Pub Date : 2025-12-27DOI: 10.3390/curroncol33010015
Christine Brezden-Masley, Katarzyna J Jerzak, Nancy A Nixon, Anne Koch, Amanda Roberts, Jean-François Boileau, May Lynn Quan, M J DeCoteau, Tulin D Cil
The 2025 Canadian Breast Cancer Symposium (CBCS) brought together patients, clinicians and researchers from across Canada to discuss advances shaping personalized breast cancer care. Key updates in systemic therapy highlighted expanding treatment options, including CDK4/6 inhibitors, oral SERDs, PI3K/AKT-targeted therapies, and antibody-drug conjugates across early and metastatic settings. Radiation oncology sessions emphasized treatment de-escalation, featuring evidence for ultra-hypofractionation, selective omission of nodal irradiation, and stereotactic strategies to manage oligoprogression. Surgical presentations focused on reducing morbidity through tailored axillary management and emerging techniques to prevent lymphedema. Advances in the management of central nervous system metastases underscored the growing synergy between stereotactic radiotherapy and CNS-active systemic therapies. Informed by patient testimony and advocacy perspectives, experts reflected on persistent gaps in diagnosis, access, and survivorship that shape priorities for future improvements. Together, these insights outline key directions that help to refine clinical practice and guide future research.
{"title":"The Canadian Breast Cancer Symposium 2025: Meeting Report.","authors":"Christine Brezden-Masley, Katarzyna J Jerzak, Nancy A Nixon, Anne Koch, Amanda Roberts, Jean-François Boileau, May Lynn Quan, M J DeCoteau, Tulin D Cil","doi":"10.3390/curroncol33010015","DOIUrl":"10.3390/curroncol33010015","url":null,"abstract":"<p><p>The 2025 Canadian Breast Cancer Symposium (CBCS) brought together patients, clinicians and researchers from across Canada to discuss advances shaping personalized breast cancer care. Key updates in systemic therapy highlighted expanding treatment options, including CDK4/6 inhibitors, oral SERDs, PI3K/AKT-targeted therapies, and antibody-drug conjugates across early and metastatic settings. Radiation oncology sessions emphasized treatment de-escalation, featuring evidence for ultra-hypofractionation, selective omission of nodal irradiation, and stereotactic strategies to manage oligoprogression. Surgical presentations focused on reducing morbidity through tailored axillary management and emerging techniques to prevent lymphedema. Advances in the management of central nervous system metastases underscored the growing synergy between stereotactic radiotherapy and CNS-active systemic therapies. Informed by patient testimony and advocacy perspectives, experts reflected on persistent gaps in diagnosis, access, and survivorship that shape priorities for future improvements. Together, these insights outline key directions that help to refine clinical practice and guide future research.</p>","PeriodicalId":11012,"journal":{"name":"Current oncology","volume":"33 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2025-12-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12839805/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146050742","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-27DOI: 10.3390/curroncol33010014
Salih Karatlı, Doğan Yazılıtaş
Background: Febrile neutropenia (FN) is a serious chemotherapy-related complication in patients with solid tumors. Identifying simple and accessible biomarkers that can predict prolonged hospitalization may support early risk stratification and clinical decision-making.
Methods: This retrospective study included 169 adults hospitalized with FN between January 2023 and January 2025. Immunonutritional indices, including the Hemoglobin-Albumin-Lymphocyte-Platelet (HALP) score, the Prognostic Nutritional Index (PNI), and the C-reactive protein/albumin ratio (CAR), as well as the Clinical Index of Stable Febrile Neutropenia (CISNE) score were calculated. HALP and PNI were categorized using ROC-derived cut-offs based on the Youden Index. Prolonged hospital stay was defined as a binary variable based on the cohort median (>9 days). Spearman correlation, univariate and multivariate logistic regression were performed to identify predictors of prolonged hospitalization.
Results: HALP showed a significant negative correlation with hospitalization duration (r = -0.469; p < 0.001), as did serum albumin (r = -0.184; p = 0.017) and PNI (r = -0.273; p < 0.001). CAR (p = 0.617) and neutrophil count (p = 0.955) demonstrated no correlation. In univariate logistic regression, low HALP (p < 0.001), low PNI (p = 0.001), intermediate CISNE (p = 0.002), high CISNE (p < 0.001), microbiological culture positivity (p < 0.001), and sex (p = 0.015) were significantly associated with prolonged hospitalization. Age, comorbidity status, metastatic stage, and CAR were not significant. In the multivariate model, low HALP (p < 0.001), intermediate CISNE (p = 0.007), high CISNE (p < 0.001), and culture positivity (p < 0.001) remained independent predictors. PNI (p = 0.400) and sex (p = 0.176) did not retain significance.
