Nationwide incidence and survival of retinoblastoma in the USA between 1996 and 2018: a review of 5730 cases.

IF 1 4区 医学 Q4 GENETICS & HEREDITY
Ophthalmic Genetics Pub Date : 2025-04-01 Epub Date: 2025-02-10 DOI:10.1080/13816810.2024.2449086
Ahmad Samir Alfaar, Hadeel Halalsheh, Abdallah E Shelil, Ibrahim Qaddoumi
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引用次数: 0

Abstract

Background: Retinoblastoma is the most common intraocular cancer in children, with significant variations in incidence and Survival. This study sought to evaluate nationwide retinoblastoma incidences and survival rates in the United States from 1996 to 2018.

Methods: We extracted data from the North American Association of Central Cancer Registries (NACCR) and the National Program of Cancer Registries between 1996 and 2018. Cases were stratified by sex, age, race, Hispanic origin, urban or rural origin, stage of the disease, and state of residence and compared by laterality. We applied SEER*Stat version 8.4.0.1 software for age-adjusted incidence rates (AAIR) and annual average per cent change (AAPC) and JoinPoint version 4.9.1.0 software to assess incidence trends. Survival trends were evaluated with JPSurv online software.

Results: The study comprised 5730 patients with a crude incidence rate (CIR) of 0.89 per million. The incidence declined from 29.6 per million in the first year of life to 16.5 in the second year. The CIR for unilateral and bilateral diseases were 0.61 and 0.27, respectively. Males had a slightly higher and significant crude incidence of 0.93 versus 0.86 for females. Hispanics had the highest rate of 1.48 in general. Treatment data revealed chemotherapy usage in 39% of unilateral and 78% of bilateral patients. The 5-year cumulative relative Survival did not significantly differ between unilateral (96.8%) and bilateral (97.0%) patients. A slight but significant annual decline in CIR was observed, with a trend toward an increase in the percentage of patients diagnosed in the first year of life.

Conclusions: This study indicated an overall decrease in incidence but a slight increase in early diagnosis. Findings underscore the need for consistent surveillance, early detection strategies, and personalized care to improve patient outcomes. The changes in the Survival in the unilateral disease require further investigations and mitigation strategies.

1996年至2018年美国视网膜母细胞瘤的全国发病率和生存率:对5730例病例的回顾
背景:视网膜母细胞瘤是儿童最常见的眼内癌,其发病率和生存率存在显著差异。本研究旨在评估1996年至2018年美国全国视网膜母细胞瘤的发病率和生存率。方法:我们从1996年至2018年期间的北美中央癌症登记协会(NACCR)和国家癌症登记计划中提取数据。病例按性别、年龄、种族、西班牙裔、城市或农村血统、疾病分期和居住状态分层,并通过侧边性进行比较。我们应用SEER*Stat版本8.4.0.1软件计算年龄调整后的发病率(AAIR)和年平均百分比变化(AAPC),使用JoinPoint版本4.9.1.0软件评估发病率趋势。使用JPSurv在线软件评估生存趋势。结果:该研究纳入了5730例患者,粗发病率(CIR)为0.89 /百万人。发病率从出生第一年的29.6 /百万人下降到第二年的16.5 /百万人。单侧疾病和双侧疾病的CIR分别为0.61和0.27。男性的粗发病率略高,为0.93,而女性为0.86。西班牙裔的比率最高,为1.48。治疗数据显示39%的单侧患者和78%的双侧患者使用化疗。单侧(96.8%)和双侧(97.0%)患者的5年累积相对生存率无显著差异。观察到轻微但显著的年度CIR下降,在生命的第一年诊断的患者百分比有增加的趋势。结论:本研究表明总体发病率下降,但早期诊断略有增加。研究结果强调需要持续的监测、早期发现策略和个性化护理来改善患者的预后。单侧疾病生存率的变化需要进一步的调查和缓解策略。
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
Ophthalmic Genetics
Ophthalmic Genetics 医学-眼科学
CiteScore
2.40
自引率
8.30%
发文量
126
审稿时长
>12 weeks
期刊介绍: Ophthalmic Genetics accepts original papers, review articles and short communications on the clinical and molecular genetic aspects of ocular diseases.
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