Introduction: The work environment of oncology nurses exposes them to patient suffering, making them vulnerable to developing Secondary Traumatic Stress (STS). Most research on STS has been conducted in high-income countries with stable healthcare systems, whereas little is known about its occurrence or risk factors in conflict-affected regions. This study aims to determine the prevalence of STS and identify its predictors among Palestinian oncology nurses who face unstable political conditions, insufficient resources, and limited mental health services.
Methods: A cross-sectional analytical study was conducted in ten oncology departments across hospitals in the West Bank and East Jerusalem between August and October 2024. A total of 293 participants completed a questionnaire assessing sociodemographic characteristics, STS, burnout, social and organizational support, and coping strategies. Data were analyzed using SPSS 27 with descriptive and inferential statistics, including regression analyses to identify significant predictors.
Results: The mean STS score was 3.13 ± 0.73, with the intrusion-related symptoms being most prominent (3.18 ± 0.94). STS levels varied significantly with age, working hours, and parental status. Regression analysis identified the number of children as a negative predictor of STS (B = -0.081, p = 0.004), while education level (B = 0.096, p = 0.034) and Personal Accomplishment (B = 0.015, p < 0.001) were positive predictors. Perceived Organizational Support remained a strong negative predictor (B = -0.109, p < 0.001).
Conclusion: This study provides the first evidence of STS among oncology nurses in a conflict-affected work environment. Strengthening organizational support and tailoring coping strategies to the local context may help reduce STS while promoting nurse well-being. These findings underscore the global relevance of integrating stress management programs into oncology education and workplace policies.
肿瘤护士的工作环境使他们暴露在病人的痛苦中,使他们容易患上继发性创伤应激(STS)。大多数关于STS的研究都是在医疗系统稳定的高收入国家进行的,而对受冲突影响地区的STS发生或风险因素知之甚少。本研究旨在确定巴勒斯坦肿瘤护士中STS的患病率,并确定其预测因素,这些护士面临不稳定的政治条件、资源不足和有限的精神卫生服务。方法:在2024年8月至10月期间在西岸和东耶路撒冷的10家医院的肿瘤科进行了横断面分析研究。共有293名参与者完成了一份社会人口学特征、STS、倦怠、社会和组织支持以及应对策略的问卷。数据分析采用SPSS 27进行描述性和推断性统计,包括回归分析以确定显著的预测因子。结果:STS平均评分为3.13±0.73,其中侵入相关症状最为突出(3.18±0.94)。STS水平随年龄、工作时间和父母身份而显著不同。回归分析发现,儿童数量是STS的负向预测因子(B = -0.081, p = 0.004),教育水平(B = 0.096, p = 0.034)和个人成就(B = 0.015, p < 0.001)是STS的正预测因子。感知组织支持仍然是一个很强的负向预测因子(B = -0.109, p < 0.001)。结论:本研究首次提供了受冲突影响的工作环境中肿瘤护士发生STS的证据。加强组织支持和根据当地情况量身定制应对策略可能有助于减少STS,同时促进护士的福祉。这些发现强调了将压力管理项目纳入肿瘤学教育和工作场所政策的全球相关性。
{"title":"Predictors of Secondary Traumatic Stress among Oncology Nurses in Palestine.","authors":"Ayman Lubbad, Mohamed Ayoub Tlili, Nawaf Amro, Nabiha Missaoui","doi":"10.31557/APJCP.2026.27.2.705","DOIUrl":"https://doi.org/10.31557/APJCP.2026.27.2.705","url":null,"abstract":"<p><strong>Introduction: </strong>The work environment of oncology nurses exposes them to patient suffering, making them vulnerable to developing Secondary Traumatic Stress (STS). Most research on STS has been conducted in high-income countries with stable healthcare systems, whereas little is known about its occurrence or risk factors in conflict-affected regions. This study aims to determine the prevalence of STS and identify its predictors among Palestinian oncology nurses who face unstable political conditions, insufficient resources, and limited mental health services.</p><p><strong>Methods: </strong>A cross-sectional analytical study was conducted in ten oncology departments across hospitals in the West Bank and East Jerusalem between August and October 2024. A total of 293 participants completed a questionnaire assessing sociodemographic characteristics, STS, burnout, social and organizational support, and coping strategies. Data were analyzed using SPSS 27 with descriptive and inferential statistics, including regression analyses to identify significant predictors.</p><p><strong>Results: </strong>The mean STS score was 3.13 ± 0.73, with the intrusion-related symptoms being most prominent (3.18 ± 0.94). STS levels varied significantly with age, working hours, and parental status. Regression analysis identified the number of children as a negative predictor of STS (B = -0.081, p = 0.004), while education level (B = 0.096, p = 0.034) and Personal Accomplishment (B = 0.015, p < 0.001) were positive predictors. Perceived Organizational Support remained a strong negative predictor (B = -0.109, p < 0.001).</p><p><strong>Conclusion: </strong>This study provides the first evidence of STS among oncology nurses in a conflict-affected work environment. Strengthening organizational support and tailoring coping strategies to the local context may help reduce STS while promoting nurse well-being. These findings underscore the global relevance of integrating stress management programs into oncology education and workplace policies.</p>","PeriodicalId":55451,"journal":{"name":"Asian Pacific Journal of Cancer Prevention","volume":"27 2","pages":"705-713"},"PeriodicalIF":0.0,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146144016","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01DOI: 10.31557/APJCP.2026.27.2.405
Camila Buziqua Dartibale, Maria Vitória Felipe De Souza, Gabriela De Castro Prado, Débora De Mello Gonçales Sant'Ana, Sandra Marisa Pelloso, Valquiria Do Carmo Alves Martins, Cláudia Martins Carneiro, Rita Goreti Amaral, Janaina Cristiana De Oliveira Crispim Freitas, Karolina Reis Dos Santos Lukachaki, Vânia Ramos Sela Da Silva, Marcia Edilaine Lopes Consolaro
Objective: To evaluate the performance of a new Brazilian self-sampling device (COARI®) compared with clinician-collected samples for high-risk human papillomavirus (hrHPV) detection and partial typing.
Methods: This diagnostic agreement study included 57 women who underwent routine cervical screening or follow-up at a private health center in Maringá, Brazil, between May and October 2023. Each participant provided two samples: a self-collected vaginal sample using the COARI® device (Kolplast, Brazil) and a clinician-collected cervical sample. Both were tested using the Cobas® HPV 4800 assay (Roche, USA), which detects HPV16, HPV18, and a pooled group of 12 other hrHPV types.
