Ketpueak Thanika, Losuriya Phumiphat, Kanthawang Thanat, Prakaikietikul Pakorn, Lumkul Lalita, Phinyo Phichayut, Tajarernmuang Pattraporn
Division of Oncology, Department of Internal Medicine, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.
Division of Pulmonary, Critical Care and Allergy, Department of Internal Medicine, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.
Cancers (Basel). 2025 Aug 3;17(15):2565. doi: 10.3390/cancers17152565.
Epidermal growth factor receptor (EGFR) mutations are presented in approximately 50% of East Asian populations with advanced non-small cell lung cancer (NSCLC). While EGFR-tyrosine kinase inhibitors (TKIs) are the standard treatment, patient outcomes are also influenced by host-related factors. This study aimed to investigate clinical and radiological factors associated with early mortality and develop a prognostic prediction model in advanced EGFR-mutated NSCLC. A retrospective cohort was conducted in patients with EGFR-mutated NSCLC treated with first line EGFR-TKIs from January 2012 to October 2022 at Chiang Mai University Hospital. Clinical data and radiologic findings at the initiation of treatment were analyzed. A multivariable flexible parametric survival model was used to determine the predictors of death at 18 months. The predicted survival probabilities at 6, 12, and 18 months were estimated, and the model performance was evaluated. Among 189 patients, 84 (44.4%) died within 18 months. Significant predictors of mortality included body mass index <18.5 or ≥23, bone metastasis, neutrophil-to-lymphocyte ratio ≥ 5, albumin-to-globulin ratio < 1, and mean pulmonary artery diameter ≥ 29 mm. The model demonstrated good performance (Harrell's C-statistic = 0.72; 95% CI: 0.66-0.78). Based on bootstrap internal validation, the optimism-corrected Harrell's C-statistic was 0.71 (95% CI: 0.71-0.71), derived from an apparent C-statistic of 0.75 (95% CI: 0.74-0.75) and an estimated optimism of 0.04 (95% CI: 0.03-0.04). Estimated 18-month survival ranged from 87.1% in those without risk factors to 2.1% in those with all predictors. A web-based tool was developed for clinical use. The prognostic model developed from fundamental clinical and radiologic parameters demonstrated promising utility in predicting 18-month mortality in patients with advanced EGFR-mutated NSCLC receiving first-line EGFR-TKI therapy.
在大约50%的东亚晚期非小细胞肺癌(NSCLC)患者中存在表皮生长因子受体(EGFR)突变。虽然EGFR酪氨酸激酶抑制剂(TKIs)是标准治疗方法,但患者的预后也受到宿主相关因素的影响。本研究旨在调查与早期死亡率相关的临床和放射学因素,并建立晚期EGFR突变NSCLC的预后预测模型。对2012年1月至2022年10月在清迈大学医院接受一线EGFR-TKIs治疗的EGFR突变NSCLC患者进行了一项回顾性队列研究。分析了治疗开始时的临床数据和放射学检查结果。使用多变量灵活参数生存模型来确定18个月时死亡的预测因素。估计了6个月、12个月和18个月时的预测生存概率,并对模型性能进行了评估。在189例患者中,84例(44.4%)在18个月内死亡。死亡率的显著预测因素包括体重指数<18.5或≥23、骨转移、中性粒细胞与淋巴细胞比值≥5、白蛋白与球蛋白比值<1以及平均肺动脉直径≥29mm。该模型表现良好(Harrell氏C统计量=0.72;95%置信区间:0.66-0.78)。基于自举内部验证,经乐观校正的Harrell氏C统计量为0.71(95%置信区间:0.71-0.71),源自表观C统计量0.75(95%置信区间:0.74-0.75)和估计乐观值0.04(95%置信区间:0.03-0.04)。估计的18个月生存率范围从无危险因素患者的87.1%到具有所有预测因素患者的2.1%。开发了一个基于网络的工具供临床使用。从基本临床和放射学参数开发的预后模型在预测接受一线EGFR-TKI治疗的晚期EGFR突变NSCLC患者的18个月死亡率方面显示出有前景的效用。