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Systematic review and meta-analysis of health-related quality of life in pediatric CNS tumor survivors.
Schulte, Fiona; Russell, K Brooke; Cullen, Patricia; Embry, Leanne; Fay-McClymont, Taryn; Johnston, Donna; Rosenberg, Abby R; Sung, Lillian.
Afiliação
  • Schulte F; Departments of Oncology and Paediatrics, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Russell KB; Haematology, Oncology and Transplant Program, Alberta Children's Hospital Research Institute, Alberta Children's Hospital, Calgary, Alberta, Canada.
  • Cullen P; Haematology, Oncology and Transplant Program, Alberta Children's Hospital, Calgary, Alberta, Canada.
  • Embry L; Departments of Oncology and Psychology, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Fay-McClymont T; Loretto Heights School of Nursing, Regis University, Denver, Colorado.
  • Johnston D; Department of Pediatrics, University of Texas Health Science Center at San Antonio, San Antonio, Texas.
  • Rosenberg AR; Departments of Oncology and Paediatrics, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Sung L; Department of Paediatrics, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
Pediatr Blood Cancer ; 64(8)2017 Aug.
Article em En | MEDLINE | ID: mdl-28266804
ABSTRACT

BACKGROUND:

Pediatric central nervous system (CNS) tumor survivors are at high risk for numerous late effects including decreased health-related quality of life (HRQOL). Our objective was to summarize studies describing HRQOL in pediatric CNS tumor survivors and compare HRQOL outcomes in studies that included a comparison group. PROCEDURE EMBASE, MEDLINE, and PsychINFO were used to identify relevant articles published until August, 2016. Eligible studies reported outcomes for pediatric CNS tumor survivors diagnosed before age 21, at least 5 years from diagnosis and/or 2 years off therapy and used a standardized measure of HRQOL. All data were abstracted by two reviewers. Random-effects meta-analyses were performed using Review Manager 5.0.

RESULTS:

Of 1,912 unique articles identified, 74 were included in this review. Papers described 29 different HRQOL tools. Meta-analyses compared pediatric CNS tumor survivors to healthy comparisons and other pediatric cancer survivors separately. HRQOL was significantly lower for CNS (n = 797) than healthy comparisons (n = 1,397) (mean difference = -0.54, 95% confidence interval [CI] = -0.72 to -0.35, P < 0.001, I2 = 35%). HRQOL was also significantly lower for CNS (n = 244) than non-CNS survivors (n = 414) (mean difference = -0.56, 95% CI = -0.73 to -0.38, P < 0.00001, I2 = 0%).

CONCLUSIONS:

Pediatric CNS tumor survivors experience worse HRQOL than healthy comparisons and non-CNS cancer survivors. Future HRQOL work should be longitudinal, and/or multisite studies that examine HRQOL by diagnosis and treatment modalities.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Qualidade de Vida / Nível de Saúde / Neoplasias do Sistema Nervoso Central / Sobreviventes Tipo de estudo: Systematic_reviews Limite: Child / Female / Humans / Male Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Qualidade de Vida / Nível de Saúde / Neoplasias do Sistema Nervoso Central / Sobreviventes Tipo de estudo: Systematic_reviews Limite: Child / Female / Humans / Male Idioma: En Ano de publicação: 2017 Tipo de documento: Article