Results: hrHPV detection was significantly higher in self-collected samples than in clinician-collected ones (52.9% vs. 37.2%; P = 0.008). The Overall agreement between sampling methods was 84.3%. All discordant cases (15.7%) were hrHPV-positive in self-collected samples and negative in clinician-collected specimens, suggesting potentially greater sensitivity for self-sampling. The COARI® device showed 100% sensitivity and a 100% negative predictive value, with an overall accuracy of 84.3%.
Conclusion: The COARI® self-sampling device demonstrated reliable and effective performance for hrHPV detection and partial typing, showing strong potential to increase access to and coverage of cervical cancer screening in Brazil. Further studies with larger and more diverse populations are needed to validate these findings and inform public health implementation.
目的:评价一种新的巴西自采样装置(COARI®)与临床采集的高危人乳头瘤病毒(hrHPV)检测和部分分型的性能。方法:这项诊断一致性研究包括57名妇女,她们于2023年5月至10月在巴西maring的一家私人健康中心接受了常规宫颈筛查或随访。每位参与者提供两份样本:使用COARI®装置(Kolplast,巴西)自行收集的阴道样本和临床收集的宫颈样本。使用Cobas®HPV 4800检测(Roche, USA)检测HPV16、HPV18和其他12种hrHPV类型。结果:自行采集标本hrHPV检出率明显高于临床采集标本(52.9% vs. 37.2%, P = 0.008)。抽样方法之间的总体一致性为84.3%。所有不一致的病例(15.7%)在自己采集的样本中呈hrhpv阳性,而在临床采集的样本中呈阴性,这表明自己采集的样本可能更敏感。COARI®装置显示100%的灵敏度和100%的阴性预测值,总体准确率为84.3%。结论:COARI®自采样装置在hrHPV检测和部分分型方面表现出可靠和有效的性能,在巴西提高宫颈癌筛查的可及性和覆盖率方面显示出强大的潜力。需要对更大、更多样化的人群进行进一步研究,以验证这些发现并为公共卫生实施提供信息。
{"title":"Performance of a New Brazilian Self-Sampling Device for High-Risk Human Papillomavirus Screening.","authors":"Camila Buziqua Dartibale, Maria Vitória Felipe De Souza, Gabriela De Castro Prado, Débora De Mello Gonçales Sant'Ana, Sandra Marisa Pelloso, Valquiria Do Carmo Alves Martins, Cláudia Martins Carneiro, Rita Goreti Amaral, Janaina Cristiana De Oliveira Crispim Freitas, Karolina Reis Dos Santos Lukachaki, Vânia Ramos Sela Da Silva, Marcia Edilaine Lopes Consolaro","doi":"10.31557/APJCP.2026.27.2.405","DOIUrl":"https://doi.org/10.31557/APJCP.2026.27.2.405","url":null,"abstract":"<p><strong>Objective: </strong>To evaluate the performance of a new Brazilian self-sampling device (COARI®) compared with clinician-collected samples for high-risk human papillomavirus (hrHPV) detection and partial typing.</p><p><strong>Methods: </strong>This diagnostic agreement study included 57 women who underwent routine cervical screening or follow-up at a private health center in Maringá, Brazil, between May and October 2023. Each participant provided two samples: a self-collected vaginal sample using the COARI® device (Kolplast, Brazil) and a clinician-collected cervical sample. Both were tested using the Cobas® HPV 4800 assay (Roche, USA), which detects HPV16, HPV18, and a pooled group of 12 other hrHPV types.</p><p><strong>Results: </strong>hrHPV detection was significantly higher in self-collected samples than in clinician-collected ones (52.9% vs. 37.2%; P = 0.008). The Overall agreement between sampling methods was 84.3%. All discordant cases (15.7%) were hrHPV-positive in self-collected samples and negative in clinician-collected specimens, suggesting potentially greater sensitivity for self-sampling. The COARI® device showed 100% sensitivity and a 100% negative predictive value, with an overall accuracy of 84.3%.</p><p><strong>Conclusion: </strong>The COARI® self-sampling device demonstrated reliable and effective performance for hrHPV detection and partial typing, showing strong potential to increase access to and coverage of cervical cancer screening in Brazil. Further studies with larger and more diverse populations are needed to validate these findings and inform public health implementation.</p>","PeriodicalId":55451,"journal":{"name":"Asian Pacific Journal of Cancer Prevention","volume":"27 2","pages":"405-409"},"PeriodicalIF":0.0,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146144732","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Objective: Breast cancer is a public health problem with increasing incidence, prevalence, and mortality worldwide. Germline variants in the DNA repair genes BRCA1/2 are involved in the pathogenesis of hereditary breast/ovarian cancer. However, for many ethnic groups that are isolated geographically worldwide, founder variants of breast cancer still have not been found. In this study, we provide whole exome sequencing data performed in a group of breast/ovarian cancer patients who belong to the Buryats.
Methods: Our study included 56 Buryat patients with histologically confirmed primary breast/ovarian cancer who completed an anonymous questionnaire about basic information and nationality. Genomic DNA was isolated from peripheral blood leukocytes. Libraries were prepared using a BGI Optimal DNA Library Prep kit (MGI, China). An Agilent SureSelect Human All Exon V6 kit (Agilent, USA) was used for hybridization. High-throughput sequencing was performed on a DNA nanoball sequencing platform DNBSeq-G400 (MGI, China). Result: In the overall group of patients with signs of hereditary breast/ovarian cancer, likely pathogenic/pathogenic variants were detected in 16% (9/56). We have discovered likely pathogenic/pathogenic variants that can either directly (BRCA2, RAD51D, FANCG) or indirectly (POLR2C, FOXL2, GDF9, CYP21A4) initiate breast/ovarian cancer. For the first time, three rare germinal variants in the BRCA2 gene were detected in a small Buryat ethnic group. Further studies are required to confirm their role in the pathogenesis of breast /ovarian cancer in this ethnic group. We found that the RAD51D gene variant c.757C>T is recurrent and was observed in 4% of Buryat patients with breast/ovarian cancer.
Conclusion: For the first time, rare germinal variants in the BRCA2, RAD51D, FANGC, CYP24A1 genes were detected in a small Buryat ethnic group. Our data are consistent with existing data showing that variants in the RAD51D gene may be involved in the pathogenesis of breast/ovarian cancer. We also showed that the Mongolic-speaking Buryat populations exhibited strong genetic resemblance to those of Chinese.
