TY - JOUR
T1 - A Definitive Prognostication System for Patients With Thoracic Malignancies Diagnosed With Coronavirus Disease 2019: An Update From the TERAVOLT Registry
AU - TERAVOLT study group
AU - Whisenant, J. G.
AU - Baena, J.
AU - Cortellini, A.
AU - Huang, L. C.
AU - Lo Russo, G.
AU - Porcu, L.
AU - Wong, S. K.
AU - Bestvina, C. M.
AU - Hellmann, M. D.
AU - Roca, E.
AU - Rizvi, H.
AU - Monnet, I.
AU - Boudjemaa, A.
AU - Rogado, J.
AU - Pasello, G.
AU - Leighl, N. B.
AU - Arrieta, O.
AU - Aujayeb, A.
AU - Batra, U.
AU - Azzam, A. Y.
AU - Unk, M.
AU - Azab, M. A.
AU - Zhumagaliyeva, A. N.
AU - Gomez-Martin, C.
AU - Blaquier, J. B.
AU - Geraedts, E.
AU - Mountzios, G.
AU - Serrano-Montero, G.
AU - Reinmuth, N.
AU - Coate, L.
AU - Marmarelis, M.
AU - Presley, C. J.
AU - Hirsch, F. R.
AU - Garrido, P.
AU - Khan, H.
AU - Baggi, A.
AU - Mascaux, C.
AU - Halmos, B.
AU - Ceresoli, G. L.
AU - Fidler, M. J.
AU - Scotti, V.
AU - Métivier, A. C.
AU - Falchero, L.
AU - Felip, E.
AU - Genova, C.
AU - Mazieres, J.
AU - Tapan, U.
AU - Brahmer, J.
AU - Dingemans, A. M.
AU - Peters, S.
N1 - Funding Information:
This study was awarded a grant from the Lung Ambition that supported database development and maintenance.
Publisher Copyright:
© 2022 International Association for the Study of Lung Cancer
PY - 2022/5
Y1 - 2022/5
N2 - Introduction: Patients with thoracic malignancies are at increased risk for mortality from coronavirus disease 2019 (COVID-19), and a large number of intertwined prognostic variables have been identified so far. Methods: Capitalizing data from the Thoracic Cancers International COVID-19 Collaboration (TERAVOLT) registry, a global study created with the aim of describing the impact of COVID-19 in patients with thoracic malignancies, we used a clustering approach, a fast-backward step-down selection procedure, and a tree-based model to screen and optimize a broad panel of demographics and clinical COVID-19 and cancer characteristics. Results: As of April 15, 2021, a total of 1491 consecutive eligible patients from 18 countries were included in the analysis. With a mean observation period of 42 days, 361 events were reported with an all-cause case fatality rate of 24.2%. The clustering procedure screened 73 covariates in 13 clusters. A further multivariable logistic regression for the association between clusters and death was performed, resulting in five clusters significantly associated with the outcome. The fast-backward step-down selection procedure then identified the following seven major determinants of death: Eastern Cooperative Oncology Group—performance status (ECOG-PS) (OR = 2.47, 1.87–3.26), neutrophil count (OR = 2.46, 1.76–3.44), serum procalcitonin (OR = 2.37, 1.64–3.43), development of pneumonia (OR = 1.95, 1.48–2.58), C-reactive protein (OR = 1.90, 1.43–2.51), tumor stage at COVID-19 diagnosis (OR = 1.97, 1.46–2.66), and age (OR = 1.71, 1.29–2.26). The receiver operating characteristic analysis for death of the selected model confirmed its diagnostic ability (area under the receiver operating curve = 0.78, 95% confidence interval: 0.75–0.81). The nomogram was able to classify the COVID-19 mortality in an interval ranging from 8% to 90%, and the tree-based model recognized ECOG-PS, neutrophil count, and c-reactive protein as the major determinants of prognosis. Conclusions: From 73 variables analyzed, seven major determinants of death have been identified. Poor ECOG-PS was found to have the strongest association with poor outcome from COVID-19. With our analysis, we provide clinicians with a definitive prognostication system to help determine the risk of mortality for patients with thoracic malignancies and COVID-19.
AB - Introduction: Patients with thoracic malignancies are at increased risk for mortality from coronavirus disease 2019 (COVID-19), and a large number of intertwined prognostic variables have been identified so far. Methods: Capitalizing data from the Thoracic Cancers International COVID-19 Collaboration (TERAVOLT) registry, a global study created with the aim of describing the impact of COVID-19 in patients with thoracic malignancies, we used a clustering approach, a fast-backward step-down selection procedure, and a tree-based model to screen and optimize a broad panel of demographics and clinical COVID-19 and cancer characteristics. Results: As of April 15, 2021, a total of 1491 consecutive eligible patients from 18 countries were included in the analysis. With a mean observation period of 42 days, 361 events were reported with an all-cause case fatality rate of 24.2%. The clustering procedure screened 73 covariates in 13 clusters. A further multivariable logistic regression for the association between clusters and death was performed, resulting in five clusters significantly associated with the outcome. The fast-backward step-down selection procedure then identified the following seven major determinants of death: Eastern Cooperative Oncology Group—performance status (ECOG-PS) (OR = 2.47, 1.87–3.26), neutrophil count (OR = 2.46, 1.76–3.44), serum procalcitonin (OR = 2.37, 1.64–3.43), development of pneumonia (OR = 1.95, 1.48–2.58), C-reactive protein (OR = 1.90, 1.43–2.51), tumor stage at COVID-19 diagnosis (OR = 1.97, 1.46–2.66), and age (OR = 1.71, 1.29–2.26). The receiver operating characteristic analysis for death of the selected model confirmed its diagnostic ability (area under the receiver operating curve = 0.78, 95% confidence interval: 0.75–0.81). The nomogram was able to classify the COVID-19 mortality in an interval ranging from 8% to 90%, and the tree-based model recognized ECOG-PS, neutrophil count, and c-reactive protein as the major determinants of prognosis. Conclusions: From 73 variables analyzed, seven major determinants of death have been identified. Poor ECOG-PS was found to have the strongest association with poor outcome from COVID-19. With our analysis, we provide clinicians with a definitive prognostication system to help determine the risk of mortality for patients with thoracic malignancies and COVID-19.
UR - http://www.scopus.com/inward/record.url?scp=85126335222&partnerID=8YFLogxK
U2 - 10.1016/j.jtho.2021.12.015
DO - 10.1016/j.jtho.2021.12.015
M3 - Article
C2 - 35121086
SN - 1556-0864
VL - 17
SP - 661
EP - 674
JO - Journal of Thoracic Oncology
JF - Journal of Thoracic Oncology
IS - 5
ER -