Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/30679
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dc.contributor.authorKiamanesh, Zahra-
dc.contributor.authorAyati, Narjess-
dc.contributor.authorSadeghi, Ramin-
dc.contributor.authorHawkes, Eliza A-
dc.contributor.authorLee, Sze Ting-
dc.contributor.authorScott, Andrew M-
dc.date2022-
dc.date.accessioned2022-08-09T07:01:17Z-
dc.date.available2022-08-09T07:01:17Z-
dc.date.issued2022-08-06-
dc.identifier.citationEuropean Journal of Nuclear Medicine and Molecular Imaging 2022en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/30679-
dc.description.abstractTreatment strategies of lymphoid malignancies have been revolutionized by immunotherapy. Because of the inherent property of Hodgkin lymphoma and some subtypes of non-Hodgkin lymphoma as a highly FDG-avid tumor, functional 18F-FDG PET/CT imaging is already embedded in their routine care. Nevertheless, the question is whether it is still valuable in the context of these tumors being treated with immunotherapy. Herein, we will review the value of 18F-FDG PET/CT imaging lymphoid tumors treated with immunotherapy regimens. A comprehensive literature search of the PubMed database was conducted on the value of the 18F-FDG PET/CT for immunotherapy response monitoring of patients with malignant lymphoma. The articles were considered eligible if they met all of the following inclusion criteria: (a) clinical studies on patients with different types of malignant lymphoma, (b) treatment with anti-CD20 antibodies, immune checkpoint inhibitors or immune cell therapies, (c) and incorporated PET/CT with 18F-FDG as the PET tracer. From the initial 1488 papers identified, 91 were ultimately included in our study. In anti-CD20 therapy, the highest pooled hazard ratios (HRs) of baseline, early, and late response monitoring parameters for progression-free survival (PFS) belong to metabolic tumor volume (MTV) (3.19 (95%CI: 2.36-4.30)), maximum standardized uptake value (SUVmax) (3.25 (95%CI: 2.08-5.08)), and Deauville score (DS) (3.73 (95%CI: 2.50-5.56)), respectively. These measurements for overall survival (OS) were MTV (4.39 (95%CI: 2.71-7.08)), DS (3.23 (95%CI: 1.87-5.58)), and DS (3.64 (95%CI: 1.40-9.43)), respectively. Early and late 18F-FDG PET/CT response assessment in immune checkpoint inhibitors (ICI) and immune cell therapy might be an effective tool for prediction of clinical outcome. For anti-CD20 therapy of lymphoma, the MTV as a baseline 18F-FDG PET/CT-derived parameter has the highest HRs for PFS and OS. The DS as visual criteria in early and late response assessment has higher HRs for PFS and OS compared to the international harmonization project (IHP) visual criteria in anti-CD20 therapy. Early changes in 18F-FDG PET parameters may be predictive of response to ICIs and cell therapy in lymphoma patients.en
dc.language.isoeng-
dc.subject18F-FDG PET/CTen
dc.subjectAnti-CD20 antibodiesen
dc.subjectImmune checkpoint inhibitorsen
dc.subjectImmunotherapyen
dc.subjectMalignant lymphomaen
dc.titleThe value of FDG PET/CT imaging in outcome prediction and response assessment of lymphoma patients treated with immunotherapy: a meta-analysis and systematic review.en
dc.typeJournal Articleen
dc.identifier.journaltitleEuropean journal of nuclear medicine and molecular imagingen
dc.identifier.affiliationSchool of Public Health & Preventative Medicine, Monash University, Melbourne, Australia..en
dc.identifier.affiliationNuclear Medicine Research Center, Mashhad University of Medical Sciences, Mashhad, Iran..en
dc.identifier.affiliationDepartment of Nuclear Medicine, Ultrasound & PET, Sydney Westmead Hospital, Sydney, NSW, Australia..en
dc.identifier.affiliationSchool of Cancer Medicine, La Trobe University, Victoria, Australia..en
dc.identifier.affiliationDepartment of Medicine, University of Melbourne, Victoria, Australia..en
dc.identifier.affiliationMolecular Imaging and Therapyen
dc.identifier.affiliationMedical Oncologyen
dc.identifier.affiliationClinical Haematologyen
dc.identifier.affiliationOlivia Newton-John Cancer Research Instituteen
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/35932329/en
dc.identifier.doi10.1007/s00259-022-05918-2en
dc.type.contentTexten
dc.identifier.orcidhttp://orcid.org/0000-0002-6656-295Xen
dc.identifier.orcidhttp://orcid.org/0000-0001-8482-4119en
dc.identifier.orcidhttp://orcid.org/0000-0002-0376-2559en
dc.identifier.orcidhttp://orcid.org/0000-0001-8641-456Xen
dc.identifier.pubmedid35932329-
local.name.researcherAyati, Narjess
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
crisitem.author.deptClinical Haematology-
crisitem.author.deptOlivia Newton-John Cancer Wellness and Research Centre-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
crisitem.author.deptMolecular Imaging and Therapy-
crisitem.author.deptMolecular Imaging and Therapy-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
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