多模式治疗视网膜母细胞瘤患者的视觉预后

Ratima Chokchaitanasin , Nattawat Asawaworarit , Wimwipa Dieosuthichat , Suradej Hongeng , Smart Pakakasama , Usanarat Anurathapan , Duantida Songdej , Pongpak Pongphitcha , Rangsima Aroonroch , Rossukon Kaewkhaw , Ekachat Chanthanaphak , Duangnate Rojanaporn
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引用次数: 0

摘要

目的本研究根据眼内视网膜母细胞瘤患者的临床特征和治疗方式,评估与球体保存和长期视觉结果相关的因素。设计回顾性审查2007年1月1日至2020年6月30日期间入组的眼内视网膜母细胞瘤患者的病历:患者或研究人群:患者或研究人群:在泰国曼谷拉玛提博迪医院接受治疗的眼内视网膜母细胞瘤患者:结果86名患者(124只眼)被纳入研究。双侧发病的中位年龄明显小于单侧。四分之三的患者处于晚期(ICRB 或 IIRC 的 D 组或 E 组,AJCC 的 cT2a 以下)。全球救治率为 54.0%(67 眼)。ICRB的D-E组、IIRC的D-E组以及AJCC的cT2a和更晚期是与摘除眼球相关的独立风险因素(调整后的几率比[AOR] [95 % CI] = 7.40 [1.36, 40.09]、8.33 [1.55, 44.73]、14.73 [1.55, 139.79])。与其他分类相比,IIRC 在单变量分析中提供了最高的统计相关性。IIRC A-C 组是一个良好的视觉盲点相关独立风险因素(AOR [95 % CI] = 4.64 [1.05, 20.43],P = 0.042)。黄斑受累是一个较差的视觉连续性相关独立危险因素(AOR [95 % CI] = 0.14 [0.02, 0.82],P = 0.03)。在我们的研究中,全身化疗(86.29%)是主要的治疗方法,也是唯一视觉效果较好的相关治疗方法。对所有接受全身化疗的眼睛进行亚组分析发现,ICRB 和 IIRC A-C 组以及 AJCC cT1a-cT1b 期的肿瘤分期对球囊摘除有统计学意义的预防因素(几率比 [95 % CI] = 15.75 [4.38, 56.65],15.67 [4.34, 56.53],9.97 [2.75, 36.18],分别;P=<0.001),并在这些分期中防止较差的视觉结果,(几率比[95 % CI] = 4.57 [1.28,16.27],6.61 [1.74,25.11],7.50 [1.86,30.16],分别;P=<0.05).结论所有最近的晚期临床分期都是全球清除结果相关的独立危险因素。IIRC分期是预测视觉结果的最佳指标。IIRC分期A-C组与良好的视觉结果相关。尽管多模式治疗成功地保留了眼球,但黄斑受累肿瘤与不良视觉预后密切相关。全身化疗仍是挽救眼球的关键治疗方法,可防止视力恶化--尤其是在ICRB和IRC A-C组以及AJCC cT1a-cT1b期。
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Visual prognosis in retinoblastoma patients with multimodality treatments

Purpose

This study evaluates factors associated with globe preservation and long-term visual outcomes according to clinical characteristics and treatment modalities in intraocular retinoblastoma patients.

Design

A retrospective review of medical records enrolled intraocular retinoblastoma patients between January 1, 2007, and June 30, 2020.

Methods

  • Setting: Single-centered.
  • Patient or study population: Intraocular retinoblastoma patients treated at Ramathibodi Hospital, Bangkok, Thailand.
  • Main outcome measure: A statistically significant factor associated with visual prognosis corresponds to baseline characteristics, staging, anatomical involvement, and multimodal treatments.

Results

86 patients (124 eyes) were included. Median age of disease bilaterality onset was significantly younger than unilaterality. Three-quarters of patients were in advanced stages (groups D or E in either ICRB or IIRC and up to cT2a from AJCC). Globe salvage rate was 54.0 % (67 eyes). ICRB Groups D-E, IIRC Groups D-E, and AJCC cT2a and more advanced stages are the globe removal-associated independent risk factors (adjusted odds ratio [AOR] [95 % CI] = 7.40 [1.36, 40.09], 8.33 [1.55, 44.73], 14.73 [1.55, 139.79], respectively). Compared to other classification, IIRC provided the highest statistical correlation from univariate analysis. IIRC Groups A-C is a good visual acuity-associated independent risk factor (AOR [95 % CI] = 4.64 [1.05, 20.43] and P = 0.042). Macular involvement is a worse visual acuity-associated independent risk factor (AOR [95 % CI] = 0.14 [0.02, 0.82] and P = 0.03). Systemic chemotherapy (86.29 %) is the mainstay treatment in our study and is the only good visual outcome-associated treatment. Subgroup analysis of all eyes receiving systemic chemotherapy reveals statistically significant preventive factors for globe removal for tumor staging with ICRB and IIRC groups A-C and AJCC stages cT1a–cT1b (odds ratio [95 % CI] = 15.75 [4.38, 56.65], 15.67 [4.34, 56.53], 9.97 [2.75, 36.18], respectively; P=<0.001) and prevents the worse visual outcome in these stages, (odds ratios [95 % CI] = 4.57 [1.28, 16.27], 6.61 [1.74, 25.11], and 7.50 [1.86, 30.16], respectively; P =< 0.05).

Conclusions

All recent advanced clinical stagings are globe removal outcome-associated independent risk factors. IIRC staging is the best visual results predictor. IIRC Groups A-C were associated with a good visual outcome. Macular involvement tumors are strongly associated with poor visual outcome, despite successful globe preservation from multimodality treatment. Systemic chemotherapy remains a crucial globe-saving treatment and prevents worse vision–especially in ICRB and IIRC Groups A-C and AJCC stage cT1a-cT1b.
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