Pub Date : 2025-01-01Epub Date: 2024-12-16DOI: 10.1016/j.bulcan.2024.12.001
Stéphane Vignot, Audrey Bellesoeur, Carole Bouleuc, Romain Cohen, Baudouin Courtier, Carolyne Crozier, Alexandre De Nonneville, Frédéric Delom, Serge Evrard, Nelly Firmin, Virginie Gandemer, Mohamed Khettab, Nicolas Magné, Daniel Orbach, Isabelle Pellier, Manuel Rodrigues, Marie Wislez, Jacques-Olivier Bay
The editorial board of the Bulletin du cancer has compiled a summary of the news from 2024 in oncology, based on the main results presented at international congresses or published over the past year. After a year marked by the success of the Olympic Games, the selection of data is presented and discussed in podiums of three main results by topic. Emphasis is placed on studies that have an immediate impact on practice and on data that raise important questions for the year 2025.
《癌症公报》(Bulletin du Cancer)编辑委员会根据过去一年在国际会议上发表或发表的主要结果,汇编了2024年肿瘤学领域的新闻摘要。在奥运会成功举办的一年之后,数据的选择被提出并按主题在三个主要结果的领奖台上进行讨论。重点放在对实践有直接影响的研究和对2025年提出重要问题的数据上。
{"title":"[A 2024 inventory in oncology news].","authors":"Stéphane Vignot, Audrey Bellesoeur, Carole Bouleuc, Romain Cohen, Baudouin Courtier, Carolyne Crozier, Alexandre De Nonneville, Frédéric Delom, Serge Evrard, Nelly Firmin, Virginie Gandemer, Mohamed Khettab, Nicolas Magné, Daniel Orbach, Isabelle Pellier, Manuel Rodrigues, Marie Wislez, Jacques-Olivier Bay","doi":"10.1016/j.bulcan.2024.12.001","DOIUrl":"10.1016/j.bulcan.2024.12.001","url":null,"abstract":"<p><p>The editorial board of the Bulletin du cancer has compiled a summary of the news from 2024 in oncology, based on the main results presented at international congresses or published over the past year. After a year marked by the success of the Olympic Games, the selection of data is presented and discussed in podiums of three main results by topic. Emphasis is placed on studies that have an immediate impact on practice and on data that raise important questions for the year 2025.</p>","PeriodicalId":93917,"journal":{"name":"Bulletin du cancer","volume":" ","pages":"19-34"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142848632","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 : 2025-01-01Epub Date: 2024-10-09DOI: 10.1016/j.bulcan.2024.08.008
Frédérique Pénault-Llorca, Clarisse Audigier-Valette, Pierre-Jean Lamy, Dominique Stoppa Lyonnet, Philippe Camparo, Sophie Beaupère, Xavier Troussard, Laure Gueroult Accolas, Gérard Raymond, Alexandre Auday, Jean-Yves Blay, François Sarkozy
The prognostic of certain cancers improved significantly in recent years thanks not only to the launch of innovative treatments but also to progress made in the diagnostic field. Thus, next-generation sequencing (NGS) became paramount to help characterizing tumors and selecting the most pertinent treatments. The survey conducted by a multi stakeholder committee, at the end of 2022, with 103 actors of the management of cancer patients (public and private centers, labs, prescribers, biologists, pathologists, direction) confirmed the heterogeneity of use of NGS tests across France due to, mainly, the lack of systematic reimbursement of related costs. Référentiel des actes innovants hors nomenclature de biologie (RIHN) covers, in a delayed and partial way, only half of costs engaged by centers. Only those with a critical mass of patients or with a sufficient funding capacity can guarantee an access to large panels. Postponing the initiation of a required treatment represents a risk of loss of opportunity for patients who cannot benefit of this technology. NGS large panels tests, an efficiency lever for cancer treatment, must be part of the care toolbox. Those with a demonstration of value created should nowadays be fully reimbursed by collectivity after HAS' evaluation, for a fair access throughout the territory. Precision diagnostic can open the way to a more personalized and efficient medicine.
