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Chemotherapy use in ovarian cancer patients diagnosed 2012–2017 in Australia, Canada, Norway and the UK: An International Cancer Benchmarking Partnership (ICBP) population-based study 澳大利亚、加拿大、挪威和英国2012-2017年诊断为卵巢癌患者的化疗使用:一项基于人群的国际癌症基准伙伴关系(ICBP)研究
IF 2.3 3区 医学 Q3 ONCOLOGY Pub Date : 2025-12-01 Epub Date: 2025-09-11 DOI: 10.1016/j.canep.2025.102903
Matthew E. Barclay , Sean McPhail , Shane A. Johnson , Ruth Swann , John Butler , Christian J. Finley , Andriana Barisic , Damien Bennett , Oliver Bucher , Nicola Creighton , Cheryl A. Denny , Ron A. Dewar , David W. Donnelly , Laura Downie , Norah Finn , Steven Habbous , Dyfed W. Huws , Leon May , Bjørn Møller , David S. Morrison , Georgios Lyratzopoulos

Objective

To describe use of chemotherapy in patients with ovarian cancer in national or sub-national populations of Australia, Canada, Norway and the UK.

Methods

Linked population-based data sources were used to describe use and time to chemotherapy initiation in ovarian cancer patients diagnosed in study periods during 2012–2017. Random-effects meta-analysis characterised the size of interjurisdictional variation.

Results

Among 39,879 patients, chemotherapy use ranged from 49 % (Wales) to 75 % (Manitoba). Across jurisdictions, chemotherapy use was higher in advanced disease (79 %, 95 %CI: 74 %–83 %), and lower for stages 1–2 or localised/regional disease (54 %, 95 %CI: 48 %–60 %). Within jurisdictions, chemotherapy use was similar in patients aged 15–64 and 65–74 and then decreased sharply with increasing age. There was large interjurisdictional variation in chemotherapy use in patients aged 85–99 years with advanced disease, being, for example, 23 % (95 %CI: 20 %–25 %) in England and 61 % (95 %CI: 51 %–70 %) in Ontario. However, jurisdictions with the highest chemotherapy use in recorded advanced stage, including Ontario, tended to have higher percentage of missing stage information. Overall, time from diagnosis to chemotherapy initiation was shorter in New South Wales and Victoria and longer in Scotland and Wales. In patients with advanced disease, interjurisdictional variation in time-to-treatment was limited.

Conclusions

Even within the same age groups and stage strata, use of chemotherapy varied substantially between jurisdictions during the mid-2010s. Future work should examine use of surgery in combination with chemotherapy. The reasons for the international variation in chemotherapy use and its contribution to international variation in survival should be established.
目的:描述澳大利亚、加拿大、挪威和英国国家或次国家人群中卵巢癌患者化疗的使用情况。方法:使用相关的基于人群的数据源来描述2012-2017年研究期间诊断的卵巢癌患者的化疗使用情况和开始化疗时间。随机效应荟萃分析表征了辖区间差异的大小。结果:在39,879例患者中,化疗使用率从49% %(威尔士)到75% %(马尼托巴)不等。在各个辖区,晚期疾病的化疗使用较高(79 %,95 %CI: 74 %-83 %),而1-2期或局部/区域疾病的化疗使用较低(54 %,95 %CI: 48 %-60 %)。在辖区内,15-64岁和65-74岁患者的化疗使用情况相似,然后随着年龄的增长急剧下降。在85-99岁的晚期疾病患者中,化疗的使用有很大的司法管辖区差异,例如,在英国为23 %(95 %CI: 20 %-25 %),在安大略省为61 %(95 %CI: 51 %-70 %)。然而,在有记录的晚期化疗使用最高的司法管辖区,包括安大略省,往往有更高的阶段信息缺失百分比。总的来说,新南威尔士州和维多利亚州从诊断到化疗开始的时间较短,苏格兰和威尔士较长。在疾病晚期的患者中,不同地区在治疗时间上的差异有限。结论:即使在相同的年龄组和阶段,2010年代中期不同司法管辖区的化疗使用也存在很大差异。未来的工作应探讨手术与化疗联合使用。应确定化疗使用的国际差异的原因及其对生存的国际差异的贡献。
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引用次数: 0
Approaches to handle missing follow-up time: A comparative analysis of contralateral breast cancer incidence 处理缺失随访时间的方法:对侧乳腺癌发病率的比较分析。
IF 2.3 3区 医学 Q3 ONCOLOGY Pub Date : 2025-12-01 Epub Date: 2025-10-15 DOI: 10.1016/j.canep.2025.102942
Sarah R. Haile , Miriam Wanner , Dimitri Korol , Sabine Rohrmann

Background

We aimed to compare various common approaches for handling missing vital status or follow-up time. As a case study for application of these methods, we estimated incidence of metachronous contralateral breast cancer (CBC).

