Department of Biomedical Engineering, Case Western Reserve University, Cleveland, OH, USA.
University Hospitals, Cleveland, OH, USA.
Lancet Digit Health. 2020 Mar;2(3):e116-e128. doi: 10.1016/S2589-7500(20)30002-9. Epub 2020 Feb 13.
Use of adjuvant chemotherapy in patients with early-stage lung cancer is controversial because no definite biomarker exists to identify patients who would receive added benefit from it. We aimed to develop and validate a quantitative radiomic risk score (QuRiS) and associated nomogram (QuRNom) for early-stage non-small cell lung cancer (NSCLC) that is prognostic of disease-free survival and predictive of the added benefit of adjuvant chemotherapy following surgery.
We did a retrospective multicohort study of individuals with early-stage NSCLC (stage I and II) who either received surgery alone or surgery plus adjuvant chemotherapy. We selected patients for whom we had available pre-treatment diagnostic CT scans and corresponding survival information. We used radiomic texture features derived from within and outside the primary lung nodule on chest CT scans of patients from the Cleveland Clinic Foundation (Cleveland, OH, USA; cohort D) to develop QuRiS. A least absolute shrinkage and selection operator-Cox regularisation model was used for data dimension reduction, feature selection, and QuRiS construction. QuRiS was independently validated on a cohort of patients from the University of Pennsylvania (Philadephia, PA, USA; cohort D) and a cohort of patients whose CT scans were derived from The Cancer Imaging Archive (cohort D). QuRNom was constructed by integrating QuRiS with tumour and node descriptors (according to the tumour, node, metastasis staging system) and lymphovascular invasion. The primary endpoint of the study was the assessment of the performance of QuRiS and QuRNom in predicting disease-free survival. The added benefit of adjuvant chemotherapy estimated using QuRiS and QuRNom was validated by comparing patients who received adjuvant chemotherapy versus patients who underwent surgery alone in cohorts D-D.
We included: 329 patients in cohort D (73 [22%] had surgery plus adjuvant chemotherapy and 256 (78%) had surgery alone); 114 patients in cohort D (33 [29%] had surgery plus adjuvant chemotherapy and 81 (71%) had surgery alone); and 82 patients in cohort D (24 [29%] had surgery plus adjuvant chemotherapy and 58 (71%) had surgery alone). QuRiS comprised three intratumoral and 10 peritumoral CT-radiomic features and was found to be significantly associated with disease-free survival (ie, prognostic validation of QuRiS; hazard ratio for predicted high-risk vs predicted low-risk groups 1·56, 95% CI 1·08-2·23, p=0·016 for cohort D; 2·66, 1·24-5·68, p=0·011 for cohort D; and 2·67, 1·39-5·11, p=0·0029 for cohort D). To validate the predictive performance of QuRiS, patients were partitioned into three risk groups (high, intermediate, and low risk) on the basis of their corresponding QuRiS. Patients in the high-risk group were observed to have significantly longer survival with adjuvant chemotherapy than patients who underwent surgery alone (0·27, 0·08-0·95, p=0·042, for cohort D; 0·08, 0·01-0·42, p=0·0029, for cohorts D and D combined). As concerns QuRNom, the nomogram-estimated survival benefit was predictive of the actual efficacy of adjuvant chemotherapy (0·25, 0·12-0·55, p<0·0001, for cohort D; 0·13, <0·01-0·99, p=0·0019 for cohort D).
QuRiS and QuRNom were validated as being prognostic of disease-free survival and predictive of the added benefit of adjuvant chemotherapy, especially in clinically defined low-risk groups. Since QuRiS is based on routine chest CT imaging, with additional multisite independent validation it could potentially be employed for decision management in non-invasive treatment of resectable lung cancer.
National Cancer Institute of the US National Institutes of Health, National Center for Research Resources, US Department of Veterans Affairs Biomedical Laboratory Research and Development Service, Department of Defence, National Institute of Diabetes and Digestive and Kidney Diseases, Wallace H Coulter Foundation, Case Western Reserve University, and Dana Foundation.
在早期肺癌患者中使用辅助化疗存在争议,因为目前尚无明确的生物标志物来确定哪些患者会从中获益。我们旨在开发和验证一种用于早期非小细胞肺癌(NSCLC)的定量放射组学风险评分(QuRiS)和相关列线图(QuRNom),该评分可以预测无病生存期,并预测手术后辅助化疗的附加益处。
我们进行了一项回顾性多队列研究,纳入了早期 NSCLC(I 期和 II 期)患者,这些患者要么单独接受手术,要么接受手术加辅助化疗。我们选择了有术前诊断性 CT 扫描和相应生存信息的患者。我们使用来自克利夫兰诊所基金会(克利夫兰,OH,美国;队列 D)的患者胸部 CT 扫描的肺结节内和周围的放射组学纹理特征来开发 QuRiS。最小绝对收缩和选择算子-Cox 正则化模型用于数据降维和特征选择,以及 QuRiS 的构建。QuRiS 在宾夕法尼亚大学(费城,PA,美国;队列 D)的患者队列和来自癌症成像档案的 CT 扫描患者队列(队列 D)上进行了独立验证。通过将 QuRiS 与肿瘤和淋巴结描述符(根据肿瘤、淋巴结、转移分期系统)和血管淋巴管侵犯相结合来构建 QuRNom。研究的主要终点是评估 QuRiS 和 QuRNom 在预测无病生存期方面的性能。通过比较队列 D-D 中接受辅助化疗的患者与单独接受手术的患者,验证了使用 QuRiS 和 QuRNom 估计辅助化疗的附加益处。
我们纳入了:队列 D 中的 329 名患者(73 名接受手术加辅助化疗,256 名接受手术单独治疗);队列 D 中的 114 名患者(33 名接受手术加辅助化疗,81 名接受手术单独治疗);队列 D 中的 82 名患者(24 名接受手术加辅助化疗,58 名接受手术单独治疗)。QuRiS 由三个肿瘤内和 10 个肿瘤周围 CT 放射组学特征组成,与无病生存期显著相关(即 QuRiS 的预后验证;预测高危组与预测低危组的危险比为 1.56,95%CI 为 1.08-2.23,p=0.016;队列 D;2.66,1.24-5.68,p=0.011;队列 D;2.67,1.39-5.11,p=0.0029;队列 D)。为了验证 QuRiS 的预测性能,根据相应的 QuRiS 将患者分为三个风险组(高、中、低风险)。与单独接受手术的患者相比,高危组患者的生存时间明显更长(队列 D 中为 0.27,0.08-0.95,p=0.042;队列 D 和 D 联合为 0.08,0.01-0.42,p=0.0029)。至于 QuRNom,nomogram 估计的生存获益可以预测辅助化疗的实际疗效(队列 D 中为 0.25,0.12-0.55,p<0.0001;队列 D 中为 0.13,<0.01-0.99,p=0.0019)。
QuRiS 和 QuRNom 被验证为无病生存期的预后指标,并可预测辅助化疗的附加益处,尤其是在临床定义的低危组中。由于 QuRiS 基于常规胸部 CT 成像,并且在多个地点进行了独立验证,因此它可能有潜力用于非侵入性治疗可切除肺癌的决策管理。
美国国立卫生研究院国家癌症研究所、国家中心研究资源、美国退伍军人事务部生物医学实验室研究和发展服务部、国防部、国家糖尿病和消化与肾脏疾病研究所、华莱士 H 库尔特基金会、凯斯西储大学和达纳基金会。