近年来,某些癌症的预后明显改善,这不仅得益于创新疗法的推出,还得益于诊断领域的进步。因此,下一代测序(NGS)在帮助确定肿瘤特征和选择最合适的治疗方法方面变得至关重要。2022 年底,一个多方利益相关者委员会对 103 名癌症患者管理参与者(公立和私立中心、实验室、处方者、生物学家、病理学家、指导者)进行了调查,证实了 NGS 测试在法国各地使用的不一致性,主要原因是缺乏系统的相关费用报销。Référentiel des actes innovants hors nomenclature de biologie(RIHN)以一种延迟和部分的方式,只报销了各中心一半的费用。只有那些拥有足够数量患者或资金充足的中心才能保证获得大样本。对于无法受益于这项技术的患者来说,推迟开始所需的治疗意味着丧失机会的风险。NGS 大样本检测是癌症治疗的高效杠杆,必须成为治疗工具箱的一部分。如今,经过 HAS 评估后,那些能够证明创造了价值的检测项目应由集体全额报销,以便在全国范围内公平使用。精准诊断可以为更个性化、更高效的医疗开辟道路。
{"title":"[Precision medicine in oncology: A reality… without equity].","authors":"Frédérique Pénault-Llorca, Clarisse Audigier-Valette, Pierre-Jean Lamy, Dominique Stoppa Lyonnet, Philippe Camparo, Sophie Beaupère, Xavier Troussard, Laure Gueroult Accolas, Gérard Raymond, Alexandre Auday, Jean-Yves Blay, François Sarkozy","doi":"10.1016/j.bulcan.2024.08.008","DOIUrl":"10.1016/j.bulcan.2024.08.008","url":null,"abstract":"<p><p>The prognostic of certain cancers improved significantly in recent years thanks not only to the launch of innovative treatments but also to progress made in the diagnostic field. Thus, next-generation sequencing (NGS) became paramount to help characterizing tumors and selecting the most pertinent treatments. The survey conducted by a multi stakeholder committee, at the end of 2022, with 103 actors of the management of cancer patients (public and private centers, labs, prescribers, biologists, pathologists, direction) confirmed the heterogeneity of use of NGS tests across France due to, mainly, the lack of systematic reimbursement of related costs. Référentiel des actes innovants hors nomenclature de biologie (RIHN) covers, in a delayed and partial way, only half of costs engaged by centers. Only those with a critical mass of patients or with a sufficient funding capacity can guarantee an access to large panels. Postponing the initiation of a required treatment represents a risk of loss of opportunity for patients who cannot benefit of this technology. NGS large panels tests, an efficiency lever for cancer treatment, must be part of the care toolbox. Those with a demonstration of value created should nowadays be fully reimbursed by collectivity after HAS' evaluation, for a fair access throughout the territory. Precision diagnostic can open the way to a more personalized and efficient medicine.</p>","PeriodicalId":93917,"journal":{"name":"Bulletin du cancer","volume":" ","pages":"15-18"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142395943","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 : 2025-01-01Epub Date: 2024-09-02DOI: 10.1016/j.bulcan.2024.07.008
Nabil Yafour, Mohamed Amine Bekadja, Ibtissam El Bejjaj, Jean El-Cheikh, Maria El Kababri, Léonardo Magro, Fati Hamzy
Management of acquired aplastic anemia (AA) in emerging countries depends on the means of prognostic stratification, treatment and logistics available. During the 13th annual harmonization workshop of the francophone Society of bone marrow transplantation and cellular therapy (SFGM-TC), a designated working group reviewed the literature in order to elaborate unified guidelines for allogeneic hematopoietic cell transplantation (Allo-HCT) in this disease. In terms of practice, the conclusions are as follows; The use of anti-tymocyte globuline (ATG) is mainly from rabbit and very little from horse. Access to bone marrow graft, total body irradiation, and the international unrelated donor registries is limited, which justifies the use of peripheral blood stem cells, chemotherapy-based conditioning, and related alternative donor. The workshop recommends matched sibling allo-HCT in all patients aged less than 40 years with acquired severe or very severe AA. For patients aged over than 40 years, or who lack an HLA-identical donor, treatment with the combination of cyclosporin, horse ATG, eltrombopag or cyclosporine, eltrombopag is recommended. If horse ATG and eltrombopag are not available, matched sibling allo-HCT may be indicated as first-line therapy in patients aged between 40-60 years, and good performance status. Although, in patients who have failed immunosuppressive treatments and thrombopoietin agonists, and in the absence of HLA-matched donor, a haplo-identical allo-HCT with modified Baltimore conditioning is recommended.
