Pub Date : 2025-10-17eCollection Date: 2025-01-01DOI: 10.3332/ecancer.2025.2017
Jyoti Brahmaiah, Usha Adiga, Alfred J Augustine, Sampara Vasishta
Background: Hepatocellular carcinoma (HCC) is a complex malignancy influenced by genetic, epigenetic and immune-related factors. The tumour immune microenvironment plays a critical role in HCC progression and response to immunotherapy. Identifying key immune-related gene signatures through clustering techniques can provide insights into tumour biology and therapeutic targets.
Methods: We employed K-means, Markov Clustering Algorithm (MCL) and density-based spatial clustering of applications with noise (DBSCAN) to analyse immune-related genes in HCC. Functional enrichment analysis was conducted using Gene Ontology (GO) biological process, cellular component and molecular function categories, along with pathway analysis from Kyoto encyclopedia of genes and genomes (KEGG) and Reactome databases. Additionally, protein-protein interaction (PPI) hub analysis and microRNAs (miRNA) target predictions were integrated to understand the regulatory networks.
Results: K-means clustering segregated immune genes into three clusters, with major histocompatibility complex (MHC) class II genes forming a distinct cluster. MCL and DBSCAN identified a more unified immune cluster incorporating both MHC class I and II molecules, suggesting their coordinated role in antigen presentation. GO analysis revealed enrichment in antigen processing and presentation pathways, immunoglobulin-mediated responses and glutamate receptor signaling. KEGG pathway analysis highlighted associations with autoimmune diseases and viral infections. PPI hub analysis identified CD4, CD74 and HLA-DQA1 as central nodes, while miRNA analysis suggested regulatory interactions affecting immune gene expression.
Conclusion: Our clustering analysis highlights distinct immune-related gene signatures in HCC, emphasising the role of antigen presentation and immune modulation in tumour progression. The findings provide a foundation for further investigation into immunotherapeutic strategies targeting key immune pathways in HCC.
{"title":"Clustering-based identification of immune-related gene signatures in hepatocellular carcinoma.","authors":"Jyoti Brahmaiah, Usha Adiga, Alfred J Augustine, Sampara Vasishta","doi":"10.3332/ecancer.2025.2017","DOIUrl":"10.3332/ecancer.2025.2017","url":null,"abstract":"<p><strong>Background: </strong>Hepatocellular carcinoma (HCC) is a complex malignancy influenced by genetic, epigenetic and immune-related factors. The tumour immune microenvironment plays a critical role in HCC progression and response to immunotherapy. Identifying key immune-related gene signatures through clustering techniques can provide insights into tumour biology and therapeutic targets.</p><p><strong>Methods: </strong>We employed K-means, Markov Clustering Algorithm (MCL) and density-based spatial clustering of applications with noise (DBSCAN) to analyse immune-related genes in HCC. Functional enrichment analysis was conducted using Gene Ontology (GO) biological process, cellular component and molecular function categories, along with pathway analysis from Kyoto encyclopedia of genes and genomes (KEGG) and Reactome databases. Additionally, protein-protein interaction (PPI) hub analysis and microRNAs (miRNA) target predictions were integrated to understand the regulatory networks.</p><p><strong>Results: </strong>K-means clustering segregated immune genes into three clusters, with major histocompatibility complex (MHC) class II genes forming a distinct cluster. MCL and DBSCAN identified a more unified immune cluster incorporating both MHC class I and II molecules, suggesting their coordinated role in antigen presentation. GO analysis revealed enrichment in antigen processing and presentation pathways, immunoglobulin-mediated responses and glutamate receptor signaling. KEGG pathway analysis highlighted associations with autoimmune diseases and viral infections. PPI hub analysis identified CD4, CD74 and HLA-DQA1 as central nodes, while miRNA analysis suggested regulatory interactions affecting immune gene expression.</p><p><strong>Conclusion: </strong>Our clustering analysis highlights distinct immune-related gene signatures in HCC, emphasising the role of antigen presentation and immune modulation in tumour progression. The findings provide a foundation for further investigation into immunotherapeutic strategies targeting key immune pathways in HCC.</p>","PeriodicalId":11460,"journal":{"name":"ecancermedicalscience","volume":"19 ","pages":"2017"},"PeriodicalIF":1.3,"publicationDate":"2025-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12812832/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146009325","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-17eCollection Date: 2025-01-01DOI: 10.3332/ecancer.2025.2018
Sudarshan Govender, Tamsin K Phillips, Fiona M Walter, Sarah Day, Bothwell Guzha, Suzanne E Scott, Zvavahera M Chirenje, John E Ataguba, Nomonde Mbatani, Nazia Fakie, Jennifer Moodley
Incidence and mortality rates of cervical cancer remain high in Southern Africa (SA). We explored awareness of cervical cancer symptoms and risk factors, as well as risk lay beliefs among women recently diagnosed with cervical cancer from SA and Zimbabwe. Patients were asked to complete a locally validated questionnaire with unprompted, open-ended questions to assess awareness of cervical cancer symptoms and risk factors. Among 501 women (SA 285, Zimbabwe 216), 46% (229) were able to recall one or more symptoms (SA 24%, Zimbabwe 76%) and 19% (93) were able to recall one or more risk factors of cervical cancer (SA 27%, Zimbabwe 73%). In SA, factors associated with increased symptom awareness included higher education level (completion of secondary education compared to not completing secondary education; adjusted odds ratios (aOR) 2.74, 95% confidence interval (CI) 1.17-6.43) as well as living in urban and peri-urban areas compared to living in rural areas (Urban: aOR 2.98, 95% CI 1.35-6.80; Peri-urban: aOR 3.28, 95% CI 1.13-9.35). Having a self-reported history of a chronic condition was associated with lower risk factor awareness compared to not having a self-reported chronic condition (aOR 0.07, 95% CI 0.00-0.42). In Zimbabwe, those who self-reported living with HIV were more likely to know one or more risk factors compared to those without HIV (aOR 2.69, 95% CI 1.31-5.67). Overall, 90 (18%) women mentioned at least one lay belief about risk factors for cervical cancer, with the most reported being inserting herbs, creams or objects into the vagina (9%, n = 43). The low levels of cervical cancer awareness in two Southern African countries highlight the urgent need to improve cervical cancer awareness, as low levels of awareness can impact timely cancer diagnosis and limit the uptake of cervical cancer prevention programs.