Conclusions: A Low HALP score, higher CISNE risk categories, and microbiological culture positivity independently predicted prolonged hospitalization in FN. HALP, as a simple and inexpensive immunonutritional marker, may enhance early FN risk assessment when used alongside validated clinical tools such as CISNE or MASCC.
{"title":"Low HALP Score Predicts Prolonged Hospitalization in Solid Tumor Patients with Febrile Neutropenia.","authors":"Salih Karatlı, Doğan Yazılıtaş","doi":"10.3390/curroncol33010014","DOIUrl":"10.3390/curroncol33010014","url":null,"abstract":"<p><strong>Background: </strong>Febrile neutropenia (FN) is a serious chemotherapy-related complication in patients with solid tumors. Identifying simple and accessible biomarkers that can predict prolonged hospitalization may support early risk stratification and clinical decision-making.</p><p><strong>Methods: </strong>This retrospective study included 169 adults hospitalized with FN between January 2023 and January 2025. Immunonutritional indices, including the Hemoglobin-Albumin-Lymphocyte-Platelet (HALP) score, the Prognostic Nutritional Index (PNI), and the C-reactive protein/albumin ratio (CAR), as well as the Clinical Index of Stable Febrile Neutropenia (CISNE) score were calculated. HALP and PNI were categorized using ROC-derived cut-offs based on the Youden Index. Prolonged hospital stay was defined as a binary variable based on the cohort median (>9 days). Spearman correlation, univariate and multivariate logistic regression were performed to identify predictors of prolonged hospitalization.</p><p><strong>Results: </strong>HALP showed a significant negative correlation with hospitalization duration (r = -0.469; <i>p</i> < 0.001), as did serum albumin (r = -0.184; <i>p</i> = 0.017) and PNI (r = -0.273; <i>p</i> < 0.001). CAR (<i>p</i> = 0.617) and neutrophil count (<i>p</i> = 0.955) demonstrated no correlation. In univariate logistic regression, low HALP (<i>p</i> < 0.001), low PNI (<i>p</i> = 0.001), intermediate CISNE (<i>p</i> = 0.002), high CISNE (<i>p</i> < 0.001), microbiological culture positivity (<i>p</i> < 0.001), and sex (<i>p</i> = 0.015) were significantly associated with prolonged hospitalization. Age, comorbidity status, metastatic stage, and CAR were not significant. In the multivariate model, low HALP (<i>p</i> < 0.001), intermediate CISNE (<i>p</i> = 0.007), high CISNE (<i>p</i> < 0.001), and culture positivity (<i>p</i> < 0.001) remained independent predictors. PNI (<i>p</i> = 0.400) and sex (<i>p</i> = 0.176) did not retain significance.</p><p><strong>Conclusions: </strong>A Low HALP score, higher CISNE risk categories, and microbiological culture positivity independently predicted prolonged hospitalization in FN. HALP, as a simple and inexpensive immunonutritional marker, may enhance early FN risk assessment when used alongside validated clinical tools such as CISNE or MASCC.</p>","PeriodicalId":11012,"journal":{"name":"Current oncology","volume":"33 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2025-12-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12840241/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146050697","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-25DOI: 10.3390/curroncol33010013
Tianyi Zhou, Chaoliu Dai
Background: We aimed to evaluate ability of a novel scoring system that combines fluorodeoxyglucose-uptake parameters and systemic inflammatory response indicators to predict hepatocellular carcinoma (HCC) prognosis. Methods: Clinical data were collected from patients with HCC who underwent hepatectomy at our hospital in 2014-2022. The tumor-to-liver ratio (TLR) was adopted as a positron emission tomography/computed tomography (PET/CT) standardized uptake value (SUV)-related indicator and calculated as the ratio of the SUVmax of tumor tissue to the SUVmean of normal liver tissue. The patients' immune microenvironment reflected the NLR. Postoperative overall survival (OS)- and disease-free survival (DFS)-related independent prognostic factors were analyzed using Cox proportional hazards regression modeling. Results: Eighty-nine patients were included. TLR, NLR, and alpha-fetoprotein levels were independently associated with OS and DFS. The OS and DFS in the zero-point group were significantly longer than those in the one- and two-point groups. Time-dependent ROC curve analyses revealed area under the curve values of 0.830 and 0.752 for 5-year OS and DFS, respectively, for the scoring system, outperforming single evaluation indices. Conclusions: The proposed scoring system, which incorporates both TLR and NLR, simultaneously reflects metabolic tumor characteristics and the host's immune microenvironment, enabling more accurate patients with early to intermediate-stage HCC undergoing hepatectomy classification and better prognostic evaluation.
