AI-driven estimation of O6 methylguanine-DNA-methyltransferase (MGMT) promoter methylation in glioblastoma patients: a systematic review with bias analysis

被引:2
作者
Samartha, Mullapudi Venkata Sai [1 ]
Dubey, Navneet Kumar [2 ,3 ]
Jena, Biswajit [4 ]
Maheswar, Gorantla [1 ]
Lo, Wen-Cheng [5 ,6 ,7 ]
Saxena, Sanjay [1 ]
机构
[1] Int Inst Informat Technol, Dept Comp Sci & Engn, Bhubaneswar 751003, India
[2] Victory Biotechnol Co Ltd, Taipei 114757, Taiwan
[3] Indian Inst Management, Execut Programme Healthcare Management, Lucknow 226013, India
[4] SOA Deemed toBe Univ, Inst Tech Educ & Res, Bhubaneswar 751030, India
[5] Taipei Med Univ, Coll Med, Sch Med, Dept Surg,Div Neurosurg, Taipei 11031, Taiwan
[6] Taipei Med Univ Hosp, Dept Neurosurg, Taipei 11031, Taiwan
[7] Taipei Med Univ, Taipei Neurosci Inst, Taipei City 11031, Taiwan
基金
英国科研创新办公室;
关键词
O(6)-methylguanine-DNA-methyltransferase (MGMT); Methylation status; Radiogenomics; Artificial intelligence (AI); Machine learning; Deep learning; STEM-CELLS; CLASSIFICATION; TEMOZOLOMIDE; BIOMARKER; PREDICTION; DIAGNOSIS; SURVIVAL; TUMORS;
D O I
10.1007/s00432-023-05566-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundAccurate and non-invasive estimation of MGMT promoter methylation status in glioblastoma (GBM) patients is of paramount clinical importance, as it is a predictive biomarker associated with improved overall survival (OS). In response to the clinical need, recent studies have focused on the development of non-invasive artificial intelligence (AI)-based methods for MGMT estimation. In this systematic review, we not only delve into the technical aspects of these AI-driven MGMT estimation methods but also emphasize their profound clinical implications. Specifically, we explore the potential impact of accurate non-invasive MGMT estimation on GBM patient care and treatment decisions.MethodsEmploying a PRISMA search strategy, we identified 33 relevant studies from reputable databases, including PubMed, ScienceDirect, Google Scholar, and IEEE Explore. These studies were comprehensively assessed using 21 diverse attributes, encompassing factors such as types of imaging modalities, machine learning (ML) methods, and cohort sizes, with clear rationales for attribute scoring. Subsequently, we ranked these studies and established a cutoff value to categorize them into low-bias and high-bias groups.ResultsBy analyzing the 'cumulative plot of mean score' and the 'frequency plot curve' of the studies, we determined a cutoff value of 6.00. A higher mean score indicated a lower risk of bias, with studies scoring above the cutoff mark categorized as low-bias (73%), while 27% fell into the high-bias category.ConclusionOur findings underscore the immense potential of AI-based machine learning (ML) and deep learning (DL) methods in non-invasively determining MGMT promoter methylation status. Importantly, the clinical significance of these AI-driven advancements lies in their capacity to transform GBM patient care by providing accurate and timely information for treatment decisions. However, the translation of these technical advancements into clinical practice presents challenges, including the need for large multi-institutional cohorts and the integration of diverse data types. Addressing these challenges will be critical in realizing the full potential of AI in improving the reliability and accessibility of MGMT estimation while lowering the risk of bias in clinical decision-making.
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页数:22
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