目的:乳腺癌是世界范围内发病率、患病率和死亡率不断上升的公共卫生问题。DNA修复基因BRCA1/2的种系变异参与了遗传性乳腺癌/卵巢癌的发病机制。然而,对于世界上许多地理上孤立的种族群体,乳腺癌的创始变异仍然没有被发现。在这项研究中,我们提供了一组布里亚特族乳腺癌/卵巢癌患者的全外显子组测序数据。方法:我们的研究纳入了56例组织学证实的原发性乳腺癌/卵巢癌患者,他们完成了一份关于基本信息和国籍的匿名问卷。从外周血白细胞中分离基因组DNA。文库采用华大基因优化DNA文库准备试剂盒(MGI,中国)制备。使用Agilent SureSelect Human All Exon V6试剂盒(Agilent, USA)进行杂交。在DNA纳米球测序平台DNBSeq-G400 (MGI, China)上进行高通量测序。结果:在所有有遗传性乳腺癌/卵巢癌体征的患者中,有16%(9/56)检测到可能的致病性/致病性变异。我们已经发现可能的致病性/致病性变异可以直接(BRCA2, RAD51D, FANCG)或间接(POLR2C, FOXL2, GDF9, CYP21A4)引发乳腺癌/卵巢癌。首次在布里亚特少数民族中检测到BRCA2基因的三种罕见的生发变异。需要进一步的研究来证实它们在该民族乳腺癌/卵巢癌发病机制中的作用。我们发现RAD51D基因变异c.757C>T是复发性的,在4%的布里亚特乳腺癌/卵巢癌患者中观察到。结论:首次在布里亚特少数民族中检测到BRCA2、RAD51D、FANGC、CYP24A1基因的罕见生发变异。我们的数据与现有数据一致,显示RAD51D基因的变异可能参与乳腺癌/卵巢癌的发病机制。我们还发现,说蒙古语的布里亚特人与中国人表现出很强的遗传相似性。
{"title":"Whole Exome Sequencing Revealed Rare Variants in BRCA2, RAD51D, FANGC, CYP24A1 Genes in Breast/Ovarian Cancer Patients from a Small Buryat Ethnic Group.","authors":"Polina Gervas, Alexey Molokov, Nataliya Babyshkina, Anna Ivanova, Olesya Kollantay, Mikhail Buldakov, Liliya Molonova, Alexey Zarubin, Evgeny Choynzonov, Nadezda Cherdyntseva","doi":"10.31557/APJCP.2026.27.2.651","DOIUrl":"https://doi.org/10.31557/APJCP.2026.27.2.651","url":null,"abstract":"<p><strong>Objective: </strong>Breast cancer is a public health problem with increasing incidence, prevalence, and mortality worldwide. Germline variants in the DNA repair genes BRCA1/2 are involved in the pathogenesis of hereditary breast/ovarian cancer. However, for many ethnic groups that are isolated geographically worldwide, founder variants of breast cancer still have not been found. In this study, we provide whole exome sequencing data performed in a group of breast/ovarian cancer patients who belong to the Buryats.</p><p><strong>Methods: </strong>Our study included 56 Buryat patients with histologically confirmed primary breast/ovarian cancer who completed an anonymous questionnaire about basic information and nationality. Genomic DNA was isolated from peripheral blood leukocytes. Libraries were prepared using a BGI Optimal DNA Library Prep kit (MGI, China). An Agilent SureSelect Human All Exon V6 kit (Agilent, USA) was used for hybridization. High-throughput sequencing was performed on a DNA nanoball sequencing platform DNBSeq-G400 (MGI, China). Result: In the overall group of patients with signs of hereditary breast/ovarian cancer, likely pathogenic/pathogenic variants were detected in 16% (9/56). We have discovered likely pathogenic/pathogenic variants that can either directly (BRCA2, RAD51D, FANCG) or indirectly (POLR2C, FOXL2, GDF9, CYP21A4) initiate breast/ovarian cancer. For the first time, three rare germinal variants in the BRCA2 gene were detected in a small Buryat ethnic group. Further studies are required to confirm their role in the pathogenesis of breast /ovarian cancer in this ethnic group. We found that the RAD51D gene variant c.757C>T is recurrent and was observed in 4% of Buryat patients with breast/ovarian cancer.</p><p><strong>Conclusion: </strong>For the first time, rare germinal variants in the BRCA2, RAD51D, FANGC, CYP24A1 genes were detected in a small Buryat ethnic group. Our data are consistent with existing data showing that variants in the RAD51D gene may be involved in the pathogenesis of breast/ovarian cancer. We also showed that the Mongolic-speaking Buryat populations exhibited strong genetic resemblance to those of Chinese.</p>","PeriodicalId":55451,"journal":{"name":"Asian Pacific Journal of Cancer Prevention","volume":"27 2","pages":"651-658"},"PeriodicalIF":0.0,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146144751","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01DOI: 10.31557/APJCP.2026.27.2.667
Passant Essam Shibel, Aya Magdy Elyamany, Galal El Shorbagy, Eman Ahmed Abd Elmaogod
Background: Urinary bladder carcinoma is one of the most immunogenic cancers. Several immune checkpoint inhibitors targeting programmed death-ligand 1 (PD-L1) have been approved by the FDA for bladder carcinoma treatment. However, additional immunotherapeutic targets are still needed. CD155 is another immune checkpoint molecule that has been shown to be overexpressed in several cancers and is associated with poor prognosis.
Aim: This study aimed to evaluate CD155 expression in cases of urinary bladder urothelial carcinoma using immunohistochemistry and to correlate this expression with the clinicopathological parameters of the cases as well as with PD-L1 expression.
Methods: Immunohistochemical staining for CD155 and PD-L1 was performed on 67 cases of urothelial carcinoma of the urinary bladder.
Results: CD155 was positive in 41.8% of cases and was significantly associated with invasive tumors and advanced T stage. PD-L1 was positive in 35.8% of cases and was significantly associated with advanced T stage, distant metastasis, muscle invasion and lymphovascular emboli. A statistically significant positive correlation was observed between the expression of both CD155 and PD-L1.
Conclusion: Our study demonstrated increased expression of CD155 in urothelial carcinoma of the urinary bladder with advancing stage, suggesting its potential as a therapeutic target. Additionally, CD155 expression correlated positively with PD-L1 expression, indicating that some patients might benefit from a combined blockade of both targets.