Methods

For 1980–2016, incidence of metachronous CBC with follow-up through 2024 was estimated using Poisson regression with overdispersion, by age at incidence, year of incidence, histology and follow-up period. Missing follow-up time was ignored in the naive approach, simulated once using the average hazard derived from published Swiss cancer registry data, or multiply imputed using 3 different imputation models.

Results

24,612 women aged 20–84 had unilateral breast cancer between 1980 and 2016 in the Swiss cantons of Zurich and Zug. Of those, 5 % (n = 1264) were lost to follow-up. Over 291,463 person-years, 1145 contralateral breast malignancies were diagnosed, corresponding to 393 per 100,000 person-years (95 % CI 353–438). Incidence rates have been decreasing over time to 238 (171−333) for the incidence period 2010–2016. The same overall pattern was observed regardless of how we handled missing follow-up times. However, using a single imputation generally produced lower incidence rates compared to the naive approach, with multiple imputation giving higher estimates. The most complex multiple imputation model gave incidence estimates that were very similar to those from the naive approach.

Conclusion

Different methods to handle missing follow-up times yielded similar results: that CBC incidence has declined in recent decades. Multiple imputation is likely an appropriate method to handle missing follow-up data, enabling researchers to include all eligible individuals in the analysis.
背景:我们的目的是比较各种常见的方法来处理遗漏的生命状态或随访时间。作为应用这些方法的一个案例研究,我们估计了异时性对侧乳腺癌(CBC)的发病率。方法:对1980-2016年随访至2024年的异时性CBC发病率,采用过分散泊松回归,按发病年龄、发病年份、组织学和随访时间进行估计。在幼稚的方法中忽略了随访时间的缺失,使用从瑞士癌症登记数据中得出的平均风险进行一次模拟,或使用3种不同的估算模型进行多次估算。结果:1980年至2016年间,瑞士苏黎世和楚格州有24,612名年龄在20-84岁之间的女性患有单侧乳腺癌。其中5 % (n = 1264)失访。在291,463人/年中,诊断出1145例对侧乳腺恶性肿瘤,相当于每10万人/年393例(95 % CI 353-438)。随着时间的推移,发病率一直在下降,2010-2016年发病率为238(171-333)。无论我们如何处理缺失的随访时间,观察到的总体模式都是一样的。然而,与单纯的方法相比,使用单一输入通常产生较低的发病率,而多次输入则给出较高的估计值。最复杂的多重imputation模型给出的发生率估计与朴素方法非常相似。结论:不同方法处理缺失随访时间的结果相似:近几十年来,CBC发病率有所下降。多重输入可能是处理缺失的随访数据的合适方法,使研究人员能够在分析中包括所有符合条件的个体。
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引用次数: 0
Temporal trends and spatial distribution of prostate cancer incidence and mortality in a northeastern Brazilian state 巴西东北部一个州前列腺癌发病率和死亡率的时间趋势和空间分布
IF 2.3 3区 医学 Q3 ONCOLOGY Pub Date : 2025-12-01 Epub Date: 2025-09-12 DOI: 10.1016/j.canep.2025.102931
Ana Clara Cruz Santos de Santana , Ellen Sabrina Ramos Santos , Jefferson Felipe Calazans Batista , Alex Rodrigues Moura , Simone Soraia Silva Sardeiro , Brenda Evelin Barreto da Silva , Carlos Anselmo Lima

Background

Prostate cancer incidence and mortality exhibit regional variation often linked to disparities in healthcare access and disease management. This study aimed to analyze temporal trends and spatial distribution of prostate cancer incidence (1996–2017) and mortality (1996–2022) in Sergipe, Brazil, to support targeted cancer control strategies.

