» Articles » PMID: 35983026

M1 Stage Subdivisions Based on F-FDG PET-CT Parameters to Identify Locoregional Radiotherapy for Metastatic Nasopharyngeal Carcinoma

Overview
Specialty Oncology
Date 2022 Aug 19
PMID 35983026
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose: To establish a risk classification of de novo metastatic nasopharyngeal carcinoma (mNPC) patients based on F-fluorodeoxyglucose positron emission tomography/computed tomography (F-FDG PET-CT) radiomics parameters to identify suitable candidates for locoregional radiotherapy (LRRT).

Methods: In all, 586 de novo mNPC patients who underwent 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 + no liver involvement), M1b (intermediate risk, PPS + liver involvement, PPS + low EBV DNA), and M1c (high risk, PPS + high EBV DNA). PCT followed by LRRT displayed favorable OS rates compared to PCT alone in M1a patients ( < 0.001). No significant survival difference was observed between PCT plus LRRT and PCT alone in M1b and M1c patients ( > 0.05).

Conclusions: The PPS-based RPA stratification model could identify suitable candidates for LRRT. Patients with stage M1a disease could benefit from LRRT.

Citing Articles

Pretreatment FDG PET in prognosis of locoregionally advanced nasopharyngeal carcinoma treated with intensity-modulated radiation therapy.

Niu X, Xue F, Ou D, Zheng Y, Hu C, Shen C Int J Med Sci. 2025; 22(4):933-939.

PMID: 39991768 PMC: 11843132. DOI: 10.7150/ijms.105995.


RadShap: An Explanation Tool for Highlighting the Contributions of Multiple Regions of Interest to the Prediction of Radiomic Models.

Captier N, Orlhac F, Hovhannisyan-Baghdasarian N, Luporsi M, Girard N, Buvat I J Nucl Med. 2024; 65(8):1307-1312.

PMID: 38906555 PMC: 11294068. DOI: 10.2967/jnumed.124.267434.


Prognostic value of pre-treatment [F] FDG PET/CT in recurrent nasopharyngeal carcinoma without distant metastasis.

Dong Z, Wang G, Dai D, Qin G, Tang L, Xu C BMC Cancer. 2024; 24(1):466.

PMID: 38622555 PMC: 11017658. DOI: 10.1186/s12885-024-12189-7.

References
1.
Eisenhauer E, Therasse P, Bogaerts J, Schwartz L, Sargent D, Ford R . New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1). Eur J Cancer. 2008; 45(2):228-47. DOI: 10.1016/j.ejca.2008.10.026. View

2.
Chen Y, Chan A, Le Q, Blanchard P, Sun Y, Ma J . Nasopharyngeal carcinoma. Lancet. 2019; 394(10192):64-80. DOI: 10.1016/S0140-6736(19)30956-0. View

3.
You R, Liu Y, Huang P, Zou X, Sun R, He Y . Efficacy and Safety of Locoregional Radiotherapy With Chemotherapy vs Chemotherapy Alone in De Novo Metastatic Nasopharyngeal Carcinoma: A Multicenter Phase 3 Randomized Clinical Trial. JAMA Oncol. 2020; 6(9):1345-1352. PMC: 7378870. DOI: 10.1001/jamaoncol.2020.1808. View

4.
Lemarignier C, Martineau A, Teixeira L, Vercellino L, Espie M, Merlet P . Correlation between tumour characteristics, SUV measurements, metabolic tumour volume, TLG and textural features assessed with F-FDG PET in a large cohort of oestrogen receptor-positive breast cancer patients. Eur J Nucl Med Mol Imaging. 2017; 44(7):1145-1154. DOI: 10.1007/s00259-017-3641-4. View

5.
Pineiro-Fiel M, Moscoso A, Pubul V, Ruibal A, Silva-Rodriguez J, Aguiar P . A Systematic Review of PET Textural Analysis and Radiomics in Cancer. Diagnostics (Basel). 2021; 11(2). PMC: 7926413. DOI: 10.3390/diagnostics11020380. View