Angiomammography and Neoadjuvant Chemotherapy
Breast NeoplasmsThe 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.
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Conditions de participation
-
Sexe:
FEMALE -
Âges admissibles:
18 and up
Critères de participation
Inclusion Criteria:
* Female aged 18 and over
* Histologically proven breast cancer by large gauge needle
* No evidence of distant metastasis
* Neoadjuvant chemotherapy with or without concomitant targeted therapy
* Breast tumor initially measurable by clinical examination
Exclusion Criteria:
* Refusal to perform the biopsy or surgery
* Pregnant or possibly pregnant woman
* Usual contraindication to contrast product
* Significant kidney failure
* Allergy to contrast medium
* frank hyperthyroidism
* Usual contraindications to MRI
Lieu de l'étude
St-Sacrement Hospital
St-Sacrement HospitalQuebec City, Quebec
Canada
Contactez l'équipe d'étude
- Étude parrainée par
- CHU de Quebec-Universite Laval
- Participants recherchés
- Plus d'informations
- ID de l'étude:
NCT05402930