Methods

We analyzed prostate cancer data from the Aracaju Cancer Registry and the Mortality Information System. Age-standardized incidence and mortality rates were calculated using the World Standard Population. Joinpoint regression estimated Annual Percent Change (APC) and Average Annual Percent Change (AAPC) to assess trends. The Mortality-to-Incidence Ratio (MIR) and its complement (1–MIR) were used as proxies for survival. Spatial distribution was examined using Empirical Bayesian Kriging and local empirical Bayes smoothing in QGIS and TerraView.

Results

Between 1996 and 2017, 10,133 incident prostate cancer cases were recorded. Incidence increased until 2007 (APC=11.9 %; p < 0.001), then declined (APC=–2.0 %; p = 0.027, with peaks in men aged ≥55. Mortality increased from 1996 to 2007 (APC=12.2 %; p < 0.001) and subsequently stabilised between 2007 and 2022 (APC=–0.8 %; p = 0.228), resulting in an overall AAPC of 2.4 % (p = 0.002) for the entire study period. By age group, mortality rose among men ≥ 75 years (AAPC=3.2 %; p = 0.001) but declined in those aged 15–54 (AAPC=–2.4 %; p = 0.004). The MIR remained flat over time, but estimated survival dropped substantially among men aged ≥ 75 years, from 63 % to 38 %. Spatial analysis revealed higher incidence in central/coastal municipalities, while elevated mortality clustered in southern/coastal areas.

Conclusions

Despite improvements in incidence rates, prostate cancer remains a significant burden in Sergipe, with persistent regional disparities in outcomes. Spatial and temporal analyses highlight the need for targeted public health interventions to improve early detection and access to care, especially in areas of high social vulnerability and among older men.
背景:前列腺癌的发病率和死亡率表现出区域差异,通常与医疗保健和疾病管理的差异有关。本研究旨在分析巴西Sergipe市前列腺癌发病率(1996-2017年)和死亡率(1996-2022年)的时间趋势和空间分布,为有针对性的癌症控制策略提供支持。方法我们分析来自阿拉卡朱癌症登记处和死亡率信息系统的前列腺癌数据。使用世界标准人口计算年龄标准化发病率和死亡率。联合点回归估计年变化百分比(APC)和平均年变化百分比(AAPC)来评估趋势。使用死亡率-发病率比(MIR)及其补体(1-MIR)作为生存指标。利用经验贝叶斯Kriging和局部经验贝叶斯平滑对QGIS和TerraView中的空间分布进行了检验。结果1996年至2017年,共记录了10133例前列腺癌病例。发病率上升至2007年(APC=11.9 %;p <; 0.001),然后下降(APC= -2.0 %;p = 0.027,年龄≥55岁的男性发病率最高。死亡率从1996增加到2007 (APC % = 12.2;p & lt; 0.001),随后企稳在2007年和2022年之间(APC % = -0.8;p = 0.228),导致整体AAPC 2.4 % (p = 0.002)为整个研究期间。按年龄组划分,≥ 75岁男性死亡率上升(AAPC=3.2 %;p = 0.001),15-54岁男性死亡率下降(AAPC= -2.4 %;p = 0.004)。随着时间的推移,MIR保持平稳,但≥ 75岁男性的估计生存率大幅下降,从63% %降至38% %。空间分析显示,中部/沿海城市发病率较高,而死亡率升高集中在南部/沿海地区。结论:尽管发病率有所改善,但前列腺癌仍然是Sergipe地区的一个重大负担,并且在结果上存在持续的地区差异。空间和时间分析突出表明,需要有针对性的公共卫生干预措施,以改善早期发现和获得护理的机会,特别是在社会脆弱性高的地区和老年男子中。
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引用次数: 0
Bridging data gaps: Methodological advances in extracting and analyzing genetic information from unstructured clinical records in hereditary cancer 弥合数据差距:从遗传性癌症的非结构化临床记录中提取和分析遗传信息的方法学进展
IF 2.3 3区 医学 Q3 ONCOLOGY Pub Date : 2025-12-01 Epub Date: 2025-10-11 DOI: 10.1016/j.canep.2025.102940
Danny Styvens Cardona , Juan Pablo Valencia-Arango , Juan Pablo Gallo , Catalina Andrea Bustamante , Richard Orlando Salazar , Carlos Andrés Carmona , Melisa Naranjo Vanegas , Carolina Jaramillo Jaramillo , Juliana Espinosa Moncada , Harvy Mauricio Velasco , Natalia Gallego Lopera

