HER2-positive breast cancer: 18F-FDG PET for early prediction of response to trastuzumab plus taxane-based neoadjuvant chemotherapy

Purpose To investigate the value of 18 F-fluorodeoxyglucose positron emission tomography ( 18 F-FDG PET/CT) to predict a pathological complete response (pCR) after neoadjuvant chemotherapy (NAC) in women with human epidermal growth factor receptor 2 (HER2)-positive breast cancer. Material and method...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:European journal of nuclear medicine and molecular imaging 2014-08, Vol.41 (8), p.1525-1533
Hauptverfasser: Humbert, Olivier, Cochet, Alexandre, Riedinger, Jean-Marc, Berriolo-Riedinger, Alina, Arnould, Laurent, Coudert, Bruno, Desmoulins, Isabelle, Toubeau, Michel, Dygai-Cochet, Inna, Guiu, Séverine, Coutant, Charles, Fumoleau, Pierre, Brunotte, François
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Purpose To investigate the value of 18 F-fluorodeoxyglucose positron emission tomography ( 18 F-FDG PET/CT) to predict a pathological complete response (pCR) after neoadjuvant chemotherapy (NAC) in women with human epidermal growth factor receptor 2 (HER2)-positive breast cancer. Material and methods Fifty-seven consecutive women with HER2-positive breast cancer, treated with trastuzumab plus taxane-based NAC, were prospectively included. Maximum Standardized Uptake Value of the primary tumor and axillary nodes were measured at baseline (PET 1 .SUV max ) and after the first course of NAC (PET 2 .SUV max ). Tumor metabolic volumes were assessed to determine Total Lesion Glycolysis (TLG). The tumor metabolic response (ΔSUV max and ΔTLG) was calculated. Results In univariate analysis, negative hormonal receptor status ( p  = 0.04), high tumor grade ( p  = 0.03), and low tumor PET 2 .SUV max ( p  = 0.001) were predictive of pCR. Tumor ΔSUV max correlated with pCR ( p  = 0.03), provided that tumors with low metabolic activity at baseline were excluded. ΔTLG did not correlate with pCR. In multivariate analysis, tumor PET 2 .SUV max  
ISSN:1619-7070
1619-7089
DOI:10.1007/s00259-014-2739-1