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临床试验/NCT06711068
NCT06711068招募中不适用

Cohort Study of Adjuvant Chemotherapy Combined With Targeted Therapy for Intermediate Risk HER2 Positive and Lymph Node Negative Early Breast Cancer

Shu Wang1 个研究点 分布在 1 个国家目标入组 8,077 人开始时间: 2019年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
8,077
试验地点
1
主要终点
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 easy recurrence and metastasis. The emergence of 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 pertuzumab 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. It is planned to explore the efficacy and safety of T1-T2, HER2 positive early breast cancer patients with negative lymph nodes to achieve chemotherapy reduction based on risk stratification.

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
All
接受健康志愿者

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 T1c, N0, HER2 positive, with other high-risk factors (G3, or hormone receptor negative); Or the pathological stage is T2, N0, and there are no high-risk factors (G3, or hormone receptor negative);
  • 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

disease free survival

时间窗: 3 years

The time from enrollment to the first occurrence of the following events defined as failure, including ipsilateral local recurrence, contralateral breast cancer, distant recurrence or death from any cause.

次要结局

  • invasive disease free survival(3 years)
  • distant disease free survival(3 years)
  • breast cancer specific survival(3 years)
  • overall survival(3 years)

研究者

发起方
Shu Wang
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Shu Wang

director of breast center

Peking University People's Hospital

研究点 (1)

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