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单侧晚期视网膜母细胞瘤低风险组织病理学诊断的临床预测因素。

Clinical Predictors at Diagnosis of Low-Risk Histopathology in Unilateral Advanced Retinoblastoma.

机构信息

Department of Ophthalmology and Vision Sciences, University of Toronto, Toronto, Canada.

Department of Ophthalmology and Vision Sciences, The Hospital for Sick Children, Toronto, Canada.

出版信息

Ophthalmology. 2019 Sep;126(9):1306-1314. doi: 10.1016/j.ophtha.2019.04.003. Epub 2019 Apr 12.

Abstract

PURPOSE

Attempted eye salvage for unilateral (cT2b/group D) retinoblastoma may risk tumor spread compared with primary enucleation. Identification of clinical features predictive of low histopathologic risk support safe trial salvage.

DESIGN

Retrospective, noncomparative single-institutional observational case series.

PARTICIPANTS

Children with unilateral cT2b/group D retinoblastoma managed with primary enucleation at the Hospital for Sick Children, Toronto, Canada, January 2008 through February 2018.

METHODS

Data included clinical features (intraocular pressure, optic nerve obscuration, macular involvement, tumor seeding, and serous retinal detachment [RD] >1 quadrant), timing to enucleation, histopathologic features, and follow-up.

MAIN OUTCOME MEASURES

Primary outcome was low-risk (LR; pT1/pT2) versus high-risk (HR; pT3/pT4) histopathologic features with clinicopathologic correlations. Secondary outcomes were positive predictive (probability that certain clinical features would predict LR histopathologic features) and negative predictive values (probability that absence of these clinical features would predict HR histopathologic features).

RESULTS

Thirty-eight eyes were eligible and showed vitreous seeding and normal intraocular pressure. The median diagnosis to enucleation interval was 4 days (range, 0-14 days). Histopathologic analysis diagnosed 4 (10.5%) HR and 34 (89.5%) LR eyes. High-risk eyes demonstrated massive choroidal invasion (4/38) or trans-scleral, extraocular, and postlaminar optic nerve invasion (1/38). Clinical findings included macular involvement (31/38), complete optic nerve obscuration (27/38), and RD (28/38). The proportion of eyes with HR histopathologic features was 13% (4/31; 95% confidence interval [CI], 1%-25%) with macular involvement, 15% (4/27; 95% CI, 1%-28%) with complete optic nerve obscuration, and 14% (4/28; 95% CI, 1%-27%) with RD. The predictability of LR histopathologic features was 100% with macular sparing (7/7; 95% CI, 47%-100%), optic nerve visibility (10/10; 95% CI, 63%-100%), and less than 1 quadrant of RD (10/10; 95% CI, 63%-100%). In 1 child lacking all 3 clinical LR predictive features with HR histopathologic features (pT3a), metastases developed and the patient died; other children are alive and well (mean follow-up, 65 months).

CONCLUSIONS

Presence of macular sparing, optic nerve visibility, less than 1 quadrant of RD, or a combination thereof predicted LR histopathologic features at primary enucleation, suggesting safe trial eye salvage. No clinical sign predicted HR histopathologic features.

摘要

目的

与初次眼球摘除相比,单侧(cT2b/分组 D)视网膜母细胞瘤的眼球保留尝试可能会增加肿瘤扩散的风险。识别出具有低组织病理学风险的临床特征可以支持安全的试验性眼球保留。

设计

回顾性、非对照性单机构观察性病例系列研究。

参与者

2008 年 1 月至 2018 年 2 月在加拿大多伦多 SickKids 医院接受初次眼球摘除治疗的单侧 cT2b/分组 D 视网膜母细胞瘤患儿。

方法

数据包括临床特征(眼内压、视神经遮挡、黄斑受累、肿瘤播散和 >1 象限浆液性视网膜脱离[RD])、初次眼球摘除的时间、组织病理学特征和随访情况。

主要观察指标

主要结局为低危(LR;pT1/pT2)与高危(HR;pT3/pT4)组织病理学特征,并进行临床病理相关性分析。次要结局为阳性预测值(特定临床特征预测 LR 组织病理学特征的概率)和阴性预测值(缺乏这些临床特征预测 HR 组织病理学特征的概率)。

结果

38 只眼符合条件,表现为玻璃体内播散和正常眼内压。初次眼球摘除的中位诊断间隔时间为 4 天(范围:0-14 天)。组织病理学分析诊断出 4 只(10.5%)HR 眼和 34 只(89.5%)LR 眼。高危眼表现为大量脉络膜侵犯(4/38)或经巩膜、眼外和视神经后段侵犯(1/38)。临床发现包括黄斑受累(31/38)、完全视神经遮挡(27/38)和 RD(28/38)。具有 HR 组织病理学特征的眼占比为 13%(4/31;95%置信区间[CI]:1%-25%)伴黄斑受累,15%(4/27;95%CI:1%-28%)伴完全视神经遮挡,14%(4/28;95%CI:1%-27%)伴 RD。LR 组织病理学特征的预测性为 100%,具体表现为黄斑未受累(7/7;95%CI:47%-100%)、视神经可见(10/10;95%CI:63%-100%)和 RD 小于 1 象限(10/10;95%CI:63%-100%)。1 例儿童缺乏所有 3 个具有 LR 预测特征的临床特征,组织病理学为 HR(pT3a),发生转移,患儿死亡;其余患儿存活且情况良好(平均随访 65 个月)。

结论

初次眼球摘除时存在黄斑未受累、视神经可见、RD 小于 1 象限或三者联合存在,可预测 LR 组织病理学特征,提示可安全进行试验性眼球保留。无任何临床特征可预测 HR 组织病理学特征。

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