Beijing Tongren Eye Centre, Beijing Tongren Hospital, Capital Medical University, Beijing, China.
J Clin Oncol. 2011 Mar 1;29(7):845-51. doi: 10.1200/JCO.2010.32.5332. Epub 2011 Jan 31.
Initial response of intraocular retinoblastoma to chemotherapy has encouraged primary chemotherapy instead of primary enucleation for eyes with clinical features suggesting high risk of extraocular extension or metastasis. Upfront enucleation of such high-risk eyes allows pathologic evaluation of extraocular extension, key to management with appropriate surveillance and adjuvant therapy. Does chemotherapy before enucleation mask histologic features of extraocular extension, potentially endangering the child's life by subsequent undertreatment?
We performed retrospective analysis of 100 eyes with advanced retinoblastoma enucleated with, or without, primary chemotherapy, in Beijing Tongren Hospital, retrospectively, from October 31, 2008. The extent of retinoblastoma invasion into optic nerve, uvea, and anterior chamber on histopathology was staged by pTNM classification. The treatment groups were compared for pathologic stage (Cochran-Armitage trend test) and disease-specific mortality (competing risks methods).
Children who received chemotherapy before enucleation had lower pTNM stage than primarily enucleated children (P = .01). Five patients who received pre-enucleation chemotherapy died as a result of extension into brain or metastasis. No patients who had primary enucleation died. For children with group E eyes, disease-specific survival (DSS) was lower with pre-enucleation chemotherapy (n = 45) than with primary enucleation (n = 37; P = .01). Enucleation longer than 3 months after diagnosis was also associated with lower DSS (P < .001).
Chemotherapy before enucleation of group E eyes with advanced retinoblastoma downstaged pathologic evidence of extraocular extension, and increased the risk of metastatic death from reduced surveillance and inappropriate management of high-risk disease, if enucleation was performed longer than 3 months after diagnosis.
眼内视网膜母细胞瘤对化疗的初步反应鼓励了对具有提示眼外扩散或转移高风险的临床特征的眼进行初次化疗而不是初次眼球摘除。对于此类高危眼进行 upfront 眼球摘除可进行眼外扩散的病理评估,这是适当监测和辅助治疗管理的关键。眼球摘除前的化疗是否会掩盖眼外扩散的组织学特征,从而因后续治疗不足而危及患儿生命?
我们对 2008 年 10 月 31 日在北京同仁医院接受过或未接受过初次化疗的 100 只晚期视网膜母细胞瘤眼球进行了回顾性分析。通过 pTNM 分类对组织病理学上视神经、葡萄膜和前房内视网膜母细胞瘤的侵犯程度进行分期。通过 Cochran-Armitage 趋势检验比较治疗组的病理分期(Cochran-Armitage 趋势检验)和疾病特异性死亡率(竞争风险方法)。
接受眼球摘除前化疗的患儿比初次眼球摘除的患儿 pTNM 分期更低(P =.01)。5 例接受化疗的患儿因脑转移或扩散而死亡。未接受初次眼球摘除的患儿均未死亡。对于 E 组患儿,接受化疗的患儿(n = 45)比接受初次眼球摘除的患儿(n = 37)的疾病特异性生存率(DSS)更低(P =.01)。诊断后眼球摘除时间超过 3 个月与较低的 DSS 相关(P <.001)。
对于具有晚期视网膜母细胞瘤的 E 组眼,在眼球摘除前进行化疗会降低眼外扩散的病理证据,并增加因监测减少和高危疾病管理不当而导致转移性死亡的风险,如果诊断后眼球摘除时间超过 3 个月。