| Literature DB >> 35121871 |
Laurence Albiges1, Stéphanie Foulon2, Arnaud Bayle1, Bertrand Gachot3, Fanny Pommeret1,3, Christophe Willekens4, Annabelle Stoclin3, Mansouria Merad3, Frank Griscelli5, Ludovic Lacroix5, Florence Netzer6, Thomas Hueso4, Corinne Balleyguier7, Samy Ammari7, Emeline Colomba1, Giulia Baciarello1, Audrey Perret1, Antoine Hollebecque1,8, Julien Hadoux7, Jean-Marie Michot8, Nathalie Chaput4, Veronique Saada5, Mathilde Hauchecorne1, Jean-Baptiste Micol4, Roger Sun9, Dominique Valteau-Couanet10, Fabrice André1, Florian Scotte3, Benjamin Besse1, Jean-Charles Soria11, Fabrice Barlesi12,13.
Abstract
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.Entities:
Mesh:
Year: 2020 PMID: 35121871 DOI: 10.1038/s43018-020-00120-5
Source DB: PubMed Journal: Nat Cancer ISSN: 2662-1347