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The Current Role of Human Papillomavirus Circulating Tumor DNA in Oropharynx Cancer. 人乳头瘤病毒循环肿瘤DNA在口咽癌症中的作用。
IF 2.2 4区 医学
Cancer journal Pub Date : 2023-07-01 DOI: 10.1097/PPO.0000000000000667
Samuel N Regan, Michelle L Mierzwa
{"title":"The Current Role of Human Papillomavirus Circulating Tumor DNA in Oropharynx Cancer.","authors":"Samuel N Regan,&nbsp;Michelle L Mierzwa","doi":"10.1097/PPO.0000000000000667","DOIUrl":"10.1097/PPO.0000000000000667","url":null,"abstract":"<p><strong>Abstract: </strong>Human papillomavirus infection is currently implicated in the majority of oropharyngeal squamous cell carcinoma cases diagnosed in the United States. Circulating tumor DNA (ctDNA) has emerged as a potential biomarker for human papillomavirus-related oropharyngeal squamous cell carcinoma and has the opportunity to improve the diagnosis, treatment, and surveillance of patients with this disease. Changes in ctDNA levels during and after primary therapy may be related to disease response, which can possibly have implications for treatment intensification or de-escalation strategies. Further, ctDNA seems to be sensitive and specific for disease recurrence and may improve upon current methods for assessing both treatment response and failure. In this review, we examine the relevant literature on the use of ctDNA for oropharyngeal cancer treatment and surveillance and discuss current limitations and future directions for this promising biomarker.</p>","PeriodicalId":9655,"journal":{"name":"Cancer journal","volume":"29 4","pages":"226-229"},"PeriodicalIF":2.2,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9835654","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}
引用次数: 0
Is Apparent Diffusion Coefficient Established as an Imaging Biomarker for Stereotactic Body Radiation Therapy Assessment in Hepatocellular Carcinoma? 表观扩散系数是否被确定为肝细胞癌立体定向放射治疗评估的成像生物标志物?
IF 2.2 4区 医学
Cancer journal Pub Date : 2023-07-01 DOI: 10.1097/PPO.0000000000000668
Yue Cao, Kyle C Cuneo, Joseph Evans, Randall K Ten Haken, Daniel T Chang, Theodore S Lawrence
{"title":"Is Apparent Diffusion Coefficient Established as an Imaging Biomarker for Stereotactic Body Radiation Therapy Assessment in Hepatocellular Carcinoma?","authors":"Yue Cao, Kyle C Cuneo, Joseph Evans, Randall K Ten Haken, Daniel T Chang, Theodore S Lawrence","doi":"10.1097/PPO.0000000000000668","DOIUrl":"10.1097/PPO.0000000000000668","url":null,"abstract":"<p><strong>Abstract: </strong>In this article, as part of this special issue on biomarkers of early response, we review currently available reports regarding magnetic resonance imaging apparent diffusion coefficient (ADC) changes in hepatocellular carcinoma (HCC) in response to stereotactic body radiation therapy. We compare diffusion image acquisition, ADC analysis, methods for HCC response assessment, and statistical methods for prediction of local tumor progression by ADC metrics. We discuss the pros and cons of these studies. Following detailed analyses of existing investigations, we cannot conclude that ADC is established as an imaging biomarker for stereotactic body radiation therapy assessment in HCC.</p>","PeriodicalId":9655,"journal":{"name":"Cancer journal","volume":"29 4","pages":"238-242"},"PeriodicalIF":2.2,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10372684/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9881984","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}
引用次数: 0
Recent Advances in Blood-Based Liquid Biopsy Approaches in Prostate Cancer. 癌症前列腺血液液体活检方法的最新进展。
IF 2.2 4区 医学
Cancer journal Pub Date : 2023-07-01 DOI: 10.1097/PPO.0000000000000672
Andi K Cani, Simpa S Salami
{"title":"Recent Advances in Blood-Based Liquid Biopsy Approaches in Prostate Cancer.","authors":"Andi K Cani, Simpa S Salami","doi":"10.1097/PPO.0000000000000672","DOIUrl":"10.1097/PPO.0000000000000672","url":null,"abstract":"<p><strong>Abstract: </strong>The advent of high-throughput technologies has enabled the analysis of minute amounts of tumor-derived material purified from body fluids, termed \"liquid biopsies.