Clinicoepidemiological Profile and Treatment Outcomes in Children with Retinoblastoma: Experience from a Cancer Care Center in Northeast India.

IF 0.6 Q4 ONCOLOGY
Munlima Hazarika, Gaurav Kumar, Bhargab Jyoti Saikia, Satya Sadhan Sarangi, Partha Sarathi Roy, Kasturi Bhattacharjee, Manabjyoti Barman
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引用次数: 1

Abstract

Gaurav KumarBackground  Retinoblastoma (RB) is the most common primary intraocular malignancy in children. We sought to provide a comprehensive assessment of epidemiological profile and treatment outcomes of children with RB. Methods  In this retrospective study, we analyzed 189 children diagnosed with RB at our center between 2004 and 2017. Survival was analyzed with the Kaplan-Meier method and log-rank test. Results  Median age at presentation was 14 months with male: female ratio 1.2:1. Mean duration between onset of symptoms and presentation was 49 days (standard deviation ± 79). Most common presenting symptom was white pupillary reflex in 60% of children. Family history of RB and other cancers was found in one (0.5%) and seven (4%) children, respectively. Primary mode of diagnosis and staging was ocular ultrasonography (bone scan) in 87% of patients. Computed tomographic scan and magnetic resonance imaging were done in 124 (66%) and 30 (16%) patients, respectively. International staging system grade E disease was found in 144 (76%), extraocular disease in 55 (29%), bilateral disease in 49 (26%), and trilateral disease in 3 (1.5%) children. Out of 189 children with RB, 33 (18%) refused treatment and 156 children received treatment (24 children [15%] abandoned treatment midway and 132 [85%] completed treatment). One hundred children (64%) received systemic therapy as neoadjuvant or adjuvant chemotherapy and 20 (13%) received local therapy. Eyeball and vision salvage rate with chemotherapy were 20 (13%) and 9 (6%), respectively. Cryotherapy was the most common modality of local treatment used in 11 (55%) children. Five-year survival for patients who received treatment was 76% (median survival not reached). In the treatment refusal group, median survival was 9 months. Conclusion  In developing countries, RB is mostly detected in advanced stages resulting in poor outcomes. Increased awareness and accessibility to dedicated centers for treating childhood malignancy can lead to early diagnosis, better prognosis, and increased vision salvage.

Abstract Image

儿童视网膜母细胞瘤的临床流行病学特征和治疗结果:来自印度东北部癌症护理中心的经验。
视网膜母细胞瘤(Retinoblastoma, RB)是儿童最常见的原发性眼内恶性肿瘤。我们试图对儿童RB的流行病学概况和治疗结果进行综合评估。方法回顾性分析2004年至2017年在本中心诊断为RB的189名儿童。生存率分析采用Kaplan-Meier法和log-rank检验。结果中位发病年龄为14个月,男女比例为1.2:1。从出现症状到出现症状的平均持续时间为49天(标准差±79)。60%的儿童以白色瞳孔反射为最常见的症状。有RB和其他癌症家族史的儿童分别为1例(0.5%)和7例(4%)。87%的患者以眼超声检查(骨扫描)为主要诊断和分期方式。分别对124例(66%)和30例(16%)患者进行了计算机断层扫描和磁共振成像。国际分期系统E级疾病144例(76%),眼外疾病55例(29%),双侧疾病49例(26%),三边疾病3例(1.5%)。189例RB患儿中,33例(18%)拒绝治疗,156例接受治疗(24例(15%)中途放弃治疗,132例(85%)完成治疗)。100名儿童(64%)接受了新辅助或辅助化疗的全身治疗,20名儿童(13%)接受了局部治疗。化疗对眼球和视力的挽回率分别为20%(13%)和9%(6%)。冷冻治疗是11名(55%)儿童最常用的局部治疗方式。接受治疗的患者5年生存率为76%(未达到中位生存率)。拒绝治疗组中位生存期为9个月。在发展中国家,RB大多在晚期才被发现,导致预后不佳。提高对儿童恶性肿瘤治疗中心的认识和可及性可以导致早期诊断,更好的预后,并增加视力恢复。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.00
自引率
0.00%
发文量
80
审稿时长
35 weeks
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