Liquid Biopsies and Imaging in Breast Cancer

NCT04223492 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 61

Last updated 2023-12-28

No results posted yet for this study

Summary

The aim of the study is to show proof of concept for combining multi-parametric MRI with liquid biopsies in addition to conventional clinical and pathologic information, to accurately predict response to neoadjuvant treatment for patients with primary breast cancer.

Conditions

Interventions

DIAGNOSTIC_TEST

Liquid biopsy

A blood sample containing circulating tumor DNA and circulating tumor cells.

DIAGNOSTIC_TEST

Multi-parametric MRI

Multi-parametric MRI combines different imaging protocols in one session to measure more functional items than perfusion alone, addressing different aspects of tumor biology.

Sponsors & Collaborators

  • Horizon 2020 - European Commission

    collaborator OTHER
  • Philips Electronics Nederland BV

    collaborator INDUSTRY
  • Agena Bioscience GmbH

    collaborator UNKNOWN
  • DiaDx

    collaborator UNKNOWN
  • Stilla Technologies

    collaborator UNKNOWN
  • ANGLE Europe Limited

    collaborator UNKNOWN
  • ALS Automated Lab Solutions GmbH

    collaborator UNKNOWN
  • Institut National de la Santé Et de la Recherche Médicale, France

    collaborator OTHER_GOV
  • Philips GmbH Innovate Technologies

    collaborator UNKNOWN
  • Institut du Cancer de Montpellier - Val d'Aurelle

    collaborator OTHER
  • UMC Utrecht

    lead OTHER

Principal Investigators

  • Kenneth GA Gilhuijs, PhD · UMC Utrecht

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-01-02
Primary Completion
2022-05-16
Completion
2022-05-16

Countries

  • Netherlands

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04223492 on ClinicalTrials.gov