跳至主要内容
临床试验/NCT06723990
NCT06723990招募中不适用

Prospective Observational Monocentric Study to Evaluate the Impact of the HER2DX Assay on Treatment Decisions in Patients With Early Stage HER2+ Breast Cancer: the HER2-BREAST-DX

European Institute of Oncology1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年10月24日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
60
试验地点
1
主要终点
Impact of HER2DX on the decision-making processes of the treating physicians and multidisciplinary tumour board, in patients with stage I-III HER2+ BC

研究概览

简要总结

To prospectively evaluate the impact of HER2DX on the decision-making processes of the treating physicians and especially among the routine multidisciplinary tumour board, in defining type and setting of systemic therapy administration in patients with stage I-III HER2+ BC, and the degree of clinician's confidence in the treatment recommendation.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • •Patients ≥ 18 years of age;
  • •Histologically confirmed HER2+ breast cancer;
  • •Stage I-III breast cancer without evidence of distant metastases;
  • •Being candidate to neoadjuvant/adjuvant therapy and locoregional treatment (surgery +/- radiotherapy);
  • •Written informed consent, signed by the patient, to study-specific procedures (the consent will consist of 2 levels: level 1 specifically for patients enrolled in the primary endpoint cohort and level 2 for all patients);

排除标准

  • •HER2- BC;
  • •Stage IV breast cancer;
  • •Lack of informed consent because of patient's incapable of discernment or unwilling to participate;

研究组 & 干预措施

NEOADJUVANT SETTING

Neoadjuvant standard treatment for HER2+: A→Tax +T/P

干预措施: Neoadjuvant standard treatment for HER2+ (Drug)

ADJUVANT SETTING

Adjuvant standard treatment for HER2+ (N0): Tax + T (+/-ET); Adjuvant standard treatment for HER2+ (N+): A→Tax +T/P (+/- ET)

干预措施: Adjuvant standard treatment for HER2+ (Drug)

结局指标

主要结局

Impact of HER2DX on the decision-making processes of the treating physicians and multidisciplinary tumour board, in patients with stage I-III HER2+ BC

时间窗: from baseline to the end of treatment at 12 month

To prospectively evaluate the impact of HER2DX on the decision-making processes of the treating physicians and especially among the routine multidisciplinary tumour board, in defining type and setting of systemic therapy administration in patients with stage I-III HER2+ BC, and the degree of clinician's confidence in the treatment recommendation.

次要结局

未报告次要终点

研究者

发起方
European Institute of Oncology
申办方类型
Other
责任方
Sponsor

研究点 (1)

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