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Population-Based Cancer Screening analysis in Northern Portugal Using Process Mining 数据驱动的弹性:优化基于人口的癌症筛查在葡萄牙北部使用过程采矿。
IF 2 Q3 HEALTH POLICY & SERVICES Pub Date : 2026-01-05 DOI: 10.1016/j.jcpo.2026.100702
Hugo Monteiro , Mariana Oliveira , Ricardo Martinho , João Reis , Fernando Tavares , Óscar Felgueiras , Carlos Martins

Background

This study focuses on the Colorectal Cancer Screening Program in Northern Portugal, aiming to evaluate the disruption effects on its performance and efficiency.

Methods

We conducted an observational analyses of 271 637 administrative records from 2020 to 2022. Administrative timestamps were converted into a step-by-step dataset of screening activities (an “event log”) and analysed using process mining and comparative performance analysis across time periods and ACeS (primary care administrative clusters).

Results

Consultation‑to‑colonoscopy time lengthened by 53 %, rising from a median 58 days (IQR 29–92) in early 2020 to 89 days (IQR 53–127) in 2021, before improving to 73 days in 2022. Conversely, referral‑to‑consultation time fell from 110 days to 26 days (−76 %), reflecting targeted backlog clearance. Screening volumes declined in 2020 but recovered above baseline levels by 2022. Performance differences across primary care administrative clusters were significant (p < 0.001), with some units outperforming regional median transition times. Early adoption of automated electronic referrals and flexible consultation scheduling may have contributed to improved programme performance during the recovery period following pandemic-related disruptions. Substantial heterogeneity across units was observed for key transitions, indicating uneven disruption and recovery patterns across administrative units.

Conclusion

Process Mining techniques revealed critical vulnerabilities in the screening program during the initial stages of the period in analysis (matching the pandemic). These findings support targeted monitoring and prioritisation of operational improvements to reduce avoidable delays and strengthen continuity of population-based screening.

Policy summary

Policies aimed at strengthening healthcare service continuity and operational capacity benefit from analytical methods like process mining. Key recommendations include standardizing workflows, enhancing coordination between primary care and hospital services, and investing in digital monitoring systems to mitigate disruptions and ensure continuity in cancer screening programs during periods of system stress.
背景:本研究以葡萄牙北部的结直肠癌筛查项目为研究对象,旨在评估干扰对其性能和效率的影响。方法:一项观察性研究分析了2020-2022年的行政记录。该筛查项目于2018年启动,包括一系列活动,从邀请患者到粪便隐血检查和必要时的结肠镜检查。使用流程挖掘技术和比较性能分析,创建事件日志以识别不同时间段和管理区域之间的变化。结果:观察到明显的工作流程中断,特别是在从咨询到结肠镜检查活动的过渡中,延误增加了40%以上,导致瓶颈。一些医疗保健服务通过缩短试剂盒分发和实验室处理活动的延迟,显示出更好的恢复能力。表现差异是显著的,协调良好的地区的过渡时间比协调不佳的地区快30%。事实证明,根据资源限制调整工作流程的能力对于减轻大流行病的影响至关重要。结论:过程挖掘技术揭示了在分析期间(与大流行相匹配)的初始阶段筛选方案中的关键漏洞。有针对性的干预措施,包括采用韧性地区的最佳做法和改进协调工作,对于提高项目的效率和韧性至关重要。策略摘要:提高医疗保健弹性和操作能力的策略受益于流程挖掘等分析方法。主要建议侧重于标准化工作流程,加强初级保健和医院服务之间的协调,以及投资于数字监测系统,以减轻危机期间癌症筛查计划的中断并确保其连续性。
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引用次数: 0
Current opinions on lung cancer screening in the Nordic countries: A survey-based study 北欧国家目前对肺癌筛查的看法:一项基于调查的研究。
IF 2 Q3 HEALTH POLICY & SERVICES Pub Date : 2026-01-05 DOI: 10.1016/j.jcpo.2026.100703
Morten Borg , Kirill Neumann , Jannie Christina Frølund , Ghida Khalife , Zaigham Saghir , Aija Knuuttila , Haseem Ashraf , Johan Isaksson , Torben Riis Rasmussen

Introduction

Lung cancer is the leading cause of cancer-related death worldwide, with early detection critical for curative treatment. Low-dose computed tomography (LDCT) can detect lung cancer at earlier stages, but its implementation in the Nordic countries remains limited. This study surveys invasive respiratory physicians in Sweden, Finland, Norway, and Denmark to explore their views on LDCT screening.

Methods

A web-based survey was conducted among invasive respiratory physicians in Denmark, Norway, Sweden, and Finland to assess opinions on lung cancer screening. Responses were analysed using descriptive statistics and the Kruskal-Wallis test.

Results

A total of 125 respondents from 54 Nordic hospitals completed the survey. The majority reported no prior experience with LDCT screening. Most physicians were familiar with LDCT and recognized its potential to improve early detection, though opinions on national implementation were mixed. Key barriers identified included financial constraints, lack of trained personnel, and limited access to CT scanners. Significant differences were observed by country, hospital type, and years of clinical experience (p < 0.05).

