Severe radiation-induced lymphopenia during concurrent chemoradiotherapy for stage III non-small cell lung cancer: external validation of two prediction models

被引:2
|
作者
van Rossum, Peter S. N. [1 ,2 ]
Juan-Cruz, Celia [1 ]
Stam, Barbara [1 ]
Rossi, Maddalena M. G. [1 ]
Lin, Steven H. [3 ]
Abravan, Azadeh [4 ,5 ]
Belderbos, Jose S. A. [1 ]
Sonke, Jan-Jakob [1 ]
机构
[1] Antoni van Leeuwenhoek Hosp, Netherlands Canc Inst, Dept Radiat Oncol, Amsterdam, Netherlands
[2] Univ Amsterdam, Dept Radiat Oncol, Med Ctr, Amsterdam, Netherlands
[3] Univ Texas MD Anderson Canc Ctr, Dept Radiat Oncol, Houston, TX USA
[4] Univ Manchester, Sch Med Sci, Div Canc Sci, Fac Biol Med & Hlth, Manchester, England
[5] Christie Natl Hlth Serv NHS Fdn Trust, Dept Radiotherapy Related Res, Manchester, England
来源
FRONTIERS IN ONCOLOGY | 2023年 / 13卷
关键词
lung cancer; radiotherapy; chemoradiotherapy; lymphopenia; hematologic toxicity; SURVIVAL; CHEMORADIATION; RADIOTHERAPY; ASSOCIATION; THERAPY; PROTON;
D O I
10.3389/fonc.2023.1278723
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundSevere radiation-induced lymphopenia (RIL) in patients undergoing chemoradiotherapy (CRT) for non-small cell lung cancer (NSCLC) is associated with decreased immunotherapy efficacy and survival. At The Christie and MD Anderson Cancer Center (MDACC), prediction models for lymphopenia were developed in lung and esophageal cancer patients, respectively. The aim of this study was to externally validate both models in patients with stage III NSCLC.MethodsPatients who underwent concurrent CRT for stage III NSCLC in 2019-2021 were studied. Outcomes were grade >= 3 and grade 4 lymphopenia during CRT. The Christie model predictors for grade >= 3 lymphopenia included age, baseline lymphocyte count, radiotherapy duration, chemotherapy, mean heart and lung doses, and thoracic vertebrae V20Gy. MDACC predictors for grade 4 lymphopenia were age, baseline lymphocyte count, planning target volume (PTV), and BMI. The external performance of both models was assessed.ResultsAmong 100 patients, 78 patients (78%) developed grade >= 3 lymphopenia, with grade 4 lymphopenia in 17 (17%). For predicting grade >= 3 lymphopenia, the Christie and MDACC models yielded c-statistics of 0.77 and 0.79, respectively. For predicting grade 4 lymphopenia, c-statistics were 0.69 and 0.80, respectively. Calibration for the Christie and MDACC models demonstrated moderate and good agreement, respectively.ConclusionThe PTV-based MDACC prediction model for severe RIL demonstrated superior external performance in NSCLC patients compared to the dosimetry-based Christie model. As such, the MDACC model can aid in identifying patients at high risk for severe lymphopenia. However, to optimize radiotherapy planning, further improvement and external validation of dosimetry-based models is desired.
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页数:10
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