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Risk factors for cataract in retinoblastoma management

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AimsTo investigate the risk factors for cataract following eye-preserving therapies for retinoblastoma.MethodsThis retrospective, single-centre cohort study included patients diagnosed with retinoblastoma receiving eye-preserving therapies between January 2017 and June 2021. Cataract by the end of the follow-up was the main outcome.ResultsCataract was found in 31 of 184 (16.8%) included eyes during a mean follow-up of 27.6 months. The cataract and control groups were similar regarding patients’ laterality, sex and disease stage. Eyes in the cataract group were more likely to present with endophytic retinoblastoma (p=0.02) and greater intraocular pressure (p=0.001). Competing risk regression analysis (univariate Fine-Gray model) showed that the growth pattern (p=0.01), intraocular pressure (p=0.01), number of intra-arterial chemotherapy (IAC) cycles (p=0.001), melphalan dose per IAC cycle (p=0.001) and number of intravitreous chemotherapy (IvitC) cycles (p=0.001) were associated with cataract occurrence. Multivariate analysis included higher intraocular pressure (p=0.003), a higher melphalan dose per IAC cycle (p=0.001) and an increasing number of IvitC cycles (p=0.04) as independent risk factors for cataract.ConclusionsRepeated IAC and/or IvitC with melphalan were the most common eye-preserving therapies that induced cataract formation. The toxic effect of melphalan was an essential factor in cataract development, as indicated by the association of cataract occurrence with the melphalan dose.
Title: Risk factors for cataract in retinoblastoma management
Description:
AimsTo investigate the risk factors for cataract following eye-preserving therapies for retinoblastoma.
MethodsThis retrospective, single-centre cohort study included patients diagnosed with retinoblastoma receiving eye-preserving therapies between January 2017 and June 2021.
Cataract by the end of the follow-up was the main outcome.
ResultsCataract was found in 31 of 184 (16.
8%) included eyes during a mean follow-up of 27.
6 months.
The cataract and control groups were similar regarding patients’ laterality, sex and disease stage.
Eyes in the cataract group were more likely to present with endophytic retinoblastoma (p=0.
02) and greater intraocular pressure (p=0.
001).
Competing risk regression analysis (univariate Fine-Gray model) showed that the growth pattern (p=0.
01), intraocular pressure (p=0.
01), number of intra-arterial chemotherapy (IAC) cycles (p=0.
001), melphalan dose per IAC cycle (p=0.
001) and number of intravitreous chemotherapy (IvitC) cycles (p=0.
001) were associated with cataract occurrence.
Multivariate analysis included higher intraocular pressure (p=0.
003), a higher melphalan dose per IAC cycle (p=0.
001) and an increasing number of IvitC cycles (p=0.
04) as independent risk factors for cataract.
ConclusionsRepeated IAC and/or IvitC with melphalan were the most common eye-preserving therapies that induced cataract formation.
The toxic effect of melphalan was an essential factor in cataract development, as indicated by the association of cataract occurrence with the melphalan dose.

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