Conclusion

Nordic respiratory physicians acknowledge the benefits of LDCT screening for early lung cancer detection but highlight substantial implementation challenges, particularly related to resources and personnel. Addressing these barriers, standardizing protocols, and exploring supportive measures such as risk-scores and AI-assisted imaging will be essential for successful adoption of national screening programs across the Nordic region.
肺癌是全球癌症相关死亡的主要原因,早期发现对治疗至关重要。低剂量计算机断层扫描(LDCT)可以在早期阶段检测肺癌,但其在北欧国家的实施仍然有限。本研究调查了瑞典、芬兰、挪威和丹麦的有创呼吸内科医生,探讨他们对LDCT筛查的看法。方法:对丹麦、挪威、瑞典和芬兰的侵入性呼吸内科医生进行了一项基于网络的调查,以评估他们对肺癌筛查的意见。采用描述性统计和Kruskal-Wallis检验对反应进行分析。结果:来自北欧54家医院的125名受访者完成了调查。大多数报告没有LDCT筛查的经验。大多数医生都熟悉LDCT,并认识到其改善早期检测的潜力,尽管对国家实施的意见不一。确定的主要障碍包括资金限制、缺乏训练有素的人员以及获得CT扫描仪的机会有限。国家、医院类型和临床经验年数的差异有统计学意义(p < 0.05)。结论:北欧呼吸内科医生承认LDCT筛查对早期肺癌检测的好处,但强调了实施方面的重大挑战,特别是与资源和人员相关的挑战。解决这些障碍,使协议标准化,并探索风险评分和人工智能辅助成像等支持性措施,对于在北欧地区成功采用国家筛查计划至关重要。
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引用次数: 0
Geographic disparities in access to oncologists and association with cancer outcomes in the United States 在美国,获得肿瘤学家的地理差异及其与癌症预后的关系。
IF 2 Q3 HEALTH POLICY & SERVICES Pub Date : 2026-01-05 DOI: 10.1016/j.jcpo.2026.100704
Ryan J. Crowley , Jag S. Lally , David M. Kline , Amanda M. Bunting

Background

Access to oncologists is crucial to quality cancer care. We aimed to assess the geospatial distribution of oncologists in the United States and its association with cancer mortality.

Methods

We used county-level oncologist data from the 2025 Doctors and Clinicians national downloadable file and county-level cancer outcome data from the 2018–2022 State Cancer Profiles. We assessed urban-rural differences in the distribution of oncologists in the United States and used Local Moran’s I to identify clusters of high and low oncologist density and cancer mortality rates. We classified counties using the 2023 Rural-Urban Continuum Codes (RUCC) with RUCC 1–3 as urban and RUCC 4–9 as rural.

Results

13,332 oncologists were identified nationwide. The median oncologist density per 100,000 population was 6.0 in urban counties and 0.0 in rural counties (p-value <0.001). The median age-adjusted cancer mortality rate per 100,000 population was 156.1 in urban counties and 166.8 in rural counties (p-value <0.001). Clusters of low oncologist density were observed in the South.

Conclusion

There are significant geospatial differences in oncologist accessibility and cancer outcomes. Targeted interventions are necessary to ensure that rural areas maintain access to oncology care.
背景:获得肿瘤学家对高质量的癌症治疗至关重要。我们旨在评估美国肿瘤学家的地理空间分布及其与癌症死亡率的关系。方法:我们使用了2025年医生和临床医生国家可下载文件中的县级肿瘤学家数据和2018-2022年国家癌症概况中的县级癌症结局数据。我们评估了美国肿瘤医生分布的城乡差异,并使用Local Moran's I来确定肿瘤医生密度高和低的集群和癌症死亡率。我们使用2023城乡连续代码(RUCC)对县进行分类,其中RUCC 1-3为城市,RUCC 4-9为农村。结果:在全国范围内确定了13332名肿瘤学家。城市县肿瘤医师密度中位数为每10万人6.0人,农村县为每10万人0.0人(p值)。结论:肿瘤医师可及性和肿瘤转归存在显著的地理空间差异。有针对性的干预措施是必要的,以确保农村地区继续获得肿瘤护理。
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引用次数: 0
Social framework to judge the importance of breast cancer 判断乳腺癌重要性的社会框架。
IF 2 Q3 HEALTH POLICY & SERVICES Pub Date : 2025-12-22 DOI: 10.1016/j.jcpo.2025.100679
Zsuzsa Réka Pozsár , Krisztina Tóth , Marianna Moizs , János Révész , Klára Tatár-Kiss , Judit Tittmann , Aliz Nikolényi , Ágnes Anna Kovács , Tamás Mátrai , Borbála Judit Szabó , Erzsébet Hajduné Kovács , Csilla Czene , Dalma Hosszú , Anna Bögös , Tu Thanh Nguyen , Júlia Zemplényiné Bartha , Tamás Ágh , Zoltán Kaló , Magdolna Dank

Background

Breast cancer (BC) has profound effects on patients, households, and society, necessitating a multidimensional approach to understand its implications fully. This study aimed to develop a conceptual model for a social framework (SF) that assists in identifying group common values and needs for BC interventions in Hungary. The SF reflects diverse perspectives, including healthcare professionals, patients, caregivers, policymakers of health and social care, health technology developers, and corporate and philanthropic supporters of BC initiatives.

Methods

A narrative literature review was conducted to identify value elements (VEs) of BC. VEs were categorized into groups and further clustered into sub-groups within each main category. This literature-based conceptual model was contextualized and adapted to the Hungarian setting through individual and group interviews with various societal group representatives. A closing validation meeting fostered stakeholders’ reflection on the draft model.

