Metabolic active tumour volume quantified on [18F]FDG PET/CT further stratifies TNM stage IV non-small cell lung cancer patients

被引:3
作者
Rocha, Ana Luisa Gomes [1 ]
da Conceicao, Mauro Alessandro Monteiro [2 ]
da Cunha Sequeira Mano, Francisco Xavier Proenca [1 ]
Martins, Helder Carvalho [3 ]
Costa, Gracinda Maria Lopes Magalhaes [1 ,2 ]
Dos Santos Oliveiros Paiva, Barbara Cecilia Bessa [4 ,5 ]
Lapa, Paula Alexandra Amado [1 ,2 ]
机构
[1] Univ Coimbra, Fac Med, Azinhaga Santa Comba, P-3000548 Coimbra, Portugal
[2] Ctr Hospitalar Univ Coimbra, Dept Nucl Med, Coimbra, Portugal
[3] Ctr Hospitalar Univ Porto, Dept Nucl Med, Porto, Portugal
[4] Univ Coimbra, Lab Biostatist & Med Informat, Fac Med, Coimbra, Portugal
[5] Univ Coimbra, Coimbra Inst Clin & Biomed Res, Coimbra, Portugal
关键词
Non-small cell lung cancer; TNM staging; PET-CT; Tumour burden; Prognostic factor; PROGNOSTIC VALUE; FDG PET/CT; BURDEN; PARAMETERS; EPIDEMIOLOGY; RECURRENCE; PREDICTS; SURVIVAL; DEATH;
D O I
10.1007/s00432-021-03799-w
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose This study aimed to assess whether the whole body metabolic active tumour volume (MTVWB), quantified on staging [F-18]FDG PET/CT, could further stratify stage IV non-small cell lung cancer (NSCLC) patients. Methods A group of 160 stage IV NSCLC patients, submitted to staging [F-18]FDG PET/CT between July 2010 and May 2020, were retrospectively evaluated. MTVWB was quantified. Univariate and multivariate Cox regressions were carried out to assess correlation with overall survival (OS). C-statistic was used to test predictive power. Kaplan-Meier survival curves with Log-Rank tests were performed to compute statistical differences between strata from dichotomized variables and to calculate the estimated mean survival times (EMST). Survival rates at 1 and 5 years were calculated. Results MTVWB was a statistically significant predictor of OS on univariate (p < 0.0001) and multivariate analyses (p < 0.0001). The multivariate model with MTVWB (Cindex +/- SE = 0.657 +/- 0.024) worked significantly better as an OS predictor than the cTNM model (Cindex +/- SE = 0.544 +/- 0.028) (p = 0.003). An EMST of 29.207 +/- 3.627(95% CI 22.099-36.316) months and an EMST of 10.904 +/- 1.171(95% CI 8.609-13.199) months (Log-Rank p < 0.0001) were determined for patients with MTVWB < 104.3 and MTVWB >= 104.3, respectively. In subsamples of stage IVA (cut-off point = 114.5) and IVB patients (cut-off point = 191.1), statistically significant differences between EMST were also reported, with p-values of 0.0001 and 0.0002, respectively. In both substages and in the entire cohort, patients with MTVWB >= cut-off points had lower EMST and survival rates. Conclusion Baseline MTVWB, measured on staging [F-18]FDG PET/CT, further stratifies stage IV NSCLC patients. This parameter is an independent predictor of OS and provides valuable prognostic information over the 8th edition of cTNM staging.
引用
收藏
页码:3601 / 3611
页数:11
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