跳至主要内容
临床试验/NL-OMON52473
NL-OMON52473已完成不适用

iquid biopsies and imaging - LIMA

niversitair Medisch Centrum Utrecht0 个研究点目标入组 100 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
100

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 64(—)

入选标准

  • •- Female patients aged 18 years or older
  • •- Histologically proven invasive breast carcinoma
  • •- Planned for neoadjuvant chemotherapy (and in case of a Her2-positive
  • •tumor: addition of trastuzumab and/or pertuzumab)

排除标准

  • •- ER-positive, HER2-negative, B&R grade 1 breast cancer
  • •- Inflammatory breast cancer
  • •- Distant metastases on PET/CT
  • •- Ipsilateral breast cancer in history (contralateral breast cancer >5 years
  • •ago is allowed)
  • •- Other active malignant disease in the past 5 years (excluded squamous cell or
  • •basal cell carcinoma of the skin)
  • •- Pregnant or lactating women.
  • •- Contra-indications for MRI according to standard hospital guidelines.
  • •- Contra-indications for gadolinium-based contrast-agent, including known prior
  • •allergic reaction to any contrastagent, and renal failure, defined by GFR < 30
  • •mL/min/1.73m2.

研究者

发起方
niversitair Medisch Centrum Utrecht

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