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临床试验/2023-508411-23-00
2023-508411-23-00招募中2 期

PREDIX HER2 - Neoadjuvant response-guided treatment of HER2 positive breast cancer. Part of a platform of translational phase II trials based on molecular subtypes

Karolinska University Hospital9 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2023年10月2日最近更新:

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
200
试验地点
9
主要终点
Pathological objective response to primary medical treatment

研究概览

简要总结

Evaluate the impact of response-guided treatment on objective response and long-term outcome.

入排标准

年龄范围
18 years 至 65+ years(18-64 Years, 65+ Years)
接受健康志愿者

入选标准

  • Written informed consent
  • Patients with breast cancer confirmed by histology, characterized by immunohistochemistry for ER, PR, HER2 and proliferation marker
  • Tumor and blood samples available. HER2 type confirmed by genomic profiling using Next-Generation Sequencing.
  • Age 18 years or older. Elderly patients in condition adequate for planned therapy
  • Primary breast cancer >20mm in diameter and/or verified lymph node metastases
  • Adequate bone marrow, renal, hepatic and cardiac functions and no other uncontrolled medical or psychiatric disorders
  • ECOG performance status 0-1
  • Primary breast cancer as defined in p. 5 plus at most 2 morphologically characterized well-defined distant metastases accessible for stereotactic radiotherapy, provided that this treatment is available.

排除标准

  • Distant metastases, including node metastases in the contralateral thoracic region or in the mediastinum
  • Other malignancy diagnosed within the last five years, except for radically treated basal or squamous cell carcinoma of the skin or CIS of the cervix
  • Patients in child-bearing age without adequate contraception
  • Pregnancy or lactation
  • Uncontrolled hypertension, heart, liver, kidney related or other medical or psychiatric disorders.

结局指标

主要结局

Pathological objective response to primary medical treatment

Pathological objective response to primary medical treatment

次要结局

  • Clinical/radiological objective response during neoadjuvant treatment
  • Morphological, functional and biological characteristics of tumors exposed to cytotoxic and targeted treatment of early breast cancer
  • Event-free survival (EFS), invasive disease-free survival (IDFS), distant disease-free survival (DDFS), breast cancer-specific survival (BCSS) and overall survival (OS)
  • Safety
  • Quality of life
  • Frequency of breast-conserving surgery

研究者

发起方
Karolinska University Hospital
申办方类型
Hospital/Clinic/Other health care facility
责任方
Principal Investigator
主要研究者

Thomas Hatschek

Scientific

Karolinska University Hospital

研究点 (9)

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