TY - JOUR
T1 - Geriatric risk factors for serious COVID-19 outcomes among older adults with cancer
T2 - a cohort study from the COVID-19 and Cancer Consortium
AU - COVID-19 and Cancer Consortium
AU - Elkrief, Arielle
AU - Hennessy, Cassandra
AU - Kuderer, Nicole M.
AU - Rubinstein, Samuel M.
AU - Wulff-Burchfield, Elizabeth
AU - Rosovsky, Rachel P.
AU - Vega-Luna, Karen
AU - Thompson, Michael A.
AU - Panagiotou, Orestis A.
AU - Desai, Aakash
AU - Rivera, Donna R.
AU - Khaki, Ali Raza
AU - Tachiki, Lisa
AU - Lynch, Ryan C.
AU - Stratton, Catherine
AU - Elias, Rawad
AU - Batist, Gerald
AU - Kasi, Anup
AU - Shah, Dimpy P.
AU - Bakouny, Ziad
AU - Cabal, Angelo
AU - Clement, Jessica
AU - Crowell, Jennifer
AU - Dixon, Becky
AU - Friese, Christopher R.
AU - Fry, Stacy L.
AU - Grover, Punita
AU - Gulati, Shuchi
AU - Gupta, Shilpa
AU - Hwang, Clara
AU - Khan, Hina
AU - Kim, Soo Jung
AU - Klein, Elizabeth J.
AU - Labaki, Chris
AU - McKay, Rana R.
AU - Nizam, Amanda
AU - Pennell, Nathan A.
AU - Puc, Matthew
AU - Schmidt, Andrew L.
AU - Shahrokni, Armin
AU - Shaya, Justin A.
AU - Su, Christopher T.
AU - Wall, Sarah
AU - Williams, Nicole
AU - Wise-Draper, Trisha M.
AU - Mishra, Sanjay
AU - Grivas, Petros
AU - French, Benjamin
AU - Warner, Jeremy L.
AU - Wildes, Tanya M.
N1 - Funding Information:
We thank all members of the CCC19 steering committee: Toni Choueiri, Petros Grivas, Gilberto Lopes, Corrie Painter, Solange Peters, Brian Rini, Dimpy Shah, Mike Thompson, Dimitrios Farmakiotis, Narjust Duma, and Jeremy Warner for their invaluable guidance of the CCC19 consortium. We also thank Gary Lyman for important contributions to the study design. The CCC19 Research Coordinating Center (CHe, SM, BF, JLW, and KV-L) is supported by the NIH National Cancer Institute (NCI) Cancer Center Support Grants P30 CA068485. AE is supported by the Canadian Institute of Health Research, the Detweiler Travelling Fellowship, and the Henry R Shibata Fellowship. AS was supported in part by the Beatriz and Samuel Seaver Foundation, the Memorial Sloan Kettering Cancer and Aging Program, and NIH NCI Cancer Center Support Grant P30 CA008748. CRF was supported by T32 CA 236621 and P30 CA 046592. OAP was supported by P01 AG027296 and R01 AG053307. PGri was supported by P30CA015704–45. REDCap is developed and supported by Vanderbilt Institute for Clinical and Translational Research grant support (UL1 TR000445 from NCATS/NIH).
