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Pre-CCRT 18-fluorodeoxyglucose PET-CT improves survival in patients with advanced stages p16-negative oropharyngeal squamous cell carcinoma via accurate radiation treatment planning

PURPOSE: No large-scale prospective randomized study with a long-term follow-up period has evaluated the survival outcomes of preconcurrent chemoradiotherapy (CCRT) 18-fluorodeoxyglucose positron emission tomography–computed tomography ((18)FDG PET–CT) in patients with non–human papillomavirus (HPV)...

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Detalles Bibliográficos
Autores principales: Chen, Tsung-Ming, Chen, Wan-Ming, Chen, Mingchih, Shia, Ben-Chang, Wu, Szu-Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9926577/
https://www.ncbi.nlm.nih.gov/pubmed/36782296
http://dx.doi.org/10.1186/s40463-023-00623-y
Descripción
Sumario:PURPOSE: No large-scale prospective randomized study with a long-term follow-up period has evaluated the survival outcomes of preconcurrent chemoradiotherapy (CCRT) 18-fluorodeoxyglucose positron emission tomography–computed tomography ((18)FDG PET–CT) in patients with non–human papillomavirus (HPV)-associated oropharyngeal squamous cell carcinoma (OPSCC). PATIENTS AND METHODS: We included patients with stage I–IVA p16-negative OPSCC receiving definitive CCRT and categorized them into two groups according to pre-CCRT (18)FDG PET–CT and compared their outcomes: the case group consisted of patients who underwent pre-CCRT (18)FDG PET–CT, whereas the comparison group consisted of patients who did not receive pre-CCRT (18)FDG PET–CT. RESULTS: The final cohort consisted of 3942 patients (1663 and 2279 in the case and comparison groups, respectively). According to multivariable Cox regression analysis, pre-CCRT (18)FDG PET–CT was not a significant prognostic factor for overall survival in patients with stages I–II of p16-negative OPSCC receiving standard CCRT. The adjusted hazard ratio (95% confidence interval) of all-cause death for the patients with advanced stages (III–IVA) of p16-negative OPSCC receiving pre-CCRT (18)FDG PET–CT was 0.75 (0.87–0.94, P = 0.0236). CONCLUSIONS: Routine use of pre-CCRT (18)FDG PET–CT is not necessary for each patient with p16-negative OPSCC. Pre-CCRT (18)FDG PET–CT is associated with improved survival in patients with stage III–IVA p16-negative OSCC, but might be not in those with stage I–II p16-negative OPSCC. CONDENSED ABSTRACT: No large-scale prospective randomized study with a long-term follow-up period has evaluated the survival outcomes of preconcurrent chemoradiotherapy (CCRT) 18-fluorodeoxyglucose positron emission tomography–computed tomography ((18)FDG PET–CT) in patients with p16-negative oropharyngeal squamous cell carcinoma (OPSCC). Our study is the first, largest, homogenous modality study on PET–CT including a long-term follow-up cohort to examine the survival outcomes of pre-CCRT (18)FDG PET–CT or non-pre-CCRT PET–CT for patients with p16-negative OPSCC receiving standard CCRT stratified by different clinical stages. Routine use of pre-CCRT (18)FDG PET–CT is not necessary for each patient with p16-negative OPSCC. Pre-CCRT (18)FDG PET–CT is associated with improved survival in patients with stage III–IVA p16-negative OPSCC, but might be not in those with stage I–II p16-negative OPSCC.