在南部非洲,子宫颈癌的发病率和死亡率仍然很高。我们探讨了南非和津巴布韦最近诊断为宫颈癌的妇女对宫颈癌症状和危险因素的认识,以及对风险的认识。患者被要求完成一份当地有效的问卷,其中包含无提示的开放式问题,以评估对宫颈癌症状和危险因素的认识。在501名妇女中(南非285名,津巴布韦216名),46%(229名)能够回忆起一种或多种症状(南非24%,津巴布韦76%),19%(93名)能够回忆起一种或多种宫颈癌危险因素(南非27%,津巴布韦73%)。在SA中,与症状意识增强相关的因素包括高等教育水平(完成中等教育与未完成中等教育相比;调整优势比(aOR) 2.74, 95%可信区间(CI) 1.17-6.43)以及生活在城市和城郊地区与生活在农村地区相比(城市:aOR 2.98, 95% CI 1.35-6.80;城郊:aOR 3.28, 95% CI 1.13-9.35)。与没有自我报告的慢性病史相比,自我报告的慢性病史与较低的危险因素意识相关(aOR 0.07, 95% CI 0.00-0.42)。在津巴布韦,与没有感染艾滋病毒的人相比,自我报告感染艾滋病毒的人更有可能知道一种或多种危险因素(aOR 2.69, 95% CI 1.31-5.67)。总体而言,90名(18%)妇女提到了至少一种关于宫颈癌风险因素的外行信念,其中报告最多的是将草药、面霜或物体插入阴道(9%,n = 43)。两个南部非洲国家对宫颈癌的认识水平较低,这凸显了提高对宫颈癌认识的迫切需要,因为认识水平低可能会影响癌症的及时诊断,并限制宫颈癌预防计划的实施。
{"title":"Cervical cancer awareness among women recently diagnosed with cervical cancer in South Africa and Zimbabwe.","authors":"Sudarshan Govender, Tamsin K Phillips, Fiona M Walter, Sarah Day, Bothwell Guzha, Suzanne E Scott, Zvavahera M Chirenje, John E Ataguba, Nomonde Mbatani, Nazia Fakie, Jennifer Moodley","doi":"10.3332/ecancer.2025.2018","DOIUrl":"10.3332/ecancer.2025.2018","url":null,"abstract":"<p><p>Incidence and mortality rates of cervical cancer remain high in Southern Africa (SA). We explored awareness of cervical cancer symptoms and risk factors, as well as risk lay beliefs among women recently diagnosed with cervical cancer from SA and Zimbabwe. Patients were asked to complete a locally validated questionnaire with unprompted, open-ended questions to assess awareness of cervical cancer symptoms and risk factors. Among 501 women (SA 285, Zimbabwe 216), 46% (229) were able to recall one or more symptoms (SA 24%, Zimbabwe 76%) and 19% (93) were able to recall one or more risk factors of cervical cancer (SA 27%, Zimbabwe 73%). In SA, factors associated with increased symptom awareness included higher education level (completion of secondary education compared to not completing secondary education; adjusted odds ratios (aOR) 2.74, 95% confidence interval (CI) 1.17-6.43) as well as living in urban and peri-urban areas compared to living in rural areas (Urban: aOR 2.98, 95% CI 1.35-6.80; Peri-urban: aOR 3.28, 95% CI 1.13-9.35). Having a self-reported history of a chronic condition was associated with lower risk factor awareness compared to not having a self-reported chronic condition (aOR 0.07, 95% CI 0.00-0.42). In Zimbabwe, those who self-reported living with HIV were more likely to know one or more risk factors compared to those without HIV (aOR 2.69, 95% CI 1.31-5.67). Overall, 90 (18%) women mentioned at least one lay belief about risk factors for cervical cancer, with the most reported being inserting herbs, creams or objects into the vagina (9%, <i>n</i> = 43). The low levels of cervical cancer awareness in two Southern African countries highlight the urgent need to improve cervical cancer awareness, as low levels of awareness can impact timely cancer diagnosis and limit the uptake of cervical cancer prevention programs.</p>","PeriodicalId":11460,"journal":{"name":"ecancermedicalscience","volume":"19 ","pages":"2018"},"PeriodicalIF":1.3,"publicationDate":"2025-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12826786/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146046281","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-17eCollection Date: 2025-01-01DOI: 10.3332/ecancer.2025.2019
Abbas A Abdus-Salam, Chiamaka G Ehiedu, Olabisi T Ojo, Atara I Ntekim, Mutiu A Jimoh, Mariam A Bashir, Daluchukwu J Obi, Abel S Anegbe
Background: Cancers in adolescents and young adults (AYAs; ages 15-39 years) differ from those in children and older adults. AYAs with cancers have received less research focus over the years despite their unique medical, psychological, socioeconomic and sexual concerns. The burden of cancer among this age group in Nigeria is unknown. This study aims to determine the pattern of cancers in AYAs seen in a radiation oncology clinic in Nigeria.
Method: A retrospective study among AYAs (15-39 years) with cancer who presented at a Radiation Oncology Clinic in Nigeria between January 2018 and December 2023.
Results: There were 529 new cancer cases among AYAs, accounting for 14.1% of all cancer cases seen during the period. The male-to-female ratio was 1:3. The majority (72.8%) were in the 30-39 age range, with a mean age of 32.06 ± 6.18 years. Females had a higher mean age (33.01 ± 5.31 years) than males (29.43 ± 7.57 years) (p < 0.001). Breast (39.1%), bone and soft tissue (12.9%) and cervix (11.6%) were the most common sites of cancer in AYAs. Among the males, bone and soft tissue (20.0%), nasopharynx (13.6%) and sinonasal (10.7%) were the most common sites, while breast (52.2%), cervix (15.4%) and bone and soft tissue (10.0%) were the most common sites among females.
Conclusion: AYAs accounted for 14.1% of all new cancer cases. Breast cancer was the most common cancer among female AYAs, while bone and soft tissue cancers were the most common among males.
