Introduction: There are multiple dose fractionation schedules for palliative radiotherapy (RT) of patients belonging to incurable locally advanced head and neck squamous cell carcinoma (LAHNSCC), but none is accepted as standard of care. In this study, we have compared three palliative RT schedules: Quad shot versus Christie versus conventional.
Aim and objectives: To assess and compare the toxicity, tolerance and effectiveness of three palliative RT regimens for incurable LAHNSCC.
Methods: A total 105 patients were randomised equally 1:1:1 in 3 arms with 35 patients each. Arm A: 14.8 Gy in 4 fractions with 3.7 Gy per fraction in 2 fractions per day 6 hours apart for 2 consecutive days for 3 sessions at 3 weekly interval. Total dose was 44.4 Gy in 12 fractions over 6.2 weeks. Arm B: 50 Gy in 16 fractions over 3.1 weeks with 3.125 Gy per fraction with 5 fractions per week.ARM C: 20 Gy in 5 fractions with 4 Gy per fraction with 5 fractions per week in 2 sessions at 3 weekly interval. Total dose was 40 Gy in 10 fractions over 3.5 weeks. All the patients were assessed pre RT, post RT and at 1 month follow up.
Results: All three arms had similar baseline characteristics 80% patients in arm A, 80% in arm B and 72% in arm C completed intended treatment. Drop out rate was 20%, 20% and 28%, respectively. Defaulters were excluded from the study. Mean ± standard deviation scores of individual domains of quality of life (QOL) (pre and post RT) have been calculated. Tumour response was partial in 92.8% patients of Arm A, 92.8% of Arm B, 96% of Arm C. Complete nodal response was seen in 71.4% patients of Arm A, 85.7% of Arm B, 60% of Arm C with Grade 3 mucositis observed in only 1 patient of Arm A and 4 patients of Arm B. Median overall survival was highest in Arm B, i.e., 6 months.
Conclusion: Statistically significant objective response and improvement in all QOL parameters, along with performance status, was observed in all the 3 arms. However, Christie arm patients had more symptomatic relief with better loco-regional control and prolonged overall survival as compared to other arms with acceptable toxicities. Therefore, as per this study, Christie schedule may be considered for adequate palliation of incurable LAHNSCC patients.
{"title":"A prospective randomised comparative study of three palliative radiotherapy schedules in incurable locally advanced head and neck cancer.","authors":"Shivani Malik, Ashok Kumar Arya, Renu Singh, Lalit Raj, Aditya Uttam","doi":"10.3332/ecancer.2025.2021","DOIUrl":"10.3332/ecancer.2025.2021","url":null,"abstract":"<p><strong>Introduction: </strong>There are multiple dose fractionation schedules for palliative radiotherapy (RT) of patients belonging to incurable locally advanced head and neck squamous cell carcinoma (LAHNSCC), but none is accepted as standard of care. In this study, we have compared three palliative RT schedules: Quad shot versus Christie versus conventional.</p><p><strong>Aim and objectives: </strong>To assess and compare the toxicity, tolerance and effectiveness of three palliative RT regimens for incurable LAHNSCC.</p><p><strong>Methods: </strong>A total 105 patients were randomised equally 1:1:1 in 3 arms with 35 patients each. Arm A: 14.8 Gy in 4 fractions with 3.7 Gy per fraction in 2 fractions per day 6 hours apart for 2 consecutive days for 3 sessions at 3 weekly interval. Total dose was 44.4 Gy in 12 fractions over 6.2 weeks. Arm B: 50 Gy in 16 fractions over 3.1 weeks with 3.125 Gy per fraction with 5 fractions per week.ARM C: 20 Gy in 5 fractions with 4 Gy per fraction with 5 fractions per week in 2 sessions at 3 weekly interval. Total dose was 40 Gy in 10 fractions over 3.5 weeks. All the patients were assessed pre RT, post RT and at 1 month follow up.</p><p><strong>Results: </strong>All three arms had similar baseline characteristics 80% patients in arm A, 80% in arm B and 72% in arm C completed intended treatment. Drop out rate was 20%, 20% and 28%, respectively. Defaulters were excluded from the study. Mean ± standard deviation scores of individual domains of quality of life (QOL) (pre and post RT) have been calculated. Tumour response was partial in 92.8% patients of Arm A, 92.8% of Arm B, 96% of Arm C. Complete nodal response was seen in 71.4% patients of Arm A, 85.7% of Arm B, 60% of Arm C with Grade 3 mucositis observed in only 1 patient of Arm A and 4 patients of Arm B. Median overall survival was highest in Arm B, i.e., 6 months.</p><p><strong>Conclusion: </strong>Statistically significant objective response and improvement in all QOL parameters, along with performance status, was observed in all the 3 arms. However, Christie arm patients had more symptomatic relief with better loco-regional control and prolonged overall survival as compared to other arms with acceptable toxicities. Therefore, as per this study, Christie schedule may be considered for adequate palliation of incurable LAHNSCC patients.</p>","PeriodicalId":11460,"journal":{"name":"ecancermedicalscience","volume":"19 ","pages":"2021"},"PeriodicalIF":1.3,"publicationDate":"2025-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12826779/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146050953","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}
Transitional cell carcinoma of the prostatic urethra was first described and reported in 1963. Primary urothelial carcinoma of the prostate is an extremely rare disease, often misdiagnosed with other entities, particularly with urothelial carcinoma of the bladder involving the prostatic tissue. There are only dozens of cases of primary urothelial carcinoma in the prostate reported in the literature. The prognosis after diagnosis is reported to be poor and there is no consensus among experts concerning its proper treatment and follow-up. Herein, we report two cases of patients diagnosed with this entity with a median follow-up of 14 months.