Results

The final conceptual model incorporates five traditional (e.g., clinical outcomes, adverse events, survival, and direct medical costs), nine patient-centric (e.g., personal milestones, patient experience, and financial burden), and seven societal (e.g., disease severity, the presence of the disease around us, and indirect costs) VEs.

Conclusion

Our study is the first to present a comprehensive SF that provides insights into key disease challenges and why different BC interventions are important to various stakeholder groups via capturing traditional, patient-centric, and societal VEs. It informs decision-making within and beyond the healthcare domain by supporting the evaluation of policies, health technologies, public and civil society initiatives in Hungary.

Policy Summary

While BC is a priority disease area for all stakeholder groups, their views on what contributes to the success of policy decisions are different. If policymakers intend to represent the interests of the whole society, they should aim to express the value of policy interventions in a comprehensive SF.
背景:乳腺癌(BC)对患者、家庭和社会都有深远的影响,需要一个多维的方法来充分了解其影响。本研究旨在为社会框架(SF)开发一个概念模型,以帮助识别匈牙利群体的共同价值观和BC干预的需求。SF反映了不同的观点,包括医疗保健专业人员、患者、护理人员、卫生和社会保健政策制定者、卫生技术开发人员以及BC倡议的企业和慈善支持者。方法:采用叙事性文献法,识别BC的价值要素。将ve分类成组,并在每个主要类别内进一步聚类成子组。通过对不同社会群体代表的个人和团体访谈,这种基于文献的概念模型被语境化并适应匈牙利的环境。最后的确认会议促进了利益相关者对模型草案的反思。结果:最终的概念模型包含五个传统的(例如,临床结果、不良事件、生存和直接医疗费用)、九个以患者为中心的(例如,个人里程碑、患者经历和经济负担)和七个社会的(例如,疾病严重程度、我们周围疾病的存在和间接费用)。结论:我们的研究首次提出了一个全面的SF,通过捕获传统的、以患者为中心的和社会的ve,提供了对关键疾病挑战的见解,以及为什么不同的BC干预对不同利益相关者群体很重要。它通过支持评估匈牙利的政策、卫生技术、公共和民间社会倡议,为保健领域内外的决策提供信息。政策摘要:虽然不列颠哥伦比亚省是所有利益相关者群体的优先疾病领域,但他们对什么有助于政策决定的成功的看法是不同的。如果政策制定者打算代表整个社会的利益,他们应该致力于在一个全面的SF中表达政策干预的价值。
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引用次数: 0
Progression-free survival is strongly associated with overall survival in relapsed/refractory diffuse large B-cell lymphoma in the CAR T-cell era 在CAR - t细胞时代,复发/难治性弥漫性大b细胞淋巴瘤的无进展生存率与总生存率密切相关。
IF 2 Q3 HEALTH POLICY & SERVICES Pub Date : 2025-12-20 DOI: 10.1016/j.jcpo.2025.100699
Alexander M. Gorzewski , Rebecca Z. Steuer , Charmi Trivedi , Kaavya Mandi , Christina A. Raker , Charles J. Milrod , Ari R. Pelcovits

Introduction

In clinical trials for diffuse large B-cell lymphoma (DLBCL), progression-free survival (PFS) has been used as a validated surrogate endpoint to help expedite drug development and regulatory approval. The advent of chimeric antigen receptor (CAR) T-cell therapies has radically changed the treatment landscape, potentially prolonging post-progression survival and weakening the correlation between PFS and overall survival (OS). This study evaluates the utility of PFS as a surrogate endpoint for OS in relapsed/refractory (R/R) DLBCL in the CAR T-cell era.

Materials and methods

A systematic review of Phase 3 randomized clinical trials for R/R DLBCL initiated after 2015 was conducted. A weighted linear regression analysis was performed to assess the correlation between PFS and OS.

Results

Six trials, comprising 1577 patients, met the inclusion criteria. Weighted linear regression demonstrated a coefficient of determination (R²) of 0.88 (p = 0.0054), indicating a strong association between PFS and OS in R/R DLBCL trials conducted since the introduction of CAR T-cell therapy.

