TY - JOUR
T1 - A Definitive Prognostication System for Patients With Thoracic Malignancies Diagnosed With Coronavirus Disease 2019
T2 - An Update From the TERAVOLT Registry
AU - TERAVOLT study group
AU - Whisenant, Jennifer G.
AU - Baena, Javier
AU - Cortellini, Alessio
AU - Huang, Li Ching
AU - Lo Russo, Giuseppe
AU - Porcu, Luca
AU - Wong, Selina K.
AU - Bestvina, Christine M.
AU - Hellmann, Matthew D.
AU - Roca, Elisa
AU - Rizvi, Hira
AU - Monnet, Isabelle
AU - Boudjemaa, Amel
AU - Rogado, Jacobo
AU - Pasello, Giulia
AU - Leighl, Natasha B.
AU - Arrieta, Oscar
AU - Aujayeb, Avinash
AU - Batra, Ullas
AU - Azzam, Ahmed Y.
AU - Unk, Mojca
AU - Azab, Mohammed A.
AU - Zhumagaliyeva, Ardak N.
AU - Gomez-Martin, Carlos
AU - Blaquier, Juan B.
AU - Geraedts, Erica
AU - Mountzios, Giannis
AU - Serrano-Montero, Gloria
AU - Reinmuth, Niels
AU - Coate, Linda
AU - Marmarelis, Melina
AU - Presley, Carolyn J.
AU - Hirsch, Fred R.
AU - Garrido, Pilar
AU - Khan, Hina
AU - Baggi, Alice
AU - Mascaux, Celine
AU - Halmos, Balazs
AU - Ceresoli, Giovanni L.
AU - Fidler, Mary J.
AU - Scotti, Vieri
AU - Métivier, Anne Cécile
AU - Falchero, Lionel
AU - Felip, Enriqueta
AU - Genova, Carlo
AU - Mazieres, Julien
AU - Tapan, Umit
AU - Brahmer, Julie
AU - Bria, Emilio
AU - Puri, Sonam
N1 - 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.
KW - COVID-19
KW - Cancer
KW - NSCLC
KW - Registry
KW - TERAVOLT
KW - Thoracic
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U2 - 10.1016/j.jtho.2021.12.015
DO - 10.1016/j.jtho.2021.12.015
M3 - Article
C2 - 35121086
AN - SCOPUS:85126335222
SN - 1556-0864
VL - 17
SP - 661
EP - 674
JO - Journal of Thoracic Oncology
JF - Journal of Thoracic Oncology
IS - 5
ER -