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The value of metabolic imaging to predict tumour response after chemoradiation in locally advanced rectal cancer

BACKGROUND: We aim to investigate the possibility of using 18F-positron emission tomography/computer tomography (PET-CT) to predict the histopathologic response in locally advanced rectal cancer (LARC) treated with preoperative chemoradiation (CRT). METHODS: The study included 50 patients with LARC...

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Detalles Bibliográficos
Autores principales: Palma, Pablo, Conde-Muíño, Raquel, Rodríguez-Fernández, Antonio, Segura-Jiménez, Inmaculada, Sánchez-Sánchez, Rocío, Martín-Cano, Javier, Gómez-Río, Manuel, Ferrón, José A, Llamas-Elvira, José M
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3012041/
https://www.ncbi.nlm.nih.gov/pubmed/21159200
http://dx.doi.org/10.1186/1748-717X-5-119
Descripción
Sumario:BACKGROUND: We aim to investigate the possibility of using 18F-positron emission tomography/computer tomography (PET-CT) to predict the histopathologic response in locally advanced rectal cancer (LARC) treated with preoperative chemoradiation (CRT). METHODS: The study included 50 patients with LARC treated with preoperative CRT. All patients were evaluated by PET-CT before and after CRT, and results were compared to histopathologic response quantified by tumour regression grade (patients with TRG 1-2 being defined as responders and patients with grade 3-5 as non-responders). Furthermore, the predictive value of metabolic imaging for pathologic complete response (ypCR) was investigated. RESULTS: Responders and non-responders showed statistically significant differences according to Mandard's criteria for maximum standardized uptake value (SUV(max)) before and after CRT with a specificity of 76,6% and a positive predictive value of 66,7%. Furthermore, SUV(max )values after CRT were able to differentiate patients with ypCR with a sensitivity of 63% and a specificity of 74,4% (positive predictive value 41,2% and negative predictive value 87,9%); This rather low sensitivity and specificity determined that PET-CT was only able to distinguish 7 cases of ypCR from a total of 11 patients. CONCLUSIONS: We conclude that 18-F PET-CT performed five to seven weeks after the end of CRT can visualise functional tumour response in LARC. In contrast, metabolic imaging with 18-F PET-CT is not able to predict patients with ypCR accurately.