{"title":"Exploring the Role Of CD155 in Urothelial Carcinoma of the Urinary Bladder: An Immunohistochemical Study & Its Correlation With PD-L1.","authors":"Passant Essam Shibel, Aya Magdy Elyamany, Galal El Shorbagy, Eman Ahmed Abd Elmaogod","doi":"10.31557/APJCP.2026.27.2.667","DOIUrl":"https://doi.org/10.31557/APJCP.2026.27.2.667","url":null,"abstract":"<p><strong>Background: </strong>Urinary bladder carcinoma is one of the most immunogenic cancers. Several immune checkpoint inhibitors targeting programmed death-ligand 1 (PD-L1) have been approved by the FDA for bladder carcinoma treatment. However, additional immunotherapeutic targets are still needed. CD155 is another immune checkpoint molecule that has been shown to be overexpressed in several cancers and is associated with poor prognosis.</p><p><strong>Aim: </strong>This study aimed to evaluate CD155 expression in cases of urinary bladder urothelial carcinoma using immunohistochemistry and to correlate this expression with the clinicopathological parameters of the cases as well as with PD-L1 expression.</p><p><strong>Methods: </strong>Immunohistochemical staining for CD155 and PD-L1 was performed on 67 cases of urothelial carcinoma of the urinary bladder.</p><p><strong>Results: </strong>CD155 was positive in 41.8% of cases and was significantly associated with invasive tumors and advanced T stage. PD-L1 was positive in 35.8% of cases and was significantly associated with advanced T stage, distant metastasis, muscle invasion and lymphovascular emboli. A statistically significant positive correlation was observed between the expression of both CD155 and PD-L1.</p><p><strong>Conclusion: </strong>Our study demonstrated increased expression of CD155 in urothelial carcinoma of the urinary bladder with advancing stage, suggesting its potential as a therapeutic target. Additionally, CD155 expression correlated positively with PD-L1 expression, indicating that some patients might benefit from a combined blockade of both targets.</p>","PeriodicalId":55451,"journal":{"name":"Asian Pacific Journal of Cancer Prevention","volume":"27 2","pages":"667-675"},"PeriodicalIF":0.0,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146144760","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01DOI: 10.31557/APJCP.2026.27.2.693
Hariyono Winarto, Glenardi Glenardi, Muhammad Habiburrahman, Fitriyadi Kusuma, Laila Nuranna, Gatot Purwoto, Tofan Widya Utami, Tricia Dewi Anggraeni, Kartiwa Hadi Nuryanto
Background: Cervical cancer remains a leading public health problem in Indonesia, with low screening and HPV vaccination coverage, particularly in rural areas where knowledge gaps and limited healthcare access persist. This study aims to assess the knowledge, attitudes, and practices (KAP) regarding HPV infection and cervical cancer, and the role of information-seeking behavior in identifying effective channels for raising awareness on these issues.
Methods: A cross-sectional study was conducted between 20 March 2023 and 20 January 2024, involving 220 women from two rural districts in North Moluccas, selected via convenience sampling. Data were collected using a validated questionnaire administered through face-to-face interviews. Data were analyzed using SPSS version 25.0 with descriptive statistics, normality testing (Kolmogorov-Smirnov), bivariate analyses (Chi-square, Fisher's Exact, Pearson's or Spearman's tests), and multivariate logistic regression (backward LR, p < 0.05), with model performance assessed using ROC curves and AUC values.
Results: Most participants demonstrated poor KAP, with 18.7% showing good knowledge, 22.7% expressing a positive attitude, and 44.5% engaging in favorable practices. KAP were found to be positively correlated (p<0.001). Key predictors of good knowledge included higher education (AOR = 7.07), family history of cancer (AOR = 15.20), private vehicle use (AOR = 4.15), and active health-information seeking behavior (HISB) (AOR = 3.41). Determinants for a positive attitude included higher education (AOR = 3.79), family history of cancer (AOR = 4.42), active HISB (AOR = 3.88), and good knowledge (OR = 10.29). Favorable practices were influenced by private vehicle use (AOR = 2.66) and positive attitude (AOR = 20.62).
Conclusion: In conclusion, KAP are influenced by HISB, and involving healthcare workers in providing information, particularly through digital platforms, has the potential to improve KAP in rural communities.
背景:在印度尼西亚,宫颈癌仍然是一个主要的公共卫生问题,筛查和HPV疫苗接种覆盖率低,特别是在知识差距和卫生保健机会有限的农村地区。本研究旨在评估有关HPV感染和宫颈癌的知识,态度和实践(KAP),以及信息寻求行为在确定有效渠道以提高对这些问题的认识方面的作用。方法:在2023年3月20日至2024年1月20日期间进行横断面研究,通过方便抽样的方式选择来自北摩鹿加群岛两个农村地区的220名妇女。数据收集使用有效的问卷,通过面对面的访谈管理。数据分析采用SPSS 25.0版,采用描述性统计、正态性检验(Kolmogorov-Smirnov)、双变量分析(卡方检验、Fisher’s Exact检验、Pearson’s检验或Spearman’s检验)和多变量logistic回归(后向LR, p < 0.05),采用ROC曲线和AUC值评估模型性能。结果:大多数参与者表现出较差的KAP,其中18.7%的人表现出良好的知识,22.7%的人表现出积极的态度,44.5%的人表现出良好的行为。结论:综上所述,KAP受到HISB的影响,让医护人员提供信息,特别是通过数字平台,有可能改善农村社区的KAP。
{"title":"Exploring Knowledge, Attitudes, Practices, and Information-Seeking on HPV Infection and Cervical Cancer Prevention in Rural Indonesia.","authors":"Hariyono Winarto, Glenardi Glenardi, Muhammad Habiburrahman, Fitriyadi Kusuma, Laila Nuranna, Gatot Purwoto, Tofan Widya Utami, Tricia Dewi Anggraeni, Kartiwa Hadi Nuryanto","doi":"10.31557/APJCP.2026.27.2.693","DOIUrl":"https://doi.org/10.31557/APJCP.2026.27.2.693","url":null,"abstract":"<p><strong>Background: </strong>Cervical cancer remains a leading public health problem in Indonesia, with low screening and HPV vaccination coverage, particularly in rural areas where knowledge gaps and limited healthcare access persist. This study aims to assess the knowledge, attitudes, and practices (KAP) regarding HPV infection and cervical cancer, and the role of information-seeking behavior in identifying effective channels for raising awareness on these issues.</p><p><strong>Methods: </strong>A cross-sectional study was conducted between 20 March 2023 and 20 January 2024, involving 220 women from two rural districts in North Moluccas, selected via convenience sampling. Data were collected using a validated questionnaire administered through face-to-face interviews. Data were analyzed using SPSS version 25.0 with descriptive statistics, normality testing (Kolmogorov-Smirnov), bivariate analyses (Chi-square, Fisher's Exact, Pearson's or Spearman's tests), and multivariate logistic regression (backward LR, p < 0.05), with model performance assessed using ROC curves and AUC values.</p><p><strong>Results: </strong>Most participants demonstrated poor KAP, with 18.7% showing good knowledge, 22.7% expressing a positive attitude, and 44.5% engaging in favorable practices. KAP were found to be positively correlated (p<0.001). Key predictors of good knowledge included higher education (AOR = 7.07), family history of cancer (AOR = 15.20), private vehicle use (AOR = 4.15), and active health-information seeking behavior (HISB) (AOR = 3.41). Determinants for a positive attitude included higher education (AOR = 3.79), family history of cancer (AOR = 4.42), active HISB (AOR = 3.88), and good knowledge (OR = 10.29). Favorable practices were influenced by private vehicle use (AOR = 2.66) and positive attitude (AOR = 20.62).</p><p><strong>Conclusion: </strong>In conclusion, KAP are influenced by HISB, and involving healthcare workers in providing information, particularly through digital platforms, has the potential to improve KAP in rural communities.</p>","PeriodicalId":55451,"journal":{"name":"Asian Pacific Journal of Cancer Prevention","volume":"27 2","pages":"693-704"},"PeriodicalIF":0.0,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146144729","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01DOI: 10.31557/APJCP.2026.27.2.433
Ajeng Viska Icanervilia, Lina Choridah, Afdina Melya G Febiyanti, Afina Azka L Kuncoro, Sita Nur Agustyana, Dhite Bayu Nugroho
Background: Breast cancer is a prevalent malignancy worldwide, with a growing number of survivors requiring post-treatment surveillance to improve outcomes. Radiologic surveillance, particularly mammography, is essential for early detection, however, there are disparities in the accuracy and effectiveness of various imaging modalities.