{"title":"Pattern of cancers among adolescents and young adults seen at a radiation oncology clinic in Nigeria.","authors":"Abbas A Abdus-Salam, Chiamaka G Ehiedu, Olabisi T Ojo, Atara I Ntekim, Mutiu A Jimoh, Mariam A Bashir, Daluchukwu J Obi, Abel S Anegbe","doi":"10.3332/ecancer.2025.2019","DOIUrl":"10.3332/ecancer.2025.2019","url":null,"abstract":"<p><strong>Background: </strong>Cancers in adolescents and young adults (AYAs; ages 15-39 years) differ from those in children and older adults. AYAs with cancers have received less research focus over the years despite their unique medical, psychological, socioeconomic and sexual concerns. The burden of cancer among this age group in Nigeria is unknown. This study aims to determine the pattern of cancers in AYAs seen in a radiation oncology clinic in Nigeria.</p><p><strong>Method: </strong>A retrospective study among AYAs (15-39 years) with cancer who presented at a Radiation Oncology Clinic in Nigeria between January 2018 and December 2023.</p><p><strong>Results: </strong>There were 529 new cancer cases among AYAs, accounting for 14.1% of all cancer cases seen during the period. The male-to-female ratio was 1:3. The majority (72.8%) were in the 30-39 age range, with a mean age of 32.06 ± 6.18 years. Females had a higher mean age (33.01 ± 5.31 years) than males (29.43 ± 7.57 years) (<i>p</i> < 0.001). Breast (39.1%), bone and soft tissue (12.9%) and cervix (11.6%) were the most common sites of cancer in AYAs. Among the males, bone and soft tissue (20.0%), nasopharynx (13.6%) and sinonasal (10.7%) were the most common sites, while breast (52.2%), cervix (15.4%) and bone and soft tissue (10.0%) were the most common sites among females.</p><p><strong>Conclusion: </strong>AYAs accounted for 14.1% of all new cancer cases. Breast cancer was the most common cancer among female AYAs, while bone and soft tissue cancers were the most common among males.</p>","PeriodicalId":11460,"journal":{"name":"ecancermedicalscience","volume":"19 ","pages":"2019"},"PeriodicalIF":1.3,"publicationDate":"2025-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12826780/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146050914","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-16eCollection Date: 2025-01-01DOI: 10.3332/ecancer.2025.2016
Imad Barjij, Meryem Meliani
<p><strong>Background: </strong>Cancer stem cells (CSCs) are increasingly recognised as pivotal drivers of tumour recurrence and treatment resistance across multiple malignancies. Despite extensive preclinical investigations, the mechanisms by which CSCs mediate relapse after therapy remain insufficiently integrated and poorly translated into clinical frameworks.</p><p><strong>Objective: </strong>This systematic review aimed to synthesise current mechanistic evidence linking CSC biology to post-therapeutic recurrence in solid and hematologic tumours, highlighting recurrent molecular pathways, experimental models and translational gaps.</p><p><strong>Methods: </strong>Following Preferred Reporting Items for Systematic Reviews and Meta-Analyses 2020 guidelines, five major databases (PubMed, Scopus, Web of Science, Embase and ResearchRabbit) were searched without time or language restriction. Eligible studies included original experimental articles investigating the mechanistic role of CSCs in tumour recurrence, therapy resistance or metastatic relapse. A total of 23 studies were included after rigorous screening and data extraction. Risk of bias was assessed using predefined methodological criteria. No meta-analysis was conducted due to mechanistic and qualitative heterogeneity.</p><p><strong>Results: </strong>Included studies spanned diverse tumour types, including glioblastoma, breast, pancreatic, hepatocellular, colorectal, lung, thyroid and hematologic cancers. CSC-related recurrence was linked to key mechanistic axes: chromatin remodeling (e.g., suppressor of variegation 3-9 Homolog 1, methyltransferase like 16), transcriptional regulators (e.g., SRY-box transcription factor 2, MYC and Transcription factor activating enhancer-binding protein 4), epithelial-to-mesenchymal transition-associated plasticity, immune evasion (Programmed death-ligand 1, stimulator of interferon genes pathway suppression), metabolic rewiring (P-element induced WImpy Testis-like 2-PDK1, ribosomal biosynthesis) and microenvironmental crosstalk (cancer-associated fibroblasts- and myeloid-derived suppressor cells-mediated niches). Across studies, CSCs demonstrated higher resistance to chemotherapy, prolonged survival under treatment stress and robust capacity for tumour regeneration.</p><p><strong>Limitations: </strong>The majority of studies were preclinical and varied in CSC definitions and recurrence models. Few incorporated longitudinal tracking or patient-level validation. Overall risk of bias was moderate due to lack of blinding, protocol registration or replication.</p><p><strong>Conclusion: </strong>CSC-driven recurrence is a multifaceted and dynamic process shaped by epigenetic, transcriptional, metabolic and immunologic adaptations. Single-target strategies are unlikely to achieve durable eradication. Future research must prioritise multi-targeted approaches, integrate CSC endpoints into clinical trials and develop predictive biomarkers of CSC burden. Addressing
背景:癌症干细胞(CSCs)越来越被认为是多种恶性肿瘤复发和治疗耐药的关键驱动因素。尽管进行了广泛的临床前研究,但CSCs介导治疗后复发的机制仍然没有充分整合,并且很难转化为临床框架。目的:本系统综述旨在综合目前将CSC生物学与实体和血液肿瘤治疗后复发联系起来的机制证据,强调复发分子途径、实验模型和翻译空白。方法:根据系统评价和元分析2020指南的首选报告项目,在没有时间和语言限制的情况下检索五大数据库(PubMed, Scopus, Web of Science, Embase和ResearchRabbit)。符合条件的研究包括研究CSCs在肿瘤复发、治疗抵抗或转移性复发中的机制作用的原始实验文章。经过严格筛选和数据提取,共纳入23项研究。使用预先确定的方法学标准评估偏倚风险。由于机制和质量异质性,未进行meta分析。结果:纳入的研究涵盖了不同的肿瘤类型,包括胶质母细胞瘤、乳腺癌、胰腺癌、肝细胞癌、结肠直肠癌、肺癌、甲状腺癌和血液癌。csc相关复发与关键的机械轴有关:染色质重塑(例如,变异抑制因子3-9同源物1,甲基转移酶样16),转录调节因子(例如,SRY-box转录因子2,MYC和转录因子激活增强子结合蛋白4),上皮到间质转化相关的可塑性,免疫逃避(程序性死亡配体1,干扰素基因通路抑制刺激物),代谢重新连接(P-element诱导的WImpy睾丸样2- pdk1,核糖体生物合成)和微环境串扰(癌症相关成纤维细胞和髓源性抑制细胞介导的生态位)。在所有研究中,CSCs表现出更高的化疗耐药性,在治疗压力下延长生存期和强大的肿瘤再生能力。局限性:大多数研究是临床前的,CSC的定义和复发模型各不相同。很少纳入纵向跟踪或患者层面的验证。由于缺乏盲法、方案注册或复制,总体偏倚风险为中等。结论:csc驱动的复发是一个多方面的动态过程,受表观遗传、转录、代谢和免疫适应的影响。单一目标战略不太可能实现持久的根除。未来的研究必须优先考虑多靶点方法,将CSC终点整合到临床试验中,并开发CSC负担的预测性生物标志物。解决csc介导的复发对于推进精准肿瘤学和实现持久的治疗反应至关重要。