{"title":"Prognostic Value of the PET/CT-Derived Maximum Standardized Uptake Value Combined with the Neutrophil-Lymphocyte Ratio in Patients with Hepatocellular Carcinoma Undergoing Hepatectomy.","authors":"Tianyi Zhou, Chaoliu Dai","doi":"10.3390/curroncol33010013","DOIUrl":"10.3390/curroncol33010013","url":null,"abstract":"<p><p><b>Background:</b> We aimed to evaluate ability of a novel scoring system that combines fluorodeoxyglucose-uptake parameters and systemic inflammatory response indicators to predict hepatocellular carcinoma (HCC) prognosis. <b>Methods:</b> Clinical data were collected from patients with HCC who underwent hepatectomy at our hospital in 2014-2022. The tumor-to-liver ratio (TLR) was adopted as a positron emission tomography/computed tomography (PET/CT) standardized uptake value (SUV)-related indicator and calculated as the ratio of the SUV<sub>max</sub> of tumor tissue to the SUV<sub>mean</sub> of normal liver tissue. The patients' immune microenvironment reflected the NLR. Postoperative overall survival (OS)- and disease-free survival (DFS)-related independent prognostic factors were analyzed using Cox proportional hazards regression modeling. <b>Results:</b> Eighty-nine patients were included. TLR, NLR, and alpha-fetoprotein levels were independently associated with OS and DFS. The OS and DFS in the zero-point group were significantly longer than those in the one- and two-point groups. Time-dependent ROC curve analyses revealed area under the curve values of 0.830 and 0.752 for 5-year OS and DFS, respectively, for the scoring system, outperforming single evaluation indices. <b>Conclusions:</b> The proposed scoring system, which incorporates both TLR and NLR, simultaneously reflects metabolic tumor characteristics and the host's immune microenvironment, enabling more accurate patients with early to intermediate-stage HCC undergoing hepatectomy classification and better prognostic evaluation.</p>","PeriodicalId":11012,"journal":{"name":"Current oncology","volume":"33 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2025-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12840277/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146050759","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: In response to the growing emotional support needs of patients in oncology, peer support was introduced into clinical teams in Quebec, Canada, in 2018. These peers, called accompanying patients (APs), are former cancer patients who use their experiential knowledge to provide support to patients during their oncology journey. This paper aims to identify APs' perceptions of the program by including a diversity of perspectives. We include inexperienced and experienced APs, APs in different facilities, and APs in different cancer programs.
Methods: We conducted a qualitative study based on 12 semi-structured interviews of APs between June and August 2024 in Quebec, Canada. We explored four themes, building on the Practice Change Model for qualitative analysis: APs' sources of motivation, influences and environmental factors, resources available for AP integration, and the program's effects.
Results: 12 APs from 5 facilities participated in an interview. All the APs, both experienced and inexperienced, were highly motivated to participate in the program. Their motivations included a desire to give back to society, to help people and to give meaning to their illness. Both experienced and inexperienced APs were confident in their ability to accompany others. They were aware of their responsibilities and its limits regarding their role as an AP. They pointed out the program's positive impact on their own emotional well-being and that of the patients. The program also benefited the clinical team, by limiting unhelpful demands from patients and saving time for clinicians. However, experienced APs did not feel well integrated into the healthcare team.
Conclusions: We concluded that APs are highly motivated to be in the program. They perceived a need for the program in the current health system. They noted its beneficial effects on patients, on themselves, and on the clinical team. However, more resources need to be directed toward integrating APs into healthcare teams.
