A prognostic and predictive computational pathology image signature for added benefit of adjuvant chemotherapy in early stage non-small-cell lung cancer

Background: We developed and validated a prognostic and predictive computational pathology risk score (CoRiS) using H&E stained tissue images from patients with early-stage non-small cell lung cancer (ES-NSCLC). Methods: 1330 patients with ES-NSCLC were acquired from 3 independent sources and di...

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Main Authors: Xiangxue Wang, Kaustav Bera, Cristian Barrera, Yu Zhou, Cheng Lu, Pranjal Vaidya, Pingfu Fu, Michael Yang, Ralph Alexander Schmid, Sabina Berezowska, Humberto Choi, Vamsidhar Velcheti, Anant Madabhushi
Format: Article
Language:English
Published: Elsevier 2021-07-01
Series:EBioMedicine
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2352396421002747
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author Xiangxue Wang
Kaustav Bera
Cristian Barrera
Yu Zhou
Cheng Lu
Pranjal Vaidya
Pingfu Fu
Michael Yang
Ralph Alexander Schmid
Sabina Berezowska
Humberto Choi
Vamsidhar Velcheti
Anant Madabhushi
author_facet Xiangxue Wang
Kaustav Bera
Cristian Barrera
Yu Zhou
Cheng Lu
Pranjal Vaidya
Pingfu Fu
Michael Yang
Ralph Alexander Schmid
Sabina Berezowska
Humberto Choi
Vamsidhar Velcheti
Anant Madabhushi
author_sort Xiangxue Wang
collection DOAJ
description Background: We developed and validated a prognostic and predictive computational pathology risk score (CoRiS) using H&E stained tissue images from patients with early-stage non-small cell lung cancer (ES-NSCLC). Methods: 1330 patients with ES-NSCLC were acquired from 3 independent sources and divided into four cohorts D1-4. D1 comprised 100 surgery treated patients and was used to identify prognostic features via an elastic-net Cox model to predict overall and disease-free survival. CoRiS was constructed using the Cox model coefficients for the top features. The prognostic performance of CoRiS was evaluated on D2 (N=331), D3 (N=657) and D4 (N=242). Patients from D2 and D3 which comprised surgery + chemotherapy were used to validate CoRiS as predictive of added benefit to adjuvant chemotherapy (ACT) by comparing survival between different CoRiS defined risk groups. Findings: CoRiS was found to be prognostic on univariable analysis, D2 (hazard ratio (HR) = 1.41, adjusted (adj.) P = .01) and D3 (HR = 1.35, adj. P < .001). Multivariable analysis showed CoRiS was independently prognostic, D2 (HR = 1.41, adj. P < .001) and D3 (HR = 1.35, adj. P < .001), after adjusting for clinico-pathologic factors. CoRiS was also able to identify high-risk patients who derived survival benefit from ACT D2 (HR = 0.42, adj. P = .006) and D3 (HR = 0.46, adj. P = .08). Interpretation: CoRiS is a tissue non-destructive, quantitative and low-cost tool that could potentially help guide management of ES-NSCLC patients.