Discussion

These findings provide evidence that PFS remains a valid and strong surrogate endpoint for OS in the contemporary R/R DLBCL treatment landscape. This supports the continued use of PFS as a primary endpoint in regulatory studies for new therapies for R/R DLBCL and provides important information for health policy discussions on drug approval, insurance coverage, and reimbursement decisions for aggressive lymphomas.
在弥漫性大b细胞淋巴瘤(DLBCL)的临床试验中,无进展生存期(PFS)已被用作有效的替代终点,以帮助加快药物开发和监管审批。嵌合抗原受体(CAR) t细胞疗法的出现从根本上改变了治疗前景,可能延长进展后生存期,削弱PFS与总生存期(OS)之间的相关性。这项研究评估了在CAR - t细胞时代,PFS作为复发/难治性(R/R) DLBCL OS的替代终点的效用。材料与方法:系统回顾2015年以后开展的R/R DLBCL的3期随机临床试验。采用加权线性回归分析评估PFS与OS的相关性。结果:6项试验,1577例患者符合纳入标准。加权线性回归显示决定系数(R²)为0.88 (p = 0.0054),表明自引入CAR - t细胞治疗以来进行的R/R DLBCL试验中PFS和OS之间存在很强的关联。讨论:这些发现提供了证据,证明在当代R/R DLBCL治疗领域,PFS仍然是OS的有效和强有力的替代终点。这支持将PFS继续作为R/R DLBCL新疗法的监管研究的主要终点,并为有关药物批准、保险覆盖和侵袭性淋巴瘤报销决策的卫生政策讨论提供重要信息。
{"title":"Progression-free survival is strongly associated with overall survival in relapsed/refractory diffuse large B-cell lymphoma in the CAR T-cell era","authors":"Alexander M. Gorzewski ,&nbsp;Rebecca Z. Steuer ,&nbsp;Charmi Trivedi ,&nbsp;Kaavya Mandi ,&nbsp;Christina A. Raker ,&nbsp;Charles J. Milrod ,&nbsp;Ari R. Pelcovits","doi":"10.1016/j.jcpo.2025.100699","DOIUrl":"10.1016/j.jcpo.2025.100699","url":null,"abstract":"<div><h3>Introduction</h3><div>In clinical trials for diffuse large B-cell lymphoma (DLBCL), progression-free survival (PFS) has been used as a validated surrogate endpoint to help expedite drug development and regulatory approval. The advent of chimeric antigen receptor (CAR) T-cell therapies has radically changed the treatment landscape, potentially prolonging post-progression survival and weakening the correlation between PFS and overall survival (OS). This study evaluates the utility of PFS as a surrogate endpoint for OS in relapsed/refractory (R/R) DLBCL in the CAR T-cell era.</div></div><div><h3>Materials and methods</h3><div>A systematic review of Phase 3 randomized clinical trials for R/R DLBCL initiated after 2015 was conducted. A weighted linear regression analysis was performed to assess the correlation between PFS and OS.</div></div><div><h3>Results</h3><div>Six trials, comprising 1577 patients, met the inclusion criteria. Weighted linear regression demonstrated a coefficient of determination (R²) of 0.88 (p = 0.0054), indicating a strong association between PFS and OS in R/R DLBCL trials conducted since the introduction of CAR T-cell therapy.</div></div><div><h3>Discussion</h3><div>These findings provide evidence that PFS remains a valid and strong surrogate endpoint for OS in the contemporary R/R DLBCL treatment landscape. This supports the continued use of PFS as a primary endpoint in regulatory studies for new therapies for R/R DLBCL and provides important information for health policy discussions on drug approval, insurance coverage, and reimbursement decisions for aggressive lymphomas.</div></div>","PeriodicalId":38212,"journal":{"name":"Journal of Cancer Policy","volume":"47 ","pages":"Article 100699"},"PeriodicalIF":2.0,"publicationDate":"2025-12-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145811053","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Innovative oncology trial designs: Time to act - A review with recommendations of the Cancer Drug Development Forum. 创新肿瘤试验设计:癌症药物发展论坛建议的回顾。
IF 2 Q3 HEALTH POLICY & SERVICES Pub Date : 2025-12-19 DOI: 10.1016/j.jcpo.2025.100696
Rosa Giuliani, Nafsika Kronidou-Horst, Christina Yap, Aáron Sosa Mejia, Lada Leyens, Theodor Framke, Fergus Sweeney, Laurence Collette, Rachel Giles, Jan Bogaerts, Peter van de Ven, Stefan N Symeonides

Introduction: Clinical oncology trial design constantly adapts and evolves to meet the needs of all stakeholders, from patients to regulators. This evolution has however also led to an increase in the complexity of clinical development, and investigators are expected to invest more time and money in planning and running their studies and overall clinical and regulatory pathway.

Methods: Here we review recent innovations in trial designs, study endpoints, and relevant regulatory guidelines, before making recommendations to enhance the clinical trial ecosystem in the EU.

Results: Innovative clinical study designs that go beyond traditional randomised, double-blinded, placebo-controlled trials often promise greater flexibility and efficiency in the conduct of oncology studies, but adoption has been slow. Furthermore, the increased complexity associated with innovative trials means that coordination between all relevant stakeholders is essential to every phase of clinical development. Despite recent advances, there is a risk that Europe is becoming seen as a less attractive location for clinical trials, and this article outlines initiatives and possible steps to improve patient access to medicines and processes across Europe.

Policy summary: Innovative trial designs promise more efficient, flexible, and inclusive clinical trials, but more needs to be done to encourage their adoption if the advantages outweigh the limitations. Partnership and coordination between all stakeholders, from patients to regulators, and at all phases, is more important than ever. Finally, effective action is needed to make Europe a more attractive destination for clinical research and to improve access to innovative medicines for patients.

(最多250个)前言:临床肿瘤试验设计不断适应和发展,以满足从患者到监管机构的所有利益相关者的需求。然而,这种演变也导致临床开发的复杂性增加,研究人员预计将投入更多的时间和金钱来规划和运行他们的研究以及整体临床和监管途径。方法:在本文中,我们回顾了最近在试验设计、研究终点和相关监管指南方面的创新,然后提出了加强欧盟临床试验生态系统的建议。结果:创新的临床研究设计超越了传统的随机、双盲、安慰剂对照试验,通常承诺在肿瘤研究中具有更大的灵活性和效率,但采用速度缓慢。此外,与创新试验相关的复杂性增加意味着所有相关利益相关者之间的协调对于临床开发的每个阶段都至关重要。尽管最近取得了进展,但欧洲有可能成为临床试验的一个不那么有吸引力的地点,部分原因可能是监管挑战和操作复杂性。需要做更多的工作来改善整个欧洲患者获得药物和治疗的机会。政策摘要:创新的试验设计有望提高临床试验的效率、灵活性和包容性,但如果其优点大于局限性,则需要做更多的工作来鼓励采用这些试验。从患者到监管机构的所有利益攸关方之间在所有阶段的伙伴关系和协调比以往任何时候都更加重要。最后,如果欧洲不希望临床试验研究的专业知识和投资落后于世界其他地区,就迫切需要采取有效行动。
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引用次数: 0
Economic burden of breast, cervical, and oral cancer in Bangladesh: a cost-of-illness study 孟加拉国乳腺癌、宫颈癌和口腔癌的经济负担:一项疾病成本研究。
IF 2 Q3 HEALTH POLICY & SERVICES Pub Date : 2025-12-18 DOI: 10.1016/j.jcpo.2025.100694
Md. Ragaul Azim , Quazi Nazmus Sakib , Md. Mahfujur Rahman , Md. Sirajul Islam , Mushfika Binta Latif , Md. Habibullah Talukder , Syed Abdul Hamid