Objectives: The aim of this systematic review and meta-analysis is to evaluate the effectiveness of radiology surveillance techniques for breast cancer survivors, focusing on diagnostic accuracy and mortality reduction.
Methods: Studies assessing radiologic surveillance (e.g. mammography, ultrasonography, magnetic resonance imaging [MRI], and digital breast tomosynthesis) were included in this review. A comprehensive literature search was conducted in Medline, Cochrane Central Register of Controlled Trials, and Scopus databases. To obtain pooled estimates for sensitivity, specificity, accuracy, and mortality, we extracted and synthesized data using a random-effects model. The Newcastle-Ottawa Scale and QUADAS-2 instruments were used to assess the risk of bias.
Results: A total of eighteen studies met the eligibility criteria for the review, of which eight were included in the meta-analysis (three for diagnostic accuracy and five for mortality. The pooled sensitivity, specificity, and accuracy of mammographic surveillance were 81% (95% CI 0.63-0.91), 71% (95% CI 0.31-0.93), and 76% (95% CI 0.59-0.88). A 50% reduction in mortality risk was linked to mammographic surveillance (OR 0.50; 95% CI 0.27-0.92). Heterogeneity was substantial for mortality analysis (I2=93%), while there was a low heterogeneity for the sensitivity analysis (I2=16%). MRI showed better sensitivity (91%) and specificity (82%) than ultrasonography and mammography.
Conclusion: Although mammographic surveillance has a lower diagnostic accuracy than that observed in the screening population, it considerably lowers mortality among breast cancer survivors. The use of adjunct imaging modalities, such as MRI, may enhance early detection. Standardized surveillance protocols and further research on imaging strategies in diverse populations are required to improve post-treatment monitoring and patient outcomes.
背景:乳腺癌是世界范围内普遍存在的恶性肿瘤,越来越多的幸存者需要治疗后监测以改善预后。放射学监测,特别是乳房x光检查,对于早期发现是必不可少的,然而,各种成像方式的准确性和有效性存在差异。目的:本系统综述和荟萃分析的目的是评估放射学监测技术对乳腺癌幸存者的有效性,重点是诊断准确性和降低死亡率。方法:本综述纳入了评估放射学监测的研究(如乳房x光检查、超声检查、磁共振成像(MRI)和数字乳房断层合成)。在Medline、Cochrane Central Register of Controlled Trials和Scopus数据库中进行了全面的文献检索。为了获得敏感性、特异性、准确性和死亡率的综合估计,我们使用随机效应模型提取和合成数据。使用纽卡斯尔-渥太华量表和QUADAS-2工具评估偏倚风险。结果:共有18项研究符合本综述的资格标准,其中8项纳入荟萃分析(3项用于诊断准确性,5项用于死亡率)。乳房x线摄影监测的敏感性、特异性和准确性分别为81% (95% CI 0.63-0.91)、71% (95% CI 0.31-0.93)和76% (95% CI 0.59-0.88)。50%的死亡风险降低与乳房x线摄影监测有关(OR 0.50; 95% CI 0.27-0.92)。死亡率分析的异质性很大(I2=93%),而敏感性分析的异质性很低(I2=16%)。MRI的敏感性(91%)和特异性(82%)优于超声和乳房x光检查。结论:尽管乳房x线摄影监测的诊断准确性低于筛查人群,但它大大降低了乳腺癌幸存者的死亡率。使用辅助成像方式,如核磁共振成像,可以加强早期发现。标准化的监测方案和对不同人群成像策略的进一步研究需要改善治疗后监测和患者预后。
{"title":"Radiology Surveillance for Breast Cancer Survivors: A Systematic Review and Meta-Analysis.","authors":"Ajeng Viska Icanervilia, Lina Choridah, Afdina Melya G Febiyanti, Afina Azka L Kuncoro, Sita Nur Agustyana, Dhite Bayu Nugroho","doi":"10.31557/APJCP.2026.27.2.433","DOIUrl":"https://doi.org/10.31557/APJCP.2026.27.2.433","url":null,"abstract":"<p><strong>Background: </strong>Breast cancer is a prevalent malignancy worldwide, with a growing number of survivors requiring post-treatment surveillance to improve outcomes. Radiologic surveillance, particularly mammography, is essential for early detection, however, there are disparities in the accuracy and effectiveness of various imaging modalities.</p><p><strong>Objectives: </strong>The aim of this systematic review and meta-analysis is to evaluate the effectiveness of radiology surveillance techniques for breast cancer survivors, focusing on diagnostic accuracy and mortality reduction.</p><p><strong>Methods: </strong>Studies assessing radiologic surveillance (e.g. mammography, ultrasonography, magnetic resonance imaging [MRI], and digital breast tomosynthesis) were included in this review. A comprehensive literature search was conducted in Medline, Cochrane Central Register of Controlled Trials, and Scopus databases. To obtain pooled estimates for sensitivity, specificity, accuracy, and mortality, we extracted and synthesized data using a random-effects model. The Newcastle-Ottawa Scale and QUADAS-2 instruments were used to assess the risk of bias.</p><p><strong>Results: </strong>A total of eighteen studies met the eligibility criteria for the review, of which eight were included in the meta-analysis (three for diagnostic accuracy and five for mortality. The pooled sensitivity, specificity, and accuracy of mammographic surveillance were 81% (95% CI 0.63-0.91), 71% (95% CI 0.31-0.93), and 76% (95% CI 0.59-0.88). A 50% reduction in mortality risk was linked to mammographic surveillance (OR 0.50; 95% CI 0.27-0.92). Heterogeneity was substantial for mortality analysis (I2=93%), while there was a low heterogeneity for the sensitivity analysis (I2=16%). MRI showed better sensitivity (91%) and specificity (82%) than ultrasonography and mammography.</p><p><strong>Conclusion: </strong>Although mammographic surveillance has a lower diagnostic accuracy than that observed in the screening population, it considerably lowers mortality among breast cancer survivors. The use of adjunct imaging modalities, such as MRI, may enhance early detection. Standardized surveillance protocols and further research on imaging strategies in diverse populations are required to improve post-treatment monitoring and patient outcomes.</p>","PeriodicalId":55451,"journal":{"name":"Asian Pacific Journal of Cancer Prevention","volume":"27 2","pages":"433-442"},"PeriodicalIF":0.0,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146144313","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01DOI: 10.31557/APJCP.2026.27.2.575
Menha Swellam, Mohamed K Khalifa, Amira M Nageeb, Magda Sayed Mahmoud, Maha Hashim, Aliaa Alisslam I A Alshazly, Magdy E Mahfouz, Lobna R Ez ElArab, Madyha H Mahmoud, Mohamed Emam Sobeih
Background: Breast cancer is the most common cancer affecting females according to WHO 2020 report, with BRCA1 and BRCA2 identified as the major tumor suppressor genes linked to disease susceptibility. Hence, the purpose of the current study was to investigate germline mutations among these genes in a group of Egyptian female breast cancer patients.