{"title":"[Acquired severe aplastic anemia in emerging countries: Management from allogeneic hematopoietic cell transplantation indication until post-transplant follow-up SFGM-TC].","authors":"Nabil Yafour, Mohamed Amine Bekadja, Ibtissam El Bejjaj, Jean El-Cheikh, Maria El Kababri, Léonardo Magro, Fati Hamzy","doi":"10.1016/j.bulcan.2024.07.008","DOIUrl":"10.1016/j.bulcan.2024.07.008","url":null,"abstract":"<p><p>Management of acquired aplastic anemia (AA) in emerging countries depends on the means of prognostic stratification, treatment and logistics available. During the 13th annual harmonization workshop of the francophone Society of bone marrow transplantation and cellular therapy (SFGM-TC), a designated working group reviewed the literature in order to elaborate unified guidelines for allogeneic hematopoietic cell transplantation (Allo-HCT) in this disease. In terms of practice, the conclusions are as follows; The use of anti-tymocyte globuline (ATG) is mainly from rabbit and very little from horse. Access to bone marrow graft, total body irradiation, and the international unrelated donor registries is limited, which justifies the use of peripheral blood stem cells, chemotherapy-based conditioning, and related alternative donor. The workshop recommends matched sibling allo-HCT in all patients aged less than 40 years with acquired severe or very severe AA. For patients aged over than 40 years, or who lack an HLA-identical donor, treatment with the combination of cyclosporin, horse ATG, eltrombopag or cyclosporine, eltrombopag is recommended. If horse ATG and eltrombopag are not available, matched sibling allo-HCT may be indicated as first-line therapy in patients aged between 40-60 years, and good performance status. Although, in patients who have failed immunosuppressive treatments and thrombopoietin agonists, and in the absence of HLA-matched donor, a haplo-identical allo-HCT with modified Baltimore conditioning is recommended.</p>","PeriodicalId":93917,"journal":{"name":"Bulletin du cancer","volume":" ","pages":"S10-S23"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142127651","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}
The advanced practice nurse (APN) has been introduced in France, following the 2016 health law and implementing decrees published in 2018. In this context, the French Society for Bone Marrow Transplantation and Cellular Therapy (SFGM-TC) has already issued guidelines regarding the allocation of APNs' new clinical competences and their collaboration with physicians. It is now providing new recommendations on the transversal activities that can be fulfilled by APNs, such as research, leadership, training and teaching. Additionally, the guidelines outline how APNs can cooperate with other professionals in departments of haematology and cellular therapy, including nurses, coordinators and health managers.
{"title":"[Clinical and transversal competencies of advanced practice nurses (APNs) within a cellular therapy team (SFGM-TC)].","authors":"Thomas Jezequel, Rezarta Ajazi Hub, Caroline Bompoint, Céline Chauvel, Elodie Colonnese, Coralie Corbineau, Claire Desmedt, Céline Kicki, Sandra Lomazzi, Anne Sirvent, Solène Evard, Karine Roux, Léonardo Magro, Fabienne Colledani","doi":"10.1016/j.bulcan.2024.06.002","DOIUrl":"10.1016/j.bulcan.2024.06.002","url":null,"abstract":"<p><p>The advanced practice nurse (APN) has been introduced in France, following the 2016 health law and implementing decrees published in 2018. In this context, the French Society for Bone Marrow Transplantation and Cellular Therapy (SFGM-TC) has already issued guidelines regarding the allocation of APNs' new clinical competences and their collaboration with physicians. It is now providing new recommendations on the transversal activities that can be fulfilled by APNs, such as research, leadership, training and teaching. Additionally, the guidelines outline how APNs can cooperate with other professionals in departments of haematology and cellular therapy, including nurses, coordinators and health managers.</p>","PeriodicalId":93917,"journal":{"name":"Bulletin du cancer","volume":" ","pages":"S92-S102"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142147115","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 : 2025-01-01Epub Date: 2024-12-09DOI: 10.1016/j.bulcan.2024.11.003
Clara Helal, Stéphane Vignot
{"title":"[Selpercatinib in advanced solid tumors with RET fusion, in the absence of therapeutic alternatives].","authors":"Clara Helal, Stéphane Vignot","doi":"10.1016/j.bulcan.2024.11.003","DOIUrl":"10.1016/j.bulcan.2024.11.003","url":null,"abstract":"","PeriodicalId":93917,"journal":{"name":"Bulletin du cancer","volume":" ","pages":"8-10"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142808677","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 : 2025-01-01Epub Date: 2024-11-18DOI: 10.1016/j.bulcan.2024.10.009
Dong Oh Moon
In the evolving landscape of cancer research, the identification of key molecular players that contribute to the disease's progression and resistance against treatments has become paramount. Among these, Maternal Embryonic Leucine Zipper Kinase (MELK) has emerged as a critical regulator of cancer cell proliferation, survival, and therapy evasion. Concurrently, the significance of non-coding RNAs (ncRNAs), including microRNAs (miRNAs) and long non-coding RNAs (lncRNAs), in modulating gene expression and cancer phenotypes has been increasingly recognized. Given the pivotal roles both MELK and ncRNAs play within cancer biology, investigating their interactions presents a compelling new frontier for therapeutic innovation. This exploration not only promises to enhance our understanding of cancer's molecular underpinnings but also opens up avenues for developing novel targeted interventions. The rationale behind focusing on MELK-ncRNA crosstalk lies in the potential to disrupt these critical molecular interactions, thereby offering a novel strategy to counteract cancer progression and improve treatment outcomes.
