Viviana Cortiana Ms, Jenna Ghazal BSc, Harshitha Vallabhaneni Bs, Ahmed Hashim Azeez Md, Kennedy Itodo Bs, Chandler H Park Md Ms Facp, Yan Leyfman Md
{"title":"Immune Modulation in Sarcoma: Targeting the Tumor Microenvironment.","authors":"Viviana Cortiana Ms, Jenna Ghazal BSc, Harshitha Vallabhaneni Bs, Ahmed Hashim Azeez Md, Kennedy Itodo Bs, Chandler H Park Md Ms Facp, Yan Leyfman Md","doi":"10.46883/2025.25921045","DOIUrl":null,"url":null,"abstract":"<p><p>Modifying the immune environment in sarcoma treatment has a critical role, which highlights the necessity to overcome inhibitory macrophages and facilitate cellular therapy modifications. A lecture by Seth M. Pollack, MD, addresses sarcomas and rare cancers that are impacting various tissues and adult health and emphasizes the importance of techniques such as T-cell receptor (TCR) therapy, cancer testis antigen (CTA), and chimeric antigen receptor (CAR) T-cell therapy for effective treatment. The study investigates the effects of altering the tumor microenvironment to support cellular therapy, aiming to understand the immune response in sarcomas. By targeting inhibitory macrophages and optimizing cellular treatment strategies, such as interferon gamma and canine CAR T cells, new therapeutic approaches can be developed to enhance patient outcomes and survival rates. This underscores how manipulating the immune environment can significantly improve treatment efficacy, offering a revolutionary approach to sarcoma therapy.</p>","PeriodicalId":51147,"journal":{"name":"Oncology-New York","volume":"null 6","pages":"232-236"},"PeriodicalIF":1.8000,"publicationDate":"2025-07-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Oncology-New York","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.46883/2025.25921045","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Modifying the immune environment in sarcoma treatment has a critical role, which highlights the necessity to overcome inhibitory macrophages and facilitate cellular therapy modifications. A lecture by Seth M. Pollack, MD, addresses sarcomas and rare cancers that are impacting various tissues and adult health and emphasizes the importance of techniques such as T-cell receptor (TCR) therapy, cancer testis antigen (CTA), and chimeric antigen receptor (CAR) T-cell therapy for effective treatment. The study investigates the effects of altering the tumor microenvironment to support cellular therapy, aiming to understand the immune response in sarcomas. By targeting inhibitory macrophages and optimizing cellular treatment strategies, such as interferon gamma and canine CAR T cells, new therapeutic approaches can be developed to enhance patient outcomes and survival rates. This underscores how manipulating the immune environment can significantly improve treatment efficacy, offering a revolutionary approach to sarcoma therapy.
期刊介绍:
Although laboratory and clinical cancer research need to be closely linked, observations at the basic level often remain removed from medical applications. This journal works to accelerate the translation of experimental results into the clinic, and back again into the laboratory for further investigation. The fundamental purpose of this effort is to advance clinically-relevant knowledge of cancer, and improve the outcome of prevention, diagnosis and treatment of malignant disease. The journal publishes significant clinical studies from cancer programs around the world, along with important translational laboratory findings, mini-reviews (invited and submitted) and in-depth discussions of evolving and controversial topics in the oncology arena. A unique feature of the journal is a new section which focuses on rapid peer-review and subsequent publication of short reports of phase 1 and phase 2 clinical cancer trials, with a goal of insuring that high-quality clinical cancer research quickly enters the public domain, regardless of the trial’s ultimate conclusions regarding efficacy or toxicity.