Use of pretreatment metabolic tumour volumes to predict the outcome of pharyngeal cancer treated by definitive radiotherapy

被引:51
作者
Kao, Chia-Hung [1 ,2 ,4 ,5 ]
Lin, Shih-Chieh [3 ]
Hsieh, Te-Chun [1 ,2 ]
Yen, Kuo-Yang [1 ,2 ,8 ]
Yang, Shih-Neng [3 ,8 ]
Wang, Yao-Ching [3 ]
Liang, Ji-An [3 ,4 ,5 ]
Hua, Chun-Hung [9 ]
Chen, Shang-Wen [3 ,4 ,5 ,6 ,7 ]
机构
[1] China Med Univ Hosp, Dept Nucl Med, Taichung 404, Taiwan
[2] China Med Univ Hosp, PET Ctr, Taichung 404, Taiwan
[3] China Med Univ Hosp, Dept Radiat Oncol, Taichung 404, Taiwan
[4] China Med Univ, Coll Med, Inst Clin Med Sci, Taichung, Taiwan
[5] China Med Univ, Coll Med, Sch Med, Taichung, Taiwan
[6] Taipei Med Univ, Inst Clin Med Sci, Taipei, Taiwan
[7] Taipei Med Univ, Sch Med, Taipei, Taiwan
[8] China Med Univ, Dept Biomed Imaging & Radiol Sci, Taichung, Taiwan
[9] China Med Univ Hosp, Dept Otorhinolaryngol, Taichung 404, Taiwan
关键词
FDG PET/CT; Pharyngeal carcinoma; Radiotherapy; Metabolic tumour volume; Prognostic factor; STANDARDIZED UPTAKE VALUE; POSITRON-EMISSION-TOMOGRAPHY; SQUAMOUS-CELL CARCINOMA; NECK-CANCER; FDG-PET; HUMAN-PAPILLOMAVIRUS; LUNG-CANCER; NASOPHARYNGEAL CARCINOMAS; OROPHARYNGEAL CANCER; RADIATION-THERAPY;
D O I
10.1007/s00259-012-2127-7
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
The aim of the study was to investigate the predictive role of pretreatment metabolic volume (MTV) in pharyngeal cancer (PC) patients treated with definitive (chemo) radiotherapy. This retrospective analysis enrolled 64 patients with PC treated with (chemo) radiotherapy. All patients received pretreatment fluorodeoxyglucose (FDG) positron emission tomography (PET)/CT. Four PET segmentation methods were used, namely applying an isocontour at a standardized uptake value (SUV) of either 2.5 or 3.0 (MTV2.5 and MTV3.0) or using fixed thresholds of either 40 or 50 % (MTV40 %, MTV50 %) of the maximum intratumoural FDG activity. Disease-free survival (DFS) and primary relapse-free survival (PRFS) were examined according to cutoffs of the median values for each MTV and the gross tumour volume (GTVp). Independent prognosticators were identified by Cox regression analysis. With a median follow-up of 24 months, 19 patients died, and 26 patients experienced tumour relapse at primary sites. Multivariate analysis of the DFS showed that MTV2.5 > 13.6 ml was the only predictor of relapse [p = 0.011, hazard ratio = 2.69, 95 % confidence interval (CI) 1.25-5.76]. The independent predictor for PRFS was MTV2.5 > 13.6 ml (p = 0.003, hazard ratio = 3.76, 95 % CI 1.57-8.92), whereas GTVp > 15.5 ml had a marginal impact on PRFS (p = 0.06, hazard ratio = 3.54, 95 % CI 0.97-11.85). Patients having tumours with MTV2.5 > 13.6 ml had a significantly inferior 2-year PRFS compared with patients who had lower MTV2.5 tumours (39 vs 72 %, respectively, p = 0.001). For PC patients treated with definitive (chemo)radiotherapy, pretreatment MTV2.5 volume achieved the best predictive value for primary recurrence, and the same value was also a prognosticator for DFS.
引用
收藏
页码:1297 / 1305
页数:9
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