Publication:
Pulsed radiation therapy to improve systemic control of metastatic cancer

dc.contributor.coauthorHe, Kewen
dc.contributor.coauthorBarsoumian, Hampartsoum B.
dc.contributor.coauthorPuebla-Osorio, Nahum
dc.contributor.coauthorHsu, Ethan Y.
dc.contributor.coauthorVerma, Vivek
dc.contributor.coauthorAbana, Chike O.
dc.contributor.coauthorChen, Dawei
dc.contributor.coauthorPatel, Roshal R.
dc.contributor.coauthorGu, Meidi
dc.contributor.coauthorCortez, Maria Angelica
dc.contributor.coauthorWelsh, James W.
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorSezen, Duygu
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2024-11-09T13:23:13Z
dc.date.issued2021
dc.description.abstractRadiation therapy (RT) is emerging as an interventional modality in the cancer-immunity cycle, augmenting the activation of an adaptive immune response against tumors. RT, particularly in combination with immunotherapy, can enhance immune memory effects and shape the tumor-directed T-cell populations. However, a single cycle of RT delivered to a limited number of polymetastatic lesions is rarely sufficient to achieve systemic control. We hypothesize that several rounds of RT, akin to several rounds of immunotherapeutic drugs, is likely to provide greater clinical benefit to patients with metastatic disease. We propose that the repeated exposure to tumor antigens released by ""pulsed-RT"" (i.e., treating 2-4 tumor lesions with 3 irradiation cycles given one month apart) may amplify the adaptive immune response by expanding the tumor-specific T-cell receptor repertoire, the production of high-affinity tumor antibodies, and the generation of memory lymphocytes and thereby improve immune control of systemic disease.</p>
dc.description.fulltextYES
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.openaccessYES
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipNational Cancer Institute
dc.description.sponsorshipNational Institutes of Health
dc.description.sponsorshipCancer Center Support (Core) Grant
dc.description.versionPublisher version
dc.description.volume11
dc.identifier.doi10.3389/fonc.2021.737425
dc.identifier.embargoNO
dc.identifier.filenameinventorynoIR03204
dc.identifier.issn2234-943X
dc.identifier.quartileQ2
dc.identifier.scopus2-s2.0-85114346555
dc.identifier.urihttps://doi.org/10.3389/fonc.2021.737425
dc.identifier.wos698695100001
dc.keywordsRadiation therapy
dc.keywordsImmunotherapy
dc.keywordsMetastatic cancer
dc.keywordsAdaptive immunity
dc.keywordsMemory effect
dc.language.isoeng
dc.publisherFrontiers
dc.relation.grantnoP30 CA016672
dc.relation.ispartofFrontiers in Oncology
dc.relation.urihttp://cdm21054.contentdm.oclc.org/cdm/ref/collection/IR/id/9966
dc.subjectOncology
dc.titlePulsed radiation therapy to improve systemic control of metastatic cancer
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorSezen, Duygu
local.publication.orgunit1SCHOOL OF MEDICINE
local.publication.orgunit2School of Medicine
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relation.isOrgUnitOfPublication.latestForDiscoveryd02929e1-2a70-44f0-ae17-7819f587bedd
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