{"title":"Role, Resources, and Integration of Accompanying Patients in Oncology: A Qualitative Study from the Accompanying Patient's Perspective.","authors":"Sarit Kang-Auger, Margaux Deroi, Khaled Katergi, Soline Bernard, Monica Iliescu Nelea, Cécile Vialaron, Louise Normandin, Marie-Andrée Côté, Mado Desforges, Marie-Pascale Pomey","doi":"10.3390/curroncol33010011","DOIUrl":"10.3390/curroncol33010011","url":null,"abstract":"<p><strong>Background: </strong>In response to the growing emotional support needs of patients in oncology, peer support was introduced into clinical teams in Quebec, Canada, in 2018. These peers, called accompanying patients (APs), are former cancer patients who use their experiential knowledge to provide support to patients during their oncology journey. This paper aims to identify APs' perceptions of the program by including a diversity of perspectives. We include inexperienced and experienced APs, APs in different facilities, and APs in different cancer programs.</p><p><strong>Methods: </strong>We conducted a qualitative study based on 12 semi-structured interviews of APs between June and August 2024 in Quebec, Canada. We explored four themes, building on the Practice Change Model for qualitative analysis: APs' sources of motivation, influences and environmental factors, resources available for AP integration, and the program's effects.</p><p><strong>Results: </strong>12 APs from 5 facilities participated in an interview. All the APs, both experienced and inexperienced, were highly motivated to participate in the program. Their motivations included a desire to give back to society, to help people and to give meaning to their illness. Both experienced and inexperienced APs were confident in their ability to accompany others. They were aware of their responsibilities and its limits regarding their role as an AP. They pointed out the program's positive impact on their own emotional well-being and that of the patients. The program also benefited the clinical team, by limiting unhelpful demands from patients and saving time for clinicians. However, experienced APs did not feel well integrated into the healthcare team.</p><p><strong>Conclusions: </strong>We concluded that APs are highly motivated to be in the program. They perceived a need for the program in the current health system. They noted its beneficial effects on patients, on themselves, and on the clinical team. However, more resources need to be directed toward integrating APs into healthcare teams.</p>","PeriodicalId":11012,"journal":{"name":"Current oncology","volume":"33 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2025-12-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12840174/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146050693","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-24DOI: 10.3390/curroncol33010012
Abdullah M Alsoghier, Bader A Alwhaibi, Abdullah F Alnuwaybit, Simon N Rogers, Saif A Aljabab
Introduction: Head and neck cancer (HNC) treatments often lead to significant post-treatment side effects that affect patients' quality of life. This study aimed to translate and validate the post-treatment Patient Concerns Inventory for head and neck (PCI-HN) into Arabic among HNC survivors.
Methods: This study employed a cross-sectional design, where PCI-HN was translated and assessed for content and face validity by clinical experts and patients, respectively. Revisions to multiple items related to 'social and religious welfare'. Patients' responses were then analysed to assess internal consistency (Cronbach's alpha) and test-retest reliability (Cohen's Kappa).
Results: Thirty-eight participants (19 males, 19 females, mean age 50.68 ± 16.13 years) were included. The Arabic PCI-HN demonstrated good overall internal consistency (α = 0.723) but fair test-retest agreement (κ = 0.22), likely reflecting dynamic changes in HNC post-treatment experiences.
Conclusion: The Ar-PCI-HN can be a helpful instrument for capturing distinct aspects of the survivorship experience among Arabic-speaking HNC survivors. Determining the clinical interpretability and ability to detect changes over time requires further multi-centre and multi-country clinical studies. This would be necessary to ensure its integration into routine outpatient consultations for Arabic-speaking patients in Arab countries and globally.
{"title":"Patient Concerns Inventory for Arabic Patients with Head and Neck Cancer: A Cross-Cultural Adaptation and Preliminary Validation.","authors":"Abdullah M Alsoghier, Bader A Alwhaibi, Abdullah F Alnuwaybit, Simon N Rogers, Saif A Aljabab","doi":"10.3390/curroncol33010012","DOIUrl":"10.3390/curroncol33010012","url":null,"abstract":"<p><strong>Introduction: </strong>Head and neck cancer (HNC) treatments often lead to significant post-treatment side effects that affect patients' quality of life. This study aimed to translate and validate the post-treatment Patient Concerns Inventory for head and neck (PCI-HN) into Arabic among HNC survivors.</p><p><strong>Methods: </strong>This study employed a cross-sectional design, where PCI-HN was translated and assessed for content and face validity by clinical experts and patients, respectively. Revisions to multiple items related to 'social and religious welfare'. Patients' responses were then analysed to assess internal consistency (Cronbach's alpha) and test-retest reliability (Cohen's Kappa).</p><p><strong>Results: </strong>Thirty-eight participants (19 males, 19 females, mean age 50.68 ± 16.13 years) were included. The Arabic PCI-HN demonstrated good overall internal consistency (α = 0.723) but fair test-retest agreement (κ = 0.22), likely reflecting dynamic changes in HNC post-treatment experiences.</p><p><strong>Conclusion: </strong>The Ar-PCI-HN can be a helpful instrument for capturing distinct aspects of the survivorship experience among Arabic-speaking HNC survivors. Determining the clinical interpretability and ability to detect changes over time requires further multi-centre and multi-country clinical studies. This would be necessary to ensure its integration into routine outpatient consultations for Arabic-speaking patients in Arab countries and globally.</p>","PeriodicalId":11012,"journal":{"name":"Current oncology","volume":"33 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2025-12-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12839732/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146050671","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-24DOI: 10.3390/curroncol33010010
Sebastian Skoczylas, Tomasz Płoszaj, Izabela Dróżdż, Hanna Moczulska, Marcin Serafin, Katarzyna Piekarska, Olga Wojtyczka, Karolina Żeżawska, Agnieszka Zmysłowska
Background/objectives: Pathogenic and likely pathogenic variants in the BRCA1 and BRCA2 genes are associated with a significantly increased risk of breast and/or ovarian cancer. We investigated genetic variants in a cohort of 450 unaffected individuals with a family history of breast and/or ovarian cancer, involving at least one first-degree relative.
