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Pediatr Blood Cancer. 2021 Jul;68(7):e28998. doi: 10.1002/pbc.28998. Epub 2021 Mar 15.

Impact of location of inpatient cancer care on patients with Ewing sarcoma and osteosarcoma-A population-based study.

Pediatric blood & cancer

Elysia Alvarez, Marcio Malogolowkin, Brad H Pollock, Qian Li, Emily Johnston, Neyssa Marina, Ted Wun, Steven Thorpe, Theresa Keegan

Affiliations

  1. Division of Pediatric Hematology/Oncology, University of California Davis School of Medicine, Sacramento, California, USA.
  2. Department of Public Health Sciences, University of California Davis School of Medicine, Sacramento, California, USA.
  3. Center for Oncology Hematology Outcomes Research and Training and Division of Hematology and Oncology, University of California Davis School of Medicine, Sacramento, California, USA.
  4. Division of Pediatric Hematology/Oncology and Institute of Cancer Outcomes and Survivorship, University of Alabama-Birmingham, Birmingham, Alabama, USA.
  5. Stanford University School of Medicine, Palo Alto, California, USA.
  6. Sarcoma Services, University of California Davis School of Medicine, Sacramento, California, USA.

PMID: 33720485 DOI: 10.1002/pbc.28998

Abstract

BACKGROUND: Ewing sarcoma (EWS) and osteosarcoma (OS) require multidisciplinary treatment. Care at specialized cancer centers (SCC: Children's Oncology Group affiliated and/or National Cancer Institute-designated cancer center) has been found to improve outcomes in patients with leukemia, but studies have not considered location of care and outcomes in EWS and OS patients, an ideal group to evaluate given their specialized multidisciplinary treatment needs.

METHODS: Patients hospitalized with primary EWS and OS (2000-2014) were identified using the California Cancer Registry linked with hospitalization data. Patients were divided into age groups (0-18, 19-39, ≥40 years), and classified on whether they received all versus part/none of their inpatient treatment at a SCC within 1 year of diagnosis. Multivariable Cox proportional hazards regression identified factors associated with survival.

RESULTS: There were 531 ES and 959 OS patients. Five-year overall survival was better for patients with EWS (all: 63% vs. part/none: 42%) and OS (all: 64% vs. part/none: 47%) who received all of their treatment at a SCC. After adjusting for sociodemographic and clinical factors, receiving all inpatient cancer treatment at a SCC was associated with superior overall survival (EWS HR: 0.49, CI 0.37-0.67; OS HR: 0.78, CI 0.63-0.97).

CONCLUSION: Our results suggest that treatment for EWS and OS at a SCC is associated with significantly improved survival even after adjustment for known prognostic factors. The superior survival among those treated at SCCs may be due to having greater access to clinical trials and services at SCCs.

© 2021 Wiley Periodicals LLC.

Keywords: Ewing sarcoma; adolescent and young adult; location of care; osteosarcoma

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