Ophthalmic Oncology Service, Memorial Sloan Kettering Cancer Center, New York City, New York, USA.
Department of Ophthalmology, Weill Cornell Medical College, New York City, New York, USA.
Br J Ophthalmol. 2019 Sep;103(9):1272-1277. doi: 10.1136/bjophthalmol-2018-312915. Epub 2018 Oct 25.
BACKGROUND/AIMS: Enucleation for retinoblastoma is performed less often in the past decade due to increasingly widespread alternative therapies, but enucleation remains an important option. There is a paucity of reports on the current incidence of metastases and metastatic deaths in unilateral retinoblastoma from US centres.
Retrospective chart review at five tertiary retinoblastoma centres in the USA for unilateral retinoblastoma patients treated with primary enucleation, 2007-2017, with 1 year of follow-up or treatment failure.
Among 228 patients (228 eyes), there were nine metastases (3.9%) and four deaths (1.7%). The Kaplan-Meier estimate at 5 years for metastasis-free survival was 96% (95% CI, 94% to 99 %), and for overall survival was 98% (95% CI 96% to 100%). All metastases were evident within 12 months. Histopathology revealed higher risk pathology (postlaminar optic nerve and/or massive choroidal invasion) in 62 of 228 eyes (27%). Of these higher risk eyes, 39 received adjuvant chemotherapy. There were four subsequent metastases in this higher risk pathology with adjuvant chemotherapy group, with three deaths. Of the nine overall with metastases, seven (78%) showed higher risk pathology. All metastatic patients were classified as Reese-Ellsworth V and International Classification of Retinoblastoma Groups D or E. Initial metastases presented as orbital invasion in seven of nine cases.
Primary enucleation for unilateral retinoblastoma results in a low rate of metastatic death, but is still associated with a 3.9% chance of metastases within a year of enucleation. Most but not all patients who developed metastases had higher risk histopathological findings.
背景/目的:由于替代疗法的广泛应用,过去十年中视网膜母细胞瘤的眼球摘除术应用减少,但眼球摘除术仍然是一个重要的选择。来自美国中心的单侧视网膜母细胞瘤转移和转移性死亡的发生率报告很少。
对美国五个三级视网膜母细胞瘤中心的 228 例(228 只眼)接受初次眼球摘除术治疗的单侧视网膜母细胞瘤患者进行回顾性图表审查,随访或治疗失败时间为 1 年。
在 228 例患者(228 只眼)中,有 9 例发生转移(3.9%),4 例死亡(1.7%)。无转移的 Kaplan-Meier 估计 5 年生存率为 96%(95%CI,94%至 99%),总生存率为 98%(95%CI,96%至 100%)。所有转移均在 12 个月内出现。组织病理学显示,228 只眼中有 62 只(27%)存在高危病理(视节后神经和/或巨大脉络膜侵犯)。在这些高危眼目中,有 39 只接受了辅助化疗。在接受辅助化疗的高危病理组中,有 4 例随后发生转移,其中 3 例死亡。在 9 例有转移的患者中,有 7 例(78%)存在高危病理。所有转移性患者均被归类为 Reese-Ellsworth V 和国际视网膜母细胞瘤分类 D 或 E 组。在 9 例初诊转移患者中,7 例(78%)出现眶内侵犯。
单侧视网膜母细胞瘤的初次眼球摘除术导致转移性死亡的发生率较低,但仍有 3.9%的患者在眼球摘除术后 1 年内发生转移。大多数(但不是全部)发生转移的患者均有高危组织病理学发现。