{"title":"Primary urothelial carcinoma of the prostate: report of two cases and review of the literature.","authors":"Panzardi Nicolás, Fernández-Alberti Joaquin, Schinoni Juan Pablo, Ares Jorge Hugo, Iotti Alejandro, Featherston Marcelo","doi":"10.3332/ecancer.2025.2022","DOIUrl":"10.3332/ecancer.2025.2022","url":null,"abstract":"<p><p>Transitional cell carcinoma of the prostatic urethra was first described and reported in 1963. Primary urothelial carcinoma of the prostate is an extremely rare disease, often misdiagnosed with other entities, particularly with urothelial carcinoma of the bladder involving the prostatic tissue. There are only dozens of cases of primary urothelial carcinoma in the prostate reported in the literature. The prognosis after diagnosis is reported to be poor and there is no consensus among experts concerning its proper treatment and follow-up. Herein, we report two cases of patients diagnosed with this entity with a median follow-up of 14 months.</p>","PeriodicalId":11460,"journal":{"name":"ecancermedicalscience","volume":"19 ","pages":"2022"},"PeriodicalIF":1.3,"publicationDate":"2025-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12826775/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146050927","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 : 2025-10-22eCollection Date: 2025-01-01DOI: 10.3332/ecancer.2025.2020
Tooba Ali, Nasir Ali, Syed Aun Hasan, Nawazish Zehra, Laraib Khan, Maham Khan, Mariam Hina, Bilal Ahmed, Fabiha Shakeel, Ahmed Nadeem Abbasi, Bilal Mazhar Qureshi, Asim Hafiz, Maria Tariq, Sehrish Abrar
Introduction: Breast cancer is the most common malignancy in women worldwide, with significant geographic variation in incidence. Adjuvant radiotherapy (RT) improves outcomes but can cause underrecognised toxicities such as radiation-induced nausea, vomiting (RINV) and esophagitis. This study aims to correlate RINV and esophagitis with organ-at-risk (OAR) dose constraints and clinical factors.
Materials and method: This prospective observational study analysed upper gastrointestinal (GI) toxicity in breast cancer patients receiving adjuvant RT. Patient demographics, clinical characteristics and dose-volume parameters for the stomach and esophagus were recorded. Statistical analyses identified predictors of RINV and esophagitis using univariate and multivariate models. Significant correlations were reported with a p-value <0.05.
Results: The study included 110 female breast cancer patients (mean age 51 years), with volumetric modulated arc therapy (VMAT) as the predominant radiation technique and moderate hypofractionation (42.56 Gy/16 fractions) as the most prescribed regimen. Acute upper GI toxicity was observed in 60.9% of patients, with 3.6% experiencing Grade 3 toxicity. Higher stomach dose exposure (D10, D30 and D60cc) significantly correlated with increased toxicity (p < 0.001). Free breathing was associated with a higher risk of GI toxicity compared to deep inspiration breath-hold (DIBH) (p = 0.035), which showed a protective effect. Dysphagia was reported in 70% of patients, with esophageal mean dose strongly predicting severity (p < 0.001). Multivariate analysis confirmed stomach D30 cc and esophageal mean dose as independent predictors of high-grade toxicity. VMAT was associated with slightly higher toxicity compared to three-dimensional conformal RT.
Conclusion: Radiation technique, dose-volume parameters and breathing strategy significantly influence acute upper GI toxicity and dysphagia in breast cancer RT. DIBH reduces GI toxicity risk, while higher stomach and esophageal doses correlate with increased toxicity. Incorporating the stomach as an OAR and optimising treatment planning can enhance tolerability and improve patient outcomes.