\" Prostate cancer (PCa) management, like in many other cancer types, has benefited from liquid biopsies at several stages of the disease. Although initially describing circulating tumor cells in blood, the term \"liquid biopsy\" has come to more prominently include cell-free, circulating tumor DNA, as well as RNA, proteins, and other molecules. They provide tumor molecular information representing the entire, often-heterogeneous disease, relatively noninvasively and longitudinally. Blood has been the main liquid biopsy specimen in PCa, and urine has also proven beneficial. Technological advances have allowed clinical implementation of some liquid biopsies in PCa, in disease monitoring and precision oncology. This narrative review introduces the main types of blood-based PCa liquid biopsies focusing on advances in the past 5 years. Clinical adoption of liquid biopsies to detect and monitor the evolving PCa tumor biology promises to deepen our understanding of the disease and improve patient outcomes.</p>","PeriodicalId":9655,"journal":{"name":"Cancer journal","volume":"29 4","pages":"220-225"},"PeriodicalIF":2.2,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10372784/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10262144","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}
引用次数: 0
The Utility of Interim Positron Emission Tomography Imaging to Inform Adaptive Radiotherapy for Head and Neck Squamous Cell Carcinoma. 中期正电子发射断层成像在头颈部鳞状细胞癌适应性放射治疗中的应用。
IF 2.2 4区 医学
Cancer journal Pub Date : 2023-07-01 DOI: 10.1097/PPO.0000000000000669
Benjamin S Rosen, Neil Vaishampayan, Yue Cao, Michelle L Mierzwa
{"title":"The Utility of Interim Positron Emission Tomography Imaging to Inform Adaptive Radiotherapy for Head and Neck Squamous Cell Carcinoma.","authors":"Benjamin S Rosen,&nbsp;Neil Vaishampayan,&nbsp;Yue Cao,&nbsp;Michelle L Mierzwa","doi":"10.1097/PPO.0000000000000669","DOIUrl":"10.1097/PPO.0000000000000669","url":null,"abstract":"<p><strong>Abstract: </strong>In this article, as part of this special issue on biomarkers of early response, we review the current evidence to support the use of positron emission tomography (PET) imaging during chemoradiation therapy to inform biologically adaptive radiotherapy for head and neck squamous cell carcinoma. We review literature covering this topic spanning nearly 3 decades, including the use of various radiotracers and discoveries of novel predictive PET biomarkers. Through understanding how observational trials have informed current interventional clinical trials, we hope that this review will encourage researchers and clinicians to incorporate PET response criteria in new trial designs to advance biologically optimized radiotherapy.</p>","PeriodicalId":9655,"journal":{"name":"Cancer journal","volume":"29 4","pages":"243-247"},"PeriodicalIF":2.2,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9845070","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}
引用次数: 0
Tumor-Derived Exosomes and the Role of Liquid Biopsy in Human Papillomavirus Oropharyngeal Squamous Cell Carcinoma. 肿瘤来源的外泌体和液体活检在人乳头瘤病毒口咽鳞状细胞癌中的作用。
IF 2.2 4区 医学
Cancer journal Pub Date : 2023-07-01 DOI: 10.1097/PPO.0000000000000671
Michael M Allevato, Joshua D Smith, Michael J Brenner, Steven B Chinn
{"title":"Tumor-Derived Exosomes and the Role of Liquid Biopsy in Human Papillomavirus Oropharyngeal Squamous Cell Carcinoma.","authors":"Michael M Allevato, Joshua D Smith, Michael J Brenner, Steven B Chinn","doi":"10.1097/PPO.0000000000000671","DOIUrl":"10.1097/PPO.0000000000000671","url":null,"abstract":"<p><strong>Abstract: </strong>The global incidence of human papillomavirus-positive (HPV+) head and neck squamous cell carcinoma (HNSCC) has surged in recent decades, with HPV+ HNSCC accounting for >70% of oropharynx cancers in the United States. Its incidence in men has surpassed that of HPV+ cervical cancer in women, and reliable assays are needed for early detection and to monitor response to therapy. Human papillomavirus-positive OPSCC has a more favorable response to therapy and prognosis than HPV-negative (HPV-) HNSCC, motivating regimens to deintensify curative surgery or chemoradiotherapy protocols. A barrier to deintensifying and personalizing therapy is lack of reliable predictive biomarkers. Furthermore, HPV- HNSCC survival rates are static without reliable surveillance biomarkers available. The emergence of circulating plasma-based biomarkers reflecting the tumor-immune microenvironment heralds a new era in HNSCC diagnosis and therapy. We review evidence on tumor-derived extracellular vesicles (exosomes) as biomarkers for diagnosis, prognostication, and treatment in HPV+ and HPV- HNSCC.</p>","PeriodicalId":9655,"journal":{"name":"Cancer journal","volume":"29 4","pages":"230-237"},"PeriodicalIF":2.2,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10372688/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9884051","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}