Background

Breast, cervical, and oral cancers are leading causes of morbidity and mortality in Bangladesh, placing a heavy economic burden on households and the health system. Yet, this burden remains poorly understood, as no prior study has comprehensively examined their economic impact. Moreover, the profound psychological suffering experienced by patients are often overlooked in existing global evidence. Therefore, this study aims to estimate the comprehensive economic burden of breast, cervical, and oral cancers in Bangladesh from the household perspective.

Methods

Using a cross-sectional design, primary data were collected through structured interviews with 346 cancer patients. A cost-of-illness approach was employed. Direct medical and direct non-medical costs were estimated based on respondent-reported expenditures. Indirect costs, i.e.income loss, were calculated using the human capital approach. Intangible costs, reflecting pain and discomfort, were quantified using the willingness-to-pay method.

Results

The average total cost per patient was US$12,117, with breast cancer accounting for the highest burden. Intangible costs comprised 47.7 % of the total, underscoring the substantial psychological impact of cancer on patients. The combined national economic burden exceeded US$1.17 billion. Catastrophic health expenditure was nearly universal (99.1 %), with average treatment costs exceeding the catastrophic threshold by 44-fold. Expenditures were significantly higher among wealthier households, patients with longer disease duration, and those seeking care from multiple facilities.

Conclusion

Breast, cervical, and oral cancers impose a major financial and psychological burden on households in Bangladesh. The near-universal catastrophic health expenditure and high intangible costs highlight the urgent need for accessible and affordable cancer care.

Policy summary

Policies should strengthen financial protection, decentralize diagnosis and treatment, introduce insurance with cancer-specific benefits, establish an effective referral system, integrate psychosocial support and strengthen early detection programs.
背景:乳腺癌、宫颈癌和口腔癌是孟加拉国发病率和死亡率的主要原因,给家庭和卫生系统带来了沉重的疾病和经济负担。然而,人们对这种负担仍然知之甚少,因为之前没有研究全面考察过它们的经济影响。此外,在现有的全球证据中,患者所经历的深刻心理痛苦往往被忽视。本研究旨在从家庭角度估计孟加拉国乳腺癌、宫颈癌和口腔癌的综合经济负担。方法:采用横断面设计,对346例成年癌症患者进行结构化访谈,收集初步资料。采用了疾病成本法。直接医疗费用和直接非医疗费用是根据答复者报告的支出估计的。间接成本,包括生产力损失,是用人力资本法计算的。反映心理痛苦的无形成本采用支付意愿法进行量化。结果:每位患者的平均总费用为12117美元,其中乳腺癌负担最高。无形成本占总成本的47.7%,强调了癌症对患者的巨大心理影响。合计国民经济负担超过11.7亿美元。灾难性卫生支出几乎普遍存在(99.1%),平均治疗费用超过灾难性阈值44倍。在较富裕的家庭、病程较长的患者以及在多个机构寻求治疗的患者中,支出明显较高。结论:乳腺癌、宫颈癌和口腔癌给孟加拉国家庭带来了巨大的经济和心理负担。近乎普遍的灾难性卫生支出和高昂的无形成本突出表明,迫切需要公平筹资和可获得、负担得起的保健。政策总结:政策应加强财政保护,分散诊断和治疗,引入针对癌症的保险,建立有效的转诊系统,整合社会心理支持,加强早期发现项目。
{"title":"Economic burden of breast, cervical, and oral cancer in Bangladesh: a cost-of-illness study","authors":"Md. Ragaul Azim ,&nbsp;Quazi Nazmus Sakib ,&nbsp;Md. Mahfujur Rahman ,&nbsp;Md. Sirajul Islam ,&nbsp;Mushfika Binta Latif ,&nbsp;Md. Habibullah Talukder ,&nbsp;Syed Abdul Hamid","doi":"10.1016/j.jcpo.2025.100694","DOIUrl":"10.1016/j.jcpo.2025.100694","url":null,"abstract":"<div><h3>Background</h3><div>Breast, cervical, and oral cancers are leading causes of morbidity and mortality in Bangladesh, placing a heavy economic burden on households and the health system. Yet, this burden remains poorly understood, as no prior study has comprehensively examined their economic impact. Moreover, the profound psychological suffering experienced by patients are often overlooked in existing global evidence. Therefore, this study aims to estimate the comprehensive economic burden of breast, cervical, and oral cancers in Bangladesh from the household perspective.</div></div><div><h3>Methods</h3><div>Using a cross-sectional design, primary data were collected through structured interviews with 346 cancer patients. A cost-of-illness approach was employed. Direct medical and direct non-medical costs were estimated based on respondent-reported expenditures. Indirect costs, i.e.income loss, were calculated using the human capital approach. Intangible costs, reflecting pain and discomfort, were quantified using the willingness-to-pay method.</div></div><div><h3>Results</h3><div>The average total cost per patient was US$12,117, with breast cancer accounting for the highest burden. Intangible costs comprised 47.7 % of the total, underscoring the substantial psychological impact of cancer on patients. The combined national economic burden exceeded US$1.17 billion. Catastrophic health expenditure was nearly universal (99.1 %), with average treatment costs exceeding the catastrophic threshold by 44-fold. Expenditures were significantly higher among wealthier households, patients with longer disease duration, and those seeking care from multiple facilities.</div></div><div><h3>Conclusion</h3><div>Breast, cervical, and oral cancers impose a major financial and psychological burden on households in Bangladesh. The near-universal catastrophic health expenditure and high intangible costs highlight the urgent need for accessible and affordable cancer care.</div></div><div><h3>Policy summary</h3><div>Policies should strengthen financial protection, decentralize diagnosis and treatment, introduce insurance with cancer-specific benefits, establish an effective referral system, integrate psychosocial support and strengthen early detection programs.</div></div>","PeriodicalId":38212,"journal":{"name":"Journal of Cancer Policy","volume":"47 ","pages":"Article 100694"},"PeriodicalIF":2.0,"publicationDate":"2025-12-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145800774","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Interventions to improve cancer screening adherence in migrants and ethnic minorities in the European Region: A systematic review. 改善欧洲地区移民和少数民族癌症筛查依从性的干预措施:一项系统综述。
IF 2 Q3 HEALTH POLICY & SERVICES Pub Date : 2025-12-11 DOI: 10.1016/j.jcpo.2025.100677
Chiara De Marchi , Federica Di Lullo , Caterina Ferrari , Valentina Pettinicchio , Alessandra Sinopoli , Paolo lombardo , Maria Elena Tosti , Silvia Declich , Scilla Pizzarelli , Franca D’Angelo , Maria Teresa Riccardi , Fabiana Arrivi , Francesca Maria Forestiero , Virginia Rosca , Alessandra Romano , Daniela Marotta

