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儿童 1 型神经纤维瘤病相关视神经胶质瘤行依维莫司靶向治疗后的视觉预后。

Visual outcomes following everolimus targeted therapy for neurofibromatosis type 1-associated optic pathway gliomas in children.

机构信息

Department of Neurology, Boston Children's Hospital, Boston, Massachusetts.

Dana-Farber/Boston Children's Cancer and Blood Disorder Center, Boston, Massachusetts.

出版信息

Pediatr Blood Cancer. 2021 Apr;68(4):e28833. doi: 10.1002/pbc.28833. Epub 2020 Dec 18.

Abstract

Data for visual acuity (VA) after treatment of neurofibromatosis type 1-associated optic pathway gliomas (NF1-OPGs) are limited. We retrospectively collected VA, converted to logMAR, before and after targeted therapy with everolimus for NF1-OPG, and compared to radiologic outcomes (14/18 with NF1-OPG, 25 eyes [three without quantifiable vision]). Upon completion of treatment, VA was stable in 19 eyes, improved in four eyes, and worsened in two eyes; visual and radiologic outcomes were discordant. In summary, the majority of children with NF1-OPG exhibited stabilization of their VA after everolimus treatment. A larger, prospective study will help delineate visual outcomes after targeted therapy.

摘要

关于神经纤维瘤病 1 型相关视神经胶质瘤(NF1-OPG)治疗后视力的数据有限。我们回顾性收集了接受依维莫司靶向治疗前后 NF1-OPG 的视力(VA)数据,将其转换为 logMAR 并进行分析,并与影像学结果进行了比较(14/18 例 NF1-OPG,25 只眼[3 只眼视力无法量化])。治疗完成后,19 只眼的 VA 稳定,4 只眼的 VA 改善,2 只眼的 VA 恶化;视力和影像学结果不一致。总之,大多数 NF1-OPG 患儿在接受依维莫司治疗后,VA 稳定。更大规模的前瞻性研究将有助于明确靶向治疗后的视力结果。

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