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dc.contributor.authorSharafeldin, Noha
dc.contributor.authorBates, Benjamin
dc.contributor.authorSong, Qianqian
dc.contributor.authorMadhira, Vithal
dc.contributor.authorYan, Yao
dc.contributor.authorDong, Sharlene
dc.contributor.authorLee, Eileen
dc.contributor.authorKuhrt, Nathaniel
dc.contributor.authorShao, Yu Raymond
dc.contributor.authorLiu, Feifan
dc.contributor.authorBergquist, Timothy
dc.contributor.authorGuinney, Justin
dc.contributor.authorSu, Jing
dc.contributor.authorTopaloglu, Umit
dc.date2022-08-11T08:08:10.000
dc.date.accessioned2022-08-23T15:45:04Z
dc.date.available2022-08-23T15:45:04Z
dc.date.issued2021-06-04
dc.date.submitted2021-06-14
dc.identifier.citation<p>Sharafeldin N, Bates B, Song Q, Madhira V, Yan Y, Dong S, Lee E, Kuhrt N, Shao YR, Liu F, Bergquist T, Guinney J, Su J, Topaloglu U. Outcomes of COVID-19 in Patients With Cancer: Report From the National COVID Cohort Collaborative (N3C). J Clin Oncol. 2021 Jun 4:JCO2101074. doi: 10.1200/JCO.21.01074. Epub ahead of print. PMID: 34085538. <a href="https://doi.org/10.1200/JCO.21.01074">Link to article on publisher's site</a></p>
dc.identifier.issn0732-183X (Linking)
dc.identifier.doi10.1200/JCO.21.01074
dc.identifier.pmid34085538
dc.identifier.urihttp://hdl.handle.net/20.500.14038/27451
dc.description.abstractPURPOSE: Variation in risk of adverse clinical outcomes in patients with cancer and COVID-19 has been reported from relatively small cohorts. The NCATS' National COVID Cohort Collaborative (N3C) is a centralized data resource representing the largest multicenter cohort of COVID-19 cases and controls nationwide. We aimed to construct and characterize the cancer cohort within N3C and identify risk factors for all-cause mortality from COVID-19. METHODS: We used 4,382,085 patients from 50 US medical centers to construct a cohort of patients with cancer. We restricted analyses to adults > /= 18 years old with a COVID-19-positive or COVID-19-negative diagnosis between January 1, 2020, and March 25, 2021. We followed N3C selection of an index encounter per patient for analyses. All analyses were performed in the N3C Data Enclave Palantir platform. RESULTS: A total of 398,579 adult patients with cancer were identified from the N3C cohort; 63,413 (15.9%) were COVID-19-positive. Most common represented cancers were skin (13.8%), breast (13.7%), prostate (10.6%), hematologic (10.5%), and GI cancers (10%). COVID-19 positivity was significantly associated with increased risk of all-cause mortality (hazard ratio, 1.20; 95% CI, 1.15 to 1.24). Among COVID-19-positive patients, age > /= 65 years, male gender, Southern or Western US residence, an adjusted Charlson Comorbidity Index score > /= 4, hematologic malignancy, multitumor sites, and recent cytotoxic therapy were associated with increased risk of all-cause mortality. Patients who received recent immunotherapies or targeted therapies did not have higher risk of overall mortality. CONCLUSION: Using N3C, we assembled the largest nationally representative cohort of patients with cancer and COVID-19 to date. We identified demographic and clinical factors associated with increased all-cause mortality in patients with cancer. Full characterization of the cohort will provide further insights into the effects of COVID-19 on cancer outcomes and the ability to continue specific cancer treatments.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=34085538&dopt=Abstract">Link to Article in PubMed</a></p>
dc.relation.urlhttps://doi.org/10.1200/jco.21.01074
dc.subjectCOVID-19
dc.subjectcancer outcomes
dc.subjectUMCCTS funding
dc.subjectEpidemiology
dc.subjectInfectious Disease
dc.subjectNeoplasms
dc.subjectOncology
dc.subjectVirus Diseases
dc.titleOutcomes of COVID-19 in Patients With Cancer: Report From the National COVID Cohort Collaborative (N3C)
dc.typeJournal Article
dc.source.journaltitleJournal of clinical oncology : official journal of the American Society of Clinical Oncology
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/covid19/251
dc.identifier.contextkey23348828
html.description.abstract<p>PURPOSE: Variation in risk of adverse clinical outcomes in patients with cancer and COVID-19 has been reported from relatively small cohorts. The NCATS' National COVID Cohort Collaborative (N3C) is a centralized data resource representing the largest multicenter cohort of COVID-19 cases and controls nationwide. We aimed to construct and characterize the cancer cohort within N3C and identify risk factors for all-cause mortality from COVID-19.</p> <p>METHODS: We used 4,382,085 patients from 50 US medical centers to construct a cohort of patients with cancer. We restricted analyses to adults > /= 18 years old with a COVID-19-positive or COVID-19-negative diagnosis between January 1, 2020, and March 25, 2021. We followed N3C selection of an index encounter per patient for analyses. All analyses were performed in the N3C Data Enclave Palantir platform.</p> <p>RESULTS: A total of 398,579 adult patients with cancer were identified from the N3C cohort; 63,413 (15.9%) were COVID-19-positive. Most common represented cancers were skin (13.8%), breast (13.7%), prostate (10.6%), hematologic (10.5%), and GI cancers (10%). COVID-19 positivity was significantly associated with increased risk of all-cause mortality (hazard ratio, 1.20; 95% CI, 1.15 to 1.24). Among COVID-19-positive patients, age > /= 65 years, male gender, Southern or Western US residence, an adjusted Charlson Comorbidity Index score > /= 4, hematologic malignancy, multitumor sites, and recent cytotoxic therapy were associated with increased risk of all-cause mortality. Patients who received recent immunotherapies or targeted therapies did not have higher risk of overall mortality.</p> <p>CONCLUSION: Using N3C, we assembled the largest nationally representative cohort of patients with cancer and COVID-19 to date. We identified demographic and clinical factors associated with increased all-cause mortality in patients with cancer. Full characterization of the cohort will provide further insights into the effects of COVID-19 on cancer outcomes and the ability to continue specific cancer treatments.</p>
dc.identifier.submissionpathcovid19/251
dc.contributor.departmentDepartment of Population and Quantitative Health Sciences
dc.source.pagesJCO2101074


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