{"title":"Cancer stem cells and post-therapy tumour recurrence: a systematic review of mechanistic pathways and translational gaps.","authors":"Imad Barjij, Meryem Meliani","doi":"10.3332/ecancer.2025.2016","DOIUrl":"10.3332/ecancer.2025.2016","url":null,"abstract":"<p><strong>Background: </strong>Cancer stem cells (CSCs) are increasingly recognised as pivotal drivers of tumour recurrence and treatment resistance across multiple malignancies. Despite extensive preclinical investigations, the mechanisms by which CSCs mediate relapse after therapy remain insufficiently integrated and poorly translated into clinical frameworks.</p><p><strong>Objective: </strong>This systematic review aimed to synthesise current mechanistic evidence linking CSC biology to post-therapeutic recurrence in solid and hematologic tumours, highlighting recurrent molecular pathways, experimental models and translational gaps.</p><p><strong>Methods: </strong>Following Preferred Reporting Items for Systematic Reviews and Meta-Analyses 2020 guidelines, five major databases (PubMed, Scopus, Web of Science, Embase and ResearchRabbit) were searched without time or language restriction. Eligible studies included original experimental articles investigating the mechanistic role of CSCs in tumour recurrence, therapy resistance or metastatic relapse. A total of 23 studies were included after rigorous screening and data extraction. Risk of bias was assessed using predefined methodological criteria. No meta-analysis was conducted due to mechanistic and qualitative heterogeneity.</p><p><strong>Results: </strong>Included studies spanned diverse tumour types, including glioblastoma, breast, pancreatic, hepatocellular, colorectal, lung, thyroid and hematologic cancers. CSC-related recurrence was linked to key mechanistic axes: chromatin remodeling (e.g., suppressor of variegation 3-9 Homolog 1, methyltransferase like 16), transcriptional regulators (e.g., SRY-box transcription factor 2, MYC and Transcription factor activating enhancer-binding protein 4), epithelial-to-mesenchymal transition-associated plasticity, immune evasion (Programmed death-ligand 1, stimulator of interferon genes pathway suppression), metabolic rewiring (P-element induced WImpy Testis-like 2-PDK1, ribosomal biosynthesis) and microenvironmental crosstalk (cancer-associated fibroblasts- and myeloid-derived suppressor cells-mediated niches). Across studies, CSCs demonstrated higher resistance to chemotherapy, prolonged survival under treatment stress and robust capacity for tumour regeneration.</p><p><strong>Limitations: </strong>The majority of studies were preclinical and varied in CSC definitions and recurrence models. Few incorporated longitudinal tracking or patient-level validation. Overall risk of bias was moderate due to lack of blinding, protocol registration or replication.</p><p><strong>Conclusion: </strong>CSC-driven recurrence is a multifaceted and dynamic process shaped by epigenetic, transcriptional, metabolic and immunologic adaptations. Single-target strategies are unlikely to achieve durable eradication. Future research must prioritise multi-targeted approaches, integrate CSC endpoints into clinical trials and develop predictive biomarkers of CSC burden. Addressing","PeriodicalId":11460,"journal":{"name":"ecancermedicalscience","volume":"19 ","pages":"2016"},"PeriodicalIF":1.3,"publicationDate":"2025-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12812827/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146009271","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-14eCollection Date: 2025-01-01DOI: 10.3332/ecancer.2025.2013
Iqbal Alamri, Zahid Almandhari, M Saiful Huq
Purpose: Modern radiotherapy is a complex, technology-driven process that requires precise planning and delivery to maximise tumour control and minimise harm to normal tissues. Errors in radiotherapy can result in underdosing tumours or overdosing healthy tissues, posing serious risks to patients. In the Eastern Mediterranean Region and Turkey (EMRO+T), variations in workforce expertise, institutional policies and regulatory frameworks contribute to inconsistencies in incident reporting and safety practices. While some centers adhere to international guidelines, others lack structured mechanisms for reporting and learning from errors. A regional incident learning system (ILS) could standardise reporting, enhance safety culture and improve patient outcomes.
Methods: A cross-sectional survey assessed the state of radiotherapy ILS in EMRO+T. Ethical approval was obtained (CCCRC-94-2023), and the survey was distributed via Research Electronic Data Capture to 671 radiation oncology professionals. It gathered data on institutional classification, patient volume, technologies, local ILS presence, adherence to guidelines and perceptions of a regional ILS. Responses from 135 participants across healthcare settings were analysed.
Results: Most respondents (66%) were from government hospitals, and 29.5% worked in private institutions. About 25% of centers treated over 2,000 patients annually, and advanced techniques such as intensity-modulated radiotherapy (75.2%) and stereotactic body radiotherapy (52%) were widely used. However, only 70.7% adhered to international reporting guidelines, and just 48.4% had a local ILS. Barriers included a lack of leadership support (51%) and confidentiality concerns. Although 62% supported reporting by all staff, opinions on confidentiality varied. Regular incident review occurred in 64% of institutions and 91.7% strongly supported a regional ILS.
Conclusion: A regional ILS would foster knowledge-sharing, encourage a non-punitive culture and enhance transparency, accountability and continuous quality improvement in patient safety.