Methods: Next-generation sequencing (NGS) was used to analyze the coding regions of these two genes, with copy number variation (CNV) analysis.
Results: A total of 16 unique to our cohort variants classified as pathogenic or likely pathogenic were identified in 22 patients, including one novel loss-of-function variant in BRCA1 gene. Furthermore, we identified a deletion of exon 21 in the BRCA1 gene in two patients.
Conclusions: These results emphasize the difficulties involved in molecular diagnostics and indicate the need for further research into new predictive models for patients with hereditary breast and ovarian cancer.
{"title":"Germline <i>BRCA1/2</i> Variants in Polish Patients with Family History of Breast and Ovarian Cancer: Prevalence, CNV Detection, and Identification of a Novel Loss-of-Function Mutation.","authors":"Sebastian Skoczylas, Tomasz Płoszaj, Izabela Dróżdż, Hanna Moczulska, Marcin Serafin, Katarzyna Piekarska, Olga Wojtyczka, Karolina Żeżawska, Agnieszka Zmysłowska","doi":"10.3390/curroncol33010010","DOIUrl":"10.3390/curroncol33010010","url":null,"abstract":"<p><strong>Background/objectives: </strong>Pathogenic and likely pathogenic variants in the <i>BRCA1</i> and <i>BRCA2</i> genes are associated with a significantly increased risk of breast and/or ovarian cancer. We investigated genetic variants in a cohort of 450 unaffected individuals with a family history of breast and/or ovarian cancer, involving at least one first-degree relative.</p><p><strong>Methods: </strong>Next-generation sequencing (NGS) was used to analyze the coding regions of these two genes, with copy number variation (CNV) analysis.</p><p><strong>Results: </strong>A total of 16 unique to our cohort variants classified as pathogenic or likely pathogenic were identified in 22 patients, including one novel loss-of-function variant in <i>BRCA1</i> gene. Furthermore, we identified a deletion of exon 21 in the <i>BRCA1</i> gene in two patients.</p><p><strong>Conclusions: </strong>These results emphasize the difficulties involved in molecular diagnostics and indicate the need for further research into new predictive models for patients with hereditary breast and ovarian cancer.</p>","PeriodicalId":11012,"journal":{"name":"Current oncology","volume":"33 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2025-12-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12839688/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146050637","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-23DOI: 10.3390/curroncol33010008
Mary-Pat Schlosser, Lea Stelter, Mike Stelter
High-grade gliomas in children continue to have a dismal prognosis. This case is of a child with a diffuse pediatric-type high-grade glioma H3 and IDH-wildtype, treated with surgery, radiation, chemotherapy, and a targeted agent without success. Physician and family perspectives are also presented. Options for treatment and research participation are limited, but there is a strong desire from patients and families to access new treatment modalities and take part in clinical trials. Treating teams and families remain hopeful that in the future, tumours like the one described in this report will be treated with much greater success.