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spelling doaj.art-e5a09d38255e45c88fe57738e7605aef2022-12-21T22:35:30ZengElsevierEBioMedicine2352-39642021-07-0169103481A prognostic and predictive computational pathology image signature for added benefit of adjuvant chemotherapy in early stage non-small-cell lung cancerXiangxue Wang0Kaustav Bera1Cristian Barrera2Yu Zhou3Cheng Lu4Pranjal Vaidya5Pingfu Fu6Michael Yang7Ralph Alexander Schmid8Sabina Berezowska9Humberto Choi10Vamsidhar Velcheti11Anant Madabhushi12Center for Computational Imaging and Personalized Diagnostics, Case Western Reserve University, OH, USACenter for Computational Imaging and Personalized Diagnostics, Case Western Reserve University, OH, USACenter for Computational Imaging and Personalized Diagnostics, Case Western Reserve University, OH, USACenter for Computational Imaging and Personalized Diagnostics, Case Western Reserve University, OH, USACenter for Computational Imaging and Personalized Diagnostics, Case Western Reserve University, OH, USACenter for Computational Imaging and Personalized Diagnostics, Case Western Reserve University, OH, USADepartment of Population and Quantitative Health Sciences, Case Western Reserve University, OH, USADepartment of Pathology-Anatomic, University Hospitals, OH, USADivision of General Thoracic Surgery, University Hospital Berne, Bern, SwitzerlandInstitute of Pathology, University of Bern, Bern, Switzerland; Department of Laboratory Medicine and Pathology, Institute of Pathology, Lausanne University Hospital and Lausanne University, Lausanne, SwitzerlandDepartment of Pulmonary and Critical Care Medicine, Respiratory Institute, Cleveland Clinic Foundation, OH, USADepartment of Hematology and Oncology, NYU Langone Health, NY, USACenter for Computational Imaging and Personalized Diagnostics, Case Western Reserve University, OH, USA; Louis Stokes Cleveland Veterans Administration Medical Center, Cleveland, OH, USA; Corresponding author at: Center for Computational Imaging and Personalized Diagnostics, Case Western Reserve University, OH, USA.Background: We developed and validated a prognostic and predictive computational pathology risk score (CoRiS) using H&E stained tissue images from patients with early-stage non-small cell lung cancer (ES-NSCLC). Methods: 1330 patients with ES-NSCLC were acquired from 3 independent sources and divided into four cohorts D1-4. D1 comprised 100 surgery treated patients and was used to identify prognostic features via an elastic-net Cox model to predict overall and disease-free survival. CoRiS was constructed using the Cox model coefficients for the top features. The prognostic performance of CoRiS was evaluated on D2 (N=331), D3 (N=657) and D4 (N=242). Patients from D2 and D3 which comprised surgery + chemotherapy were used to validate CoRiS as predictive of added benefit to adjuvant chemotherapy (ACT) by comparing survival between different CoRiS defined risk groups. Findings: CoRiS was found to be prognostic on univariable analysis, D2 (hazard ratio (HR) = 1.41, adjusted (adj.) P = .01) and D3 (HR = 1.35, adj. P < .001). Multivariable analysis showed CoRiS was independently prognostic, D2 (HR = 1.41, adj. P < .001) and D3 (HR = 1.35, adj. P < .001), after adjusting for clinico-pathologic factors. CoRiS was also able to identify high-risk patients who derived survival benefit from ACT D2 (HR = 0.42, adj. P = .006) and D3 (HR = 0.46, adj. P = .08). Interpretation: CoRiS is a tissue non-destructive, quantitative and low-cost tool that could potentially help guide management of ES-NSCLC patients.http://www.sciencedirect.com/science/article/pii/S2352396421002747Early-stage non-small cell lung cancerComputational pathologyPrognostic and predictive
spellingShingle Xiangxue Wang
Kaustav Bera
Cristian Barrera
Yu Zhou
Cheng Lu
Pranjal Vaidya
Pingfu Fu
Michael Yang
Ralph Alexander Schmid
Sabina Berezowska
Humberto Choi
Vamsidhar Velcheti
Anant Madabhushi
A prognostic and predictive computational pathology image signature for added benefit of adjuvant chemotherapy in early stage non-small-cell lung cancer
EBioMedicine
Early-stage non-small cell lung cancer
Computational pathology
Prognostic and predictive
title A prognostic and predictive computational pathology image signature for added benefit of adjuvant chemotherapy in early stage non-small-cell lung cancer
title_full A prognostic and predictive computational pathology image signature for added benefit of adjuvant chemotherapy in early stage non-small-cell lung cancer
title_fullStr A prognostic and predictive computational pathology image signature for added benefit of adjuvant chemotherapy in early stage non-small-cell lung cancer
title_full_unstemmed A prognostic and predictive computational pathology image signature for added benefit of adjuvant chemotherapy in early stage non-small-cell lung cancer
title_short A prognostic and predictive computational pathology image signature for added benefit of adjuvant chemotherapy in early stage non-small-cell lung cancer
title_sort prognostic and predictive computational pathology image signature for added benefit of adjuvant chemotherapy in early stage non small cell lung cancer
topic Early-stage non-small cell lung cancer
Computational pathology
Prognostic and predictive
url http://www.sciencedirect.com/science/article/pii/S2352396421002747
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