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Clinical presentation and treatment outcome of retinoblastoma in children of South Western China

机译:西南地区儿童视网膜母细胞瘤的临床表现和治疗结果

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摘要

To study the clinical presentation and treatment outcome among children in South Western China with retinoblastoma (RB) and to determine factors predictive of poor outcome.A retrospective review of children diagnosed with RB from 2006 to 2015 at West China Hospital was undertaken. Demographic and clinical characteristics and treatment outcomes were studied.A total of 253 patients (unilateral 80.2%, bilateral 19.8%) were studied. Twenty six patients (10.3%) were from minority ethnic groups of China. The median onset age was 21 months. Leukocoria was the most common presenting sign (71%). Tumors were intraocular in 91.3% cases, extraocular in 8.7% cases. Extraocular RB patients had a longer median lag period than intraocular patients (9 months vs 2 months, P < 0.0001). In the intraocular group, 89.5% were advanced group D or E diseases. Enucleation was the major treatment for intraocular RB. However, over 10 years, the enucleation rate decreased constantly while more patients received chemotherapy. The Kaplan–Meier survival probability was 87.8%, 81.4%, and 74.8% at 3 years, 5 years, and 10 years, respectively. On Cox regression analysis, extraocular RB (P = 0.0008) and treatment abandonment (P < 0.0001) were associated with poor outcome; bilateral RB (P = 0.0116) and advanced pathological grade pT4 (P = 0.0011) were associated with poor outcome of intraocular RB.Most RB patients from South Western China were diagnosed at advanced clinical stage. Delayed presentation is related to extraocular RB which is a risk factor for poor outcome. Chemotherapy increased the eye salvage but had no effects to overall survival. Education for parents and general physicians for the early signs of RB (such as leukocoria), therapeutic strategy and treatment outcomes of RB may promote early diagnosis, improve the compliance, and outcome.
机译:为了研究中国西南地区视网膜母细胞瘤(RB)儿童的临床表现和治疗结果,并确定预后不良的因素.2006年至2015年,在中国西部医院对诊断为RB的儿童进行了回顾性研究。研究了人口统计学和临床​​特征以及治疗结果。共研究了253例患者(单侧80.2%,双侧19.8%)。二十六名患者(10.3%)来自中国少数民族。中位发病年龄为21个月。白细胞减少症是最常见的表现体征(71%)。眼内肿瘤占91.3%,眼外肿瘤占8.7%。眼外RB患者的中位滞后期比眼内患者更长(9个月比2个月,P <0.0001)。眼内组中,晚期D或E组疾病占89.5%。去核是眼内RB的主要治疗方法。然而,十多年来,去核率不断下降,而更多的患者接受了化疗。在3年,5年和10年时,Kaplan-Meier生存率分别为87.8%,81.4%和74.8%。经Cox回归分析,眼外RB(P = 0.0008)和治疗放弃(P <0.0001)与不良预后相关。双侧RB(P = 0.0116)和晚期病理分级pT4(P = 0.0011)与眼内RB的不良预后有关。西南地区大多数RB患者被诊断为处于晚期临床阶段。延迟出现与眼外RB有关,后者是不良预后的危险因素。化学疗法可增加挽救眼睛的能力,但对整体生存没有影响。对父母和普通医师进行RB早期征兆(例如白斑),RB的治疗策略和治疗结果的教育可能会促进早期诊断,改善依从性和结果。

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