Bladder cancer in Africa, 2010-2023: burden, geographic heterogeneity, demographic drivers, pandemic-era temporal changes, and projections to 2030.

IF 3.2 2区 医学 Q3 IMMUNOLOGY
Yongli Jin, Yan Jin, Yan Cui
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引用次数: 0

Abstract

Purpose: To characterize the burden, temporal trends, geographic heterogeneity, demographic components, pandemic-era deviations, and projected age-standardized rates of bladder cancer across Africa.

Methods: We conducted an ecological secondary analysis of modeled Global Burden of Disease Study 2023 estimates for the GBD aggregate labeled "African Union" and 54 African country locations from 2010 to 2023. Incidence, prevalence, deaths, and disability-adjusted life-years (DALYs) were assessed as counts and age-standardized rates (ASRs) per 100,000 population for both sexes combined. Trends were summarized using estimated annual percentage changes. Incidence trajectories were descriptively grouped using dynamic time warping, and changes in counts were partitioned into population-size, age-structure, and age-specific rate components using Das Gupta decomposition. Exploratory autoregressive integrated moving average models compared GBD-estimated rates in 2020-2023 with trajectories extrapolated from 2010 to 2019. Country-specific ASRs were projected through 2030 using log-linear models.

Results: For the GBD aggregate labeled "African Union," incident cases increased from 16,357 in 2010 to 31,503 in 2023, prevalent cases from 73,806 to 147,599, deaths from 9,261 to 16,467, and DALYs from 232,414 to 415,746. Corresponding ASRs increased from 3.5 to 4.4 for incidence, 13.9 to 18.3 for prevalence, 2.2 to 2.6 for deaths, and 48.1 to 56.1 for DALYs. The highest estimated incidence ASRs in 2023 occurred in Tunisia, Malawi, Libya, Egypt, and Mali, while several countries with low estimated baseline rates had rapid relative increases. Population-size change was the largest decomposition component, accounting for 39.8%-58.8% of the increase across outcomes, with additional contributions from age structure and age-specific rates. GBD-estimated incidence, mortality, and DALY rates during 2020-2023 were above the extrapolated point forecasts; however, this exploratory analysis did not establish a causal pandemic effect. The primary projection models yielded higher fitted 2030 ASRs in a majority of countries, although results varied across training windows.

Conclusion: GBD 2023 estimates indicate an increasing but geographically heterogeneous bladder cancer burden across Africa. Population growth was the largest contributor to increasing counts, while age-structure and age-specific rate changes also contributed. Regionally tailored prevention, diagnostic and treatment capacity, and improved cancer surveillance are needed. Pandemic-era deviations and 2030 projections should be interpreted as model-dependent rather than causal or definitive forecasts.

2010-2023年非洲膀胱癌:负担、地理异质性、人口驱动因素、大流行时期的时间变化以及到2030年的预测。
目的:描述整个非洲膀胱癌的负担、时间趋势、地理异质性、人口组成、大流行时代偏差和预测的年龄标准化发病率。方法:我们对2010年至2023年标记为“非洲联盟”的GBD总量和54个非洲国家地点的全球疾病负担研究模型进行了生态二次分析。发病率、患病率、死亡率和残疾调整生命年(DALYs)以每10万人口中男女合计的计数和年龄标准化率(ASRs)进行评估。使用估计的年度百分比变化来总结趋势。使用动态时间扭曲对发病率轨迹进行描述性分组,并使用Das Gupta分解将计数变化划分为人口规模、年龄结构和年龄特异性比率组成部分。探索性自回归综合移动平均模型将2020-2023年gbd估计的费率与2010 - 2019年推断的轨迹进行了比较。使用对数线性模型预测到2030年的具体国家asr。结果:对于标记为“非洲联盟”的GBD总量,事件病例从2010年的16,357例增加到2023年的31,503例,流行病例从73,806例增加到147,599例,死亡病例从9,261例增加到16,467例,DALYs从232,414例增加到415,746例。相应的asr发生率从3.5增加到4.4,患病率从13.9增加到18.3,死亡从2.2增加到2.6,DALYs从48.1增加到56.1。2023年ASRs估计发病率最高的国家为突尼斯、马拉维、利比亚、埃及和马里,而一些估计基线率较低的国家则出现了相对快速增长。人口规模变化是最大的分解成分,占所有结果增加的39.8%-58.8%,年龄结构和年龄特定率也有额外的贡献。gbd估计的2020-2023年期间的发病率、死亡率和DALY率高于外推点预测;然而,这一探索性分析并没有建立因果大流行效应。主要预测模型在大多数国家产生了更高的拟合2030年asr,尽管结果因培训窗口而异。结论:GBD 2023估计表明,非洲各地膀胱癌负担不断增加,但地理上存在差异。人口增长是增加数量的最大因素,而年龄结构和特定年龄的比率变化也有贡献。有必要根据地区情况制定预防、诊断和治疗能力,并改进癌症监测。大流行时期的偏差和2030年的预测应被解释为依赖于模型的预测,而不是因果或确定的预测。
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来源期刊
Infectious Agents and Cancer
Infectious Agents and Cancer ONCOLOGY-IMMUNOLOGY
CiteScore
5.80
自引率
2.70%
发文量
54
期刊介绍: Infectious Agents and Cancer is an open access, peer-reviewed online journal that encompasses all aspects of basic, clinical, epidemiological and translational research providing an insight into the association between chronic infections and cancer. The journal welcomes submissions in the pathogen-related cancer areas and other related topics, in particular: • HPV and anogenital cancers, as well as head and neck cancers; • EBV and Burkitt lymphoma; • HCV/HBV and hepatocellular carcinoma as well as lymphoproliferative diseases; • HHV8 and Kaposi sarcoma; • HTLV and leukemia; • Cancers in Low- and Middle-income countries. The link between infection and cancer has become well established over the past 50 years, and infection-associated cancer contribute up to 16% of cancers in developed countries and 33% in less developed countries. Preventive vaccines have been developed for only two cancer-causing viruses, highlighting both the opportunity to prevent infection-associated cancers by vaccination and the gaps that remain before vaccines can be developed for other cancer-causing agents. These gaps are due to incomplete understanding of the basic biology, natural history, epidemiology of many of the pathogens that cause cancer, the mechanisms they exploit to cause cancer, and how to interrupt progression to cancer in human populations. Early diagnosis or identification of lesions at high risk of progression represent the current most critical research area of the field supported by recent advances in genomics and proteomics technologies.
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