Methods: Blood samples from primary breast cancer patients (n=22), benign breast lesions (n=5) and healthy controls (n=7) were sequenced for BRCA genes by next generation sequencer.
Results: A total of 135 genetic variations were detected, 59 in BRCA1 and 76 BRCA2, 2 indels (insertion-deletion) and 133 SNV (single nucleotide variation), nearly 55% of those variants were missense variants, 38% were synonymous and 7% were nonsense. A total of 59 variations were detected in BRCA1 and they were categorized as exonic (n=10) and intronic (n=49) regions, BRCA1 exonic variants were categorized into: missense (n=12), non-coding transcript (n=11) synonymous (n=6), splice region synonymous (n=2), stop gain (n=2) and 3-prime UTR (n=1) variants. Regarding variations detected in BRCA2, 55 intronic and 21 exonic variants were identified. Among these 21 variants; 13 novel mutations and 8 formally reported as follows: 7 as benign and one previously reported with contradictory pathogenicity according to the Clinvar database which is a freely available, public archive of reports of the relationships between human variations and phenotypes hosted by the National Center for Biotechnology Information (NCBI) and funded by intramural National Institutes of Health (NIH) funding.
Conclusion: BRCA1 and BRCA2 germline profiling based on next-generation sequencing technology among Egyptian breast cancer female patients revealed 135 germline variations -104 intronic and 31 exonic, respectively. Among the exonic variants; 13 were newly reported mutations. Hence further study is required to enhance mutational analysis which may benefit clinical system.
{"title":"Identification of BRCA1 and BRCA2 Germline Mutations in Female Breast Cancer Patients Using Next Generation Sequencing.","authors":"Menha Swellam, Mohamed K Khalifa, Amira M Nageeb, Magda Sayed Mahmoud, Maha Hashim, Aliaa Alisslam I A Alshazly, Magdy E Mahfouz, Lobna R Ez ElArab, Madyha H Mahmoud, Mohamed Emam Sobeih","doi":"10.31557/APJCP.2026.27.2.575","DOIUrl":"https://doi.org/10.31557/APJCP.2026.27.2.575","url":null,"abstract":"<p><strong>Background: </strong>Breast cancer is the most common cancer affecting females according to WHO 2020 report, with BRCA1 and BRCA2 identified as the major tumor suppressor genes linked to disease susceptibility. Hence, the purpose of the current study was to investigate germline mutations among these genes in a group of Egyptian female breast cancer patients.</p><p><strong>Methods: </strong>Blood samples from primary breast cancer patients (n=22), benign breast lesions (n=5) and healthy controls (n=7) were sequenced for BRCA genes by next generation sequencer.</p><p><strong>Results: </strong>A total of 135 genetic variations were detected, 59 in BRCA1 and 76 BRCA2, 2 indels (insertion-deletion) and 133 SNV (single nucleotide variation), nearly 55% of those variants were missense variants, 38% were synonymous and 7% were nonsense. A total of 59 variations were detected in BRCA1 and they were categorized as exonic (n=10) and intronic (n=49) regions, BRCA1 exonic variants were categorized into: missense (n=12), non-coding transcript (n=11) synonymous (n=6), splice region synonymous (n=2), stop gain (n=2) and 3-prime UTR (n=1) variants. Regarding variations detected in BRCA2, 55 intronic and 21 exonic variants were identified. Among these 21 variants; 13 novel mutations and 8 formally reported as follows: 7 as benign and one previously reported with contradictory pathogenicity according to the Clinvar database which is a freely available, public archive of reports of the relationships between human variations and phenotypes hosted by the National Center for Biotechnology Information (NCBI) and funded by intramural National Institutes of Health (NIH) funding.</p><p><strong>Conclusion: </strong>BRCA1 and BRCA2 germline profiling based on next-generation sequencing technology among Egyptian breast cancer female patients revealed 135 germline variations -104 intronic and 31 exonic, respectively. Among the exonic variants; 13 were newly reported mutations. Hence further study is required to enhance mutational analysis which may benefit clinical system.</p>","PeriodicalId":55451,"journal":{"name":"Asian Pacific Journal of Cancer Prevention","volume":"27 2","pages":"575-581"},"PeriodicalIF":0.0,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146144695","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01DOI: 10.31557/APJCP.2026.27.2.685
Ajithkumar M, Subhankar Show, Sneha Jha, Aaditya Prakash, Chitra S
Purpose: This study aims to evaluate the impact of varying Aperture Shape Controller (ASC) settings on the optimization of VMAT plans for tongue carcinoma (Ca-Tongue), focusing on their role in modulating plan complexity, maintaining dosimetric integrity, and ensuring accurate treatment delivery.
Materials and methods: Twenty Ca-Tongue patients were retrospectively planned using four ASC settings: Off, Very Low, Moderate, and Very High, totaling 80 plans. Complexity metrics such as Modulation Complexity Score (MCSv), Small Aperture Score (SAS), and Monitor Units per cGy (MU/cGy) were computed using MATLAB from exported DICOM RT files. Each plan underwent portal dosimetry QA with gamma analysis (3%/3mm and 2%/2mm). Dosimetric quality was evaluated using Conformity Index (CI), Homogeneity Index (HI), and PTV D98%, along with doses to organs-at-risk (OARs). Statistical analysis included the Wilcoxon signed-rank test and linear regression.
