Prediction of Severe Lymphopenia During Chemoradiation Therapy for Esophageal Cancer: Development and Validation of a Pretreatment Nomogram

被引:58
作者
van Rossum, Peter S. N. [1 ,2 ]
Deng, Wei [1 ]
Routman, David M. [3 ]
Liu, Amy Y. [4 ]
Xu, Cai [1 ]
Shiraishi, Yutaka [1 ]
Peters, Max [2 ]
Merrell, Kenneth W. [3 ]
Hallemeier, Christopher L. [3 ]
Mohan, Radhe [4 ]
Lin, Steven H. [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Radiat Oncol, Houston, TX 77030 USA
[2] Univ Med Ctr Utrecht, Dept Radiat Oncol, Utrecht, Netherlands
[3] Mayo Clin, Dept Radiat Oncol, Rochester, MN USA
[4] Univ Texas MD Anderson Canc Ctr, Dept Radiat Phys, Houston, TX 77030 USA
关键词
MODULATED RADIATION-THERAPY; GROWTH-FACTOR-BETA; SURVIVAL OUTCOMES; LYMPHOCYTE COUNT; PROTON THERAPY; VOLUME; RADIOTHERAPY; ASSOCIATION; CONCURRENT; CHEMORADIOTHERAPY;
D O I
10.1016/j.prro.2019.07.010
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: In patients with esophageal cancer, occurrence of severe radiation-induced lymphopenia during chemoradiation therapy has been associated with worse progression-free and overall survival. The aim of this study was to develop and validate a pretreatment clinical nomogram for the prediction of grade 4 lymphopenia. Methods and Materials: A development set of consecutive patients who underwent chemoradiation therapy for esophageal cancer and an independent validation set of patients from another institution were identified. Grade 4 lymphopenia was defined as an absolute lymphocyte count nadir during chemoradiation therapy of <0.2 x 10(3)/mu L. Multivariable logistic regression analysis was used to create a prediction model for grade 4 lymphopenia in the development set, which was internally validated using bootstrapping and externally validated by applying the model to the validation set. The model was presented as a nomogram yielding 4 risk groups. Results: Among 860 included patients, 322 (37%) experienced grade 4 lymphopenia. Higher age, larger planning target volume in interaction with lower body mass index, photon-rather than proton-based therapy, and lower baseline absolute lymphocyte count were predictive in the final model (corrected c-statistic, 0.76). External validation in 144 patients, among whom 58 (40%) had grade 4 lymphopenia, yielded a c-statistic of 0.71. Four nomogram-based risk groups yielded predicted risk rates of 10%, 24%, 43%, and 70%, respectively. Conclusions: A pretreatment clinical nomogram was developed and validated for the prediction of grade 4 radiation-induced lymphopenia during chemoradiation therapy for esophageal cancer. The nomogram can risk stratify individual patients suitable for lymphopenia-mitigating strategies or potential future therapeutic approaches to ultimately improve survival. (C) 2019 American Society for Radiation Oncology. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:E16 / E26
页数:11
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