Introduction

The global impact of cancer, driven by both acquired and hereditary mutations, underscores the necessity for extensive research efforts. Despite the increasing volume of genetic data, significant gaps remain in data science research, particularly in Latinos and admixed populations. This study utilizes advanced data science techniques to integrate genetic and clinical data, aiming to improve the understanding of hereditary cancer in Colombia and demonstrating the transformative potential of data-driven approaches in cancer research.

Methods

This observational study analyzed healthcare databases from four regions and 11 cities in Colombia. Genetic data were extracted from PDF reports within SURA Colombia's Electronic Health Records (a Latin American health insurance provider) for individuals referred for hereditary cancer testing between October 2019 and November 2021. Variants in 30 genes, aligned with NCCN guidelines, were examined using Next-Generation Sequencing (NGS). Data extraction was automated using Python and R, followed by integration and analysis of genetic, clinical, and sociodemographic data using advanced data science tools hosted on Azure infrastructure. These tools enabled predictive modeling and cross-referencing to explore correlations between genetic variants and clinical outcomes.

Results

The study included 1377 patients, with a predominance of women (92.81 %) and 63 % from the northwestern region of Colombia. The largest age group (40.37 %) was between 31 and 44 years, and 95.35 % had a personal cancer history, primarily breast cancer (75.86 %). Hereditary cancer testing revealed 145 positive results and 587 uncertain outcomes. Data science-driven analysis identified higher positivity rates in patients aged 31–44 and over 50, particularly in the northeast and central regions. Among positive results, 42.6 % included variants of uncertain significance, with 95.9 % of these patients having a personal cancer history.