Publisher Copyright:
© 2022 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY-NC-ND 4.0 license
PY - 2022/3
Y1 - 2022/3
N2 - Background: Older age is associated with poorer outcomes of SARS-CoV-2 infection, although the heterogeneity of ageing results in some older adults being at greater risk than others. The objective of this study was to quantify the association of a novel geriatric risk index, comprising age, modified Charlson comorbidity index, and Eastern Cooperative Oncology Group performance status, with COVID-19 severity and 30-day mortality among older adults with cancer. Methods: In this cohort study, we enrolled patients aged 60 years and older with a current or previous cancer diagnosis (excluding those with non-invasive cancers and premalignant or non-malignant conditions) and a current or previous laboratory-confirmed COVID-19 diagnosis who reported to the COVID-19 and Cancer Consortium (CCC19) multinational, multicentre, registry between March 17, 2020, and June 6, 2021. Patients were also excluded for unknown age, missing data resulting in unknown geriatric risk measure, inadequate data quality, or incomplete follow-up resulting in unknown COVID-19 severity. The exposure of interest was the CCC19 geriatric risk index. The primary outcome was COVID-19 severity and the secondary outcome was 30-day all-cause mortality; both were assessed in the full dataset. Adjusted odds ratios (ORs) and 95% CIs were estimated from ordinal and binary logistic regression models. Findings: 5671 patients with cancer and COVID-19 were included in the analysis. Median follow-up time was 56 days (IQR 22–120), and median age was 72 years (IQR 66–79). The CCC19 geriatric risk index identified 2365 (41·7%) patients as standard risk, 2217 (39·1%) patients as intermediate risk, and 1089 (19·2%) as high risk. 36 (0·6%) patients were excluded due to non-calculable geriatric risk index. Compared with standard-risk patients, high-risk patients had significantly higher COVID-19 severity (adjusted OR 7·24; 95% CI 6·20–8·45). 920 (16·2%) of 5671 patients died within 30 days of a COVID-19 diagnosis, including 161 (6·8%) of 2365 standard-risk patients, 409 (18·5%) of 2217 intermediate-risk patients, and 350 (32·1%) of 1089 high-risk patients. High-risk patients had higher adjusted odds of 30-day mortality (adjusted OR 10·7; 95% CI 8·54–13·5) than standard-risk patients. Interpretation: The CCC19 geriatric risk index was strongly associated with COVID-19 severity and 30-day mortality. Our CCC19 geriatric risk index, based on readily available clinical factors, might provide clinicians with an easy-to-use risk stratification method to identify older adults most at risk for severe COVID-19 as well as mortality. Funding: US National Institutes of Health National Cancer Institute Cancer Center.
AB - Background: Older age is associated with poorer outcomes of SARS-CoV-2 infection, although the heterogeneity of ageing results in some older adults being at greater risk than others. The objective of this study was to quantify the association of a novel geriatric risk index, comprising age, modified Charlson comorbidity index, and Eastern Cooperative Oncology Group performance status, with COVID-19 severity and 30-day mortality among older adults with cancer. Methods: In this cohort study, we enrolled patients aged 60 years and older with a current or previous cancer diagnosis (excluding those with non-invasive cancers and premalignant or non-malignant conditions) and a current or previous laboratory-confirmed COVID-19 diagnosis who reported to the COVID-19 and Cancer Consortium (CCC19) multinational, multicentre, registry between March 17, 2020, and June 6, 2021. Patients were also excluded for unknown age, missing data resulting in unknown geriatric risk measure, inadequate data quality, or incomplete follow-up resulting in unknown COVID-19 severity. The exposure of interest was the CCC19 geriatric risk index. The primary outcome was COVID-19 severity and the secondary outcome was 30-day all-cause mortality; both were assessed in the full dataset. Adjusted odds ratios (ORs) and 95% CIs were estimated from ordinal and binary logistic regression models. Findings: 5671 patients with cancer and COVID-19 were included in the analysis. Median follow-up time was 56 days (IQR 22–120), and median age was 72 years (IQR 66–79). The CCC19 geriatric risk index identified 2365 (41·7%) patients as standard risk, 2217 (39·1%) patients as intermediate risk, and 1089 (19·2%) as high risk. 36 (0·6%) patients were excluded due to non-calculable geriatric risk index. Compared with standard-risk patients, high-risk patients had significantly higher COVID-19 severity (adjusted OR 7·24; 95% CI 6·20–8·45). 920 (16·2%) of 5671 patients died within 30 days of a COVID-19 diagnosis, including 161 (6·8%) of 2365 standard-risk patients, 409 (18·5%) of 2217 intermediate-risk patients, and 350 (32·1%) of 1089 high-risk patients. High-risk patients had higher adjusted odds of 30-day mortality (adjusted OR 10·7; 95% CI 8·54–13·5) than standard-risk patients. Interpretation: The CCC19 geriatric risk index was strongly associated with COVID-19 severity and 30-day mortality. Our CCC19 geriatric risk index, based on readily available clinical factors, might provide clinicians with an easy-to-use risk stratification method to identify older adults most at risk for severe COVID-19 as well as mortality. Funding: US National Institutes of Health National Cancer Institute Cancer Center.
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U2 - 10.1016/S2666-7568(22)00009-5
DO - 10.1016/S2666-7568(22)00009-5
M3 - Article
C2 - 35187516
AN - SCOPUS:85125705178
SN - 2666-7568
VL - 3
SP - e143-e152
JO - The Lancet Healthy Longevity
JF - The Lancet Healthy Longevity
IS - 3
ER -