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眼内注射拓扑替康治疗视网膜母细胞瘤难治性和复发性玻璃体内播散。

Intravitreal topotecan in the management of refractory and recurrent vitreous seeds in retinoblastoma.

机构信息

Department of Ocular Oncology Service, National Retinoblastoma Foundation, Centre for Sight, Hyderabad, India.

出版信息

Br J Ophthalmol. 2018 Apr;102(4):490-495. doi: 10.1136/bjophthalmol-2017-310641. Epub 2017 Aug 26.

Abstract

BACKGROUND/AIM: To evaluate the efficacy of intravitreal topotecan for refractory or recurrent vitreous seeds in retinoblastoma.

METHODS

Intravitreal injection of topotecan hydrochloride (30 µg/0.15 mL) was provided every 3 weeks by the safety enhanced technique.

RESULTS

The study included 17 consecutive patients with retinoblastoma with refractory or recurrent vitreous seeds. Five eyes (29%) belonged to International Classification of Retinoblastoma group C and 12 eyes (71%) belonged to group D. Primary treatment included triple drug intravenous chemotherapy for a mean of 10 cycles (median, 9 cycles; range, 6-18 cycles). Fifteen patients (88%) had undergone 56 periocular carboplatin injections with a mean of 4 injections (median, 3 injections; range, 1-8 injections), concurrent with intravenous chemotherapy. A total of 53 intravitreal topotecan injections were performed in 17 eyes of 17 consecutive patients with refractory or recurrent vitreous seeds with a mean of 3 injections (median, 3 injections; range, 2-6 injections). Complete regression of vitreous seeds was achieved in 17 of 17 eyes (100%). At a mean follow-up of 23.8 months (median, 24 months; range, 15.1-34.1 months), one eye (6%) with a recurrent retinal tumour needed enucleation, and the rest of the 16 eyes (94%) maintained complete regression. Final visual acuity could be reliably assessed in all 16 eyes (100%), of whom 12 eyes (75%) had visual acuity ≥20/200. None of the patients developed ocular or systemic complications.

CONCLUSION

Three-weekly intravitreal topotecan appears effective and safe in controlling focal or diffuse refractory or recurrent vitreous seeds in retinoblastoma.

摘要

背景/目的:评估拓扑替康玻璃体腔内注射治疗视网膜母细胞瘤难治性或复发性玻璃体内种子的疗效。

方法

采用安全增强技术,每 3 周玻璃体腔内注射盐酸拓扑替康(30μg/0.15mL)。

结果

本研究纳入了 17 例患有难治性或复发性玻璃体内种子的视网膜母细胞瘤连续患者。5 只眼(29%)属于国际视网膜母细胞瘤分类 C 组,12 只眼(71%)属于 D 组。一线治疗包括三药静脉化疗,平均 10 个周期(中位数,9 个周期;范围,6-18 个周期)。15 例(88%)患者接受了 56 次眶周卡铂注射,平均 4 次(中位数,3 次;范围,1-8 次),同时进行静脉化疗。17 例连续难治性或复发性玻璃体内种子患者的 17 只眼共进行了 53 次玻璃体腔内拓扑替康注射,平均 3 次(中位数,3 次;范围,2-6 次)。17 只眼(100%)的玻璃体内种子完全消退。平均随访 23.8 个月(中位数,24 个月;范围,15.1-34.1 个月)后,1 只眼(6%)因视网膜肿瘤复发而需要眼球摘除,其余 16 只眼(94%)保持完全消退。16 只眼(100%)的最终视力均可可靠评估,其中 12 只眼(75%)视力≥20/200。所有患者均未出现眼部或全身并发症。

结论

三周一次的玻璃体腔内拓扑替康治疗视网膜母细胞瘤难治性或复发性玻璃体内种子具有疗效和安全性。

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