Shan Gao , Yu-tong Wang , Guang-yu Ma , Min-qiu Lu , Bin Chu , Lei Shi , Li-juan Fang , Qiu-qing Xiang , Yue-hua Ding , Li Bao
{"title":"Solitary bone plasmacytoma: Long-term clinical outcomes in a single center","authors":"Shan Gao , Yu-tong Wang , Guang-yu Ma , Min-qiu Lu , Bin Chu , Lei Shi , Li-juan Fang , Qiu-qing Xiang , Yue-hua Ding , Li Bao","doi":"10.1016/j.currproblcancer.2024.101095","DOIUrl":"https://doi.org/10.1016/j.currproblcancer.2024.101095","url":null,"abstract":"<div><h3>Background</h3><p>A solitary plasmacytoma is classified into a solitary plasmacytoma of the bone (SBP) and a solitary extramedullary (soft tissue mass) plasmacytoma, based on the site of the lesion. Despite the high local control rate with radiotherapy, approximately half of patients’ conditions progress to multiple myeloma (MM) within 3–5 years after diagnosis, with SBP having a worse prognosis.</p></div><div><h3>Patients and methods</h3><p>We retrospectively assessed the treatment and outcomes of patients with SBP in a hospital in China from 2008 to 2021. Twenty-four patients treated over 13 years with SBP were enrolled in this retrospective study.</p></div><div><h3>Results</h3><p>The most common sites for SBP were the axial skeleton and femur. The M protein was detected in 11 patients (46 %), of which 8 (33 %) had light chains, 2 (8 %) had immunoglobulin G kappa and 1 (4 %) had immunoglobulin D kappa. Flow cytometry revealed that 5 patients (21 %) had minimal bone marrow involvement. The treatment included chemotherapy, surgery, and radiotherapy in 18 (75 %), 12 (50 %), and 9 (38 %) patients, respectively, of whom 13 (54 %) received combined treatment. Over a median follow-up period of 67.2 months, 9 patients (38 %) developed MM in a median time of 101.5 months. The 5- and 10-year progression-free survival rates were 67.3 % and 37.4 %, respectively. One patient died due to pneumonia without progression and the other died due to relapse.</p></div><div><h3>Conclusion</h3><p>This study confirmed the high rate of progression of SBP to MM, indicating a need for adjunct chemotherapy for the management of SBP.</p></div>","PeriodicalId":55193,"journal":{"name":"Current Problems in Cancer","volume":"50 ","pages":"Article 101095"},"PeriodicalIF":2.6,"publicationDate":"2024-04-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140535547","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Current management of uncommon EGFR mutations in non-small cell lung cancer","authors":"Jonathan Q. Trinh , Omar Abughanimeh","doi":"10.1016/j.currproblcancer.2024.101064","DOIUrl":"10.1016/j.currproblcancer.2024.101064","url":null,"abstract":"<div><p>Epidermal growth factor receptor (EGFR) mutations are frequently implicated in non-small cell lung cancer (NSCLC). Though these typically involve exon 19 in-frame deletions or L858R mutations in exon 21, uncommon EGFR mutations comprise 10-15 % of all EGFR mutations. These most frequently include G719X mutations in exon 18, L861Q mutations in exon 21, S768I mutations in exon 20, and in-frame insertions and/or duplications in exon 20. It is crucial to understand these distinct variants and their specific responses to active treatment options to optimize care. In this review, we discuss these uncommon mutations in depth and dissect the current literature regarding their treatment outcomes and subsequent evidence-based management guidelines.</p></div>","PeriodicalId":55193,"journal":{"name":"Current Problems in Cancer","volume":"49 ","pages":"Article 101064"},"PeriodicalIF":2.6,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139667882","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Kavitha Munuswamy Selvaraj , Sumathy Gnanagurusubbiah , Reena Roy Roby Roy , Jasmine Hephzipah John peter , Sarala Balu
{"title":"Enhancing skin lesion classification with advanced deep learning ensemble models: a path towards accurate medical diagnostics","authors":"Kavitha Munuswamy Selvaraj , Sumathy Gnanagurusubbiah , Reena Roy Roby Roy , Jasmine Hephzipah John peter , Sarala Balu","doi":"10.1016/j.currproblcancer.2024.101077","DOIUrl":"10.1016/j.currproblcancer.2024.101077","url":null,"abstract":"<div><p>Skin cancer, including the highly lethal malignant melanoma, poses a significant global health challenge with a rising incidence rate. Early detection plays a pivotal role in improving survival rates. This study aims to develop an advanced deep learning-based approach for accurate skin lesion classification, addressing challenges such as limited data availability, class imbalance, and noise. Modern deep neural network designs, such as ResNeXt101, SeResNeXt101, ResNet152V2, DenseNet201, GoogLeNet, and Xception, which are used in the study and ze optimised using the SGD technique. The dataset comprises diverse skin lesion images from the HAM10000 and ISIC datasets. Noise