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Retinoblastoma Presentation, Treatment and Outcome in a Large Referral Centre in Tehran: A 10-Year Retrospective Analysis Publisher Pubmed



Faranoush M1, 2 ; Mehrvar N1, 3 ; Tashvighi M1 ; Fabian ID4 ; Zloto O5 ; Bascaran C4 ; Ghorbani R6 ; Ghasemi F7 ; Naseripour M8 ; Sedaghat A8 ; Alebouyeh M1 ; Mehrvar A1, 9
Authors
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Authors Affiliations
  1. 1. MAHAK Hematology Oncology Research Center (MAHAK-HORC), MAHAK Hospital, Tehran, Iran
  2. 2. Pediatric Growth and Development Research Center, Institute of Endocrinology and Metabolism, Iran University of Medical Sciences, Tehran, Iran
  3. 3. Cancer Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  4. 4. International Centre for Eye Health, London School of Hygiene and Tropical Medicine, London, United Kingdom
  5. 5. SIREDO Oncology Center (Care, Innovation and Research for Children, Adolescents and Young Adults with Cancer), Institute Curie, Paris, France
  6. 6. Social Determinants of Health Research Center, Semnan University of Medical Sciences, Semnan, Iran
  7. 7. Farabi Eye Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  8. 8. Eye Research Center, Rassoul Akram Hospital, Iran University of Medical Sciences, Tehran, Iran
  9. 9. AJA Cancer Epidemiology Research and Treatment Center (AJA-CERTC), AJA University of Medical Sciences, Tehran, Iran

Source: Eye (Basingstoke) Published:2021


Abstract

Background/objectives: Early diagnosis, care and treatment of retinoblastoma is a challengeable issue for Iranian health system. This study was designed and conducted in a referral multidisciplinary centre in the capital city of Iran to evaluate management, care, prognosis and survival rates of paediatric patients with retinoblastoma. Methods: In this retrospective study, a total number of 309 patients younger than 15 years, diagnosed with retinoblastoma, who referred for diagnosis and treatment to MAHAK’s Pediatric Cancer Treatment and Research Center (MPCTRC) from 2007 to 2017 were evaluated. All data were analyzed via SPSS version 22 software in regard of parametric and non-parametric data. Survival rates were analyzed using the Kaplan–Meyer method. Results: The mean age of patients was 20 months and the majority of patients (77%) had leukocoria as a common clinical symptom at the time of diagnosis. Primary treatment methods were systemic chemotherapy (94%), laser (35%) and primary enucleation (28%). Relapses occurred in nearly 42% of cases, and the median time from diagnosis to the first relapse was 9 months. At the time analyzing the data, 11% of patients died. Patients’ 5-year OS and RFS rates were 79.6% and 41.5%, respectively. Conclusion: Comparing results with other conducted studies identifies that the recurrence rate was high in our considered patients. Also, OS and RFS rates in our study were not as considerable as other reports. Screening methods, updating protocols and follow-up of patients may lead to improvements in survival rates of patients with retinoblastoma. © 2020, The Author(s), under exclusive licence to The Royal College of Ophthalmologists.