目的:现代放射治疗是一个复杂的、技术驱动的过程,需要精确的计划和交付,以最大限度地控制肿瘤,最大限度地减少对正常组织的伤害。放射治疗中的错误可能导致肿瘤剂量不足或健康组织剂量过大,对患者构成严重风险。在东地中海区域和土耳其(EMRO+T),劳动力专业知识、体制政策和监管框架的差异导致事故报告和安全实践不一致。虽然一些中心遵守国际准则,但其他中心缺乏结构化的报告和从错误中吸取教训的机制。区域事故学习系统(ILS)可以使报告标准化,加强安全文化并改善患者的预后。方法:通过横断面调查评估EMRO+T放疗后ILS的状态。获得伦理批准(CCCRC-94-2023),并通过Research Electronic Data Capture将调查分发给671名放射肿瘤学专业人员。它收集了关于机构分类、患者数量、技术、当地ILS存在、遵守指南和对区域ILS的看法的数据。分析了来自135名医疗机构参与者的回答。结果:受访者中公立医院工作人员占66%,民办医院工作人员占29.5%。约25%的中心每年治疗超过2,000名患者,并广泛使用调强放疗(75.2%)和立体定向放疗(52%)等先进技术。然而,只有70.7%的人遵守了国际报告准则,只有48.4%的人拥有当地的ILS。障碍包括缺乏领导支持(51%)和保密问题。尽管62%的人支持全体员工报告,但对保密问题的看法各不相同。64%的机构进行了定期事件审查,91.7%的机构强烈支持区域性ILS。结论:区域性ILS将促进知识共享,鼓励非惩罚性文化,提高透明度,问责制和患者安全的持续质量改进。
{"title":"Call to action: the need for an incident learning system in Eastern Mediterranean Region and Turkey (EMRO+T).","authors":"Iqbal Alamri, Zahid Almandhari, M Saiful Huq","doi":"10.3332/ecancer.2025.2013","DOIUrl":"10.3332/ecancer.2025.2013","url":null,"abstract":"<p><strong>Purpose: </strong>Modern radiotherapy is a complex, technology-driven process that requires precise planning and delivery to maximise tumour control and minimise harm to normal tissues. Errors in radiotherapy can result in underdosing tumours or overdosing healthy tissues, posing serious risks to patients. In the Eastern Mediterranean Region and Turkey (EMRO+T), variations in workforce expertise, institutional policies and regulatory frameworks contribute to inconsistencies in incident reporting and safety practices. While some centers adhere to international guidelines, others lack structured mechanisms for reporting and learning from errors. A regional incident learning system (ILS) could standardise reporting, enhance safety culture and improve patient outcomes.</p><p><strong>Methods: </strong>A cross-sectional survey assessed the state of radiotherapy ILS in EMRO+T. Ethical approval was obtained (CCCRC-94-2023), and the survey was distributed via Research Electronic Data Capture to 671 radiation oncology professionals. It gathered data on institutional classification, patient volume, technologies, local ILS presence, adherence to guidelines and perceptions of a regional ILS. Responses from 135 participants across healthcare settings were analysed.</p><p><strong>Results: </strong>Most respondents (66%) were from government hospitals, and 29.5% worked in private institutions. About 25% of centers treated over 2,000 patients annually, and advanced techniques such as intensity-modulated radiotherapy (75.2%) and stereotactic body radiotherapy (52%) were widely used. However, only 70.7% adhered to international reporting guidelines, and just 48.4% had a local ILS. Barriers included a lack of leadership support (51%) and confidentiality concerns. Although 62% supported reporting by all staff, opinions on confidentiality varied. Regular incident review occurred in 64% of institutions and 91.7% strongly supported a regional ILS.</p><p><strong>Conclusion: </strong>A regional ILS would foster knowledge-sharing, encourage a non-punitive culture and enhance transparency, accountability and continuous quality improvement in patient safety.</p>","PeriodicalId":11460,"journal":{"name":"ecancermedicalscience","volume":"19 ","pages":"2013"},"PeriodicalIF":1.3,"publicationDate":"2025-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12812822/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146009231","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-14eCollection Date: 2025-01-01DOI: 10.3332/ecancer.2025.2015
Israel Gabriel, Andy Emmanuel, P Pratitha, Divitha Subramanian, Thilaka Chandanee, Fariba Hosseinisazi
Background: ehealth improves the health-related quality of life for cancer patients and their families by providing easier access to medical information, promoting self-management, and providing personalised care through digital platforms. However, there is still a dearth of comprehensive understanding of their influences in developing countries.
Objectives: To identify several ehealth interventions accessible to family caregivers of people with cancer in developing countries and to assess the impact of these interventions on their health-related quality of life.
Methods: The review will adhere to the Preferred Reporting Items for Systematic Reviews and Meta-Analysis Protocols. Health databases and search engines, including PubMed, Medline via Ovid, Embase via Ovid, and CINAHL via EBSCOhost, will be used. We will include quantitative or mixed method research evaluating e-health, with a particular emphasis on the health-related quality of life of family caregivers of cancer patients. Studies from developing countries, including peer-reviewed journals and grey literature, will be considered without regard to publication date.The study selection process involves screening titles and abstracts for relevance, then, doing a full-text assessment against the inclusion criteria. The Cochrane Risk of Bias tool for randomised controlled trials and ROBINS-I V2 for non-randomised studies will be employed to assess the quality of the included studies. The A Measurement Tool to Assess Systematic Reviews will assess the quality of this systematic review.
Implications: This review offers a thorough and impartial summary of current research on e-health tools and their impact on the health-related quality of life of family caregivers of cancer patients. It seeks to inform evidence-based decision-making across healthcare, policy development, and research design by identifying knowledge gaps, emphasising areas requiring further investigation, and steering future research.
