A Cohort Study of Adjuvant Therapy With Taxane Combined Targeted Therapy for Low-risk HER2 Positive and Lymph Node Negative Breast Cancer
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 285
- 试验地点
- 1
- 主要终点
- invasive disease free survival
研究概览
简要总结
Human epidermal growth factor receptor 2 (HER2) positive breast cancer is a molecular subtype with high malignancy and high risk of recurrence and metastasis. HER2 targeted drugs has greatly improved the prognosis and survival of such patients. At present, for HER2 positive breast cancer patients with negative lymph nodes, chemotherapy drugs combined with trastuzumab is the current standard treatment scheme, and in most cases, chemotherapy uses a combination of two drugs, while the main beneficiaries of the trastuzumab and paltuzumab are concentrated in the group of patients with positive lymph nodes. Can targeted therapy be used to reduce the progression of chemotherapy and further achieve efficient and low toxicity strategies. To explore the efficacy and safety of adjuvant therapy of taxane chemotherapy combined with trastuzumab targeting therapy for low-risk HER2 positive and lymph node negative early breast cancer.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Other
入排标准
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Treatment in Peking University People's Hospital for radical resection of breast cancer and had hospitalization records;
- •Postoperative pathology confirmed invasive breast cancer, and the pathological stage was T1a-b (T ≤ 1cm), N0, HER2 positive, with high-risk factors (G3, or hormone receptor negative); Or the pathological stage is T1c (1cm < T ≤ 2cm), N0, and there are no high-risk factors (G1/G2, hormone receptor positive);
- •Signed an agreement to participate in the PKUPH Breast Disease Cohort study at Peking University People's Hospital.
排除标准
- •Lack of clinical pathological data (such as imaging data, pathological data);
- •Preoperative neoadjuvant therapy;
- •Patients with metastatic breast cancer or bilateral breast cancer;
- •Failed to undergo curative surgery.
结局指标
主要结局
invasive disease free survival
时间窗: 5 years
The time from enrollment to the first occurrence of the following events defined as failure: local recurrence of ipsilateral invasive breast cancer, contralateral invasive breast cancer, distant recurrence or death from any cause.
次要结局
- disease free survival(5 years)
- distant disease free survival(5 years)
- breast cancer specific survival(5 years)
- overall survival(5 years)
研究者
Shu Wang
director of breast center
Peking University People's Hospital