Multifactorial risk factors for mortality after chemotherapy and radiotherapy for non-small cell lung cancer

被引:29
作者
Defraene, Gilles [1 ]
Dankers, Frank J. W. M. [2 ,3 ]
Price, Gareth [4 ]
Schuit, Ewoud [5 ]
van Elmpt, Wouter [3 ]
Arredouani, Soumia [1 ]
Lambrecht, Maarten [1 ]
Nuyttens, Joost [6 ]
Faivre-Finn, Corinne [4 ]
De Ruysscher, Dirk [1 ,3 ]
机构
[1] KU Leuven Univ Leuven, Dept Oncol, Expt Radiat Oncol, B-3000 Leuven, Belgium
[2] Radboud Univ Nijmegen, Dept Radiat Oncol, Med Ctr, Nijmegen, Netherlands
[3] Maastricht Univ, Med Ctr, GROW Sch Oncol & Dev Biol, Dept Radiat Oncol MAASTRO, Maastricht, Netherlands
[4] Univ Manchester, Christie NHS Fdn Trust, Div Canc Sci, Manchester, Lancs, England
[5] Univ Utrecht, Univ Med Ctr Utrecht, Julius Ctr Hlth Sci & Primary Care, Utrecht, Netherlands
[6] Erasmus MC Canc Inst, Dept Radiotherapy, Rotterdam, Netherlands
关键词
Mean heart dose; Overall survival; Prediction model; Lung cancer; Proton therapy; RADIATION-THERAPY; DOSE-ESCALATION; TUMOR VOLUME; SECONDARY ANALYSIS; PROGNOSTIC-FACTOR; PROTON THERAPY; PHASE-III; RTOG; 0617; STAGE; HEART;
D O I
10.1016/j.radonc.2019.09.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background and purpose: A higher radiation dose to the heart is known to be associated with increased mortality in non-small cell lung cancer (NSCLC) patients. It is however unknown what the contribution of the heart dose is when other risk factors for mortality are also accounted for. Materials and methods: We constructed and externally validated prediction models of mortality after definitive chemoradiotherapy for NSCLC. Models were developed in 145 stage I-IIIB NSCLC patients. Clinical (performance status, age, gross tumour volume (GTV) combining primary tumour and involved lymph nodes, current smoker) and dosimetric (mean lung (MLD) and heart (MHD) dose) variables were considered. Multivariable logistic regression models predicting 12 and 24 month mortality were built in 5-fold cross-validation. Discrimination and calibration was assessed in 3 external validation datasets containing 878 (via distributed learning), 127 and 96 NSCLC patients. Results: The best discriminating prediction models combined GTV, smoker and/or MHD: bootstrapping AUC (95% CI) of 0.74 (0.66-0.78) and 0.69 (0.55-0.74) at 12 and 24 months. At external validation, the 24 month mortality GTV-smoker-MHD model robustly showed moderate discrimination (AUC = 0.61- 0.64 before and 0.64-0.65 after model update) with limited 0.01-0.07 improvement over a GTV-only model, and calibration slope (0.64-0.65). This model can identify patients for whom a MHD reduction may be useful (e.g. PPV = 77%, NPV = 52% (60% cut-off)). Conclusions: Tumour volume is strongly related to mortality risk in the first 2 years after chemoradiotherapy for NSCLC. Modelling indicates that efforts to reduce cardiac dose may be relevant for small tumours and that smoking has an important negative association with survival. (C) 2019 Elsevier B.V. All rights reserved.
引用
收藏
页码:117 / 125
页数:9
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