Outcomes of COVID-19 in Patients With Cancer: Report From the National COVID Cohort Collaborative (N3C)

Author:

Sharafeldin Noha1ORCID,Bates Benjamin2ORCID,Song Qianqian3ORCID,Madhira Vithal4ORCID,Yan Yao56ORCID,Dong Sharlene3ORCID,Lee Eileen2ORCID,Kuhrt Nathaniel2ORCID,Shao Yu Raymond7ORCID,Liu Feifan8ORCID,Bergquist Timothy6ORCID,Guinney Justin6ORCID,Su Jing9ORCID,Topaloglu Umit3ORCID

Affiliation:

1. School of Medicine, University of Alabama at Birmingham, Birmingham, AL

2. Rutgers University, New Brunswick, NJ

3. Wake Forest School of Medicine, Winston-Salem, NC

4. Palila Software LLC, Reno, NV

5. University of Washington, Seattle, WA

6. Sage Bionetworks, Seattle, WA

7. Duke University Medical Center, Durham, NC

8. University of Massachusetts Medical School, Boston, MA

9. Department of Biostatistics, Indiana University School of Medicine, Indianapolis, IN

Abstract

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. 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.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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