Introduction

Adherence to cancer screening programs is crucial for reducing cancer-related mortality, yet migrant and ethnic minorities (MEMs) often show lower participation rates compared to the general population. This systematic review aims to identify effective strategies to improve cancer screening adherence among MEMs in the WHO European Region.

Methods

A systematic review was conducted following PRISMA guidelines, searching Medline, Embase, Scisearch, and Biosis for studies published up to October 13th, 2025. Eligible studies included quantitative and quali-quantitative studies focused on interventions aimed to increase adherence to cancer screening among MEMs. Study quality was assessed using the Joanna Briggs Institute Critical Appraisal Tools.

Results

We included 12 studies, conducted in the United Kingdom, Norway, Israel, and Turkey. All of the interventions focused on breast and cervical cancer screening, with no studies addressing colorectal cancer screening. Effective interventions incorporated culturally and linguistically tailored strategies, such as community-based education, use of cultural mediators, multilingual reminds and information, free transport service and language support. Community-based and informal health education approaches significantly increased screening uptake, particularly among South Asian and ultraOrthodox Jewish women. However, interventions targeting men or colorectal cancer screening were lacking, indicating a significant research gap.

Policy Summary

This review highlights the need for gender-inclusive, culturally sensitive policies to improve screening adherence among MEMs. Policymakers should develop integrated screening campaigns that address multiple cancer types, particularly colorectal cancer, and ensure the inclusion of male populations. Enhancing community involvement is essential to achieve equitable screening coverage in line with EU health targets.
导读:坚持癌症筛查计划对于降低癌症相关死亡率至关重要,然而与普通人群相比,移民和少数民族(MEMs)的参与率往往较低。本系统综述旨在确定提高世卫组织欧洲区域MEMs癌症筛查依从性的有效策略。方法:按照PRISMA指南进行系统评价,检索Medline、Embase、Scisearch和Biosis,检索截至2025年10月13日发表的研究。符合条件的研究包括定量和定性定量研究,重点关注旨在提高MEMs癌症筛查依从性的干预措施。使用乔安娜布里格斯研究所关键评估工具评估研究质量。结果:我们纳入了在英国、挪威、以色列和土耳其进行的12项研究。所有的干预措施都集中在乳腺癌和宫颈癌筛查上,没有针对结直肠癌筛查的研究。有效的干预措施包括针对文化和语言的战略,如基于社区的教育、使用文化媒介、多语种提醒和信息、免费交通服务和语言支持。以社区为基础和非正式的健康教育方法显著提高了筛查的接受程度,特别是在南亚和极端正统派犹太妇女中。然而,针对男性或结直肠癌筛查的干预措施缺乏,表明研究存在重大空白。政策总结:本综述强调需要制定性别包容、文化敏感的政策,以提高MEMs的筛查依从性。决策者应开展针对多种癌症类型的综合筛查活动,特别是结肠直肠癌,并确保纳入男性人群。加强社区参与对于实现符合欧盟卫生目标的公平筛查覆盖率至关重要。
{"title":"Interventions to improve cancer screening adherence in migrants and ethnic minorities in the European Region: A systematic review.","authors":"Chiara De Marchi ,&nbsp;Federica Di Lullo ,&nbsp;Caterina Ferrari ,&nbsp;Valentina Pettinicchio ,&nbsp;Alessandra Sinopoli ,&nbsp;Paolo lombardo ,&nbsp;Maria Elena Tosti ,&nbsp;Silvia Declich ,&nbsp;Scilla Pizzarelli ,&nbsp;Franca D’Angelo ,&nbsp;Maria Teresa Riccardi ,&nbsp;Fabiana Arrivi ,&nbsp;Francesca Maria Forestiero ,&nbsp;Virginia Rosca ,&nbsp;Alessandra Romano ,&nbsp;Daniela Marotta","doi":"10.1016/j.jcpo.2025.100677","DOIUrl":"10.1016/j.jcpo.2025.100677","url":null,"abstract":"<div><h3>Introduction</h3><div>Adherence to cancer screening programs is crucial for reducing cancer-related mortality, yet migrant and ethnic minorities (MEMs) often show lower participation rates compared to the general population. This systematic review aims to identify effective strategies to improve cancer screening adherence among MEMs in the WHO European Region.</div></div><div><h3>Methods</h3><div>A systematic review was conducted following PRISMA guidelines, searching Medline, Embase, Scisearch, and Biosis for studies published up to October 13th, 2025. Eligible studies included quantitative and quali-quantitative studies focused on interventions aimed to increase adherence to cancer screening among MEMs. Study quality was assessed using the Joanna Briggs Institute Critical Appraisal Tools.</div></div><div><h3>Results</h3><div>We included 12 studies, conducted in the United Kingdom, Norway, Israel, and Turkey. All of the interventions focused on breast and cervical cancer screening, with no studies addressing colorectal cancer screening. Effective interventions incorporated culturally and linguistically tailored strategies, such as community-based education, use of cultural mediators, multilingual reminds and information, free transport service and language support. Community-based and informal health education approaches significantly increased screening uptake, particularly among South Asian and ultraOrthodox Jewish women. However, interventions targeting men or colorectal cancer screening were lacking, indicating a significant research gap.