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视网膜母细胞瘤治疗中白内障的风险因素。

Risk factors for cataract in retinoblastoma management.

机构信息

Department of Ophthalmology, Shanghai Key Laboratory of Orbital Diseases and Ocular Oncology, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

Department of Ophthalmology, Shanghai Key Laboratory of Orbital Diseases and Ocular Oncology, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China

出版信息

Br J Ophthalmol. 2024 Mar 20;108(4):571-577. doi: 10.1136/bjo-2022-321723.

Abstract

AIMS

To investigate the risk factors for cataract following eye-preserving therapies for retinoblastoma.

METHODS

This 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.

RESULTS

Cataract 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.

CONCLUSIONS

Repeated 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.

摘要

目的

探讨眼保存疗法治疗视网膜母细胞瘤后白内障发生的危险因素。

方法

本回顾性单中心队列研究纳入了 2017 年 1 月至 2021 年 6 月期间接受眼保存疗法治疗的视网膜母细胞瘤患者。以随访结束时发生白内障为主要结局。

结果

在平均 27.6 个月的随访中,184 只眼中有 31 只(16.8%)发现白内障。白内障组和对照组在患者的侧别、性别和疾病分期方面相似。白内障组的眼更有可能出现内生性视网膜母细胞瘤(p=0.02)和更高的眼内压(p=0.001)。竞争风险回归分析(单变量 Fine-Gray 模型)显示,生长模式(p=0.01)、眼内压(p=0.01)、动脉内化疗(IAC)周期数(p=0.001)、每个 IAC 周期的氨甲喋呤剂量(p=0.001)和玻璃体内化疗(IvitC)周期数(p=0.001)与白内障发生有关。多变量分析包括更高的眼内压(p=0.003)、每个 IAC 周期更高的氨甲喋呤剂量(p=0.001)和更多的 IvitC 周期(p=0.04)是白内障的独立危险因素。

结论

反复的 IAC 和/或 IvitC 联合氨甲喋呤是最常见的眼保存疗法,会导致白内障形成。氨甲喋呤的毒性作用是白内障发生的一个重要因素,这表明白内障的发生与氨甲喋呤剂量有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dd2/10958276/5310cb3011d5/bjo-2022-321723f01.jpg

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