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Outcome, pathologic findings, and compliance in orbital retinoblastoma (International Retinoblastoma Staging System stage III) treated with neoadjuvant chemotherapy: A prospective study

机译:新辅助化疗治疗眼眶视网膜母细胞瘤(国际视网膜母细胞瘤分期系统III期)的结局,病理学发现和顺应性:一项前瞻性研究

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Purpose: The present study prospectively evaluated outcome, pathologic findings, and compliance in orbital retinoblastoma patients (International Retinoblastoma Staging System [IRSS] stage III). Design: Prospective study and case series. Participants: Twenty-eight consecutive IRSS stage III retinoblastoma patients were enrolled prospectively in the study after ethics committee approval and written informed consent. Methods: Planned therapy for patients included treatment with a uniform protocol consisting of neoadjuvant chemotherapy followed by enucleation, adjuvant radiotherapy, and chemotherapy. Prospective computerized data entry and telephone contact were undertaken to improve compliance, a major issue in treatment of orbital retinoblastoma. Main Outcome Measures: Event-free survival (EFS) and overall survival (OS) were calculated using Kaplan-Meier survival analysis. The difference between groups was analyzed using the log-rank test. Results: Median follow-up was 14.75 months (range, 2.23-26.3 months). The OS for all patients was 40.4% and the EFS was 33.33% at a follow-up of 26.3 months. The median EFS and OS were 10.37 months and 15.73 months, respectively. At baseline, bilateral retinoblastoma predicted inferior EFS (P = 0.0006) and OS (P = 0.0081). Twenty-two of 28 patients underwent enucleation, and viable tumor was present in 21 of 22 enucleated specimens (95%). Neoadjuvant chemotherapy prevented orbital exenterations. Presence of tumor in the cut end of the optic nerve significantly correlated with inferior EFS (P = 0.012) and OS (P = 0.0098). Central nervous system metastasis was the most common site of relapse and death. The overall rate of compliance with treatment was 67.8% (19/28), which was twice the compliance rate at the authors' center before initiation of the present study. Conclusions: There is a paucity of information in the literature on outcomes and pathologic findings after neoadjuvant chemotherapy in IRSS stage III retinoblastoma treated with a uniform treatment protocol, and as far as the authors are aware, there has been no prospective study. Neoadjuvant chemotherapy was able to avoid exenteration in all operated patients; however, residual viable tumor was present in 95% of enucleated specimens. Bilaterality and tumor in the optic nerve cut end after neoadjuvant chemotherapy were associated with inferior outcome. Compliance could be improved with computerized data entry and regular telephone contact. Financial Disclosure(s): The author(s) have no proprietary or commercial interest in any materials discussed in this article.
机译:目的:本研究前瞻性评估眼眶视网膜母细胞瘤患者的结局,病理学发现和依从性(国际视网膜母细胞瘤分期系统[IRSS] III期)。设计:前瞻性研究和案例系列。参与者:在伦理委员会批准并获得知情同意后,连续入选了28名IRSS III期视网膜母细胞瘤患者。方法:针对患者的计划治疗包括统一的治疗方案,包括新辅助化疗,摘除,辅助放疗和化疗。进行了前瞻性的计算机数据输入和电话联系以提高依从性,这是治疗眼眶视网膜母细胞瘤的主要问题。主要结果指标:使用Kaplan-Meier生存分析计算无事件生存(EFS)和总体生存(OS)。使用对数秩检验分析组之间的差异。结果:中位随访时间为14.75个月(范围:2.23-26.3个月)。随访26.3个月,所有患者的OS为40.4%,EFS为33.33%。 EFS和OS的中位数分别为10.37个月和15.73个月。在基线时,双侧视网膜母细胞瘤预测的EFS(P = 0.0006)和OS(P = 0.0081)较差。 28例患者中有22例接受了摘除术,22例摘除标本中有21例存在活体肿瘤(95%)。新辅助化疗可防止眼眶脱落。视神经切口末端的肿瘤存在与EFS差(P = 0.012)和OS(P = 0.0098)显着相关。中枢神经系统转移是复发和死亡的最常见部位。治疗的总依从率为67.8%(19/28),是本研究开始之前作者中心的依从率的两倍。结论:文献中缺乏关于采用统一治疗方案治疗的IRSS III期视网膜母细胞瘤新辅助化疗后的结局和病理发现的信息,据作者所知,尚无前瞻性研究。新辅助化疗能够避免所有手术患者的肿瘤消退。但是,在95%的去核标本中仍存在残留的存活肿瘤。新辅助化疗后视神经切断端的双侧性和肿瘤与不良预后相关。可以通过计算机化的数据输入和定期的电话联系来提高合规性。财务披露:作者对本文讨论的任何材料均没有所有权或商业利益。

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