{"title":"The role of MELK in cancer and its interactions with non-coding RNAs: Implications for therapeutic strategies.","authors":"Dong Oh Moon","doi":"10.1016/j.bulcan.2024.10.009","DOIUrl":"10.1016/j.bulcan.2024.10.009","url":null,"abstract":"<p><p>In the evolving landscape of cancer research, the identification of key molecular players that contribute to the disease's progression and resistance against treatments has become paramount. Among these, Maternal Embryonic Leucine Zipper Kinase (MELK) has emerged as a critical regulator of cancer cell proliferation, survival, and therapy evasion. Concurrently, the significance of non-coding RNAs (ncRNAs), including microRNAs (miRNAs) and long non-coding RNAs (lncRNAs), in modulating gene expression and cancer phenotypes has been increasingly recognized. Given the pivotal roles both MELK and ncRNAs play within cancer biology, investigating their interactions presents a compelling new frontier for therapeutic innovation. This exploration not only promises to enhance our understanding of cancer's molecular underpinnings but also opens up avenues for developing novel targeted interventions. The rationale behind focusing on MELK-ncRNA crosstalk lies in the potential to disrupt these critical molecular interactions, thereby offering a novel strategy to counteract cancer progression and improve treatment outcomes.</p>","PeriodicalId":93917,"journal":{"name":"Bulletin du cancer","volume":" ","pages":"35-53"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142677991","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 : 2025-01-01Epub Date: 2024-09-03DOI: 10.1016/j.bulcan.2024.05.008
Stéphane Oudard, Marc-Olivier Timsit, Denis Maillet, Guillaume Mouillet, Luca Campedel, Émeline Colomba, Louis Marie Dourthe, Jean-Christophe Eymard, Aurélien Gobert, Claire Jamet, Charlotte Joly, Camille Serrate, Guillaume Ploussard
Castration-resistant metastatic prostate cancer remains lethal and a therapeutic challenge. Current strategies are geared towards the personalization of treatments based on the identification of relevant molecular targets, including genomic alterations involved in tumoral processes. Among these novel targeted therapies, poly-ADP-ribose polymerase inhibitors (PARPi), by blocking the action of enzymes involved in deoxyribonucleic acid (DNA) repair, induce the destruction of cells carrying defects in homologous recombination repair, often associated with alterations in genes involved in this mechanism. Thus, determining the presence of a molecular anomaly, particularly alterations in the BRCA1/2 genes, is a prerequisite for initiating PARPi monotherapy. In patients with metastatic castration-resistant prostate cancer , around 20-30 % carry this type of mutation. In this population, single-agent studies have demonstrated PARPi ability to prolong overall survival, and to improve symptom control, including pain. Other studies are underway to assess their effectiveness in combination with other therapies, and it already appears that association with new-generation hormone therapy can further prolong radiological progression-free survival, regardless of the mutation status of the genes involved in DNA repair, indicating a synergistic action between PARPi and new-generation hormone therapy.