and artifacts are tackled using image inpainting, and data augmentation techniques enhance training sample diversity. The ensemble technique is utilized, creating both average and weighted average ensemble models. Grid search optimizes model weight distribution. The individual models exhibit varying performance, with metrics including recall, precision, F1 score, and MCC. The \"Average ensemble model\" achieves harmonious balance, emphasizing precision, F1 score, and recall, yielding high performance. The \"Weighted ensemble model\" capitalizes on individual models' strengths, showcasing heightened precision and MCC, yielding outstanding performance. The ensemble models consistently outperform individual models, with the average ensemble model attaining a macro-average ROC-AUC score of 96 % and the weighted ensemble model achieving a macro-average ROC-AUC score of 97 %. This research demonstrates the efficacy of ensemble techniques in significantly improving skin lesion classification accuracy. By harnessing the strengths of individual models and addressing their limitations, the ensemble models exhibit robust and reliable performance across various metrics. The findings underscore the potential of ensemble techniques in enhancing medical diagnostics and contributing to improved patient outcomes in skin lesion diagnosis.</p></div>","PeriodicalId":55193,"journal":{"name":"Current Problems in Cancer","volume":"49 ","pages":"Article 101077"},"PeriodicalIF":2.6,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140121460","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Gabriel Cavalcante Lima Chagas , Amanda Ribeiro Rangel , Badi El Osta
{"title":"MET alterations in advanced non-small cell lung cancer","authors":"Gabriel Cavalcante Lima Chagas , Amanda Ribeiro Rangel , Badi El Osta","doi":"10.1016/j.currproblcancer.2024.101075","DOIUrl":"10.1016/j.currproblcancer.2024.101075","url":null,"abstract":"<div><p>Precision medicine has helped identify several tumor molecular aberrations to be treated with targeted therapies. These therapies showed substantial improvement in efficacy without excessive toxicity in patients with specific oncogenic drivers with advanced cancers. In metastatic lung cancers, the implementation of broad platforms for molecular tumor sequencing has helped oncology providers identify oncogenic drivers linked with better outcomes when treated upfront with targeted therapies. Mesenchymal-epithelial transition factor (<em>MET</em>) alterations are present in up to 60% of non-small cell lung cancer and are associated with a poor prognosis. Capmatinib and tepotinib are currently the only two approved targeted therapies by the U.S. Food and Drug Administration (FDA) for patients with <em>MET exon 14 skipping</em> mutation. Several agents are being developed to tackle an unmet need in patients with <em>MET</em> alterations. Some of these agents are being used in combination with <em>EGFR</em> targeted therapy to mitigate resistance to <em>EGFR</em> inhibitor. These agents are poised to provide new hope for these patients.</p></div>","PeriodicalId":55193,"journal":{"name":"Current Problems in Cancer","volume":"49 ","pages":"Article 101075"},"PeriodicalIF":2.6,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140121461","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Familial and Social Implications of Breast and Gynaecological cancer in Kerala, India","authors":"Lorane Scaria , Saju Madavanakadu Devassy , Lynette Joubert","doi":"10.1016/j.currproblcancer.2024.101080","DOIUrl":"10.1016/j.currproblcancer.2024.101080","url":null,"abstract":"<div><h3>Background</h3><p>Due to the paucity of reliable data to determine the components of family-based comprehensive care for cancer in India, we explored the familial implications of gynaecological and breast cancer diagnosis and treatment through a mixed-method study.</p></div><div><h3>Methods</h3><p>The mixed method study included 130 women aged above 18 with a confirmed diagnosis of gynaecological or breast cancer recruited from three selected tertiary hospitals in Kerala, India. Information on quality of life (36-Item Short Form Survey (SF-36)), psychological distress (distress thermometer), and the familial, interpersonal, social, and community impacts of cancer (semi-structured interview guide) were elicited. Linear regression was used to identify the factors associated with distress and the factors were explored further using thematic analysis.</p></div><div><h3>Results</h3><p>Patients included in the study (n = 130; mean age 57.5 years) had moderate or mild (66.9%) to severe (25.4%) distress. Concerns about work (93%), difficulty in; home care and housing (82%), care for dependents (65%), unempathetic family (87.6%), isolation (70%), and body image (65%) were major reasons for their distress. Physiological, social, and family-related stressors among the respondents included challenges in physical functioning, intense physical symptoms like fatigue, loss of appetite and sleep, role restrictions, alterations in family responsibilities, functional dependency, inadequate family support, challenges in social and interpersonal interactions, and an unsupportive work environment.