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化疗降低风险联合低剂量调强放疗挽救治疗后双眼视网膜母细胞瘤 D 组眼的长期疗效

Long-term outcomes of Group D eyes in bilateral retinoblastoma patients treated with chemoreduction and low-dose IMRT salvage.

机构信息

Doheny Eye Institute, Los Angeles, California 90033, USA.

出版信息

Pediatr Blood Cancer. 2013 Apr;60(4):688-93. doi: 10.1002/pbc.24303. Epub 2012 Sep 19.

Abstract

BACKGROUND

To evaluate outcomes of Group D eyes of bilateral retinoblastoma patients treated with primary chemoreduction and external beam radiation as salvage.

PROCEDURE

Retrospective chart review of patients diagnosed with bilateral retinoblastoma and designated Group D in at least one eye from January 1, 2000 to December 31, 2009. Overall, 62 Group D eyes of 49 patients were included; 13 had bilateral Group D disease. Primary chemoreduction with vincristine, etoposide, and carboplatin with local consolidation was administered, followed by external beam radiation in the form of intensity-modulated radiation therapy (IMRT) as salvage for recurrent tumor. Primary outcome measure was globe salvage.

RESULTS

Of 62 Group D eyes, 7 were enucleated primarily; 55 were treated with systemic chemoreduction, and local therapy. Chemoreduction cured 26 of 55 eyes (47%). Recurrences were found in 29 eyes; 5 underwent enucleation and 24 were treated with IMRT at a dose of 24 Gy (2 eyes) or 36 Gy (22 eyes). Of the 24 irradiated eyes, 19 (79%) were salvaged and 5 required enucleation. Final visual acuity ranged from 20/20 to light perception with 10 eyes having 20/80 or better visual acuity. Average follow-up was 54.2 months.

CONCLUSION

Kaplan-Meier estimates of eye survival of Group D eyes in bilateral patients at 12 months is 82% (95% confidence interval [CI] 70.1-89.7%); at 60 months eye survival is estimated to be 68% (95% confidence interval [CI] 55.4-82.8%). Systemic treatment for retinoblastoma demonstrated a high rate of globe preservation with acceptable complications and many eyes retaining functional vision.

摘要

背景

评估 2000 年 1 月 1 日至 2009 年 12 月 31 日期间至少一只眼被诊断为双侧视网膜母细胞瘤且被归类为 D 组的双侧视网膜母细胞瘤患者经初次化学减瘤和外照射作为挽救治疗后的结局。

方法

对至少一眼被诊断为双侧视网膜母细胞瘤且至少一眼被归类为 D 组的患者进行回顾性图表分析。共纳入 49 例患者的 62 只 D 组眼,其中 13 例为双眼 D 组疾病。给予长春新碱、依托泊苷和顺铂的初次化学减瘤治疗,并进行局部巩固治疗,然后作为复发性肿瘤的挽救治疗,采用调强放疗(IMRT)进行外照射。主要结局指标为眼球保存。

结果

62 只 D 组眼中,7 只眼最初行眼球摘除术;55 只眼行全身化学减瘤和局部治疗。化学减瘤治愈 55 只眼中的 26 只(47%)。29 只眼出现复发;5 只眼行眼球摘除术,24 只眼行 IMRT 治疗,剂量为 24 Gy(2 只眼)或 36 Gy(22 只眼)。24 只接受放疗的眼中,19 只(79%)得以挽救,5 只需要行眼球摘除术。最终视力范围从 20/20 到光感,其中 10 只眼的视力为 20/80 或更好。平均随访时间为 54.2 个月。

结论

12 个月时双侧患者 D 组眼的生存估计为 82%(95%置信区间[CI]70.1-89.7%);60 个月时眼生存估计为 68%(95%置信区间[CI]55.4-82.8%)。用于治疗视网膜母细胞瘤的全身治疗具有较高的眼球保留率,并发症可接受,许多眼保留了有用的视力。

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