法语非洲儿童癌症流行病学研究。GFAOP医院登记]。

IF 0.8
Brenda Mallon, Aissata Barry, Rolande Kabore, Erick Mbokoya Kokanya, Francis Diedhiou, Thomas Nihouarn, Isabelle Champenois, Anne Gagnepain Lacheteau, Laila Hessissen, Catherine Patte
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引用次数: 0

摘要

在非洲法语区(2024年有3.43亿居民,其中42%在15岁以下),儿童癌症的记录不足。法国非洲儿科肿瘤小组(GFAOP)于2016年启动了一项集中医院注册项目(RFAOP),以改善知识,构建儿科肿瘤单位的需求,并解决缺乏可靠信息的问题。在这里,我们描述了这个独特的注册表,解释了我们学到的东西及其影响。对登记处的分析(2016-2019年)揭示了诊断差异,病例数与人口之间缺乏相关性,突出了人力和物质资源的巨大需求,并强调了有针对性投资的必要性。该登记处追踪癌症趋势,并记录了流行的癌症类型,例如某些地区的伯基特淋巴瘤,以及非常低数量的脑肿瘤,特别是在撒哈拉以南地区。在诊断时也讨论了疾病的分期和程度。注意到单位间的异质性和医院登记偏差。分期指南的应用提高了数据质量,但晚期诊断仍然存在很高比例的晚期疾病。12个月的随访生存率为57%,但对某些癌症观察到令人鼓舞的生存率。放弃治疗是一个主要问题,正在利用社会经济和癌症类型作为可能的影响因素进行研究。尽管在诊断和后续行动方面存在局限性,但该登记处对资源规划至关重要。持续的培训和支持对于保持该项目的质量至关重要。它揭示了与全球数据之间的差异,强调需要建立与高质量诊断和护理相关的强有力的基于人口的登记,并需要提供可持续的资金,以确保产生持久的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Epidemiology of paediatric cancers in French-speaking Africa. The GFAOP hospital register].

In Francophone Africa (343 million inhabitants in 2024, 42% under 15 years of age), childhood cancer is under-documented. The French African Paediatric Oncology Group (GFAOP) launched a centralized hospital registry project (RFAOP) in 2016 to improve knowledge, structure the needs of paediatric oncology units, and address the lack of reliable information. Here, we describe this unique Registry, explaining what has been learned and its impact. Analyses of the Registry (2016-2019) reveal diagnostic disparities and a lack of correlation between the number of cases and the population, highlighting significant needs in human and material resources and underscoring the necessity for targeted investments. The Registry tracks cancer trends, and documents prevalent types of cancer, such as Burkitt's lymphoma in some regions, and very low numbers of brain tumours especially in the sub-Saharan region. The stage and extent of the disease at diagnosis is also discussed. Inter-unit heterogeneities and a hospital registry bias are noted. The application of staging guidelines has improved data quality, but late diagnoses persist with high percentages of advanced stage disease. Follow-up of survival 57% at 12 months is discussed, but encouraging rates are observed for certain cancers. Treatment abandonment is a major problem being studied using socio-economic and cancer type as possible contributing factors. This Registry is crucial for resource planning despite limitations in diagnosis and follow-up. On-going training and support are essential to maintain the quality of this project. It reveals disparities with global data, emphasizing the need for robust population-based registries linked to quality diagnostics and care, and for sustainable funding to ensure a lasting impact.

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