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<metadata xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/"><dc:title>Retinoblastoma with and without extraocular tumor extension</dc:title><dc:creator>Kaliki,	Swathi	(Avtor)
	</dc:creator><dc:creator>Vempuluru,	Vijitha S.	(Avtor)
	</dc:creator><dc:creator>Fabian,	Ido Didi	(Avtor)
	</dc:creator><dc:creator>Lavrič Groznik,	Alenka	(Sodelavec pri raziskavi)
	</dc:creator><dc:creator>Tekavčič Pompe,	Manca	(Sodelavec pri raziskavi)
	</dc:creator><dc:subject>external beam radiotherapy</dc:subject><dc:subject>extraocular extension</dc:subject><dc:subject>multimodal treatment</dc:subject><dc:subject>retinoblastoma</dc:subject><dc:subject>tumor</dc:subject><dc:description>Purpose
To study the treatment and outcomes of children with retinoblastoma (RB) with extraocular tumor extension (RB-EOE) and compare them with RB without extraocular tumor extension (RB-w/o-EOE).
Design
Multicenter intercontinental collaborative prospective study from 2017 to 2020. RB-EOE cases included those with overt orbital tumor extension in treatment-naive patients. Cases with microscopic orbital extension detected postenucleation were excluded from the study.
Participants
A total of 319 children with RB-EOE and 3116 children with RB-w/o-EOE.
Intervention
Chemotherapy, enucleation, exenteration, radiotherapy.
Main Outcome Measures
Systemic metastasis and death.
Results
Of the 3435 RB patients included in this study, 309 (9%) were from low-income countries (LIC), 1448 (42%) from lower-middle income, 1012 (29%) from upper-middle income, and 666 (19%) patients from high-income countries. There was an inverse relationship between the percentage of RB-EOE and national income level, with 96 (31%) patients from LIC, 197 (6%) lower-middle income, 20 (2%) upper-middle income, and 6 (1%) patients from high-income countries (P = 0.0001). The outcomes were statistically significant for RB-EOE compared with RB-w/o-EOE: systemic metastasis (32% vs. 4% respectively; P = 0.0001) and metastasis-related death (63% vs. 6% respectively; P = 0.0001). Multimodal treatment was the most common form of treatment (n = 177; 54%) for RB-EOE, with most cases undergoing a combination of intravenous chemotherapy and enucleation (n = 97; 30%). Adjuvant external beam radiotherapy (EBRT) after surgery (enucleation/orbital exenteration) was given in only 68 (21%) cases. Kaplan–Meier analysis for systemic metastasis and metastasis-related death in RB-EOE was 28% and 57% at 1 year, 29% and 60% at 2 years, and 29% and 61% at 3 years, respectively. Cox regression analysis revealed that the risk of death from RB-EOE was greater in patients aged &gt;4 years than &lt;2 years (hazard ratio, 2.912; P &lt; 0.001) and for unimodal (surgery or intravenous chemotherapy) and bimodal (surgery and intravenous chemotherapy) treatment than trimodal treatment (surgery, intravenous chemotherapy, and EBRT) (hazard ratio, 2.023; P = 0.004 and hazard ratio, 1.819; P = 0.027, respectively).
Conclusions
Retinoblastoma with extraocular tumor extension is associated with a higher risk of metastasis and death. Patients with RB-EOE are likely to benefit from trimodal treatment (intravenous chemotherapy, surgery, and EBRT) rather than treatment protocols excluding EBRT.</dc:description><dc:date>2025</dc:date><dc:date>2026-03-10 11:02:40</dc:date><dc:type>Neznano</dc:type><dc:identifier>28105</dc:identifier><dc:identifier>UDK: 617.7</dc:identifier><dc:identifier>ISSN pri članku: 2666-9145</dc:identifier><dc:identifier>DOI: 10.1016/j.xops.2024.100637</dc:identifier><dc:identifier>COBISS_ID: 240654851</dc:identifier><dc:language>sl</dc:language></metadata>
