Patient-related factors and outcome of retinoblastoma in Calabar, Nigeria: A single-center, retrospective study

Elizabeth D. Nkanga , Anthony C. Nlemadim , Mattan Arazi , Dennis G. Nkanga , Roseline E. Duke , Ido D. Fabian , Essemfon D. Nkanga , Friday A. Odey , Martin M. Meremikwu
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Abstract

Background

Retinoblastoma is associated with mortality in resource-poor nations due to disparities and poor access to treatment. The aim was to determine the relationships between patient-related factors and clinical outcomes of retinoblastoma in a tertiary hospital in Nigeria.

Material and methods

It was a retrospective study of all children diagnosed and treated for retinoblastoma from January 2017 through December 2022. Information obtained from their records included bio-socioeconomic data, symptoms, lag time from initial symptoms, staging, treatment, and survival outcome.

Results

Fifty-three patients, aged 6–88 months on first hospital presentation were recruited. There were 29 (54.7%) females. Twenty (37.7%) patients died. The majority were the last child of their parents (62.3%) with a low socioeconomic class (86.8%) and lived in rural areas (50.9%). The median (interquartile) age at diagnosis [24 (18–36) months, p = 0.005] and lag time [13 (6–20) months, p = 0.274] were lower in those who survived than in those who died. The prevalence of bilateral disease (20.8%, p = 0.002), brain metastasis (22.6%, p < 0.001), stage IV disease (18.9%, p = 0.01) and relapse (34%, p < 0.001) was higher among the patients who died. The median (interquartile) overall survival (OS) was 22 (11.8–32.2) months with a 1-year OS of 63%. Treatment with only chemotherapy [HR 4.76 (95% CI: 1.7–13.1)], incomplete chemotherapy [HR 5.61 (95% CI: 1.3–24.7)], relapse [HR 5.98 (95% CI: 1.4–25.9)] and eye surgery delayed after 3 chemotherapy cycles [HR 8.22 (95% CI: 1.1–62.2)] were predictors of mortality.

Conclusion

Most patients with retinoblastoma arrived at our treatment center approximately 14 months following the first symptom. Most (84.9%) presented with proptosis. The majority were of a low social class (86.8%), had a secondary level of education only (47.2%), and lived in rural areas (50.9%). The 3-year overall survival was 29%.

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尼日利亚卡拉巴尔视网膜母细胞瘤的患者相关因素和临床治疗效果:单中心回顾性研究
背景视网膜母细胞瘤与资源贫乏国家的死亡率有关,原因是存在差异和难以获得治疗。该研究旨在确定尼日利亚一家三级医院视网膜母细胞瘤患者相关因素与临床结果之间的关系。材料和方法这是一项回顾性研究,研究对象是2017年1月至2022年12月期间诊断和治疗视网膜母细胞瘤的所有儿童。从他们的病历中获取的信息包括生物-社会经济数据、症状、从最初症状开始的滞后时间、分期、治疗和生存结果。其中女性 29 人(54.7%)。20名(37.7%)患者死亡。大多数患者是父母的最后一个孩子(62.3%),社会经济阶层较低(86.8%),居住在农村地区(50.9%)。存活患者的诊断年龄中位数(四分位数)[24(18-36)个月,p = 0.005]和滞后时间[13(6-20)个月,p = 0.274]均低于死亡患者。死亡患者中,双侧疾病(20.8%,p = 0.002)、脑转移(22.6%,p <0.001)、IV 期疾病(18.9%,p = 0.01)和复发(34%,p <0.001)的发病率较高。中位(四分位间)总生存期(OS)为 22(11.8-32.2)个月,1 年 OS 为 63%。仅接受化疗[HR 4.76 (95% CI: 1.7-13.1)]、化疗不完全[HR 5.61 (95% CI: 1.3-24.7)]、复发[HR 5.98 (95% CI: 1.4-25.9)]和眼部手术推迟到3个化疗周期后[HR 8.22 (95% CI: 1.1-62.2)]是预测死亡率的因素。大多数患者(84.9%)伴有突眼。大多数患者社会阶层较低(86.8%),仅受过中等教育(47.2%),居住在农村地区(50.9%)。3年总存活率为29%。
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