4.7 Article

CT derived radiomic score for predicting the added benefit of adjuvant chemotherapy following surgery in stage I, II resectable non-small cell lung cancer: a retrospective multicohort study for outcome prediction

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LANCET DIGITAL HEALTH
卷 2, 期 3, 页码 E116-E128

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DOI: 10.1016/S2589-7500(20)30002-9

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资金

  1. National Cancer Institute of the NIH [1U24CA199374-01, R01CA202752-01A1, R01CA208236-01A1, R01 CA216579-01A1, R01 CA220581-01A1, 1U01 CA239055-01, 1P20 CA233216-01]
  2. National Center for Research Resources [1 C06 RR12463-01]
  3. VA Merit Review Award from the US Department of Veterans Affairs Biomedical Laboratory Research and Development Service [IBX004121A]
  4. DOD Prostate Cancer Idea Development Award [W81XWH-15-1-0558]
  5. DOD Lung Cancer Investigator-Initiated Translational Research Award [W81XWH-18-1-0440]
  6. DOD Peer Reviewed Cancer Research Program [W81XWH-16-1-0329]
  7. National Institute of Diabetes and Digestive and Kidney Diseases [1K25 DK115904-01A1]
  8. Ohio Third Frontier Technology Validation Fund
  9. Wallace H Coulter Foundation Program in the Department of Biomedical Engineering
  10. DOD PRCRP Career Development Award
  11. Dana Foundation David Mahoney Neuroimaging Program
  12. CTSA at Case Western Reserve University

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Background 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. Methods 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 pretreatment 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-1) 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-2) and a cohort of patients whose CT scans were derived from The Cancer Imaging Archive (cohort D-3). 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-1-D-3. Findings We included: 329 patients in cohort D-1 (73 [22%] had surgery plus adjuvant chemotherapy and 256 (78%) had surgery alone); 114 patients in cohort D-2 (33 [29%] had surgery plus adjuvant chemotherapy and 81 (71%) had surgery alone); and 82 patients in cohort D-3 (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-1; 2.66, 1.24-5.68, p=0.011 for cohort D-2; and 2.67, 1.39-5.11, p=0.0029 for cohort D-3). 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-1; 0.08, 0.01-0.42, p=0.0029, for cohorts D-2 and D-3 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-1; 0.13, <0.01-0.99, p=0.0019 for cohort D-3). Interpretation 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. Copyright (C) 2020 The Author(s). Published by Elsevier Ltd.

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