{"title":"Family and Physician Perspectives: Unassailable, a p53 and PIK3CA Mutant Glioblastoma in a Child.","authors":"Mary-Pat Schlosser, Lea Stelter, Mike Stelter","doi":"10.3390/curroncol33010008","DOIUrl":"10.3390/curroncol33010008","url":null,"abstract":"<p><p>High-grade gliomas in children continue to have a dismal prognosis. This case is of a child with a diffuse pediatric-type high-grade glioma H3 and IDH-wildtype, treated with surgery, radiation, chemotherapy, and a targeted agent without success. Physician and family perspectives are also presented. Options for treatment and research participation are limited, but there is a strong desire from patients and families to access new treatment modalities and take part in clinical trials. Treating teams and families remain hopeful that in the future, tumours like the one described in this report will be treated with much greater success.</p>","PeriodicalId":11012,"journal":{"name":"Current oncology","volume":"33 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2025-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12839620/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146050622","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-23DOI: 10.3390/curroncol33010009
Stephanie A Maier, Frédéric Barabé, Tobias Berg, Jonathan Bramson, Gwynivere A Davies, Mahmoud Elsawy, Alejandro Garcia-Horton, Alix Lapworth, Christopher Lemieux, Kylie Lepic, Kristjan Paulson, Michael Radford, Mégane Tanguay, Ram Vasudevan Nampoothiri, Darrell White, Charles Yin, Jonas Mattsson
On behalf of Cell Therapy Transplant Canada (CTTC), we are pleased to present the Abstracts of the CTTC 2024 Annual Conference. The conference was held on 1-3 May 2024 in beautiful Victoria, British Columbia, at the Victoria Conference Centre, and attracted 293 in-person delegates and five virtual attendees. Several plenary sessions were held on topics such as gene therapy for hemoglobin disorders, optimizing donor selection, graft-versus-host disease (GvHD) strategies, collaborative care, survivorship, graft failure, and CAR-T therapy. Poster authors presented their work during a lively and engaging networking reception on Thursday, 2 May, and oral abstract authors were featured during the oral abstract session in the afternoon of Friday, 3 May 2024. Forty-nine (49) abstracts were selected for presentation as posters and six (6) as oral presentations. Abstracts were submitted within four categories: (1) Basic/Translational Sciences, (2) Clinical Trials/Observations, (3) Laboratory/Quality, and (4) Pharmacy/Nursing/Other Transplant Support. The top six (6) abstract authors were invited to give an oral presentation, and the top four (4) poster abstracts were selected to receive an award. All of these were marked as "Award Recipient" within the relevant category. Three abstracts were determined by the peer review panel to be inappropriate for this conference and were not invited to present at the conference, and two authors withdrew their abstract; therefore, five abstract numbers are missing from the list. We congratulate all the 2024 abstract presenters on their research and contributions to the field.
{"title":"Abstracts of the Cell Therapy Transplant Canada 2024 Annual Conference.","authors":"Stephanie A Maier, Frédéric Barabé, Tobias Berg, Jonathan Bramson, Gwynivere A Davies, Mahmoud Elsawy, Alejandro Garcia-Horton, Alix Lapworth, Christopher Lemieux, Kylie Lepic, Kristjan Paulson, Michael Radford, Mégane Tanguay, Ram Vasudevan Nampoothiri, Darrell White, Charles Yin, Jonas Mattsson","doi":"10.3390/curroncol33010009","DOIUrl":"10.3390/curroncol33010009","url":null,"abstract":"<p><p>On behalf of Cell Therapy Transplant Canada (CTTC), we are pleased to present the Abstracts of the CTTC 2024 Annual Conference. The conference was held on 1-3 May 2024 in beautiful Victoria, British Columbia, at the Victoria Conference Centre, and attracted 293 in-person delegates and five virtual attendees. Several plenary sessions were held on topics such as gene therapy for hemoglobin disorders, optimizing donor selection, graft-versus-host disease (GvHD) strategies, collaborative care, survivorship, graft failure, and CAR-T therapy. Poster authors presented their work during a lively and engaging networking reception on Thursday, 2 May, and oral abstract authors were featured during the oral abstract session in the afternoon of Friday, 3 May 2024. Forty-nine (49) abstracts were selected for presentation as posters and six (6) as oral presentations. Abstracts were submitted within four categories: (1) Basic/Translational Sciences, (2) Clinical Trials/Observations, (3) Laboratory/Quality, and (4) Pharmacy/Nursing/Other Transplant Support. The top six (6) abstract authors were invited to give an oral presentation, and the top four (4) poster abstracts were selected to receive an award. All of these were marked as \"Award Recipient\" within the relevant category. Three abstracts were determined by the peer review panel to be inappropriate for this conference and were not invited to present at the conference, and two authors withdrew their abstract; therefore, five abstract numbers are missing from the list. We congratulate all the 2024 abstract presenters on their research and contributions to the field.