TY - JOUR
T1 - Determinants of the outcomes of patients with cancer infected with SARS-CoV-2
T2 - results from the Gustave Roussy cohort
AU - Albiges, Laurence
AU - Foulon, Stéphanie
AU - Bayle, Arnaud
AU - Gachot, Bertrand
AU - Pommeret, Fanny
AU - Willekens, Christophe
AU - Stoclin, Annabelle
AU - Merad, Mansouria
AU - Griscelli, Frank
AU - Lacroix, Ludovic
AU - Netzer, Florence
AU - Hueso, Thomas
AU - Balleyguier, Corinne
AU - Ammari, Samy
AU - Colomba, Emeline
AU - Baciarello, Giulia
AU - Perret, Audrey
AU - Hollebecque, Antoine
AU - Hadoux, Julien
AU - Michot, Jean Marie
AU - Chaput, Nathalie
AU - Saada, Veronique
AU - Hauchecorne, Mathilde
AU - Micol, Jean Baptiste
AU - Sun, Roger
AU - Valteau-Couanet, Dominique
AU - André, Fabrice
AU - Scotte, Florian
AU - Besse, Benjamin
AU - Soria, Jean Charles
AU - Barlesi, Fabrice
N1 - Publisher Copyright:
© 2020, The Author(s), under exclusive licence to Springer Nature America, Inc.
PY - 2020/10/1
Y1 - 2020/10/1
N2 - Patients with cancer are presumed to be at increased risk of severe COVID-19 outcomes due to underlying malignancy and treatment-induced immunosuppression. Of the first 178 patients managed for COVID-19 at the Gustave Roussy Cancer Centre, 125 (70.2%) were hospitalized, 47 (26.4%) developed clinical worsening and 31 (17.4%) died. An age of over 70 years, smoking status, metastatic disease, cytotoxic chemotherapy and an Eastern Cooperative Oncology Group score of ≥2 at the last visit were the strongest determinants of increased risk of death. In multivariable analysis, the Eastern Cooperative Oncology Group score remained the only predictor of death. In contrast, immunotherapy, hormone therapy and targeted therapy did not increase clinical worsening or death risk. Biomarker studies found that C-reactive protein and lactate dehydrogenase levels were significantly associated with an increased risk of clinical worsening, while C-reactive protein and D-dimer levels were associated with an increased risk of death. COVID-19 management impacted the oncological treatment strategy, inducing a median 20 d delay in 41% of patients and adaptation of the therapeutic strategy in 30% of patients.
AB - Patients with cancer are presumed to be at increased risk of severe COVID-19 outcomes due to underlying malignancy and treatment-induced immunosuppression. Of the first 178 patients managed for COVID-19 at the Gustave Roussy Cancer Centre, 125 (70.2%) were hospitalized, 47 (26.4%) developed clinical worsening and 31 (17.4%) died. An age of over 70 years, smoking status, metastatic disease, cytotoxic chemotherapy and an Eastern Cooperative Oncology Group score of ≥2 at the last visit were the strongest determinants of increased risk of death. In multivariable analysis, the Eastern Cooperative Oncology Group score remained the only predictor of death. In contrast, immunotherapy, hormone therapy and targeted therapy did not increase clinical worsening or death risk. Biomarker studies found that C-reactive protein and lactate dehydrogenase levels were significantly associated with an increased risk of clinical worsening, while C-reactive protein and D-dimer levels were associated with an increased risk of death. COVID-19 management impacted the oncological treatment strategy, inducing a median 20 d delay in 41% of patients and adaptation of the therapeutic strategy in 30% of patients.
UR - http://www.scopus.com/inward/record.url?scp=85092346857&partnerID=8YFLogxK
U2 - 10.1038/s43018-020-00120-5
DO - 10.1038/s43018-020-00120-5
M3 - Article
C2 - 35121871
AN - SCOPUS:85092346857
SN - 2662-1347
VL - 1
SP - 965
EP - 975
JO - Nature Cancer
JF - Nature Cancer
IS - 10
ER -