Results: Increasing ASC level significantly reduced plan complexity: MCSv increased from 0.32±0.02 (Off) to 0.38±0.03 (Very High), SAS decreased from 0.47±0.04 to 0.37±0.07, and MU/cGy dropped from 2.25±0.09 to 2.03±0.12 (p < 0.05). However, higher ASC levels were associated with minor but consistent reductions in PTV coverage (D98%: 96.66% to 94.94%) and increases in OAR doses (e.g., spinal cord Dmax: 30.46 Gy to 34.90 Gy). CI and HI remained clinically acceptable across all settings. Gamma pass rates were uniformly high (≥98.85%), with no significant improvement across ASC levels. Weak or negligible correlations (R² < 0.323) were found between complexity metrics and gamma outcomes.
Conclusion: The ASC effectively reduces plan complexity in VMAT for Ca-Tongue without compromising delivery accuracy. While Very High ASC yields the greatest complexity reduction, it also introduces modest trade-offs in PTV coverage and OAR sparing. The Moderate ASC setting appears optimal, offering a balance between complexity control and dosimetric quality. Clinical implementation of ASC should be tailored to tumor site and anatomy, with Moderate ASC recommended for head and neck VMAT to ensure safety, efficiency, and robust QA performance.
{"title":"A Multidimensional Assessment of the Aperture Shape Controller in VMAT for Ca Tongue: Implications for Plan Complexity and Quality Assurance.","authors":"Ajithkumar M, Subhankar Show, Sneha Jha, Aaditya Prakash, Chitra S","doi":"10.31557/APJCP.2026.27.2.685","DOIUrl":"https://doi.org/10.31557/APJCP.2026.27.2.685","url":null,"abstract":"<p><strong>Purpose: </strong>This study aims to evaluate the impact of varying Aperture Shape Controller (ASC) settings on the optimization of VMAT plans for tongue carcinoma (Ca-Tongue), focusing on their role in modulating plan complexity, maintaining dosimetric integrity, and ensuring accurate treatment delivery.</p><p><strong>Materials and methods: </strong>Twenty Ca-Tongue patients were retrospectively planned using four ASC settings: Off, Very Low, Moderate, and Very High, totaling 80 plans. Complexity metrics such as Modulation Complexity Score (MCSv), Small Aperture Score (SAS), and Monitor Units per cGy (MU/cGy) were computed using MATLAB from exported DICOM RT files. Each plan underwent portal dosimetry QA with gamma analysis (3%/3mm and 2%/2mm). Dosimetric quality was evaluated using Conformity Index (CI), Homogeneity Index (HI), and PTV D98%, along with doses to organs-at-risk (OARs). Statistical analysis included the Wilcoxon signed-rank test and linear regression.</p><p><strong>Results: </strong>Increasing ASC level significantly reduced plan complexity: MCSv increased from 0.32±0.02 (Off) to 0.38±0.03 (Very High), SAS decreased from 0.47±0.04 to 0.37±0.07, and MU/cGy dropped from 2.25±0.09 to 2.03±0.12 (p < 0.05). However, higher ASC levels were associated with minor but consistent reductions in PTV coverage (D98%: 96.66% to 94.94%) and increases in OAR doses (e.g., spinal cord Dmax: 30.46 Gy to 34.90 Gy). CI and HI remained clinically acceptable across all settings. Gamma pass rates were uniformly high (≥98.85%), with no significant improvement across ASC levels. Weak or negligible correlations (R² < 0.323) were found between complexity metrics and gamma outcomes.</p><p><strong>Conclusion: </strong>The ASC effectively reduces plan complexity in VMAT for Ca-Tongue without compromising delivery accuracy. While Very High ASC yields the greatest complexity reduction, it also introduces modest trade-offs in PTV coverage and OAR sparing. The Moderate ASC setting appears optimal, offering a balance between complexity control and dosimetric quality. Clinical implementation of ASC should be tailored to tumor site and anatomy, with Moderate ASC recommended for head and neck VMAT to ensure safety, efficiency, and robust QA performance.</p>","PeriodicalId":55451,"journal":{"name":"Asian Pacific Journal of Cancer Prevention","volume":"27 2","pages":"685-691"},"PeriodicalIF":0.0,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146144384","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: Colorectal cancer (CRC) is one of the most prevalent malignancies worldwide. Variability in patient response to fluoropyrimidine-based neoadjuvant chemotherapy remains a critical challenge. We aimed to develop a nomogram that integrated dihydropyrimidine dehydrogenase (DPD) and methylenetetrahydrofolate reductase (MTHFR) expression to predict CapeOX (Capecitabine-Oxaliplatin) neoadjuvant chemotherapy outcomes in colorectal cancer.
Methods: A prospective cohort of 36 advanced-stage CRC patients who received CapeOX neoadjuvant chemotherapy at Wahidin Sudirohusodo Hospital from 2024 to 2025 was analyzed. mRNA expression levels of TS, DPD, and MTHFR were measured in tissue and blood using quantitative RT-PCR. The chemotherapy response was evaluated by RECIST 1.1. Statistical analysis was performed to identify predictors of response, which were incorporated into a nomogram with bootstrap validation.
Results: Among the 36 patients with advanced colorectal cancer, response to CapeOX chemotherapy was observed in 50%. Blood-based gene profiling revealed that responders had significantly lower DPD and MTHFR expression compared with non-responders (both p<0.001), while TS showed no predictive relevance. A nomogram that integrated only blood DPD and MTHFR achieved outstanding discrimination (AUC 0.932, C-index 0.78) and demonstrated strong calibration, accurately predicting treatment response across probability ranges. These results established circulating DPD and MTHFR as powerful non-invasive biomarkers and validated the nomogram as a robust tool for individualized response prediction.
Conclusion: A predictive nomogram that incorporated DPD and MTHFR has improved individualized estimation of CapeOX neoadjuvant chemotherapy response in CRC, supporting precision oncology strategies. .
