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Contribution of MRI in the Evaluation of Apparent Diffusion Coefficient and Prediction of Response to Neoadjuvant Chemotherapy in Breast Cancer

Etude ADC Apport de l'IRM Dans l'évaluation du Coefficient de Diffusion Apparent et prédiction de la réponse à la chimiothérapie néoadjuvante Dans le Cancer du Sein

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01956513
Acronym
ADC
Enrollment
0
Registered
2013-10-08
Start date
2012-03-31
Completion date
2013-10-31
Last updated
2013-10-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Assess the Variation of Apparent Diffusion Coefficient

Keywords

ADC, breast cancer, complete pathological response

Brief summary

The main objective of the study is to assess the sensitivity and the specificity of the variation of apparent diffusion coefficient for prediction, after a course of neoadjuvant chemotherapy or after modification of the treatment sequence, the pathological response at the end of chemotherapy

Interventions

MRI will be realised at the beginning of the study, after a cycle of chemotherapy or at changement of sequence and at the end of chemotherapy.

Sponsors

Centre Jean Perrin
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age\> 18 years. * Patient suffering from a breast tumor, regardless of the stage and size * Patient requiring neoadjuvant chemotherapy * Patient has the ability to undergo 18F-FDG-PET at baseline, at end of cycle 1 and at the end of neoadjuvant treatment before surgery * Compulsory affiliation to a social security system. * Obtaining informed consent in writing, signed and dated.

Exclusion criteria

* Patient with cognitive or psychiatric disorders. * Patient deprived of liberty by a court or administrative. * Patient with signs against the achievement of MRI, mammography and ultrasound * Patient metastatic * Patient with prior chemotherapy, radiotherapy and hormone therapy for her breast cancer * Pregnant women, current lactation * Patient suffering from uncontrolled diabetes (\> 11 mmol / L)

Design outcomes

Primary

MeasureTime frame
Variation of apparent diffusion coefficient before / after a cycle of neoadjuvant chemotherapy or before / after modification of the treatment sequence and correlated with histologic responseOne year

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026