</p>","PeriodicalId":11012,"journal":{"name":"Current oncology","volume":"33 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2025-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12839565/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146050617","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-22DOI: 10.3390/curroncol33010007
Linda E Carlson, Harriet Richardson, Ron Shore, Christopher P Albertyn, Lynda G Balneaves, Alan Bates, Margot Burnell, Harvey Max Chochinov, David Clements, Julie Deleemans, Hilary Horlock, Jean Mathews, Michael McKenzie, Chantal Savard, Claudio N Soares, Wei Tu, Monnica Williams
The CAnadian Network for Psychedelic-Assisted Cancer Therapy (CAN-PACT) was launched in 2025 to address urgent gaps in supportive care for Canadians with cancer experiencing demoralization syndrome (loss of meaning, dysphoria, disheartenment, helplessness, a sense of failure) and related psychosocial distress. CAN-PACT has six major objectives: (1) to develop a national interdisciplinary research and practice network; (2) to set research priorities through structured stakeholder engagement; (3) to develop and provide PAT training and education for clinicians, researchers, and patients; (4) to pilot test the feasibility of intervention and assessment procedures; (5) to conduct a multi-center, randomized controlled trial of PAT for people with advanced cancer; and (6) to inform and influence healthcare policy on PAT in Canada. We discuss the background and need for PAT in cancer, describe challenges currently limiting its use, and outline CAN-PACT's strategy for building capacity, generating Canadian evidence, and preparing the oncology healthcare environment for potential implementation. This manuscript presents a summary overview of CAN-PACT as a multi-objective research program; detailed protocols for each discrete study component will be published separately as the research program progresses. Through environmental scans, national engagement, targeted training, rigorous research, and ongoing collaboration with policymakers, CAN-PACT aims to enable equitable access to safe, evidence-based PAT for people with advanced cancer in Canada's publicly funded cancer centers.
{"title":"The CAnadian Network for Psychedelic-Assisted Cancer Therapy (CAN-PACT): A Multi-Phase Program Overview.","authors":"Linda E Carlson, Harriet Richardson, Ron Shore, Christopher P Albertyn, Lynda G Balneaves, Alan Bates, Margot Burnell, Harvey Max Chochinov, David Clements, Julie Deleemans, Hilary Horlock, Jean Mathews, Michael McKenzie, Chantal Savard, Claudio N Soares, Wei Tu, Monnica Williams","doi":"10.3390/curroncol33010007","DOIUrl":"10.3390/curroncol33010007","url":null,"abstract":"<p><p>The CAnadian Network for Psychedelic-Assisted Cancer Therapy (CAN-PACT) was launched in 2025 to address urgent gaps in supportive care for Canadians with cancer experiencing demoralization syndrome (loss of meaning, dysphoria, disheartenment, helplessness, a sense of failure) and related psychosocial distress. CAN-PACT has six major objectives: (1) to develop a national interdisciplinary research and practice network; (2) to set research priorities through structured stakeholder engagement; (3) to develop and provide PAT training and education for clinicians, researchers, and patients; (4) to pilot test the feasibility of intervention and assessment procedures; (5) to conduct a multi-center, randomized controlled trial of PAT for people with advanced cancer; and (6) to inform and influence healthcare policy on PAT in Canada. We discuss the background and need for PAT in cancer, describe challenges currently limiting its use, and outline CAN-PACT's strategy for building capacity, generating Canadian evidence, and preparing the oncology healthcare environment for potential implementation. This manuscript presents a summary overview of CAN-PACT as a multi-objective research program; detailed protocols for each discrete study component will be published separately as the research program progresses. Through environmental scans, national engagement, targeted training, rigorous research, and ongoing collaboration with policymakers, CAN-PACT aims to enable equitable access to safe, evidence-based PAT for people with advanced cancer in Canada's publicly funded cancer centers.</p>","PeriodicalId":11012,"journal":{"name":"Current oncology","volume":"33 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2025-12-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12840114/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146050677","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-21DOI: 10.3390/curroncol33010006
