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M1 stage subdivisions based on (18)F-FDG PET-CT parameters to identify locoregional radiotherapy for metastatic nasopharyngeal carcinoma
PURPOSE: To establish a risk classification of de novo metastatic nasopharyngeal carcinoma (mNPC) patients based on (18)F-fluorodeoxyglucose positron emission tomography/computed tomography ((18)F-FDG PET-CT) radiomics parameters to identify suitable candidates for locoregional radiotherapy (LRRT)....
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9379565/ https://www.ncbi.nlm.nih.gov/pubmed/35983026 http://dx.doi.org/10.1177/17588359221118785 |
Sumario: | PURPOSE: To establish a risk classification of de novo metastatic nasopharyngeal carcinoma (mNPC) patients based on (18)F-fluorodeoxyglucose positron emission tomography/computed tomography ((18)F-FDG PET-CT) radiomics parameters to identify suitable candidates for locoregional radiotherapy (LRRT). METHODS: In all, 586 de novo mNPC patients who underwent (18)F-FDG PET-CT prior to palliative chemotherapy (PCT) were involved. A Cox regression model was performed to identify prognostic factors for overall survival (OS). Candidate PET-CT parameters were incorporated into the PET-CT parameter score (PPS). Recursive partitioning analysis (RPA) was applied to construct a risk stratification system. RESULTS: Multivariate Cox regression analyses revealed that total lesion glycolysis of locoregional lesions (LRL-TLG), the number of bone metastases (BMs), metabolic tumor volume of distant soft tissue metastases (DSTM-MTV), pretreatment Epstein–Barr virus DNA (EBV DNA), and liver involvement were independent prognosticators for OS. The number of BMs, LRL-TLG, and DSTM-MTV were incorporated as the PPS. Eligible patients were divided into three stages by the RPA-risk stratification model: M1a (low risk, PPS(low) + no liver involvement), M1b (intermediate risk, PPS(low) + liver involvement, PPS(high) + low EBV DNA), and M1c (high risk, PPS(high) + high EBV DNA). PCT followed by LRRT displayed favorable OS rates compared to PCT alone in M1a patients (p < 0.001). No significant survival difference was observed between PCT plus LRRT and PCT alone in M1b and M1c patients (p > 0.05). CONCLUSIONS: The PPS-based RPA stratification model could identify suitable candidates for LRRT. Patients with stage M1a disease could benefit from LRRT. |
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