</div></div><div><h3>Policy Summary</h3><div>This review highlights the need for gender-inclusive, culturally sensitive policies to improve screening adherence among MEMs. Policymakers should develop integrated screening campaigns that address multiple cancer types, particularly colorectal cancer, and ensure the inclusion of male populations. Enhancing community involvement is essential to achieve equitable screening coverage in line with EU health targets.</div></div>","PeriodicalId":38212,"journal":{"name":"Journal of Cancer Policy","volume":"47 ","pages":"Article 100677"},"PeriodicalIF":2.0,"publicationDate":"2025-12-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145752305","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The health and economic burden of lung cancer in Australia: A dynamic model of quality of life and productivity loss 澳大利亚肺癌的健康和经济负担:生活质量和生产力损失的动态模型。
IF 2 Q3 HEALTH POLICY & SERVICES Pub Date : 2025-12-10 DOI: 10.1016/j.jcpo.2025.100674
Mohammad Afshar Ali , Christine Y. Lu

Background

Prior studies estimated lung cancer costs; none examined quality of life and work productivity in Australia via population-based models.

Objective

Quantify lung cancer’s burden in working-age Australians using a dynamic Markov lifetable, estimating quality-adjusted life years (QALYs) and productivity-adjusted life years (PALYs) lost.

Methods

We developed a dynamic comparative Markov lifetable model to simulate both incident and prevalent cases of lung cancer among Australians aged 20–64 years from 2022 to 2031. Two parallel scenarios were modelled: (i) a base-case scenario reflecting individuals diagnosed in 2022 (incident model) and those living with lung cancer from 2012 to 2021 (prevalent model), and (ii) a counterfactual scenario in which no individuals had lung cancer. The differences between these simulations were used to estimate life years, QALYs, and PALYs lost. Model inputs were derived from previously published data. The economic value of productivity losses was estimated using the 2022 Australian gross domestic product (GDP) per full-time equivalent worker, applying a 5 % annual discount rate.

Results

Over the twenty-year period, lung cancer is projected to result in the loss of 28,430 life years, 55,964 QALYs, and 60,310 PALYs, equating to AU$14.45 billion in lost GDP. Sensitivity analyses confirmed the robustness of the model to variations in key parameters.

Conclusion

Lung cancer imposes a substantial health and economic burden among working-age Australians. By combining QALY and PALY metrics within a dynamic modelling framework, this study provides a comprehensive assessment of the burden faced by this population and may inform future research and economic evaluations.
背景:先前的研究估算了肺癌的成本;没有人通过基于人口的模型来研究澳大利亚的生活质量和工作效率。目的:使用动态马尔可夫生命表量化工作年龄澳大利亚人的肺癌负担,估计质量调整生命年(QALYs)和生产力调整生命年(PALYs)损失。方法:我们开发了一个动态比较马尔可夫生命表模型来模拟2022年至2031年间20-64岁澳大利亚人肺癌发病率和流行病例。模拟了两种平行情景:(i)反映2022年确诊的个体(事件模型)和2012年至2021年患有肺癌的个体(流行模型)的基本情景情景,以及(ii)没有个体患有肺癌的反事实情景。这些模拟之间的差异被用来估计生命年、QALYs和PALYs的损失。模型输入来自先前发布的数据。生产力损失的经济价值是用2022年澳大利亚每个全职等效工人的国内生产总值(GDP)来估算的,采用5%的年折扣率。结果:在20年的时间里,肺癌预计将导致28430个生命年、55,964个质量年和60,310个paly年的损失,相当于144.5亿澳元的GDP损失。敏感性分析证实了模型对关键参数变化的鲁棒性。结论:肺癌给工作年龄的澳大利亚人带来了巨大的健康和经济负担。通过在动态建模框架内结合QALY和PALY指标,本研究对这一人群面临的负担进行了全面评估,并可能为未来的研究和经济评估提供信息。
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引用次数: 0
Ensuring equitable access to cancer medicine and care in Australia: A human-rights lens, including people experiencing homelessness 确保在澳大利亚公平获得癌症药物和护理:人权视角,包括无家可归者
IF 2 Q3 HEALTH POLICY & SERVICES Pub Date : 2025-12-09 DOI: 10.1016/j.jcpo.2025.100678
Rashidul Alam Mahumud
Australia has strong cancer survival. Yet many people still struggle to get timely diagnosis, medicines, and supportive care. Gaps are widest for Aboriginal and Torres Strait Islander peoples, rural and remote communities, culturally and linguistically diverse groups, people with disability, temporary visa holders, and people experiencing homelessness.