Conclusion

This study highlights the significant role of data science in analyzing hereditary cancer data. Advanced computational techniques can aid in genetic variant reclassification, uncover patterns in underrepresented populations, and inform personalized interventions for hereditary cancer management in Latin America.
由获得性和遗传性突变驱动的癌症的全球影响强调了广泛研究工作的必要性。尽管基因数据量不断增加,但数据科学研究仍存在重大差距,特别是在拉丁裔和混合人口中。本研究利用先进的数据科学技术整合遗传和临床数据,旨在提高对哥伦比亚遗传性癌症的了解,并展示数据驱动方法在癌症研究中的变革潜力。方法本观察性研究分析了哥伦比亚4个地区和11个城市的卫生保健数据库。遗传数据提取自2019年10月至2021年11月期间转诊进行遗传性癌症检测的个人的SURA哥伦比亚电子健康记录(拉丁美洲健康保险提供商)中的PDF报告。根据NCCN指南,使用下一代测序(NGS)检测了30个基因的变异。使用Python和R自动提取数据,然后使用托管在Azure基础设施上的高级数据科学工具集成和分析遗传、临床和社会人口数据。这些工具使预测建模和交叉参考能够探索遗传变异和临床结果之间的相关性。结果共纳入1377例患者,其中以女性为主(92.81 %),63 %来自哥伦比亚西北部地区。最大年龄组(40.37 %)为31 - 44岁,95.35 %有个人癌症病史,主要是乳腺癌(75.86 %)。遗传性癌症检测显示145个阳性结果和587个不确定结果。数据科学驱动的分析发现,31-44岁和50岁以上患者的阳性率较高,特别是在东北部和中部地区。在阳性结果中,42.6 %包含不确定意义的变异,其中95.9% %的患者有个人癌症史。结论本研究突出了数据科学在遗传肿瘤数据分析中的重要作用。先进的计算技术可以帮助基因变异重新分类,揭示代表性不足人群的模式,并为拉丁美洲的遗传性癌症管理提供个性化干预措施。
{"title":"Bridging data gaps: Methodological advances in extracting and analyzing genetic information from unstructured clinical records in hereditary cancer","authors":"Danny Styvens Cardona ,&nbsp;Juan Pablo Valencia-Arango ,&nbsp;Juan Pablo Gallo ,&nbsp;Catalina Andrea Bustamante ,&nbsp;Richard Orlando Salazar ,&nbsp;Carlos Andrés Carmona ,&nbsp;Melisa Naranjo Vanegas ,&nbsp;Carolina Jaramillo Jaramillo ,&nbsp;Juliana Espinosa Moncada ,&nbsp;Harvy Mauricio Velasco ,&nbsp;Natalia Gallego Lopera","doi":"10.1016/j.canep.2025.102940","DOIUrl":"10.1016/j.canep.2025.102940","url":null,"abstract":"<div><h3>Introduction</h3><div>The global impact of cancer, driven by both acquired and hereditary mutations, underscores the necessity for extensive research efforts. Despite the increasing volume of genetic data, significant gaps remain in data science research, particularly in Latinos and admixed populations. This study utilizes advanced data science techniques to integrate genetic and clinical data, aiming to improve the understanding of hereditary cancer in Colombia and demonstrating the transformative potential of data-driven approaches in cancer research.</div></div><div><h3>Methods</h3><div>This observational study analyzed healthcare databases from four regions and 11 cities in Colombia. Genetic data were extracted from PDF reports within SURA Colombia's Electronic Health Records (a Latin American health insurance provider) for individuals referred for hereditary cancer testing between October 2019 and November 2021. Variants in 30 genes, aligned with NCCN guidelines, were examined using Next-Generation Sequencing (NGS). Data extraction was automated using Python and R, followed by integration and analysis of genetic, clinical, and sociodemographic data using advanced data science tools hosted on Azure infrastructure. These tools enabled predictive modeling and cross-referencing to explore correlations between genetic variants and clinical outcomes.</div></div><div><h3>Results</h3><div>The study included 1377 patients, with a predominance of women (92.81 %) and 63 % from the northwestern region of Colombia. The largest age group (40.37 %) was between 31 and 44 years, and 95.35 % had a personal cancer history, primarily breast cancer (75.86 %). Hereditary cancer testing revealed 145 positive results and 587 uncertain outcomes. Data science-driven analysis identified higher positivity rates in patients aged 31–44 and over 50, particularly in the northeast and central regions. Among positive results, 42.6 % included variants of uncertain significance, with 95.9 % of these patients having a personal cancer history.</div></div><div><h3>Conclusion</h3><div>This study highlights the significant role of data science in analyzing hereditary cancer data. Advanced computational techniques can aid in genetic variant reclassification, uncover patterns in underrepresented populations, and inform personalized interventions for hereditary cancer management in Latin America.</div></div>","PeriodicalId":56322,"journal":{"name":"Cancer Epidemiology","volume":"99 ","pages":"Article 102940"},"PeriodicalIF":2.3,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145267981","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
10 Years of breast cancer treatment trends in Fars Province, report of Shiraz Breast Cancer Registry 法尔斯省10年乳腺癌治疗趋势,设拉子乳腺癌登记处报告
IF 2.3 3区 医学 Q3 ONCOLOGY Pub Date : 2025-12-01 Epub Date: 2025-09-27 DOI: 10.1016/j.canep.2025.102937
Majid Akrami , Amirhesam Moosazadeh , Mehrdad Taghva , Nastaran Tavakolian , Marzieh Karami Rad , Zahra Keumarsi , Masoumeh Ghoddusi Johari , Vahid Zangouri

Background

Despite global recommendations favoring breast-conserving surgery (BCS) with radiotherapy for early-stage breast cancer, there is limited long-term evidence on surgical trends and survival outcomes in low- and middle-income countries such as Iran. Understanding these patterns is crucial to improving treatment equity and patient outcomes. This study aimed to evaluate two-decade trends in surgical approach selection for breast cancer and to compare survival outcomes between BCS and mastectomy in Fars province, Iran.

Methods

Data from 10,091 women diagnosed with breast cancer between 2000 and 2022 were extracted from the Shiraz Breast Cancer Registry. Patients were categorized into four groups based on type of surgery (BCS or mastectomy) and receipt of radiotherapy. Logistic regression was used to identify factors influencing treatment selection. Survival and recurrence were analyzed using Kaplan-Meier and factors affecting survival were evaluated using the Cox regression model.

