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

Prajwal Ghimire, Ben Kinnersley, Golestan Karami, Prabhu Arumugam, Richard Houlston, Keyoumars Ashkan, Marc Modat, Thomas C Booth
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摘要

免疫疗法是治疗多种癌症的有效精准医疗手段。胶质母细胞瘤患者潜在基因组(放射基因组学)的成像特征可作为肿瘤-宿主免疫装置的术前生物标志物。经过验证的生物标志物将有可能在免疫疗法临床试验期间对患者进行分层,如果试验有益,还能促进个性化的新辅助治疗。随着全基因组测序数据使用的增加以及生物信息学和机器学习的进步,这种发展是有可能的。我们进行了一项系统综述,以确定胶质母细胞瘤免疫相关放射基因组生物标记物的开发和验证程度。我们按照 PRISMA 指南,使用 PubMed、Medline 和 Embase 数据库进行了系统性综述。定性分析采用了 QUADAS 2 工具和 CLAIM 核对表,PROSPERO 注册号为 CRD42022340968。提取的数据不够均匀,无法进行荟萃分析。结果 共纳入九项研究,均为回顾性研究。从磁共振成像相关体积中提取的生物标志物包括表观扩散系数值、相对脑血容量值和图像衍生特征。这些生物标志物与肿瘤细胞或免疫细胞的基因组标志物或患者存活率存在相关性。放射基因组免疫生物标志物有可能为胶质母细胞瘤患者提供早期治疗方案。根据这些生物标志物进行分层的靶向免疫疗法有可能在临床试验中提供个体化的新辅助精准治疗方案。然而,目前还没有前瞻性研究对这些生物标志物进行验证,而且由于研究的偏差,对这些生物标志物的解释也很有限,几乎没有证据表明它们具有普遍性。
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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.
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