Prajwal Ghimire, Ben Kinnersley, Golestan Karami, Prabhu Arumugam, Richard Houlston, Keyoumars Ashkan, Marc Modat, Thomas C Booth
{"title":"胶质母细胞瘤免疫疗法的放射基因组生物标志物:磁共振成像研究系统综述","authors":"Prajwal Ghimire, Ben Kinnersley, Golestan Karami, Prabhu Arumugam, Richard Houlston, Keyoumars Ashkan, Marc Modat, Thomas C Booth","doi":"arxiv-2405.07858","DOIUrl":null,"url":null,"abstract":"Immunotherapy is an effective precision medicine treatment for several\ncancers. Imaging signatures of the underlying genome (radiogenomics) in\nglioblastoma patients may serve as preoperative biomarkers of the tumor-host\nimmune apparatus. Validated biomarkers would have the potential to stratify\npatients during immunotherapy clinical trials, and if trials are beneficial,\nfacilitate personalized neo-adjuvant treatment. The increased use of whole\ngenome sequencing data, and the advances in bioinformatics and machine learning\nmake such developments plausible. We performed a systematic review to determine\nthe extent of development and validation of immune-related radiogenomic\nbiomarkers for glioblastoma. A systematic review was performed following PRISMA\nguidelines using the PubMed, Medline, and Embase databases. Qualitative\nanalysis was performed by incorporating the QUADAS 2 tool and CLAIM checklist.\nPROSPERO registered CRD42022340968. Extracted data were insufficiently\nhomogenous to perform a meta-analysis. Results Nine studies, all retrospective,\nwere included. Biomarkers extracted from magnetic resonance imaging volumes of\ninterest included apparent diffusion coefficient values, relative cerebral\nblood volume values, and image-derived features. These biomarkers correlated\nwith genomic markers from tumor cells or immune cells or with patient survival.\nThe majority of studies had a high risk of bias and applicability concerns\nregarding the index test performed. Radiogenomic immune biomarkers have the\npotential to provide early treatment options to patients with glioblastoma.\nTargeted immunotherapy, stratified by these biomarkers, has the potential to\nallow individualized neo-adjuvant precision treatment options in clinical\ntrials. However, there are no prospective studies validating these biomarkers,\nand interpretation is limited due to study bias with little evidence of\ngeneralizability.","PeriodicalId":501572,"journal":{"name":"arXiv - QuanBio - Tissues and Organs","volume":"133 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-05-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Radiogenomic biomarkers for immunotherapy in glioblastoma: A systematic review of magnetic resonance imaging studies\",\"authors\":\"Prajwal Ghimire, Ben Kinnersley, Golestan Karami, Prabhu Arumugam, Richard Houlston, Keyoumars Ashkan, Marc Modat, Thomas C Booth\",\"doi\":\"arxiv-2405.07858\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Immunotherapy is an effective precision medicine treatment for several\\ncancers. Imaging signatures of the underlying genome (radiogenomics) in\\nglioblastoma patients may serve as preoperative biomarkers of the tumor-host\\nimmune apparatus. Validated biomarkers would have the potential to stratify\\npatients during immunotherapy clinical trials, and if trials are beneficial,\\nfacilitate personalized neo-adjuvant treatment. The increased use of whole\\ngenome sequencing data, and the advances in bioinformatics and machine learning\\nmake such developments plausible. We performed a systematic review to determine\\nthe extent of development and validation of immune-related radiogenomic\\nbiomarkers for glioblastoma. A systematic review was performed following PRISMA\\nguidelines using the PubMed, Medline, and Embase databases. Qualitative\\nanalysis was performed by incorporating the QUADAS 2 tool and CLAIM checklist.\\nPROSPERO registered CRD42022340968. Extracted data were insufficiently\\nhomogenous to perform a meta-analysis. Results Nine studies, all retrospective,\\nwere included. Biomarkers extracted from magnetic resonance imaging volumes of\\ninterest included apparent diffusion coefficient values, relative cerebral\\nblood volume values, and image-derived features. These biomarkers correlated\\nwith genomic markers from tumor cells or immune cells or with patient survival.\\nThe majority of studies had a high risk of bias and applicability concerns\\nregarding the index test performed. Radiogenomic immune biomarkers have the\\npotential to provide early treatment options to patients with glioblastoma.\\nTargeted immunotherapy, stratified by these biomarkers, has the potential to\\nallow individualized neo-adjuvant precision treatment options in clinical\\ntrials. However, there are no prospective studies validating these biomarkers,\\nand interpretation is limited due to study bias with little evidence of\\ngeneralizability.\",\"PeriodicalId\":501572,\"journal\":{\"name\":\"arXiv - QuanBio - Tissues and Organs\",\"volume\":\"133 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-05-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"arXiv - QuanBio - Tissues and Organs\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/arxiv-2405.07858\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"arXiv - QuanBio - Tissues and Organs","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/arxiv-2405.07858","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Radiogenomic biomarkers for immunotherapy in glioblastoma: A systematic review of magnetic resonance imaging studies
Immunotherapy is an effective precision medicine treatment for several
cancers. Imaging signatures of the underlying genome (radiogenomics) in
glioblastoma patients may serve as preoperative biomarkers of the tumor-host
immune apparatus. Validated biomarkers would have the potential to stratify
patients during immunotherapy clinical trials, and if trials are beneficial,
facilitate personalized neo-adjuvant treatment. The increased use of whole
genome sequencing data, and the advances in bioinformatics and machine learning
make such developments plausible. We performed a systematic review to determine
the extent of development and validation of immune-related radiogenomic
biomarkers for glioblastoma. A systematic review was performed following PRISMA
guidelines using the PubMed, Medline, and Embase databases. Qualitative
analysis was performed by incorporating the QUADAS 2 tool and CLAIM checklist.
PROSPERO registered CRD42022340968. Extracted data were insufficiently
homogenous to perform a meta-analysis. Results Nine studies, all retrospective,
were included. Biomarkers extracted from magnetic resonance imaging volumes of
interest included apparent diffusion coefficient values, relative cerebral
blood volume values, and image-derived features. These biomarkers correlated
with genomic markers from tumor cells or immune cells or with patient survival.
The majority of studies had a high risk of bias and applicability concerns
regarding the index test performed. Radiogenomic immune biomarkers have the
potential to provide early treatment options to patients with glioblastoma.
Targeted immunotherapy, stratified by these biomarkers, has the potential to
allow individualized neo-adjuvant precision treatment options in clinical
trials. However, there are no prospective studies validating these biomarkers,
and interpretation is limited due to study bias with little evidence of
generalizability.