Results

Between 2000 and 2022, the proportion of patients undergoing BCS plus radiotherapy increased from 30.5 % to 73.8 %, surpassing mastectomy. The BCS plus radiotherapy group showed the most favorable outcomes, with the lowest breast cancer-specific mortality (6.2 %), recurrence rate (10.2 %), and the highest 10-year BCSS (96.01 %). These associations remained significant after multivariable adjustment.

Conclusion

This study reveals a significant shift toward BCS plus radiotherapy in southern Iran over the past two decades. BCS with radiotherapy is associated with superior survival outcomes compared to mastectomy. However, access barriers continue to prevent many women from receiving the optimal surgical approach, indicating the need for policy and health system interventions.
尽管全球推荐早期乳腺癌保乳手术(BCS)加放疗,但在伊朗等中低收入国家,关于手术趋势和生存结果的长期证据有限。了解这些模式对于改善治疗公平性和患者预后至关重要。本研究旨在评估伊朗法尔斯省乳腺癌手术入路选择的20年趋势,并比较BCS和乳房切除术的生存结果。方法从设拉子乳腺癌登记处提取2000年至2022年间诊断为乳腺癌的10091名妇女的数据。根据手术类型(BCS或乳房切除术)和放射治疗的接受情况将患者分为四组。采用Logistic回归分析确定影响治疗方案选择的因素。采用Kaplan-Meier分析生存率和复发率,采用Cox回归模型评价影响生存率的因素。结果2000年至2022年间,接受BCS +放疗的患者比例从30.5% %增加到73.8 %,超过了乳房切除术。BCS +放疗组预后最佳,乳腺癌特异性死亡率最低(6.2 %),复发率最低(10.2 %),10年BCS最高(96.01 %)。这些关联在多变量调整后仍然显著。结论:这项研究揭示了过去20年来伊朗南部向BCS加放疗的重大转变。与乳房切除术相比,BCS联合放疗具有更好的生存结果。然而,获得手术的障碍仍然使许多妇女无法获得最佳手术方法,这表明需要政策和卫生系统干预措施。
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引用次数: 0
Aspirin use associated with a decreased risk of gastric cancer 阿司匹林的使用与胃癌风险降低有关
IF 2.3 3区 医学 Q3 ONCOLOGY Pub Date : 2025-12-01 Epub Date: 2025-09-11 DOI: 10.1016/j.canep.2025.102929
Kuan-Fu Liao, Shih-Wei Lai
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引用次数: 0
Self-assessment of melanoma risk factors versus expert assessment: A systematic review of agreement 黑色素瘤风险因素的自我评估与专家评估:一项系统的协议回顾
IF 2.3 3区 医学 Q3 ONCOLOGY Pub Date : 2025-12-01 Epub Date: 2025-10-31 DOI: 10.1016/j.canep.2025.102954
Lena Friederike Kopplin, Isabelle Kaiser
The number of melanoma cases has been rising over the past decades. Hence, screening is essential to provide early and effective patient management. However, screening for risk factors binds medical resources and may be conducted by patients. To evaluate the quality and validity of such a self-assessment, a systematic review of patient-expert agreement in dermatologic examinations is presented. A systematic review of studies examining participant-expert agreement on melanoma risk factors that were published until May 2025 was conducted. Included sources were retrieved from PubMed, the Web of Science Core Collection, and Scopus. Publications in languages other than English were excluded from the analysis. Of the 3562 records identified, 29 were eligible for evaluation. Six melanoma risk factors dominated the results: Typical and atypical nevi, skin phototype, freckles, hair and eye color., with typical nevi being the most frequently assessed risk factor (22 studies). Agreement is highly heterogeneous, ranging from predominantly weaker to scarcely reported substantial agreement, casting doubts on whether individuals should be tasked with self-assessment. Individual self-assessment may currently serve as a first indication of elevated melanoma risk but cannot substitute for dermatologic screening.