Youzhao Ma, Yan Yang, Mingda Zhu, Yue Yu, Xin Wang
Purpose: This study investigates receptor status changes following neoadjuvant chemotherapy (NAC) in breast cancer, aiming to identify new therapeutic opportunities and improve human epidermal growth factor receptor 2 (HER2) detection and categorization methods. Methods: This retrospective analysis was conducted on patients with breast cancer who underwent NAC and surgery between July 2022 and June 2024. Chi-square tests and logistic regression models were applied to assess the associations between HER2 status changes and clinicopathological features. Results: Among 508 patients, the receptor discordance rates after NAC were 5.3% for estrogen receptor (ER), 21.3% for progesterone receptor (PR), and 43.7% for HER2. Ki-67 expression decreased in 64.6% of cases and increased in 6.8%. Of the 103 patients with HER2-0, 47 (45.6%) transitioned to IHC 1+, 9 (8.7%) to IHC 2+/ISH-, and 1 (1.0%) to IHC 2+/ISH+. Among 256 patients with HER2 IHC 1+, 58 (22.7%) transitioned to IHC 2+/ISH-, 36 (14.1%) to IHC 0, and 9 (3.5%) to IHC 2+/ISH+. For 149 patients with HER2 IHC 2+/ISH-, 50 (33.6%) transitioned to IHC 1+, 6 (4.0%) to IHC 2+/ISH+, 5 (3.4%) to IHC 0, and 1 (0.7%) to IHC 3+. Univariate analysis revealed that, when compared to grade III tumors, grade I-II tumors exhibited a higher rate of HER2-0 to HER2-low conversion (66.7% vs. 36.8%, p = 0.027). HER2-low to HER2-0 conversion was associated with ER negativity (p = 0.028), PR negativity (p = 0.021), HER2 IHC 1+ (vs. IHC 2+, p = 0.001), and TIL >10% (p = 0.049). Multivariate analysis revealed that tumors with HER2 IHC 1+ were more likely to convert to HER2-0 after NAC than those with HER2 IHC 2+ (p = 0.020). Conclusions: Following NAC, ER gain, PR loss, and Ki-67 reduction were common. HER2 and ER status changes predominantly occurred within adjacent expression intensity levels.
{"title":"Changes in HER2, ER, PR, and Ki-67 in HER2-Negative Breast Cancer After Neoadjuvant Chemotherapy: A Case-Control Study.","authors":"Youzhao Ma, Yan Yang, Mingda Zhu, Yue Yu, Xin Wang","doi":"10.3390/curroncol33010006","DOIUrl":"10.3390/curroncol33010006","url":null,"abstract":"<p><p><b>Purpose</b>: This study investigates receptor status changes following neoadjuvant chemotherapy (NAC) in breast cancer, aiming to identify new therapeutic opportunities and improve human epidermal growth factor receptor 2 (HER2) detection and categorization methods. <b>Methods</b>: This retrospective analysis was conducted on patients with breast cancer who underwent NAC and surgery between July 2022 and June 2024. Chi-square tests and logistic regression models were applied to assess the associations between HER2 status changes and clinicopathological features. <b>Results</b>: Among 508 patients, the receptor discordance rates after NAC were 5.3% for estrogen receptor (ER), 21.3% for progesterone receptor (PR), and 43.7% for HER2. Ki-67 expression decreased in 64.6% of cases and increased in 6.8%. Of the 103 patients with HER2-0, 47 (45.6%) transitioned to IHC 1+, 9 (8.7%) to IHC 2+/ISH-, and 1 (1.0%) to IHC 2+/ISH+. Among 256 patients with HER2 IHC 1+, 58 (22.7%) transitioned to IHC 2+/ISH-, 36 (14.1%) to IHC 0, and 9 (3.5%) to IHC 2+/ISH+. For 149 patients with HER2 IHC 2+/ISH-, 50 (33.6%) transitioned to IHC 1+, 6 (4.0%) to IHC 2+/ISH+, 5 (3.4%) to IHC 0, and 1 (0.7%) to IHC 3+. Univariate analysis revealed that, when compared to grade III tumors, grade I-II tumors exhibited a higher rate of HER2-0 to HER2-low conversion (66.7% vs. 36.8%, <i>p</i> = 0.027). HER2-low to HER2-0 conversion was associated with ER negativity (<i>p</i> = 0.028), PR negativity (<i>p</i> = 0.021), HER2 IHC 1+ (vs. IHC 2+, <i>p</i> = 0.001), and TIL >10% (<i>p</i> = 0.049). Multivariate analysis revealed that tumors with HER2 IHC 1+ were more likely to convert to HER2-0 after NAC than those with HER2 IHC 2+ (<i>p</i> = 0.020). <b>Conclusions</b>: Following NAC, ER gain, PR loss, and Ki-67 reduction were common. HER2 and ER status changes predominantly occurred within adjacent expression intensity levels.</p>","PeriodicalId":11012,"journal":{"name":"Current oncology","volume":"33 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2025-12-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12840446/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146050591","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}