{"title":"Predictors of acute upper GI toxicity and its correlation with dosimetric analysis in patients receiving adjuvant radiation therapy for breast cancer.","authors":"Tooba Ali, Nasir Ali, Syed Aun Hasan, Nawazish Zehra, Laraib Khan, Maham Khan, Mariam Hina, Bilal Ahmed, Fabiha Shakeel, Ahmed Nadeem Abbasi, Bilal Mazhar Qureshi, Asim Hafiz, Maria Tariq, Sehrish Abrar","doi":"10.3332/ecancer.2025.2020","DOIUrl":"10.3332/ecancer.2025.2020","url":null,"abstract":"<p><strong>Introduction: </strong>Breast cancer is the most common malignancy in women worldwide, with significant geographic variation in incidence. Adjuvant radiotherapy (RT) improves outcomes but can cause underrecognised toxicities such as radiation-induced nausea, vomiting (RINV) and esophagitis. This study aims to correlate RINV and esophagitis with organ-at-risk (OAR) dose constraints and clinical factors.</p><p><strong>Materials and method: </strong>This prospective observational study analysed upper gastrointestinal (GI) toxicity in breast cancer patients receiving adjuvant RT. Patient demographics, clinical characteristics and dose-volume parameters for the stomach and esophagus were recorded. Statistical analyses identified predictors of RINV and esophagitis using univariate and multivariate models. Significant correlations were reported with a <i>p</i>-value <0.05.</p><p><strong>Results: </strong>The study included 110 female breast cancer patients (mean age 51 years), with volumetric modulated arc therapy (VMAT) as the predominant radiation technique and moderate hypofractionation (42.56 Gy/16 fractions) as the most prescribed regimen. Acute upper GI toxicity was observed in 60.9% of patients, with 3.6% experiencing Grade 3 toxicity. Higher stomach dose exposure (D10, D30 and D60cc) significantly correlated with increased toxicity (<i>p</i> < 0.001). Free breathing was associated with a higher risk of GI toxicity compared to deep inspiration breath-hold (DIBH) (<i>p</i> = 0.035), which showed a protective effect. Dysphagia was reported in 70% of patients, with esophageal mean dose strongly predicting severity (<i>p</i> < 0.001). Multivariate analysis confirmed stomach D30 cc and esophageal mean dose as independent predictors of high-grade toxicity. VMAT was associated with slightly higher toxicity compared to three-dimensional conformal RT.</p><p><strong>Conclusion: </strong>Radiation technique, dose-volume parameters and breathing strategy significantly influence acute upper GI toxicity and dysphagia in breast cancer RT. DIBH reduces GI toxicity risk, while higher stomach and esophageal doses correlate with increased toxicity. Incorporating the stomach as an OAR and optimising treatment planning can enhance tolerability and improve patient outcomes.</p>","PeriodicalId":11460,"journal":{"name":"ecancermedicalscience","volume":"19 ","pages":"2020"},"PeriodicalIF":1.3,"publicationDate":"2025-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12826783/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146046251","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.2025.2014
Manuel Bazan, Claudia Gutiérrez-Villamil, Amalia Peix, Saurabh Malhotra, Fernando Dettori, Roberto N Agüero, Belén Flores, Claudio Tinoco Mesquita, Enrique Hiplan, Teresa Massardo, Isabel Berrocal, José A Coss, Verónica Gómez, María C Fonseca, Karla Abadí, Adriana Puente, Víctor Rosales, Luis F Chen, Yariela Herrera, Marina Arnal, Aurelio Mendoza, Omar Alonso, Jorge E Aguiar, Carla Cueva, Enrique Estrada, Diana Páez
Health problems in the Latin American and Caribbean (LAC) region are mainly associated with noncommunicable diseases, with cardiovascular disease and cancer being the leading causes of death. However, knowledge and training opportunities in cardio-oncology, as well as active cardio-oncology groups, are mainly limited to large academic institutions or isolated private groups. To contribute to the implementation of viable strategies to ensure equitable access to care for all, it is essential to understand the current situation. This publication assesses the epidemiological situation of cancer in LAC and discusses the development of cardio-oncology in the region. It analyses the results of the survey on knowledge and medical action in cardio-oncology carried out among a group of physicians involved in the care of oncology patients and proposes recommendations based on the results obtained.
{"title":"Cardio-oncology in Latin America and the Caribbean. Current state.","authors":"Manuel Bazan, Claudia Gutiérrez-Villamil, Amalia Peix, Saurabh Malhotra, Fernando Dettori, Roberto N Agüero, Belén Flores, Claudio Tinoco Mesquita, Enrique Hiplan, Teresa Massardo, Isabel Berrocal, José A Coss, Verónica Gómez, María C Fonseca, Karla Abadí, Adriana Puente, Víctor Rosales, Luis F Chen, Yariela Herrera, Marina Arnal, Aurelio Mendoza, Omar Alonso, Jorge E Aguiar, Carla Cueva, Enrique Estrada, Diana Páez","doi":"10.3332/ecancer.2025.2014","DOIUrl":"10.3332/ecancer.2025.2014","url":null,"abstract":"<p><p>Health problems in the Latin American and Caribbean (LAC) region are mainly associated with noncommunicable diseases, with cardiovascular disease and cancer being the leading causes of death. However, knowledge and training opportunities in cardio-oncology, as well as active cardio-oncology groups, are mainly limited to large academic institutions or isolated private groups. To contribute to the implementation of viable strategies to ensure equitable access to care for all, it is essential to understand the current situation. This publication assesses the epidemiological situation of cancer in LAC and discusses the development of cardio-oncology in the region. It analyses the results of the survey on knowledge and medical action in cardio-oncology carried out among a group of physicians involved in the care of oncology patients and proposes recommendations based on the results obtained.</p>","PeriodicalId":11460,"journal":{"name":"ecancermedicalscience","volume":"19 ","pages":"2014"},"PeriodicalIF":1.3,"publicationDate":"2025-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12812807/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146009244","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.2025.2017
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}