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(18)F-FDG PET/CT Metrics Are Correlated to the Pathological Response in Esophageal Cancer Patients Treated With Induction Chemotherapy Followed by Neoadjuvant Chemo-Radiotherapy

BACKGROUND AND OBJECTIVE: The aim of this study was to assess the ability of Fluorodeoxyglucose Positron Emission Tomography/Computed Tomography ((18)F-FDG PET/CT) to provide functional information useful in predicting pathological response to an intensive neoadjuvant chemo-radiotherapy (nCRT) proto...

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Detalles Bibliográficos
Autores principales: Simoni, Nicola, Rossi, Gabriella, Benetti, Giulio, Zuffante, Michele, Micera, Renato, Pavarana, Michele, Guariglia, Stefania, Zivelonghi, Emanuele, Mengardo, Valentina, Weindelmayer, Jacopo, Giacopuzzi, Simone, de Manzoni, Giovanni, Cavedon, Carlo, Mazzarotto, Renzo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7729075/
https://www.ncbi.nlm.nih.gov/pubmed/33330097
http://dx.doi.org/10.3389/fonc.2020.599907
Descripción
Sumario:BACKGROUND AND OBJECTIVE: The aim of this study was to assess the ability of Fluorodeoxyglucose Positron Emission Tomography/Computed Tomography ((18)F-FDG PET/CT) to provide functional information useful in predicting pathological response to an intensive neoadjuvant chemo-radiotherapy (nCRT) protocol for both esophageal squamous cell carcinoma (SCC) and adenocarcinoma (ADC) patients. MATERIAL AND METHODS: Esophageal carcinoma (EC) patients, treated in our Center between 2014 and 2018, were retrospectively reviewed. The nCRT protocol schedule consisted of an induction phase of weekly administered docetaxel, cisplatin, and 5-fluorouracil (TCF) for 3 weeks, followed by a concomitant phase of weekly TCF for 5 weeks with concurrent radiotherapy (50–50.4 Gy in 25–28 fractions). Three (18)F-FDG PET/CT scans were performed: before (PET(1)) and after (PET(2)) induction chemotherapy (IC), and prior to surgery (PET(3)). Correlation between PET parameters [maximum and mean standardized uptake value (SUV(max) and SUV(mean)), metabolic tumor volume (MTV), and total lesion glycolysis (TLG)], radiomic features and tumor regression grade (TGR) was investigated. RESULTS: Fifty-four patients (35 ADC, 19 SCC; 48 cT3/4; 52 cN+) were eligible for the analysis. Pathological response to nCRT was classified as major (TRG1-2, 41/54, 75.9%) or non-response (TRG3-4, 13/54, 24.1%). A major response was statistically correlated with SCC subtype (p = 0.02) and smaller tumor length (p = 0.03). MTV and TLG measured prior to IC (PET(1)) were correlated to TRG1-2 response (p = 0.02 and p = 0.02, respectively). After IC (PET(2)), SUV(mean) and TLG correlated with major response (p = 0.03 and p = 0.04, respectively). No significance was detected when relative changes of metabolic parameters between PET(1) and PET(2) were evaluated. At textural quantitative analysis, three independent radiomic features extracted from PET(1) images ([JointEnergy and InverseDifferenceNormalized of GLCM and LowGrayLevelZoneEmphasis of GLSZM) were statistically correlated with major response (p < 0.0002). CONCLUSIONS: (18)F-FDG PET/CT traditional metrics and textural features seem to predict pathologic response (TRG) in EC patients treated with induction chemotherapy followed by neoadjuvant chemo-radiotherapy. Further investigations are necessary in order to obtain a reliable predictive model to be used in the clinical practice.