Actively Recruiting

Phase Not Applicable
Age: 18Years - 75Years
FEMALE
NCT06879704

Radiological Prediction of Response to Neoadjuvant Chemoimmunotherapy for Triple-negative Breast Cancer

Led by Centre Henri Becquerel · Updated on 2026-01-02

115

Participants Needed

1

Research Sites

235 weeks

Total Duration

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AI-Summary

What this Trial Is About

The aim of our study is to find the best imaging technique, alone or in combination, that can best predict a complete response (absence of tumour cells). It also seems important to identify blood markers able to predict which patients will benefit most from treatment, with a view to personalising them, or which patients will be most at risk of toxicities, particularly related to immunotherapy, with a view to personalising monitoring.

CONDITIONS

Official Title

Radiological Prediction of Response to Neoadjuvant Chemoimmunotherapy for Triple-negative Breast Cancer

Who Can Participate

Age: 18Years - 75Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Signed informed consent
  • Histologically confirmed triple-negative breast cancer
  • Planned to receive neoadjuvant chemo-immunotherapy
  • Age between 18 and 75 years
  • Affiliated with or beneficiary of a social protection scheme
Not Eligible

You will not qualify if you...

  • Pregnant or breastfeeding women
  • Contraindication to immunotherapy
  • Inflammatory breast cancer (T4d)
  • Metastatic disease
  • Allergies to iodine or gadolinium
  • Presence of breast augmentation prosthesis (for angiography/mammography)
  • Claustrophobia
  • Renal contraindication to contrast agents
  • Presence of ferromagnetic material
  • Uncontrolled diabetes (blood glucose >10 mmol/L)
  • Inability to understand or comply with study requirements
  • Under guardianship, curatorship, or judicial protection

AI-Screening

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Trial Site Locations

Total: 1 location

1

Centre Henri Becquerel

Rouen, France, 76038

Actively Recruiting

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Research Team

F

Florian Clatot, MD, PhD

CONTACT

D

Doriane Richard, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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