跳至主要内容
临床试验/NCT05404087
NCT05404087尚未招募不适用

Clinical Evaluation of Contrast Enhanced Breast CT to Improve Staging and Treatment Follow up in Women With Breast Cancer

Radboud University Medical Center0 个研究点目标入组 413 人开始时间: 2022年8月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
413
主要终点
Non-inferiority of CEBCT error rate vs DCE MRI error rate, both as compared to the golden standard for tumor staging.

研究概览

简要总结

Contrast-enhanced breast CT is a novel high resolution and fully 3D imaging method to document abnormalities within the breast. I will establish its value for breast cancer staging and in monitoring therapy response.

详细描述

Breast CT is a novel modality that has not been largely evaluated in a clinical setting. Only recently FDA and CE marked BCT machines have been released, and the number of installed bases internationally is below 10 (although rapidly rising).

Internationally only a few studies on contrast enhanced breast CT have been performed in small numbers of patients, albeit with excellent results. Nevertheless, substantial evidence for this novel modality is still absent. In particular, the correlation of enhancement and histological grade of DCIS, correlation of CEBCT findings with histopathology, and prediction and assessment of primary systemic treatment are open fields for which more substantial evaluation is clearly needed. In this study we want to establish the value of CEBCT in staging of women with breast cancer, particularly those with extensive carcinoma in situ (DCIS), and in the evaluation of women treated with primary systemic therapy.

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
Female
接受健康志愿者

入选标准

  • Diagnoses of breast cancer
  • Scheduled for a pre-surgery staging contrast enhanced breast MRI
  • Eligible for primary systemic therapy

排除标准

  • Women with suspected or confirmed pregnancy
  • Women with prior history of breast cancer
  • Women who are breastfeeding
  • Women who are very frail and unable to cooperate
  • Women who cannot give informed consent
  • Contra indication of iodine contrast (i.e. untreatable contrast allergy, renal function impairment (GFR <60 ml/min/1.73m2))
  • Contra indication for irradiation (i.e. genetic mutation that predispose to breast cancer)
  • Male subjects

结局指标

主要结局

Non-inferiority of CEBCT error rate vs DCE MRI error rate, both as compared to the golden standard for tumor staging.

时间窗: 3 years

Non-inferiority of CEBCT error rate against the golden standard, i.e. histopathology, to DCE MRI error rate against the golden standard for tumor staging. i.e. histopathology, to DCE MRI error rate against the golden standard for tumor staging.

Non-inferiority of CEBCT to predict pCR after primary systemic therapy as compared to DCE MRI.

时间窗: 3 years

Non-inferiority of CEBCT to predict pCR after primary systemic therapy as compared to DCE MRI computed from the area under the receiver operating characteristic (ROC) curve (AUC) (or AUROC).

次要结局

  • Concordance of tumor extent between CEBCT and large section histopathology(3 years)
  • Frequency of detection of contralateral cancers with CEBCT(3 years)
  • Concordance between morphological and enhancement characteristics of cancers on CEBCT to their expected response to primary systemic therapy.(3 years)
  • Potential of CEBCT predicting the response to primary systemic therapy early in treatment(3 years)

研究者

申办方类型
Other
责任方
Sponsor

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