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Poverty, race, ethnicity, and survival in pediatric nonmetastatic osteosarcoma: a Children's Oncology Group report.
Ilcisin, Lenka; Han, Ruxu; Krailo, Mark; Shulman, David S; Weil, Brent R; Weldon, Christopher B; Umaretiya, Puja; Aziz-Bose, Rahela; Greenzang, Katie A; Gorlick, Richard; Reed, Damon R; Randall, R Lor; Nadel, Helen; Binitie, Odion; Dubois, Steven G; Janeway, Katherine A; Bona, Kira.
Afiliação
  • Ilcisin L; Department of Pediatric Oncology, Division of Population Sciences, Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Harvard Medical School, Boston, MA, USA.
  • Han R; Department of Surgery, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Krailo M; Children's Oncology Group, Monrovia, CA, USA.
  • Shulman DS; Children's Oncology Group, Arcadia, CA, USA.
  • Weil BR; Department of Population and Public Health Sciences Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
  • Weldon CB; Department of Pediatric Oncology, Division of Population Sciences, Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Harvard Medical School, Boston, MA, USA.
  • Umaretiya P; Department of Surgery, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Aziz-Bose R; Department of Surgery, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Greenzang KA; Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • Gorlick R; Department of Pediatric Oncology, Division of Population Sciences, Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Harvard Medical School, Boston, MA, USA.
  • Reed DR; Department of Pediatric Oncology, Division of Population Sciences, Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Harvard Medical School, Boston, MA, USA.
  • Randall RL; Division of Pediatrics, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
  • Nadel H; Division of Pediatric Solid Tumors, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Binitie O; Department of Orthopaedic Surgery, University of California Davis Health, Sacramento, CA, USA.
  • Dubois SG; Division of Radiology, Lucille Packard Children's Hospital at Stanford University, Stanford, CA, USA.
  • Janeway KA; Department of Surgery, Moffitt Cancer Center, Tampa, FL, USA.
  • Bona K; Department of Pediatric Oncology, Division of Population Sciences, Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Harvard Medical School, Boston, MA, USA.
J Natl Cancer Inst ; 2024 Jun 26.
Article em En | MEDLINE | ID: mdl-38926133
ABSTRACT

BACKGROUND:

Children living in poverty and those of marginalized race or ethnicity experience inferior disease outcomes across many cancers. Whether survival disparities exist in osteosarcoma is poorly defined. We investigated the association between race, ethnicity, and proxied poverty exposures and event-free and overall survival for children with nonmetastatic osteosarcoma receiving care on a cooperative group trial.

METHODS:

We conducted a retrospective cohort study of US patients with nonmetastatic, osteosarcoma aged 5-21 years enrolled on the Children's Oncology Group trial AOST0331. Race and ethnicity were categorized to reflect historically marginalized populations, as Hispanic, non-Hispanic Black, non-Hispanic Other, and non-Hispanic White. Poverty was proxied at the household and neighborhood levels. Overall survival and event-free survival functions of time from trial enrollment were estimated using the Kaplan-Meier method. Hypotheses of associations between risks for event-free survival, death, and postrelapse death with race and ethnicity were assessed using log-rank tests.

RESULTS:

Among 758 patients, 25.6% were household-poverty and 28.5% neighborhood-poverty exposed. Of the patients, 21% of children identified as Hispanic, 15.4% non-Hispanic Black, 5.3% non-Hispanic Other, and 54.0% non-Hispanic White. Neither household or neighborhood poverty nor race and ethnicity were statistically significantly associated with risks for event-free survival or death. Postrelapse risk for death differed statistically significantly across race and ethnicity with non-Hispanic Black patients at greatest risk (4-year postrelapse survival 35.7% Hispanic vs 13.0% non-Hispanic Black vs 43.8% non-Hispanic Other vs 38.9% non-Hispanic White; P = .0046).

CONCLUSIONS:

Neither proxied poverty exposures or race and ethnicity were associated with event-free survival or overall survival, suggesting equitable outcomes following frontline osteosarcoma trial-delivered therapy. Non-Hispanic Black children experienced statistically significant inferior postrelapse survival. Investigation of mechanisms underlying postrelapse disparities are paramount.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Natl Cancer Inst Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Natl Cancer Inst Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos