Pub Date : 2024-12-01Epub Date: 2024-11-08DOI: 10.1016/j.bulcan.2024.09.006
Dominique Levêque
{"title":"Discrepancy in withdrawn accelerated approvals of anticancer agents in the United States (US) and Europe: Approval does not mean access.","authors":"Dominique Levêque","doi":"10.1016/j.bulcan.2024.09.006","DOIUrl":"10.1016/j.bulcan.2024.09.006","url":null,"abstract":"","PeriodicalId":93917,"journal":{"name":"Bulletin du cancer","volume":" ","pages":"1154-1155"},"PeriodicalIF":0.0,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142634495","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 : 2024-12-01Epub Date: 2024-10-10DOI: 10.1016/j.bulcan.2024.08.009
Clara Tasseau, Claire Gallois
{"title":"[Trifluridine-tipiracil plus bevacizumab in refractory metastatic colorectal cancer].","authors":"Clara Tasseau, Claire Gallois","doi":"10.1016/j.bulcan.2024.08.009","DOIUrl":"10.1016/j.bulcan.2024.08.009","url":null,"abstract":"","PeriodicalId":93917,"journal":{"name":"Bulletin du cancer","volume":" ","pages":"1087-1088"},"PeriodicalIF":0.0,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142402333","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 : 2024-12-01Epub Date: 2024-10-07DOI: 10.1016/j.bulcan.2024.08.014
Noémie Drappier, Thomas Pierret
{"title":"[Amivantamab with chemotherapy - Non-small cell lung cancer with EGFR exon 20 insertions].","authors":"Noémie Drappier, Thomas Pierret","doi":"10.1016/j.bulcan.2024.08.014","DOIUrl":"10.1016/j.bulcan.2024.08.014","url":null,"abstract":"","PeriodicalId":93917,"journal":{"name":"Bulletin du cancer","volume":" ","pages":"1085-1087"},"PeriodicalIF":0.0,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142397007","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 : 2024-12-01Epub Date: 2024-10-24DOI: 10.1016/j.bulcan.2024.08.018
Chloé Chatelet, Stanislas Quesada
{"title":"[Fruquintinib for patients with metastatic colorectal cancer previously treated with standard treatments].","authors":"Chloé Chatelet, Stanislas Quesada","doi":"10.1016/j.bulcan.2024.08.018","DOIUrl":"10.1016/j.bulcan.2024.08.018","url":null,"abstract":"","PeriodicalId":93917,"journal":{"name":"Bulletin du cancer","volume":" ","pages":"1084-1085"},"PeriodicalIF":0.0,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142514600","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 : 2024-12-01Epub Date: 2024-11-07DOI: 10.1016/j.bulcan.2024.10.002
Élise Chartier, Dauphine D'Andigné, Marie-Hélène Ducoin, Pénélope Fay, Adrien Calmus, Armel Reffet, Jean Michel Peloni, Maguelonne De La Hautière, François Blot, Julie Pouget
{"title":"[Onco-palliative ecotone: More than \"supportive care\", a frontier rich in diversity for holistic medicine and rational humanism].","authors":"Élise Chartier, Dauphine D'Andigné, Marie-Hélène Ducoin, Pénélope Fay, Adrien Calmus, Armel Reffet, Jean Michel Peloni, Maguelonne De La Hautière, François Blot, Julie Pouget","doi":"10.1016/j.bulcan.2024.10.002","DOIUrl":"10.1016/j.bulcan.2024.10.002","url":null,"abstract":"","PeriodicalId":93917,"journal":{"name":"Bulletin du cancer","volume":" ","pages":"1089-1094"},"PeriodicalIF":0.0,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142607676","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}
Purpose: This study aims to evaluate the efficacy and safety of combining androgen deprivation therapy (ADT) with stereotactic body radiation therapy (SBRT) in the treatment of localized prostate cancer.
Methods: A retrospective analysis was conducted on 30 patients treated with SBRT for localized prostate cancer at Cheikh Khalifa Hospital between 2017 and 2022. All patients presented with intermediate prognostic risk prostate cancer, as classified by the D'Amico criteria. Each patient received a total dose of 36.25Gy in five fractions using the TrueBeam STX system, along with six months of ADT. Patient outcomes were assessed based on relapse-free survival, biochemical recurrence, overall survival, and adverse effects, including gastrointestinal (GI) and genitourinary (GU) toxicities. Quality of life was evaluated using the EPIC-26 questionnaire.
Results: Over a median follow-up period of 33months, the relapse-free survival rate was 96.7%, with a biochemical recurrence rate of 3.3%. The overall survival rate at four years was 100%. Acute GI toxicities were minimal and transient, while GU toxicities were primarily grades 1 and 2, with no grade 3 or higher events reported. Erectile dysfunction was noted in 87% of patients. Quality of life assessments indicated low levels of urinary and bowel side effects but moderate impact on sexual function.
Conclusion: These findings suggest that the combination of ADT with SBRT approach offers favorable relapse-free and overall survival rates with manageable toxicity profiles. Further long-term studies are needed to confirm these results and better understand the impact on patient quality of life.
{"title":"Efficiency and safety of androgen deprivation therapy combined with stereotactic body radiation therapy for localized prostate cancer: A Moroccan experience.","authors":"Fadila Kouhen, Malak Chahid, Hanae El Gouache, Othmane Kaanouch, Abdeljalil Heddat, Younes Houry, Abdelhak Maghous","doi":"10.1016/j.bulcan.2024.10.004","DOIUrl":"10.1016/j.bulcan.2024.10.004","url":null,"abstract":"<p><strong>Purpose: </strong>This study aims to evaluate the efficacy and safety of combining androgen deprivation therapy (ADT) with stereotactic body radiation therapy (SBRT) in the treatment of localized prostate cancer.</p><p><strong>Methods: </strong>A retrospective analysis was conducted on 30 patients treated with SBRT for localized prostate cancer at Cheikh Khalifa Hospital between 2017 and 2022. All patients presented with intermediate prognostic risk prostate cancer, as classified by the D'Amico criteria. Each patient received a total dose of 36.25Gy in five fractions using the TrueBeam STX system, along with six months of ADT. Patient outcomes were assessed based on relapse-free survival, biochemical recurrence, overall survival, and adverse effects, including gastrointestinal (GI) and genitourinary (GU) toxicities. Quality of life was evaluated using the EPIC-26 questionnaire.</p><p><strong>Results: </strong>Over a median follow-up period of 33months, the relapse-free survival rate was 96.7%, with a biochemical recurrence rate of 3.3%. The overall survival rate at four years was 100%. Acute GI toxicities were minimal and transient, while GU toxicities were primarily grades 1 and 2, with no grade 3 or higher events reported. Erectile dysfunction was noted in 87% of patients. Quality of life assessments indicated low levels of urinary and bowel side effects but moderate impact on sexual function.</p><p><strong>Conclusion: </strong>These findings suggest that the combination of ADT with SBRT approach offers favorable relapse-free and overall survival rates with manageable toxicity profiles. Further long-term studies are needed to confirm these results and better understand the impact on patient quality of life.</p>","PeriodicalId":93917,"journal":{"name":"Bulletin du cancer","volume":" ","pages":"1102-1110"},"PeriodicalIF":0.0,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142607687","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}
{"title":"[Preventing the risks of interaction between cancer treatments and complementary care strategies].","authors":"Grégory Ninot, Dominique Granier, Caroline Perrier, Fanny Leenhardt, Jean-Luc Faillie, Pierre Senesse","doi":"10.1016/j.bulcan.2024.10.008","DOIUrl":"10.1016/j.bulcan.2024.10.008","url":null,"abstract":"","PeriodicalId":93917,"journal":{"name":"Bulletin du cancer","volume":" ","pages":"1155-1157"},"PeriodicalIF":0.0,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142645330","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}
Therapies targeting HER2 and immune checkpoint inhibitors have improved survival in patients with metastatic gastric or gastro-oesophageal junction adenocarcinoma, but the prognosis associated with these cancers remains poor. Claudin 18.2 is a tight junction protein expressed in the oeso-gastric mucosa. Some gastric and gastro-oesophageal junction adenocarcinoma overexpress this protein, as well as some pancreatic, ovarian and pulmonary cancers. In pathological context, its epitope may be exposed at the surface of cells and therefore makes it an interesting therapeutic target. Zolbetuximab, a monoclonal antibody targeting claudin 18.2, showed a survival benefit in first line metastatic treatment in patients with claudin 18.2 positive gastric and gastro-oesophageal junction adénocarcinoma, in two phase III studies. CAR T-cells specifically targeting this protein have also shown promising efficacy from the second line of treatment. Considering the probable impact of the expression status of claudin 18.2 in future treatment algorithms, this review aims to present the pathophysiology underlying the targeting of claudin 18.2, summarize state of the art results of anti-claudin 18.2 therapies and discuss future challenges for the management of patients with claudin 18.2 positive gastric and gastro-oesophageal junction adenocarcinoma.
针对HER2和免疫检查点抑制剂的疗法提高了转移性胃癌或胃食管交界腺癌患者的生存率,但这些癌症的预后仍然很差。Claudin 18.2 是一种在卵巢-胃黏膜中表达的紧密连接蛋白。一些胃癌和胃食管交界处腺癌以及一些胰腺癌、卵巢癌和肺癌会过表达这种蛋白。在病理情况下,它的表位可能暴露在细胞表面,因此成为一个有趣的治疗靶点。唑贝妥昔单抗(Zolbetuximab)是一种靶向claudin 18.2的单克隆抗体,在两项III期研究中显示,claudin 18.2阳性的胃癌和胃食管交界腺癌患者在一线转移性治疗中的生存率有所提高。在二线治疗中,特异性靶向该蛋白的 CAR T 细胞也显示出了良好的疗效。考虑到Claudin 18.2的表达状态可能会对未来的治疗算法产生影响,本综述旨在介绍靶向Claudin 18.2的病理生理学基础,总结抗Claudin 18.2疗法的最新成果,并讨论未来治疗Claudin 18.2阳性胃癌和胃食管交界腺癌患者所面临的挑战。
{"title":"[Claudine 18.2: A new therapeutic target in digestive cancers].","authors":"Laure Blondet, Baptiste Cervantes, Florence Renaud, Romain Cohen, Thierry André, Thomas Samaille","doi":"10.1016/j.bulcan.2024.10.006","DOIUrl":"10.1016/j.bulcan.2024.10.006","url":null,"abstract":"<p><p>Therapies targeting HER2 and immune checkpoint inhibitors have improved survival in patients with metastatic gastric or gastro-oesophageal junction adenocarcinoma, but the prognosis associated with these cancers remains poor. Claudin 18.2 is a tight junction protein expressed in the oeso-gastric mucosa. Some gastric and gastro-oesophageal junction adenocarcinoma overexpress this protein, as well as some pancreatic, ovarian and pulmonary cancers. In pathological context, its epitope may be exposed at the surface of cells and therefore makes it an interesting therapeutic target. Zolbetuximab, a monoclonal antibody targeting claudin 18.2, showed a survival benefit in first line metastatic treatment in patients with claudin 18.2 positive gastric and gastro-oesophageal junction adénocarcinoma, in two phase III studies. CAR T-cells specifically targeting this protein have also shown promising efficacy from the second line of treatment. Considering the probable impact of the expression status of claudin 18.2 in future treatment algorithms, this review aims to present the pathophysiology underlying the targeting of claudin 18.2, summarize state of the art results of anti-claudin 18.2 therapies and discuss future challenges for the management of patients with claudin 18.2 positive gastric and gastro-oesophageal junction adenocarcinoma.</p>","PeriodicalId":93917,"journal":{"name":"Bulletin du cancer","volume":" ","pages":"1133-1141"},"PeriodicalIF":0.0,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142634503","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 : 2024-12-01Epub Date: 2024-11-07DOI: 10.1016/j.bulcan.2024.09.007
Jennifer Cautela, Carolyne Croizier, Luca Inchiappa, Trecy Goncalves, Nicolas Stocker, Emmanuelle Tchernonog
The covalent Bruton tyrosine kinase inhibitors (iBTKs) have profoundly transformed the management of B-cell lymphoid malignancies, particularly chronic lymphocytic leukemia (CLL). These targeted therapies, with ibrutinib as the pioneer, have paved the way for significant improvement in the prognosis of many patients. With second-generation iBTKs such as acalabrutinib and zanubrutinib, the therapeutic landscape has expanded, offering potential new options for patients with CLL. This review focuses on the cardiovascular adverse effects associated with these treatments. It delves into the underlying pathophysiological mechanisms of these effects, highlighting the complex interactions between these molecules and the cardiovascular system. Additionally, it examines the frequency of adverse effects according to the type of iBTK, drawing on data from clinical trials and real-world clinical practice. Finally, the importance of close cardio-oncological monitoring is emphasized, with essential collaboration between hematologists and cardiologists. Strategies for screening and managing cardiovascular adverse effects are also discussed, emphasizing the need for a proactive approach in managing these complications. Experts propose a pragmatic follow-up of these patients, through a central illustration and a figure adapted from European cardio-oncology guidelines, to simplify hematologists' practice.
{"title":"[Cardiovascular adverse effects of Bruton tyrosine kinase inhibitors: Pathophysiological mechanisms, screening, and management].","authors":"Jennifer Cautela, Carolyne Croizier, Luca Inchiappa, Trecy Goncalves, Nicolas Stocker, Emmanuelle Tchernonog","doi":"10.1016/j.bulcan.2024.09.007","DOIUrl":"10.1016/j.bulcan.2024.09.007","url":null,"abstract":"<p><p>The covalent Bruton tyrosine kinase inhibitors (iBTKs) have profoundly transformed the management of B-cell lymphoid malignancies, particularly chronic lymphocytic leukemia (CLL). These targeted therapies, with ibrutinib as the pioneer, have paved the way for significant improvement in the prognosis of many patients. With second-generation iBTKs such as acalabrutinib and zanubrutinib, the therapeutic landscape has expanded, offering potential new options for patients with CLL. This review focuses on the cardiovascular adverse effects associated with these treatments. It delves into the underlying pathophysiological mechanisms of these effects, highlighting the complex interactions between these molecules and the cardiovascular system. Additionally, it examines the frequency of adverse effects according to the type of iBTK, drawing on data from clinical trials and real-world clinical practice. Finally, the importance of close cardio-oncological monitoring is emphasized, with essential collaboration between hematologists and cardiologists. Strategies for screening and managing cardiovascular adverse effects are also discussed, emphasizing the need for a proactive approach in managing these complications. Experts propose a pragmatic follow-up of these patients, through a central illustration and a figure adapted from European cardio-oncology guidelines, to simplify hematologists' practice.</p>","PeriodicalId":93917,"journal":{"name":"Bulletin du cancer","volume":" ","pages":"1142-1153"},"PeriodicalIF":0.0,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142634465","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 : 2024-12-01Epub Date: 2024-11-12DOI: 10.1016/j.bulcan.2024.10.005
Kylian Masse, Jean-François Huon, Pierre Chapron, Pierre Nizet
Introduction: The care of cancer patients involves a large number of healthcare professionals. Communication at the transition points between healthcare establishments and primary care providers needs to be improved. The aim of this study is to evaluate the satisfaction of community pharmacists regarding the transmission of the discharge letter when their patient is discharged from an oncology ward.
Methods: The patients included were those discharged from hospital with one or more changes in treatment during their hospitalization in the Multidisciplinary Medial Oncology Unit of the University Hospital Center of Nantes and who returned home. From April 1, 2023 to December 1, 2023, a seventeen-question questionnaire was e-mailed to the community pharmacists of the patients included in the study.
Results: Forty-eight patients benefited from medication reconciliation at discharge. Thirty-eight pharmacists (79%) responded to the questionnaire. Of the 35 pharmacists that indicated they had received the discharge letter, 32 found it useful (42.9%) or very useful (48.6%), and were in favor of receiving it via e-mail (97.2%). For 94.3% of pharmacists, the document provided sufficient information.
Discussion: Transmitting the discharge letter to dispensing pharmacists would seem to be an interesting option for fostering the city-hospital link. Its presentation and content seemed to meet the expectations of community pharmacists. The pharmacists felt that the continuity of care was important for ensuring their patient's care, but that it required improvement.
{"title":"[Implementation and evaluation satisfaction of the city-hospital link in a medical oncology department of a university hospital: An observational prospective study].","authors":"Kylian Masse, Jean-François Huon, Pierre Chapron, Pierre Nizet","doi":"10.1016/j.bulcan.2024.10.005","DOIUrl":"10.1016/j.bulcan.2024.10.005","url":null,"abstract":"<p><strong>Introduction: </strong>The care of cancer patients involves a large number of healthcare professionals. Communication at the transition points between healthcare establishments and primary care providers needs to be improved. The aim of this study is to evaluate the satisfaction of community pharmacists regarding the transmission of the discharge letter when their patient is discharged from an oncology ward.</p><p><strong>Methods: </strong>The patients included were those discharged from hospital with one or more changes in treatment during their hospitalization in the Multidisciplinary Medial Oncology Unit of the University Hospital Center of Nantes and who returned home. From April 1, 2023 to December 1, 2023, a seventeen-question questionnaire was e-mailed to the community pharmacists of the patients included in the study.</p><p><strong>Results: </strong>Forty-eight patients benefited from medication reconciliation at discharge. Thirty-eight pharmacists (79%) responded to the questionnaire. Of the 35 pharmacists that indicated they had received the discharge letter, 32 found it useful (42.9%) or very useful (48.6%), and were in favor of receiving it via e-mail (97.2%). For 94.3% of pharmacists, the document provided sufficient information.</p><p><strong>Discussion: </strong>Transmitting the discharge letter to dispensing pharmacists would seem to be an interesting option for fostering the city-hospital link. Its presentation and content seemed to meet the expectations of community pharmacists. The pharmacists felt that the continuity of care was important for ensuring their patient's care, but that it required improvement.</p>","PeriodicalId":93917,"journal":{"name":"Bulletin du cancer","volume":" ","pages":"1122-1132"},"PeriodicalIF":0.0,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142634443","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}