Ophthalmic Oncology Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA
Scheie Eye Institute, Philadelphia, Pennsylvania, USA.
Br J Ophthalmol. 2021 Jul;105(7):1016-1018. doi: 10.1136/bjophthalmol-2020-316588. Epub 2020 Jul 14.
Intravitreal injections of topotecan are used in the management of retinoblastoma with vitreous seeds. This study evaluated whether intravitreal topotecan was associated with retinal toxicity.
Retrospective cohort study of patients with retinoblastoma who were treated with intravitreal topotecan at Memorial Sloan Kettering Cancer Center between December 2014 and May 2019. Electroretinogram (ERG) responses under anaesthesia were measured immediately before treatment with intravitreal topotecan and at the next visitor approximately one-month. Ocular toxicity was defined by a decrease in the ERG response at 30 Hz at follow-up.
Ocular toxicity was evaluated by ERG on 50 evaluable injections administered to 28 eyes. 22 (44.0%) injections were performed with concurrent intravitreal melphalan. The median time to ERG measurement following an injection was 27 days. By using a paired t-test, intravitreal topotecan combined with melphalan (n=22) at a dose of 25 μg or 30 μg was associated with a significant decrease in ERG amplitude at follow-up (p=0.046, 95% CI -20.4 μV to -0.2 μV). Among eyes that only received topotecan (n=28) at doses of 20 μg or 30 μg, there was not a significant difference in ERG amplitude measured (p=0.85, 95% CI -7.0 μV to 5.8 μV).
Intravitreal topotecan combined with intravitreal melphalan was associated with a decrease in ERG amplitude; there was not a significant decrease in ERG amplitude observed in patients who received topotecan alone. These findings suggest that intravitreal topotecan injections at doses of 20 μg or 30 μg are not associated with retinal toxicity in patients with retinoblastoma.
眼内注射拓扑替康用于治疗伴有玻璃体内种子的视网膜母细胞瘤。本研究评估眼内注射拓扑替康是否与视网膜毒性相关。
对 2014 年 12 月至 2019 年 5 月期间在 Memorial Sloan Kettering 癌症中心接受眼内注射拓扑替康治疗的视网膜母细胞瘤患者进行回顾性队列研究。在眼内注射拓扑替康治疗前和下一次就诊时(约一个月后),在麻醉下测量视网膜电图(ERG)反应。根据随访时 ERG 反应下降定义为眼毒性。
在对 28 只眼的 50 次可评估注射中,通过 ERG 评估眼毒性。22(44.0%)次注射与眼内注射美法仑同时进行。注射后进行 ERG 测量的中位时间为 27 天。使用配对 t 检验,眼内注射拓扑替康联合美法仑(n=22)剂量为 25μg 或 30μg 与随访时 ERG 振幅显著下降相关(p=0.046,95%CI-20.4μV 至-0.2μV)。仅接受拓扑替康(n=28)剂量为 20μg 或 30μg 的眼,测量的 ERG 振幅无显著差异(p=0.85,95%CI-7.0μV 至 5.8μV)。
眼内注射拓扑替康联合眼内注射美法仑与 ERG 振幅下降相关;接受单纯眼内注射拓扑替康的患者中,未观察到 ERG 振幅显著下降。这些发现表明,在患有视网膜母细胞瘤的患者中,眼内注射拓扑替康剂量为 20μg 或 30μg 不与视网膜毒性相关。