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Time to diagnosis of retinoblastoma in Latin America: A systematic review.
Mattosinho, Clarissa Campolina De Sá; Moura, Anna Tereza M S; Oigman, Gabriela; Ferman, Sima E; Grigorovski, Nathália.
Afiliação
  • Mattosinho CCS; a Instituto Nacional de Câncer José Gomes de Alencar - Ocular Oncology , Universidade Estadual do Rio de Janeiro - Pediatric.
  • Moura ATMS; b Instituto Nacional de Câncer José Gomes de Alencar - Pediatric Oncology.
  • Oigman G; b Instituto Nacional de Câncer José Gomes de Alencar - Pediatric Oncology.
  • Ferman SE; b Instituto Nacional de Câncer José Gomes de Alencar - Pediatric Oncology.
  • Grigorovski N; b Instituto Nacional de Câncer José Gomes de Alencar - Pediatric Oncology.
Pediatr Hematol Oncol ; 36(2): 55-72, 2019 Mar.
Article em En | MEDLINE | ID: mdl-31014139
ABSTRACT
Retinoblastoma (RB) is the most common intraocular tumor of childhood. In low income countries, Time to diagnosis (TTD interval between first symptom and diagnosis) has been associated with extraocular disease, metastasis and mortality. However, the relationship between TTD and prognosis is complex and not simply a linear correlation, particularly if TTD is <6 months. This systematic review aims to identify studies reporting TTD of retinoblastoma in Latin America, highlighting factors affecting TTD, alongside proposals and initiatives to obtain shorter intervals. The review also aims to discuss the methodology linked to cancer pathways studies. The study respected PRISMA recommendations, was registered on Prospero, an international database for systematic review registries under number CRD42017076777. MEDLINE/PUBMED, LILACS and SCIELO databases were searched. Studies from Latin America and the Caribbean, published between 1997 and 2017, reporting TTD and age at diagnosis of patients with retinoblastoma were selected. Nine studies were selected, concerning 1560 patients from Argentina, Brazil, Chile, Honduras, Mexico and Peru. The median TTD ranged from 3 to 5 months and the median age at diagnosis ranged from 16.5 to 22.2 months. A prolonged TTD was observed and was associated to damaging results on retinoblastoma outcomes, particularly increasing extraocular disease, and mortality rates. Methodological heterogeneity was observed and reiterates the importance of standardization of TTD studies, allowing more reliable comparisons and greater knowledge about retinoblastoma pathways before diagnosis. Reports on successful initiatives against delayed diagnosis were scarce, emphasizing a need for further studies.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Retinoblastoma / Neoplasias Oculares Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies / Screening_studies / Systematic_reviews Limite: Child, preschool / Humans / Infant / Newborn Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Retinoblastoma / Neoplasias Oculares Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies / Screening_studies / Systematic_reviews Limite: Child, preschool / Humans / Infant / Newborn Idioma: En Ano de publicação: 2019 Tipo de documento: Article