{"title":"[Metastatic castration-resistant prostate cancer and PARP inhibitors: From tumor genomics to new therapeutic combinations].","authors":"Stéphane Oudard, Marc-Olivier Timsit, Denis Maillet, Guillaume Mouillet, Luca Campedel, Émeline Colomba, Louis Marie Dourthe, Jean-Christophe Eymard, Aurélien Gobert, Claire Jamet, Charlotte Joly, Camille Serrate, Guillaume Ploussard","doi":"10.1016/j.bulcan.2024.05.008","DOIUrl":"10.1016/j.bulcan.2024.05.008","url":null,"abstract":"<p><p>Castration-resistant metastatic prostate cancer remains lethal and a therapeutic challenge. Current strategies are geared towards the personalization of treatments based on the identification of relevant molecular targets, including genomic alterations involved in tumoral processes. Among these novel targeted therapies, poly-ADP-ribose polymerase inhibitors (PARPi), by blocking the action of enzymes involved in deoxyribonucleic acid (DNA) repair, induce the destruction of cells carrying defects in homologous recombination repair, often associated with alterations in genes involved in this mechanism. Thus, determining the presence of a molecular anomaly, particularly alterations in the BRCA1/2 genes, is a prerequisite for initiating PARPi monotherapy. In patients with metastatic castration-resistant prostate cancer , around 20-30 % carry this type of mutation. In this population, single-agent studies have demonstrated PARPi ability to prolong overall survival, and to improve symptom control, including pain. Other studies are underway to assess their effectiveness in combination with other therapies, and it already appears that association with new-generation hormone therapy can further prolong radiological progression-free survival, regardless of the mutation status of the genes involved in DNA repair, indicating a synergistic action between PARPi and new-generation hormone therapy.</p>","PeriodicalId":93917,"journal":{"name":"Bulletin du cancer","volume":" ","pages":"61-81"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142134770","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 : 2025-01-01Epub Date: 2024-11-16DOI: 10.1016/j.bulcan.2024.10.007
Alexandre Olivier, Clémence Basse
{"title":"[Tislelizumab as monotherapy or in combination with chemotherapy in locally advanced or metastatic non-small cell lung cancer].","authors":"Alexandre Olivier, Clémence Basse","doi":"10.1016/j.bulcan.2024.10.007","DOIUrl":"10.1016/j.bulcan.2024.10.007","url":null,"abstract":"","PeriodicalId":93917,"journal":{"name":"Bulletin du cancer","volume":" ","pages":"6-8"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142649595","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 : 2025-01-01Epub Date: 2024-12-17DOI: 10.1016/j.bulcan.2024.12.002
Hervé Maisonneuve
With the advent of the author-pays business model replacing subscription, mercantile publishers have created journals. They respond to the dissatisfaction of naive researchers faced with the difficulties of publishing quickly and widely. These publishers favour commercial interests over knowledge and do not respect good publication practices. The network of science academies and UNESCO distinguish three groups of publishers: fraudulent (predatory journals), of poor quality (journals of complacency that are not to be recommended) and of good quality (legitimate journals). Good and bad articles can be found in all journals. Quality journals have created special issues with rapid reviews to remain competitive. The proliferation of these journals is a source of misinformation. Paper mills are commercial scientific writing and communication companies that sell articles to researchers in order to put their name among the authors. There are social networks accounts to promote these articles and sell the authors' positions. Review and citation mills are also scams. Five factors have influenced these abuses: the monetisation of research results; the value of publishing a lot; the shortcomings of peer review; the lack of international certification of scientific journals; and artificial intelligence with its best and worst. The system can continue as long as there are satisfied researchers and institutional leaders do nothing. Fortunately, awareness is growing, but we are all waiting for our neighbours to change their practices.
{"title":"[Predatory journals and paper mills jeopardise knowledge management].","authors":"Hervé Maisonneuve","doi":"10.1016/j.bulcan.2024.12.002","DOIUrl":"10.1016/j.bulcan.2024.12.002","url":null,"abstract":"<p><p>With the advent of the author-pays business model replacing subscription, mercantile publishers have created journals. They respond to the dissatisfaction of naive researchers faced with the difficulties of publishing quickly and widely. These publishers favour commercial interests over knowledge and do not respect good publication practices. The network of science academies and UNESCO distinguish three groups of publishers: fraudulent (predatory journals), of poor quality (journals of complacency that are not to be recommended) and of good quality (legitimate journals). Good and bad articles can be found in all journals. Quality journals have created special issues with rapid reviews to remain competitive. The proliferation of these journals is a source of misinformation. Paper mills are commercial scientific writing and communication companies that sell articles to researchers in order to put their name among the authors. There are social networks accounts to promote these articles and sell the authors' positions. Review and citation mills are also scams. Five factors have influenced these abuses: the monetisation of research results; the value of publishing a lot; the shortcomings of peer review; the lack of international certification of scientific journals; and artificial intelligence with its best and worst. The system can continue as long as there are satisfied researchers and institutional leaders do nothing. Fortunately, awareness is growing, but we are all waiting for our neighbours to change their practices.</p>","PeriodicalId":93917,"journal":{"name":"Bulletin du cancer","volume":" ","pages":"100-110"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142857320","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}