{"title":"eHealth tools to improve the health-related quality of life of family caregivers of cancer patients in developing countries: a systematic review protocol.","authors":"Israel Gabriel, Andy Emmanuel, P Pratitha, Divitha Subramanian, Thilaka Chandanee, Fariba Hosseinisazi","doi":"10.3332/ecancer.2025.2015","DOIUrl":"10.3332/ecancer.2025.2015","url":null,"abstract":"<p><strong>Background: </strong>ehealth improves the health-related quality of life for cancer patients and their families by providing easier access to medical information, promoting self-management, and providing personalised care through digital platforms. However, there is still a dearth of comprehensive understanding of their influences in developing countries.</p><p><strong>Objectives: </strong>To identify several ehealth interventions accessible to family caregivers of people with cancer in developing countries and to assess the impact of these interventions on their health-related quality of life.</p><p><strong>Methods: </strong>The review will adhere to the Preferred Reporting Items for Systematic Reviews and Meta-Analysis Protocols. Health databases and search engines, including PubMed, Medline via Ovid, Embase via Ovid, and CINAHL via EBSCOhost, will be used. We will include quantitative or mixed method research evaluating e-health, with a particular emphasis on the health-related quality of life of family caregivers of cancer patients. Studies from developing countries, including peer-reviewed journals and grey literature, will be considered without regard to publication date.The study selection process involves screening titles and abstracts for relevance, then, doing a full-text assessment against the inclusion criteria. The Cochrane Risk of Bias tool for randomised controlled trials and ROBINS-I V2 for non-randomised studies will be employed to assess the quality of the included studies. The A Measurement Tool to Assess Systematic Reviews will assess the quality of this systematic review.</p><p><strong>Implications: </strong>This review offers a thorough and impartial summary of current research on e-health tools and their impact on the health-related quality of life of family caregivers of cancer patients. It seeks to inform evidence-based decision-making across healthcare, policy development, and research design by identifying knowledge gaps, emphasising areas requiring further investigation, and steering future research.</p><p><strong>Systematic review registration: </strong>PROSPERO CRD42024622302 https://www.crd.york.ac.uk/PROSPERO/view/CRD42024622302.</p>","PeriodicalId":11460,"journal":{"name":"ecancermedicalscience","volume":"19 ","pages":"2015"},"PeriodicalIF":1.3,"publicationDate":"2025-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12812838/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146009323","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-09eCollection Date: 2025-01-01DOI: 10.3332/ecancer.2025.2012
Anupama Kurup, Deepak Charles
We report a case of pyrexia of unknown origin presenting with lactic acidosis and hypoglycaemia. He further developed Guillain-Barre syndrome (GBS) and Hemophagocytic lymphohistiocytosis (HLH). The bone marrow biopsy ultimately reported Diffuse large B cell lymphoma (DLBCL). A 74-year-old gentleman visited the hospital in January 2024 with a fever since 2 weeks. He further developed hypoglycemic episodes and lower limb followed by upper limb weakness. On physical examination, he was febrile, tachypnoec with hepatomegaly and bilateral lower limb weakness with grade 3 power proximally and extensor plantar reflexes. Peripheral smear showed a leucoerythroblastic picture and 3% atypical lymphoid cells. Procalcitonin, lactate dehydrogenase and Ferritin were markedly elevated, suggestive of HLH. The bone marrow biopsy ultimately revealed DLBCL. He was diagnosed with GBS, Warburg phenomenon and HLH secondary to DLBCL. Intravenous steroids were started for secondary HLH and after he became hemodynamically stable was initiated on chemotherapy with Rituximab, Cyclophosphamide, Doxorubicin, Vincristine, Prednisolone (R-CHOP) regimen. After four cycles of R mini-CHOP, positron emission tomography-computed tomography showed a good response. Further two cycles of R mini-CHOP was given with methotrexate for central nervous system prophylaxis. This case portrays an atypical presentation of DLBCL with Warburg syndrome, GBS and HLH. Despite the adverse clinical course, the patient responded favourably to chemotherapy.
{"title":"A rare case of diffuse large B-cell lymphoma masquerading as Guillain Barre syndrome, Warburg phenomenon and hemophagocytic lymphohistiocytosis.","authors":"Anupama Kurup, Deepak Charles","doi":"10.3332/ecancer.2025.2012","DOIUrl":"10.3332/ecancer.2025.2012","url":null,"abstract":"<p><p>We report a case of pyrexia of unknown origin presenting with lactic acidosis and hypoglycaemia. He further developed Guillain-Barre syndrome (GBS) and Hemophagocytic lymphohistiocytosis (HLH). The bone marrow biopsy ultimately reported Diffuse large B cell lymphoma (DLBCL). A 74-year-old gentleman visited the hospital in January 2024 with a fever since 2 weeks. He further developed hypoglycemic episodes and lower limb followed by upper limb weakness. On physical examination, he was febrile, tachypnoec with hepatomegaly and bilateral lower limb weakness with grade 3 power proximally and extensor plantar reflexes. Peripheral smear showed a leucoerythroblastic picture and 3% atypical lymphoid cells. Procalcitonin, lactate dehydrogenase and Ferritin were markedly elevated, suggestive of HLH. The bone marrow biopsy ultimately revealed DLBCL. He was diagnosed with GBS, Warburg phenomenon and HLH secondary to DLBCL. Intravenous steroids were started for secondary HLH and after he became hemodynamically stable was initiated on chemotherapy with Rituximab, Cyclophosphamide, Doxorubicin, Vincristine, Prednisolone (R-CHOP) regimen. After four cycles of R mini-CHOP, positron emission tomography-computed tomography showed a good response. Further two cycles of R mini-CHOP was given with methotrexate for central nervous system prophylaxis. This case portrays an atypical presentation of DLBCL with Warburg syndrome, GBS and HLH. Despite the adverse clinical course, the patient responded favourably to chemotherapy.</p>","PeriodicalId":11460,"journal":{"name":"ecancermedicalscience","volume":"19 ","pages":"2012"},"PeriodicalIF":1.3,"publicationDate":"2025-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12812808/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146009209","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-09eCollection Date: 2025-01-01DOI: 10.3332/ecancer.2025.2010
Cassio Murilo Hidalgo Filho, Mateus Marinho Nogueira Soares, Wesley Antonio Lopes de Lima, Laura Testa, Marcela Simonis Martins Ferrari, Renata Colombo Bonadio
Background: Adenoid cystic carcinoma of the breast (ACCB) is a rare histological subtype of breast cancer characterised by unique clinical features and management challenges. ACCB remains poorly understood, with limited data on its epidemiology, treatment outcomes and prognostic factors. This study aimed to elucidate the landscape of ACCB in a real-world context.
Methods: A retrospective cohort study was conducted on patients diagnosed with ACCB in a Brazilian cancer center between January 2007 and October 2021. Clinical and pathological data were systematically collected from electronic medical records. Statistical analyses were performed to identify factors associated with prognosis and assess the impact of treatment interventions.