</p></div><div><h3>Conclusion</h3><p>Cancer is a health crisis that involves psychological, social, and economic distress, compelling professionals to design multifaceted individualized care packages rather than only concentrating on medical management to alleviate their distress.</p></div>","PeriodicalId":55193,"journal":{"name":"Current Problems in Cancer","volume":"49 ","pages":"Article 101080"},"PeriodicalIF":2.6,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140137439","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Information for Readers","authors":"","doi":"10.1016/S0147-0272(24)00025-4","DOIUrl":"https://doi.org/10.1016/S0147-0272(24)00025-4","url":null,"abstract":"","PeriodicalId":55193,"journal":{"name":"Current Problems in Cancer","volume":"49 ","pages":"Article 101084"},"PeriodicalIF":2.6,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140645835","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Megan Rutherford , Margaret Wheless , Katharine Thomas , Robert A. Ramirez
{"title":"Current and emerging strategies for the management of advanced/metastatic lung neuroendocrine tumors","authors":"Megan Rutherford , Margaret Wheless , Katharine Thomas , Robert A. Ramirez","doi":"10.1016/j.currproblcancer.2024.101061","DOIUrl":"10.1016/j.currproblcancer.2024.101061","url":null,"abstract":"<div><p><span><span><span>Pulmonary neuroendocrine tumors<span> represent a spectrum of disease ranging from typical carcinoid tumors to </span></span>small cell lung cancers<span><span>. The incidence of low-grade pulmonary NETs has been increasing, leading to improved awareness and the need for more treatment options for this rare cancer. </span>Somatostatin analogs continue to be the </span></span>backbone<span><span><span> of therapy and may be followed or accompanied by targeted therapy, chemotherapy, and </span>immune therapy. The recent addition of </span>peptide receptor<span> radionuclide therapy (PRRT) to the treatment armamentarium of NETs has led to the development of targeted alpha therapy to overcome PRRT resistance and minimize off-target adverse effects. Herein, we aim to highlight current treatment options for patients with advanced low grade pulmonary NETs along with emerging therapies, sequencing of therapies, upcoming </span></span></span>clinical trials, and the importance of a multidisciplinary team to improve patient outcomes.</p></div>","PeriodicalId":55193,"journal":{"name":"Current Problems in Cancer","volume":"49 ","pages":"Article 101061"},"PeriodicalIF":2.6,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139572217","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Targeting RET alterations in non-small cell lung cancer","authors":"Go Nishikawa , Mark A. Klein","doi":"10.1016/j.currproblcancer.2024.101074","DOIUrl":"10.1016/j.currproblcancer.2024.101074","url":null,"abstract":"<div><p>Rearranged during transfection (RET) alterations, which lead to aberrant activation of the <em>RET</em> proto-oncogene, have been identified in various cancers. In non-small cell lung cancer (NSCLC), <em>RET</em> mutations often manifest as <em>RET</em> fusion genes and are observed in 1–2 % of patients with NSCLC. In recent years, selective RET inhibitors such as selpercatinib and pralsetinib, approved by the Food and Drug Administration (FDA) in 2020, have been part of the revolutionary changes in the treatment landscape for non-small cell lung cancer. While first-generation RET inhibitors have become part of the standard of care for <em>RET</em>-fusion positive NSCLC, a new challenge has emerged: acquired resistance to RET inhibitors. RET resistance is a complex phenomenon that can manifest as either on-target or off-target resistance. Numerous studies have been conducted to identify the mechanisms behind this resistance. This review provides an overview of the biology of <em>RET</em> in NSCLC, methods of <em>RET</em> testing, and a comprehensive analysis of the clinical outcomes associated with multikinase and selective RET inhibitors for NSCLC. Additionally, we will explore future perspectives for <em>RET</em> fusion-positive NSCLC, including ongoing trials and the challenges involved in overcoming resistance to RET inhibitors.</p></div>","PeriodicalId":55193,"journal":{"name":"Current Problems in Cancer","volume":"49 ","pages":"Article 101074"},"PeriodicalIF":2.6,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140144722","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}