引用次数: 0
Circulating Tumor DNA in Human Papillomavirus-Mediated Oropharynx Cancer: Leveraging Early Data to Inform Future Directions. 人类乳头瘤病毒介导的口咽癌症中的循环肿瘤DNA:利用早期数据为未来方向提供信息。
IF 2.2 4区 医学
Cancer journal Pub Date : 2023-07-01 DOI: 10.1097/PPO.0000000000000670
Molly E Heft Neal, Heather M Walline, Catherine T Haring
{"title":"Circulating Tumor DNA in Human Papillomavirus-Mediated Oropharynx Cancer: Leveraging Early Data to Inform Future Directions.","authors":"Molly E Heft Neal,&nbsp;Heather M Walline,&nbsp;Catherine T Haring","doi":"10.1097/PPO.0000000000000670","DOIUrl":"10.1097/PPO.0000000000000670","url":null,"abstract":"<p><strong>Abstract: </strong>Circulating tumor DNA (ctDNA) has become an area of intense study in many solid malignancies including head and neck cancer. This is of particular interest for human papillomavirus-mediated oropharyngeal squamous cell carcinoma as this cohort of patients has excellent survival and is undergoing current clinical trials aimed at treatment de-escalation. Recent studies have demonstrated the prognostic implications of pretreatment ctDNA and the utility of monitoring ctDNA during and posttreatment; however, there is a need for a more critical understanding of ctDNA as it is beginning to be incorporated into clinical trials. This review discusses the current state of ctDNA in oropharynx cancer focusing on ctDNA kinetics and minimal residual disease detection and ends with a discussion of future applications.</p>","PeriodicalId":9655,"journal":{"name":"Cancer journal","volume":"29 4","pages":"215-219"},"PeriodicalIF":2.2,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9845066","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}
引用次数: 0
Novel Approaches and Future Directions in Myelodysplastic Syndrome Treatment. 骨髓增生异常综合征治疗的新方法和未来方向。
IF 2.2 4区 医学
Cancer journal Pub Date : 2023-05-01 DOI: 10.1097/PPO.0000000000000658
Jan Philipp Bewersdorf, Zhuoer Xie, Amer M Zeidan
{"title":"Novel Approaches and Future Directions in Myelodysplastic Syndrome Treatment.","authors":"Jan Philipp Bewersdorf,&nbsp;Zhuoer Xie,&nbsp;Amer M Zeidan","doi":"10.1097/PPO.0000000000000658","DOIUrl":"https://doi.org/10.1097/PPO.0000000000000658","url":null,"abstract":"<p><strong>Abstract: </strong>Myelodysplastic syndromes/neoplasms (MDSs) constitute a heterogeneous group of clonal disorders that are clinically characterized by dysplastic changes in multiple hematopoietic lineages, cytopenias, and a variable risk of progression to acute myeloid leukemia. Patients with MDS are classified as either lower- or higher-risk based on risk stratification tools such as the International Prognostic Scoring System and its revised version, which continue to be the basis for prognosis and treatment selection. Although anemic patients with lower-risk MDS are currently treated with an erythropoiesis-stimulating agent, luspatercept, and transfusions, the telomerase inhibitor imetelstat and the hypoxia-inducible factor α inhibitor roxadustat have shown encouraging early results and are now in phase III clinical trials. For higher-risk MDS patients, hypomethylating agent monotherapy continues to be the standard of care. However, with various novel hypomethylating agent-based combination therapies in advanced clinical testing and an increased emphasis on individualized biomarker-driven treatment decisions, the standard therapy paradigms might change in the future.</p>","PeriodicalId":9655,"journal":{"name":"Cancer journal","volume":"29 3","pages":"195-202"},"PeriodicalIF":2.2,"publicationDate":"2023-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9498193","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}
引用次数: 0
Updates in Classification of Myelodysplastic Syndrome. 骨髓增生异常综合征分类的最新进展。
IF 2.2 4区 医学
Cancer journal Pub Date : 2023-05-01 DOI: 10.1097/PPO.0000000000000659
Mina L Xu, Robert P Hasserjian
