SARS-CoV-2 in Childhood Cancer in 2020: A Disease of Disparities

Author:

Johnston Emily E.12ORCID,Martinez Isaac1ORCID,Davis Elizabeth S.1,Caudill Caroline1,Richman Joshua13ORCID,Brackett Julienne4,Dickens David S.5ORCID,Kahn Alissa6,Schwalm Carla7,Sharma Archana8,Patel Pratik A.9ORCID,Bhatia Smita12ORCID,Levine Jennifer M.10ORCID,Wolfson Julie A.12ORCID,

Affiliation:

1. Institute for Cancer Outcomes and Survivorship, University of Alabama at Birmingham, Birmingham, AL

2. Pediatric Hematology-Oncology, Department of Pediatrics, University of Alabama at Birmingham, Birmingham, AL

3. Department of Surgery, University of Alabama at Birmingham, Birmingham, AL

4. Pediatric Hematology-Oncology, Department of Pediatrics, Texas Children's Hospital, Houston, TX

5. Pediatric Hematology-Oncology, Department of Pediatrics, University of Iowa, Iowa City, IA

6. Pediatric Hematology-Oncology, Department of Pediatrics, Saint Joseph's University Medical Center, Paterson, NJ

7. Pediatric Hematology-Oncology, Department of Pediatrics, Bronson Methodist Hospital, Kalamazoo, MI

8. Pediatric Hematology-Oncology, Department of Pediatrics, Rutgers Cancer Institute of New Jersey, New Brunswick, NJ

9. Pediatric Hematology-Oncology, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA

10. Pediatric Hematology-Oncology, Department of Pediatrics, Weill Cornell Medicine, New York, NY

Abstract

PURPOSE The Pediatric Oncology COVID-19 Case Report registry supplies pediatric oncologists with data surrounding the clinical course and outcomes in children with cancer and SARS-CoV-2. METHODS This observational study captured clinical and sociodemographic characteristics for children (≤ 21 years) receiving cancer therapy and infected with SARS-CoV-2 from the pandemic onset through February 19, 2021. The demographic and clinical characteristics of the cohort were compared with population-level pediatric oncology data (SEER). Multivariable binomial regression models evaluated patient characteristics associated with hospitalization, intensive care unit (ICU) admission, and changes in cancer therapy. RESULTS Ninety-four institutions contributed details on 917 children with cancer and SARS-CoV-2. Median age at SARS-CoV-2 infection was 11 years (range, 0-21 years). Compared with SEER, there was an over-representation of Hispanics (43.6% v 29.7%, P < .01), publicly insured (59.3% v 33.5%, P < .01), and patients with hematologic malignancies (65.8% v 38.3%, P < .01) in our cohort. The majority (64.1%) were symptomatic; 31.2% were hospitalized, 10.9% required respiratory support, 9.2% were admitted to the ICU, and 1.6% died because of SARS-CoV-2. Cancer therapy was modified in 44.9%. Hispanic ethnicity was associated with changes in cancer-directed therapy (adjusted risk ratio [aRR] = 1.3; 95% CI, 1.1 to 1.6]). Presence of comorbidities was associated with hospitalization (aRR = 1.3; 95% CI, 1.1 to 1.6) and ICU admission (aRR = 2.3; 95% CI, 1.5 to 3.6). Hematologic malignancies were associated with hospitalization (aRR = 1.6; 95% CI, 1.3 to 2.1). CONCLUSION These findings provide critical information for decision making among pediatric oncologists, including inpatient versus outpatient management, cancer therapy modifications, consideration of monoclonal antibody therapy, and counseling families on infection risks in the setting of the SARS-CoV-2 pandemic. The over-representation of Hispanic and publicly insured patients in this national cohort suggests disparities that require attention.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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