{"title":"Towards Precision Oncology: A Predictive Nomogram Incorporating DPD and MTHFR for CapeOX Neoadjuvant Chemotherapy in Colorectal Cancer.","authors":"Elvida Christy Imelda Tahiya, Ronald Erasio Lusikooy, Ilhamjaya Pattelongi, Warsinggih Raharjo, Julianus Aboyaman Uwuratuw, Erwin Syarifuddin, Citra Aryanti","doi":"10.31557/APJCP.2026.27.2.731","DOIUrl":"https://doi.org/10.31557/APJCP.2026.27.2.731","url":null,"abstract":"<p><strong>Background: </strong>Colorectal cancer (CRC) is one of the most prevalent malignancies worldwide. Variability in patient response to fluoropyrimidine-based neoadjuvant chemotherapy remains a critical challenge. We aimed to develop a nomogram that integrated dihydropyrimidine dehydrogenase (DPD) and methylenetetrahydrofolate reductase (MTHFR) expression to predict CapeOX (Capecitabine-Oxaliplatin) neoadjuvant chemotherapy outcomes in colorectal cancer.</p><p><strong>Methods: </strong>A prospective cohort of 36 advanced-stage CRC patients who received CapeOX neoadjuvant chemotherapy at Wahidin Sudirohusodo Hospital from 2024 to 2025 was analyzed. mRNA expression levels of TS, DPD, and MTHFR were measured in tissue and blood using quantitative RT-PCR. The chemotherapy response was evaluated by RECIST 1.1. Statistical analysis was performed to identify predictors of response, which were incorporated into a nomogram with bootstrap validation.</p><p><strong>Results: </strong>Among the 36 patients with advanced colorectal cancer, response to CapeOX chemotherapy was observed in 50%. Blood-based gene profiling revealed that responders had significantly lower DPD and MTHFR expression compared with non-responders (both p<0.001), while TS showed no predictive relevance. A nomogram that integrated only blood DPD and MTHFR achieved outstanding discrimination (AUC 0.932, C-index 0.78) and demonstrated strong calibration, accurately predicting treatment response across probability ranges. These results established circulating DPD and MTHFR as powerful non-invasive biomarkers and validated the nomogram as a robust tool for individualized response prediction.</p><p><strong>Conclusion: </strong>A predictive nomogram that incorporated DPD and MTHFR has improved individualized estimation of CapeOX neoadjuvant chemotherapy response in CRC, supporting precision oncology strategies.<br />.</p>","PeriodicalId":55451,"journal":{"name":"Asian Pacific Journal of Cancer Prevention","volume":"27 2","pages":"731-736"},"PeriodicalIF":0.0,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146144698","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01DOI: 10.31557/APJCP.2026.27.2.601
Arindam Ray, Arindam Karmakar, Moumita Maiti, Soumyabroto Banerjee, Swati Dasgupta, Sayan Dey, Umar Faruk, Priyabrata Das, Prosenjit Saha
Objective: This study aims at develop and evaluate an artificial intelligence programming software, an integrated system that automatically detects and classifies cells from microscopic Pap smear slide images taken on Android phones or tabs to diagnose the cervical cell morphology in a time-efficient and cost-effective manner.
Methods: This study presents an integrated system designed to automatically detect and classify cells in Pap smear slide images, differentiating cellular morphologies. The system leverages three deep learning (DL) and one machine learning (ML) models, each tailored to specific tasks in the image analysis pipeline. The analysis of 292 hospital in-house microscopic Pap smear images was conducted from July 2023 to December 2024 at CliniMed LifeSciences, Kolkata, India. The following article describes the datasets used, the training procedures and the performance metrics for each model. Results: Pap smear images have been validated and standardized by using SipakMed, Herlev (public datasets) and hospital in-house data. A total of 292 in-house Pap smear images have been analysed through the newly developed AI software. Standardization and validation include an Intersection-over-Union score of cell-nuclei boundary extraction model of 71.14%, the accuracy of cell classification model and morphological feature based ML model are 99.213% and 91.23% respectively. The custom AI model could successfully classify 98.09% and 80.49% of normal and abnormal cells in hospital in-house samples respectively. Also a significant meaningful correlation is observed between biopsy (gold standard) and AI reports.
Conclusion: AI offers a lot of promise for diagnosing cervical cancer, and its uses in cervical cytology screening are particularly well-established. Manual screening of cervical cytology smears is a time-tested method, but AI is set to revolutionize the process by improving outreach, availability, accuracy and economy. A total of 292 hospital in-house Pap smear images have been validated and examined in this study with significant accuracy percentages between AI and expert eyes.
{"title":"Evaluation of the Diagnostic Accuracy of Cervical Cell Morphologies from Android Device-Captured Cytopathological Microscopic Images through Artificial Intelligence in Mainly Rural or Resource-Constraint Areas of India.","authors":"Arindam Ray, Arindam Karmakar, Moumita Maiti, Soumyabroto Banerjee, Swati Dasgupta, Sayan Dey, Umar Faruk, Priyabrata Das, Prosenjit Saha","doi":"10.31557/APJCP.2026.27.2.601","DOIUrl":"https://doi.org/10.31557/APJCP.2026.27.2.601","url":null,"abstract":"<p><strong>Objective: </strong>This study aims at develop and evaluate an artificial intelligence programming software, an integrated system that automatically detects and classifies cells from microscopic Pap smear slide images taken on Android phones or tabs to diagnose the cervical cell morphology in a time-efficient and cost-effective manner.</p><p><strong>Methods: </strong>This study presents an integrated system designed to automatically detect and classify cells in Pap smear slide images, differentiating cellular morphologies. The system leverages three deep learning (DL) and one machine learning (ML) models, each tailored to specific tasks in the image analysis pipeline. The analysis of 292 hospital in-house microscopic Pap smear images was conducted from July 2023 to December 2024 at CliniMed LifeSciences, Kolkata, India. The following article describes the datasets used, the training procedures and the performance metrics for each model. Results: Pap smear images have been validated and standardized by using SipakMed, Herlev (public datasets) and hospital in-house data. A total of 292 in-house Pap smear images have been analysed through the newly developed AI software. Standardization and validation include an Intersection-over-Union score of cell-nuclei boundary extraction model of 71.14%, the accuracy of cell classification model and morphological feature based ML model are 99.213% and 91.23% respectively. The custom AI model could successfully classify 98.09% and 80.49% of normal and abnormal cells in hospital in-house samples respectively. Also a significant meaningful correlation is observed between biopsy (gold standard) and AI reports.</p><p><strong>Conclusion: </strong>AI offers a lot of promise for diagnosing cervical cancer, and its uses in cervical cytology screening are particularly well-established. Manual screening of cervical cytology smears is a time-tested method, but AI is set to revolutionize the process by improving outreach, availability, accuracy and economy. A total of 292 hospital in-house Pap smear images have been validated and examined in this study with significant accuracy percentages between AI and expert eyes.</p>","PeriodicalId":55451,"journal":{"name":"Asian Pacific Journal of Cancer Prevention","volume":"27 2","pages":"601-612"},"PeriodicalIF":0.0,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146144697","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}