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全身化疗和延迟眼摘术对晚期眼内视网膜母细胞瘤患儿生存的影响。

Impact of Systemic Chemotherapy and Delayed Enucleation on Survival of Children with Advanced Intraocular Retinoblastoma.

机构信息

Pediatric Oncology Center, Beijing Children's Hospital, Beijing, China.

Faculty of Medicine, University of Ottawa, Ottawa, Canada.

出版信息

Ophthalmol Retina. 2020 Jun;4(6):630-639. doi: 10.1016/j.oret.2020.02.015. Epub 2020 Mar 4.

Abstract

PURPOSE

Primary enucleation is a well-established method to achieve cure for advanced intraocular retinoblastoma. Recent treatment advances have induced a trend toward trial eye salvage using chemotherapy or other modalities. We investigated how pre-enucleation/postenucleation systemic chemotherapy and the resulting delayed enucleation affect patient survival after failed trial eye salvage.

DESIGN

Multicenter, retrospective cohort study.

PARTICIPANTS

Children with Group D and E retinoblastoma primarily or secondarily enucleated at 29 Chinese treatment centers.

METHODS

Data reviewed included clinical staging, time from diagnosis to enucleation, numbers of cycles of carboplatin, etoposide/teniposide and vincristine chemotherapy, disease-specific survival (DSS), histopathology, and follow-up.

MAIN OUTCOME MEASURES

Primary outcome was DSS. Secondary outcome was histopathology of enucleated eyes.

RESULTS

Primarily enucleated eyes had significantly shorter delay from diagnosis to enucleation than eyes treated with pre-enucleation chemotherapy (P < 0.001). Delay between diagnosis and enucleation >3.5 months (Group D) and >2 months (Group E) decreased survival (Group D: P = 0.018; Group E: P = 0.017). Compared with primarily enucleated children, children with 1 to 3 cycles of pre-enucleation chemotherapy for Group E eyes had no significant difference in survival (P = 0.74), but those who received ≥4 cycles had worse survival (P = 0.025). After pre-enucleation chemotherapy, more children with Group E (but not Group D) eyes had high-risk histopathology (pT3/pT4) (Group D: P = 0.076; Group E: P < 0.001) and worse survival than those primarily enucleated (P < 0.001). Postenucleation chemotherapy improved survival of children with high-risk histopathology (pT3/pT4) (P = 0.001) but did not change survival of children with low-risk histopathology (pT1/pT2) (P = 0.52).

CONCLUSIONS

We observed that pre-enucleation chemotherapy offered no survival benefit and timely enucleation minimized risk of metastatic death. Postenucleation chemotherapy improved survival of children with high-risk histopathology but was not useful for those with low-risk histopathology. These findings facilitate informed discussion on the risks and benefits of delayed enucleation, the use of systemic chemotherapy for trial salvage of eyes with advanced intraocular retinoblastoma, and the specific children who benefit from postenucleation chemotherapy.

摘要

目的

眼球摘除术是治疗眼内晚期视网膜母细胞瘤的一种成熟方法。最近的治疗进展促使人们倾向于使用化疗或其他方式进行试验性眼保存。我们研究了眼球摘除术前/后全身化疗以及由此导致的延迟性眼球摘除术对试验性眼保存失败后患者生存的影响。

设计

多中心回顾性队列研究。

参与者

29 家中国治疗中心的 D 型和 E 型视网膜母细胞瘤患儿,行初次或二次眼球摘除术。

方法

回顾性分析的临床分期、从诊断到眼球摘除的时间、卡铂、依托泊苷/替尼泊苷和长春新碱化疗周期数、疾病特异性生存率(DSS)、组织病理学和随访。

主要观察指标

主要观察指标为 DSS。次要观察指标为眼球摘除眼的组织病理学。

结果

初次眼球摘除组与眼球摘除术前化疗组相比,从诊断到眼球摘除的时间明显缩短(P < 0.001)。诊断与眼球摘除间隔时间>3.5 个月(D 组)和>2 个月(E 组)会降低生存率(D 组:P = 0.018;E 组:P = 0.017)。与初次眼球摘除的患儿相比,E 组眼球接受 1 至 3 个周期的眼球摘除术前化疗的患儿生存率无显著差异(P = 0.74),但接受≥4 个周期化疗的患儿生存率较差(P = 0.025)。眼球摘除术前化疗后,更多的 E 组(而非 D 组)患儿有高危组织病理学(pT3/pT4)(D 组:P = 0.076;E 组:P < 0.001),且生存率较初次眼球摘除患儿差(P < 0.001)。眼球摘除术后化疗改善了高危组织病理学(pT3/pT4)患儿的生存率(P = 0.001),但对低危组织病理学(pT1/pT2)患儿的生存率无影响(P = 0.52)。

结论

我们发现眼球摘除术前化疗并不能提高生存率,及时进行眼球摘除术可降低转移性死亡的风险。眼球摘除术后化疗可提高高危组织病理学患儿的生存率,但对低危组织病理学患儿无效。这些发现有助于就延迟性眼球摘除的风险和益处、晚期眼内视网膜母细胞瘤试验性眼保存中全身化疗的应用以及从眼球摘除术后化疗中获益的特定患儿进行知情讨论。

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