Results: Twenty-one female patients with confirmed ACCB were included in the study. The median age at diagnosis was 55.2 years. Most patients had basaloid (38.1%) or classic (19.0%) histological subtypes. Adjuvant radiotherapy was associated with a trend towards better recurrence-free survival among patients with localised disease HR 0.21, CI 95% 0.04-1.06, p = 0.059). In the metastatic setting, systemic chemotherapy used for breast cancer demonstrated limited efficacy, with a median progression-free survival of 1.8 to 2.8 months. Despite the overall poor prognosis, two patients with low-volume metastatic disease had long-term survival following local therapy.
Conclusion: Given the rarity of ACCB and the absence of a standard management approach, this small study suggests a potential benefit of local therapies in adjuvant and metastatic settings while indicating the limited efficacy of systemic chemotherapy. Personalised treatment strategies tailored to ACCB are essential to optimising patient outcomes.
背景:乳腺腺样囊性癌(ACCB)是一种罕见的乳腺癌组织学亚型,具有独特的临床特征和治疗挑战。ACCB仍然知之甚少,关于其流行病学、治疗结果和预后因素的数据有限。本研究旨在阐明在现实世界背景下的ACCB景观。方法:对2007年1月至2021年10月在巴西癌症中心诊断为ACCB的患者进行回顾性队列研究。系统地从电子病历中收集临床和病理资料。进行统计分析以确定与预后相关的因素并评估治疗干预措施的影响。结果:21例确诊的女性ACCB患者纳入研究。诊断时的中位年龄为55.2岁。大多数患者为基底细胞样(38.1%)或经典(19.0%)组织学亚型。辅助放疗与局部疾病患者更好的无复发生存相关(HR 0.21, CI 95% 0.04-1.06, p = 0.059)。在转移性情况下,用于乳腺癌的全身化疗显示出有限的疗效,中位无进展生存期为1.8至2.8个月。尽管总体预后较差,但两例小体积转移性疾病患者在局部治疗后长期生存。结论:考虑到ACCB的罕见性和缺乏标准的治疗方法,这项小型研究表明局部治疗在辅助和转移性情况下有潜在的益处,同时表明全身化疗的疗效有限。针对ACCB量身定制的个性化治疗策略对于优化患者结果至关重要。
{"title":"Real-world insights on a rare disease: adenoid cystic carcinoma of the breast.","authors":"Cassio Murilo Hidalgo Filho, Mateus Marinho Nogueira Soares, Wesley Antonio Lopes de Lima, Laura Testa, Marcela Simonis Martins Ferrari, Renata Colombo Bonadio","doi":"10.3332/ecancer.2025.2010","DOIUrl":"10.3332/ecancer.2025.2010","url":null,"abstract":"<p><strong>Background: </strong>Adenoid cystic carcinoma of the breast (ACCB) is a rare histological subtype of breast cancer characterised by unique clinical features and management challenges. ACCB remains poorly understood, with limited data on its epidemiology, treatment outcomes and prognostic factors. This study aimed to elucidate the landscape of ACCB in a real-world context.</p><p><strong>Methods: </strong>A retrospective cohort study was conducted on patients diagnosed with ACCB in a Brazilian cancer center between January 2007 and October 2021. Clinical and pathological data were systematically collected from electronic medical records. Statistical analyses were performed to identify factors associated with prognosis and assess the impact of treatment interventions.</p><p><strong>Results: </strong>Twenty-one female patients with confirmed ACCB were included in the study. The median age at diagnosis was 55.2 years. Most patients had basaloid (38.1%) or classic (19.0%) histological subtypes. Adjuvant radiotherapy was associated with a trend towards better recurrence-free survival among patients with localised disease HR 0.21, CI 95% 0.04-1.06, <i>p</i> = 0.059). In the metastatic setting, systemic chemotherapy used for breast cancer demonstrated limited efficacy, with a median progression-free survival of 1.8 to 2.8 months. Despite the overall poor prognosis, two patients with low-volume metastatic disease had long-term survival following local therapy.</p><p><strong>Conclusion: </strong>Given the rarity of ACCB and the absence of a standard management approach, this small study suggests a potential benefit of local therapies in adjuvant and metastatic settings while indicating the limited efficacy of systemic chemotherapy. Personalised treatment strategies tailored to ACCB are essential to optimising patient outcomes.</p>","PeriodicalId":11460,"journal":{"name":"ecancermedicalscience","volume":"19 ","pages":"2010"},"PeriodicalIF":1.3,"publicationDate":"2025-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12812819/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146009039","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-09eCollection Date: 2025-01-01DOI: 10.3332/ecancer.2025.2011
Eduardo Paulino, Guilherme Gomes de Mesquita, Andreia Cristina de Melo
Endometrial cancer (EC) treatment changed substantially with the introduction of molecular classification. There is a paucity of data regarding the added value of L1CAM in patients with p53 aberrant tumours. The present study aimed to analyse the prognostic value of L1CAM associated with p53 aberrant EC. Patients with EC treated between 2010 and 2016 were retrospectively evaluated. Patients included in this analysis must have reviewed high-grade histologies (endometrioid grade 3, serous, clear cell, carcinosarcoma, mixed and undiffrentiated). Samples were subjected to immunohistochemistry for L1CAM and p53. Recurrence-free survival (RFS) and overall survival (OS) were analysed by the Kaplan-Meier method and log-rank test. Cox proportional hazards regression was performed for multivariable analysis. From 2010 to 2016, 464 patients met the inclusion criteria. Patients with p53 wild type and L1CAM negative (p53wt/L1CAMneg) corresponded to 13.6% (59 patients) of the population, p53 wild type and L1CAM positive (p53wt/L1CAMpos) to 11.7 % (51 patients), aberrant p53 and L1CAM negative (p53ab/L1CAMneg) to 32.9% (143 patients) and aberrant p53 with L1CAM positive (p53ab/L1CAMpos) to 41.8% (182 patients). In univariate and multivariate analysis, compared to patients with p53wt/L1CAMneg, the presence of p53wt/L1CAMpos, p53ab/L1CAMneg and p53ab/L1CAMpos was statistically associated with a worse RFS (HR 2.02; HR 2.20 and HR 2.99, respectively) and OS (HR 2.39; RH 2.31 and RH 2.94, respectively). In the present analysis of a high histological risk population, stages I-IV, we observed that the presence of p53ab/L1CAMpos was associated with a worse RFS and OS when comparing p53wt/L1CAMneg patients. Patients with L1CAMpos had the same worse prognosis as p53ab tumours.
