跳至主要内容
临床试验/NCT05314114
NCT05314114招募中不适用

Selective Omission of Axillary Surgery in Distinct Responders With Triple-negative and HER2-positive Breast Cancer After NACT

Peking University1 个研究点 分布在 1 个国家目标入组 136 人开始时间: 2020年7月3日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
136
试验地点
1
主要终点
ipsilateral axillary recurrence-free survival

研究概览

简要总结

Neoadjuvant chemotherapy (NACT) is standard treatment for many triple-negative (TNBC) and HER2-positive breast cancer. Study showed about half of the biopsy-proven axillary disease will be eradicated by NACT and converted to ypN0 indicating the efficacy of systemic treatment in local disease control.

According to current guidelines, all initial cN0 patients will undergo sentinel lymph node biopsy (SLNB) after NACT and further axillary dissection (ALND) if tumor residual is discovered after SLNB. Data suggest patients who underwent SLNB have a significantly higher rate of disability in the early post-operative period compared to patients who did not and the avoidance of SLNB might translate into a considerable reduction of physical and emotional distress. Recent studies revealed the association between breast pCR and ypN0 status after NACT. Initially cN0 TNBC and HER2-positive breast cancer patients who achieve pCR in breast after NACT have a very low risk of positive lymph node residual and are very unlikely to benefit from further axillary surgery including SLNB.

The investigators designed a clinical trial to test the hypothesis that selective omission of axillary surgery in distinct responders after NACT will not deteriorate survival. In the planned trial, axillary surgery will be completely eliminated for initially cN0 TNBC and HER2-positive breast cancer patients who achieve pCR in breast after NACT determined by lumpectomy.

The trial is designed as a prospective, single-center, single-arm study with a limited number of patients (N=136). Patients will be recruited in China over a period of 36 months. Our results, together with other ongoing studies in other parts of the world with a similar design, might give practice-changing results and spare the time and the costs of a randomized comparison.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
Female
接受健康志愿者
否

入选标准

  • •Written informed consent
  • •Core biopsy confirmed unicentric primary invasive triple-negative or HER2-positive breast cancer. Multifocal or multicentric tumors allowed only if breast-conserving surgery is deemed feasible.
  • •At least 18 years of age
  • •Initial tumor stage cT1c-T3N0M0 prior to NACT. cN0 stage established by clinical examination and ultrasonography
  • •In cases with suspicious lymph node, a negative core biopsy or fine needle aspiration (FNA) biopsy of the sonographically suspected lymph node is required
  • •Standard NACT with evident radiologic response
  • •Planned breast-conserving surgery with postoperative external whole-breast irradiation

排除标准

  • •History of previous malignancy
  • •Histologically proven N1 patients, patients with distant metastasis (M1)
  • •Pregnant or lactating patients
  • •Inflammatory breast cancer
  • •Radiologically non-responsive after NACT
  • •Mastectomy planned after NACT
  • •planned intraoperative radiotherapy (e.g. Intrabeam) or postoperative partial breast irradiation (e.g. multicatheter technique) alone; both procedures are allowed as boost techniques
  • •Written informed consent not obtained

研究组 & 干预措施

No Axillary Surgery

Experimental

No axillary surgery including SLNB

干预措施: No axillary surgery (Procedure)

结局指标

主要结局

ipsilateral axillary recurrence-free survival

时间窗: 5-year

time between randomization and confirmed ipsilateral axillary recurrence

次要结局

  • distant metastasis-free survival(5-year)
  • locoregional lymph node recurrence-free survival(5-year)

研究者

发起方
Peking University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Tao OUYANG

Professor, Director of the Breast Cancer Department

Peking University

研究点 (1)

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