在过去的几十年里,黑色素瘤病例的数量一直在上升。因此,筛查对于提供早期和有效的患者管理至关重要。然而,筛查危险因素限制了医疗资源,可能由患者进行。为了评估这种自我评估的质量和有效性,提出了皮肤病检查中患者-专家协议的系统综述。对截至2025年5月发表的关于黑色素瘤风险因素的参与者-专家共识的研究进行了系统回顾。纳入的来源检索自PubMed、Web of Science Core Collection和Scopus。以英文以外语文出版的出版物不包括在分析之内。在确定的3562个记录中,有29个有资格进行评估。结果显示,6个黑色素瘤风险因素占主导地位:典型和非典型痣、皮肤光型、雀斑、头发和眼睛颜色。典型痣是最常被评估的风险因素(22项研究)。共识是高度异质的,从明显较弱到几乎没有报道的实质性共识,这让人怀疑个人是否应该承担自我评估的任务。个体自我评估目前可以作为黑色素瘤风险升高的第一个指标,但不能代替皮肤科筛查。
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引用次数: 0
Response to ‘reverse causality’ comment 对“反向因果关系”评论的回应。
IF 2.3 3区 医学 Q3 ONCOLOGY Pub Date : 2025-12-01 Epub Date: 2025-09-29 DOI: 10.1016/j.canep.2025.102928
Shan Zhang , Hongwei Wang , Jingjing Ji, Ruiyu Chai, Shiyi Song, Jikang Shi, Siyu Liu
This document is the authors' response to the received comments for manuscript CANEP-D-25–00912.
本文是作者对CANEP-D-25-00912稿件评论的回复。
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引用次数: 0
Further dose-response association exploration could enhance the causal inference between benzene exposure and risk of nervous system cancers 进一步的剂量-反应关联探索可以加强苯暴露与神经系统癌症风险之间的因果推理。
IF 2.3 3区 医学 Q3 ONCOLOGY Pub Date : 2025-10-01 Epub Date: 2025-07-18 DOI: 10.1016/j.canep.2025.102892
Yachen Liang, Jingya Chen, Tianyou Chen, Xiao Li, Junjie Fang, Lefu Wu
Occupational benzene exposure is a known carcinogen; however, the dose-response relationship with cancers of the nervous system, particularly glioma, requires clarification. Based on the systematic review by Mangiaterra et al., this paper conducted a secondary analysis of the results and utilized original supplementary data to assess risk ratios (RRs) for high, medium, and low benzene exposure levels. This aimed to evaluate both linear and non-linear dose-response relationships. We observed a significantly increased risk for nervous system cancers only at high exposure levels. Risks associated with moderate and low exposure levels showed no significant increase. Both dose-response curves indicated no clear upward trend with increasing exposure. Limitations include the frequent lack of confounder adjustment in source estimates, potential publication bias, and limited original data, all of which impact the heterogeneity and accuracy of the findings. While high-concentration benzene exposure may pose a risk for nervous system cancers and potentially exhibit dose-dependency, these limitations constrain the robustness of the dose-response assessment. Future research should validate this association using high-quality, multi-level exposure data with adequate confounder adjustment. Such studies are crucial to provide a scientific basis for occupational health protection measures.
职业性接触苯是一种已知的致癌物;然而,剂量-反应关系与神经系统癌症,特别是胶质瘤,需要澄清。基于Mangiaterra等人的系统综述,本文对结果进行了二次分析,并利用原始补充数据评估高、中、低苯暴露水平的风险比(rr)。目的是评估线性和非线性剂量-反应关系。我们观察到,只有在高暴露水平下,患神经系统癌症的风险才会显著增加。与中等和低暴露水平相关的风险没有显著增加。两种剂量-反应曲线均未显示出随暴露量增加而明显上升的趋势。局限性包括来源估计中经常缺乏混杂因素调整、潜在的发表偏倚和有限的原始数据,所有这些都会影响研究结果的异质性和准确性。虽然高浓度苯暴露可能造成神经系统癌症的风险,并可能表现出剂量依赖性,但这些局限性限制了剂量-反应评估的稳健性。未来的研究应该使用高质量、多层次的暴露数据来验证这种关联,并进行适当的混杂校正。这些研究对制定职业健康防护措施具有重要的科学依据。
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引用次数: 0
Commentary: The significance of dose-response relationships in elucidating benzene’s neurocarcinogenicity 评论:剂量-反应关系在阐明苯的神经致癌性中的意义。
IF 2.3 3区 医学 Q3 ONCOLOGY Pub Date : 2025-10-01 Epub Date: 2025-07-19 DOI: 10.1016/j.canep.2025.102893
Monireh Sadat Seyyedsalehi, Paolo Boffetta
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引用次数: 0
期刊
Cancer Epidemiology
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