Objective

To set out practical, rights-aligned actions that turn universal coverage into universal access.

Approach

This short communication applies a rights-based analytic framing, distinct from a checklist, to reinterpret policy choices through the lenses of accountability, justiciability, and participation.

Actionable implications

Using this framing, synthesising recent evidence on affordability, diagnostics, and service capacity, we prioritise four actionable levers: cap financial toxicity (with standardised travel/accommodation support and public OOP reporting); fund and benchmark companion diagnostics (national turnaround and equity dashboards); scale tele-oncology/tele-trials with minimum local capacity and travel stipends (monitoring priority populations); and adopt distributional cost-effectiveness analysis in HTA and program design to make equity trade-offs explicit. This framing specifies who must act, by when, and with what evidence, offering a practical route to equitable, sustainable cancer.

Conclusion

Universal coverage alone does not guarantee equity. Implementing a rights-aligned plan with clear duty-bearers, timelines, and the four actionable levers we outline can narrow access gaps and support timely, affordable, culturally safe cancer care, including for people experiencing homelessness.
澳大利亚的癌症存活率很高。然而,许多人仍然难以获得及时的诊断、药物和支持性护理。土著人和托雷斯海峡岛民、农村和偏远社区、文化和语言多样化群体、残疾人、临时签证持有人和无家可归者的差距最大。目标:制定切合实际、符合权利的行动,将全民覆盖转变为普遍可及。方法本简短沟通采用基于权利的分析框架,不同于清单,通过问责制、可诉性和参与的视角重新解释政策选择。可操作的影响利用这一框架,综合最近关于可负担性、诊断和服务能力的证据,我们优先考虑了四个可操作的杠杆:限制财务毒性(通过标准化的旅行/住宿支持和公共OOP报告);基金和基准配套诊断(国家周转和股票仪表板);以最低限度的当地能力和旅费津贴进行远程肿瘤学/远程试验(监测重点人群);并在HTA和方案设计中采用分配成本效益分析,以明确股权权衡。这一框架规定了谁必须采取行动,在什么时候采取行动,以什么证据采取行动,为实现公平、可持续的癌症提供了一条切实可行的途径。结论仅全民覆盖并不能保证公平。实施一项与权利相一致的计划,明确责任承担者、时间表和我们概述的四个可操作杠杆,可以缩小获取差距,并支持及时、负担得起、文化上安全的癌症治疗,包括为无家可归者提供癌症治疗。
{"title":"Ensuring equitable access to cancer medicine and care in Australia: A human-rights lens, including people experiencing homelessness","authors":"Rashidul Alam Mahumud","doi":"10.1016/j.jcpo.2025.100678","DOIUrl":"10.1016/j.jcpo.2025.100678","url":null,"abstract":"<div><div>Australia has strong cancer survival. Yet many people still struggle to get timely diagnosis, medicines, and supportive care. Gaps are widest for Aboriginal and Torres Strait Islander peoples, rural and remote communities, culturally and linguistically diverse groups, people with disability, temporary visa holders, and people experiencing homelessness.</div></div><div><h3>Objective</h3><div>To set out practical, rights-aligned actions that turn universal coverage into universal access.</div></div><div><h3>Approach</h3><div>This short communication applies a rights-based analytic framing, distinct from a checklist, to reinterpret policy choices through the lenses of accountability, justiciability, and participation.</div></div><div><h3>Actionable implications</h3><div>Using this framing, synthesising recent evidence on affordability, diagnostics, and service capacity, we prioritise four actionable levers: cap financial toxicity (with standardised travel/accommodation support and public OOP reporting); fund and benchmark companion diagnostics (national turnaround and equity dashboards); scale tele-oncology/tele-trials with minimum local capacity and travel stipends (monitoring priority populations); and adopt distributional cost-effectiveness analysis in HTA and program design to make equity trade-offs explicit. This framing specifies who must act, by when, and with what evidence, offering a practical route to equitable, sustainable cancer.</div></div><div><h3>Conclusion</h3><div>Universal coverage alone does not guarantee equity. Implementing a rights-aligned plan with clear duty-bearers, timelines, and the four actionable levers we outline can narrow access gaps and support timely, affordable, culturally safe cancer care, including for people experiencing homelessness.</div></div>","PeriodicalId":38212,"journal":{"name":"Journal of Cancer Policy","volume":"47 ","pages":"Article 100678"},"PeriodicalIF":2.0,"publicationDate":"2025-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145737669","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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Journal of Cancer Policy
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