{"title":"The prognostic value of L1CAM in association with p53 in high-grade endometrial cancer.","authors":"Eduardo Paulino, Guilherme Gomes de Mesquita, Andreia Cristina de Melo","doi":"10.3332/ecancer.2025.2011","DOIUrl":"10.3332/ecancer.2025.2011","url":null,"abstract":"<p><p>Endometrial cancer (EC) treatment changed substantially with the introduction of molecular classification. There is a paucity of data regarding the added value of L1CAM in patients with p53 aberrant tumours. The present study aimed to analyse the prognostic value of L1CAM associated with p53 aberrant EC. Patients with EC treated between 2010 and 2016 were retrospectively evaluated. Patients included in this analysis must have reviewed high-grade histologies (endometrioid grade 3, serous, clear cell, carcinosarcoma, mixed and undiffrentiated). Samples were subjected to immunohistochemistry for L1CAM and p53. Recurrence-free survival (RFS) and overall survival (OS) were analysed by the Kaplan-Meier method and log-rank test. Cox proportional hazards regression was performed for multivariable analysis. From 2010 to 2016, 464 patients met the inclusion criteria. Patients with p53 wild type and L1CAM negative (p53wt/L1CAMneg) corresponded to 13.6% (59 patients) of the population, p53 wild type and L1CAM positive (p53wt/L1CAMpos) to 11.7 % (51 patients), aberrant p53 and L1CAM negative (p53ab/L1CAMneg) to 32.9% (143 patients) and aberrant p53 with L1CAM positive (p53ab/L1CAMpos) to 41.8% (182 patients). In univariate and multivariate analysis, compared to patients with p53wt/L1CAMneg, the presence of p53wt/L1CAMpos, p53ab/L1CAMneg and p53ab/L1CAMpos was statistically associated with a worse RFS (HR 2.02; HR 2.20 and HR 2.99, respectively) and OS (HR 2.39; RH 2.31 and RH 2.94, respectively). In the present analysis of a high histological risk population, stages I-IV, we observed that the presence of p53ab/L1CAMpos was associated with a worse RFS and OS when comparing p53wt/L1CAMneg patients. Patients with L1CAMpos had the same worse prognosis as p53ab tumours.</p>","PeriodicalId":11460,"journal":{"name":"ecancermedicalscience","volume":"19 ","pages":"2011"},"PeriodicalIF":1.3,"publicationDate":"2025-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12812821/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146009095","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-07eCollection Date: 2025-01-01DOI: 10.3332/ecancer.2025.2008
Adeniyi K Akiseku, Taiwo O Adenuga, Olusoji E Jagun, Mutiu A Popoola, Adetola O Olatunji
Background: Cervical cancer remains a significant public health issue, particularly in low-income countries. It is the fourth most common cancer among women globally, with an estimated 570,000 new cases and 311,000 deaths in 2018.
Objective: This study aimed to examine the stages of cervical cancer at diagnosis and identify factors contributing to late-stage presentation among women in a tertiary care hospital in Nigeria.
Methods: A retrospective study analysed data from women diagnosed with cervical cancer between 2017 and 2021. Demographic, reproductive and clinical data were extracted from medical records.
Results: Of the 102 women who presented during the study period, only 57 (55.9%) had complete staging, clinical and demographic data; these complete cases were included to ensure data integrity. From this population, 73.7% were aged 50 years or older and 56.1% presented with late-stage disease. Additionally, anaemia (packed cell volume <30%) was present in 75.4% of women. Postcoital bleeding was reported in 35.1% of cases. Women with no formal education had higher odds of late-stage diagnosis odds ratios (OR: 4.40, 95% CI: 1.08-17.82). Postmenopausal women also had higher odds of late-stage diagnosis (OR: 4.46, 95% CI: 1.27-15.70).
Conclusion: A late-stage cervical cancer diagnosis is prevalent among women in Nigeria, particularly among those with lower educational levels and postmenopausal women. Targeted awareness programmes, expanded screening (including integration into well-woman/postmenopausal care) and improved healthcare infrastructure, including consistent documentation of screening history and human papillomavirus vaccination, are essential for reducing the burden of cervical cancer in this context.
{"title":"Individual-level determinants of late-stage cervical cancer diagnosis and their implications for prevention and control.","authors":"Adeniyi K Akiseku, Taiwo O Adenuga, Olusoji E Jagun, Mutiu A Popoola, Adetola O Olatunji","doi":"10.3332/ecancer.2025.2008","DOIUrl":"10.3332/ecancer.2025.2008","url":null,"abstract":"<p><strong>Background: </strong>Cervical cancer remains a significant public health issue, particularly in low-income countries. It is the fourth most common cancer among women globally, with an estimated 570,000 new cases and 311,000 deaths in 2018.</p><p><strong>Objective: </strong>This study aimed to examine the stages of cervical cancer at diagnosis and identify factors contributing to late-stage presentation among women in a tertiary care hospital in Nigeria.</p><p><strong>Methods: </strong>A retrospective study analysed data from women diagnosed with cervical cancer between 2017 and 2021. Demographic, reproductive and clinical data were extracted from medical records.</p><p><strong>Results: </strong>Of the 102 women who presented during the study period, only 57 (55.9%) had complete staging, clinical and demographic data; these complete cases were included to ensure data integrity. From this population, 73.7% were aged 50 years or older and 56.1% presented with late-stage disease. Additionally, anaemia (packed cell volume <30%) was present in 75.4% of women. Postcoital bleeding was reported in 35.1% of cases. Women with no formal education had higher odds of late-stage diagnosis odds ratios (OR: 4.40, 95% CI: 1.08-17.82). Postmenopausal women also had higher odds of late-stage diagnosis (OR: 4.46, 95% CI: 1.27-15.70).</p><p><strong>Conclusion: </strong>A late-stage cervical cancer diagnosis is prevalent among women in Nigeria, particularly among those with lower educational levels and postmenopausal women. Targeted awareness programmes, expanded screening (including integration into well-woman/postmenopausal care) and improved healthcare infrastructure, including consistent documentation of screening history and human papillomavirus vaccination, are essential for reducing the burden of cervical cancer in this context.</p>","PeriodicalId":11460,"journal":{"name":"ecancermedicalscience","volume":"19 ","pages":"2008"},"PeriodicalIF":1.3,"publicationDate":"2025-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12812806/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146009362","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}