{"title":"Updates in Classification of Myelodysplastic Syndrome.","authors":"Mina L Xu,&nbsp;Robert P Hasserjian","doi":"10.1097/PPO.0000000000000659","DOIUrl":"https://doi.org/10.1097/PPO.0000000000000659","url":null,"abstract":"<p><strong>Abstract: </strong>Myelodysplastic syndrome includes a broad range of myeloid neoplasms characterized by cytopenia and morphologic dysplasia. Recently, 2 new classification systems emerged to further define how these diseases are diagnosed and risk stratified. This review compares these models, provides detailed approaches, and reveals practical ways to move forward in clinical practice of myelodysplastic syndrome diagnosis.</p>","PeriodicalId":9655,"journal":{"name":"Cancer journal","volume":"29 3","pages":"122-129"},"PeriodicalIF":2.2,"publicationDate":"2023-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9498186","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}
引用次数: 0
Epidemiology and Pathogenesis of Myelodysplastic Syndrome. 骨髓增生异常综合征的流行病学和发病机制。
IF 2.2 4区 医学
Cancer journal Pub Date : 2023-05-01 DOI: 10.1097/PPO.0000000000000665
Lara K Rotter, Shai Shimony, Kelly Ling, Evan Chen, Rory M Shallis, Amer M Zeidan, Maximilian Stahl
{"title":"Epidemiology and Pathogenesis of Myelodysplastic Syndrome.","authors":"Lara K Rotter,&nbsp;Shai Shimony,&nbsp;Kelly Ling,&nbsp;Evan Chen,&nbsp;Rory M Shallis,&nbsp;Amer M Zeidan,&nbsp;Maximilian Stahl","doi":"10.1097/PPO.0000000000000665","DOIUrl":"https://doi.org/10.1097/PPO.0000000000000665","url":null,"abstract":"Abstract Myelodysplastic syndrome (MDS) is a clonal disorder characterized by ineffective hematopoiesis and variable cytopenias with a considerable risk of progression to acute myeloid leukemia. Epidemiological assessment of MDS remains challenging because of evolving classification systems, but the overall incidence in the United States is estimated to be approximately 4 per 100,000 and increases with age. The sequential accumulation of mutations drives disease evolution from asymptomatic clonal hematopoiesis (CH) to CH of indeterminate potential, clonal cytopenia of unknown significance, to frank MDS. The molecular heterogeneity seen in MDS is highly complex and includes mutations of genes involved in splicing machinery, epigenetic regulation, differentiation, and cell signaling. Recent advances in the understanding of the molecular landscape of MDS have led to the development of improved risk assessment tools and novel therapies. Therapies targeting the underlying pathophysiology will hopefully further expand the armamentarium of MDS therapeutics, bringing us closer to a more individualized therapeutic approach based on the unique molecular profile of each patient and eventually improving the outcomes of patients with MDS. We review the epidemiology of MDS and the newly described MDS precursor conditions CH, CH of indeterminate potential, and CCUS. We then discuss central aspects of MDS pathophysiology and outline specific strategies targeting hallmarks of MDS pathophysiology, including ongoing clinical trials examining the efficacy of these therapeutic modalities.","PeriodicalId":9655,"journal":{"name":"Cancer journal","volume":"29 3","pages":"111-121"},"PeriodicalIF":2.2,"publicationDate":"2023-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9498187","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}
引用次数: 0
Spectrum From Clonal Hematopoiesis to Myelodysplastic Neoplasm/Syndromes and Other Myeloid Neoplasms. 从克隆造血到骨髓增生异常肿瘤/综合征和其他髓系肿瘤的频谱。
IF 2.2 4区 医学
Cancer journal Pub Date : 2023-05-01 DOI: 10.1097/PPO.0000000000000656
Zhuoer Xie, Evan C Chen, Lourdes M Mendez, Rami Komrokji, Amer M Zeidan
{"title":"Spectrum From Clonal Hematopoiesis to Myelodysplastic Neoplasm/Syndromes and Other Myeloid Neoplasms.","authors":"Zhuoer Xie,&nbsp;Evan C Chen,&nbsp;Lourdes M Mendez,&nbsp;Rami Komrokji,&nbsp;Amer M Zeidan","doi":"10.1097/PPO.0000000000000656","DOIUrl":"https://doi.org/10.1097/PPO.0000000000000656","url":null,"abstract":"<p><strong>Abstract: </strong>Clonal hematopoiesis (CH) confers a high risk of aging-related diseases and hematologic malignancy. There are still significant knowledge gaps in identifying high-risk patients with CH and managing such patients. In this review, we focus on 3 areas: (1) the natural history of CH; (2) the risks of progression of CH, including CH of indeterminate potential, clonal cytopenia of undetermined significance, and therapy-related CH, to myeloid malignancy; and (3) the challenges and unmet needs of CH management and research.</p>","PeriodicalId":9655,"journal":{"name":"Cancer journal","volume":"29 3","pages":"130-137"},"PeriodicalIF":2.2,"publicationDate":"2023-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9498188","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}
引用次数: 0
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