 干预措施
No SLNB group
Experimental
The study arm - BCS without SLNB
干预措施: No axillary surgery (Procedure)
SLNB group
Other
The control arm - BCS with SLNB(+/-ALND)
干预措施: Axillary surgery (Procedure)
结局指标
主要结局
Invasive Disease Free Survival (iDFS)
时间窗: 5 years
Evaluate invasive disease free survivals
次要结局
- Overall Survival (OS)(5 years)
- Distant Metastasis Free Survival (DMFS)(5 years)
- Axillary recurrence rate(5 years)
- Locoregional Recurrence Rate (LRR)(5 years)
- QoL(1 year)
研究者
Wonshik Han
Professor
Seoul National University Hospital
研究点 (1)
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