Clinical Trials Directory

Trials / Completed

CompletedNCT05402930

Angiomammography and Neoadjuvant Chemotherapy

Usefulness of Angiomammography for Predicting the Response to Neoadjuvant Chemotherapy in Breast Cancer

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
67 (actual)
Sponsor
CHU de Quebec-Universite Laval · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

The best prognostic factor following neoadjuvant chemotherapy is the pathological complete response (pCR). pCR is defined as the absence of invading cells in the breast and lymph nodes following neoadjuvant chemotherapy treatment. Since patients with pCR have a better prognosis than those without pCR, some studies have evaluated different methods to predict pCR early in treatment. Thus, patients who do not respond optimally to treatment could be identified early and changed treatment in order to maximize the chances of pCR and avoid the morbidity of poorly effective treatments. To do this, several modalities have been proposed, including MRI, mammography, ultrasound, positron emission tomography, elastography, and serial biopsies, but these techniques have shown predictive and sometimes expensive. Nevertheless, assessment of tumor response after cycle 2 has been suggested to be appropriate for the prediction of pCR. The main objective of this study is to compare the performance of two diagnostic modalities, namely CESM and MRI, in the evaluation of the response of a malignant breast tumor to neoadjuvant chemotherapy and the prediction of pCR. The radiological response will also be compared to the clinical response.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTAngiomammographyPatients will receive their care in a standard manner. Breast MRI is one modality used by physicians to monitor response to neoadjuvant chemotherapy and will therefore be used as standard. A CESM exam will be added at the same time as the MRI. Patients will have a physical exam, breast MRI and CESM before the start of chemotherapy (less than 2 weeks). These examinations will be repeated after cycle 2 (±1 week) and at the end of chemotherapy. After each cycle of chemotherapy, the tumor will be measured in two axes by the attending physician. Histological examination of the surgical specimen will be used to determine the pCR. Responses observed on MRI and CESM will be compared to pCR.

Timeline

Start date
2018-01-03
Primary completion
2025-12-31
Completion
2025-12-31
First posted
2022-06-02
Last updated
2026-03-19

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT05402930. Inclusion in this directory is not an endorsement.