Abstract

Simple SummaryCerebral diffuse gliomas present peculiar molecular features tightly linked to phenotypic characteristics that are not readily appreciated by means of standard neuroimaging. In the present Part B of our two-review series, the potential of exploiting glioma vascular and hemodynamic alterations for a better characterization of tumor subtype, differentiation of tumor recurrence from treatment effects, and prognosis prediction is critically discussed together with the advancements related to radiomics and machine learning for innovative imaging biomarkers development.Gliomas, and glioblastoma in particular, exhibit an extensive intra- and inter-tumoral molecular heterogeneity which represents complex biological features correlating to the efficacy of treatment response and survival. From a neuroimaging point of view, these specific molecular and histopathological features may be used to yield imaging biomarkers as surrogates for distinct tumor genotypes and phenotypes. The development of comprehensive glioma imaging markers has potential for improved glioma characterization that would assist in the clinical work-up of preoperative treatment planning and treatment effect monitoring. In particular, the differentiation of tumor recurrence or true progression from pseudoprogression, pseudoresponse, and radiation-induced necrosis can still not reliably be made through standard neuroimaging only. Given the abundant vascular and hemodynamic alterations present in diffuse glioma, advanced hemodynamic imaging approaches constitute an attractive area of clinical imaging development. In this context, the inclusion of objective measurable glioma imaging features may have the potential to enhance the individualized care of diffuse glioma patients, better informing of standard-of-care treatment efficacy and of novel therapies, such as the immunotherapies that are currently increasingly investigated. In Part B of this two-review series, we assess the available evidence pertaining to hemodynamic imaging for molecular feature prediction, in particular focusing on isocitrate dehydrogenase (IDH) mutation status, MGMT promoter methylation, 1p19q codeletion, and EGFR alterations. The results for the differentiation of tumor progression/recurrence from treatment effects have also been the focus of active research and are presented together with the prognostic correlations identified by advanced hemodynamic imaging studies. Finally, the state-of-the-art concepts and advancements of hemodynamic imaging modalities are reviewed together with the advantages derived from the implementation of radiomics and machine learning analyses pipelines.

Highlights

  • In recent decades, the traditional histopathological grading of diffuse gliomas has bee1n. cIonmtropdleumctieonnted by a more refined molecular analysis of tumor markers

  • Similar to traditional hemodynamic imaging, Intravoxel Incoherent Motion (IVIM)-MRI has been used for differential diagnosis [178–180], glioma grading, and isocitrate dehydrogenase (IDH) mutation prediction [181–184] to monitor the treatment effects [185–187], to identify tumor progression [109], and to predict survival [188–190]

  • Advanced hemodynamic imaging research has provided yet another promising imaging development to complement traditional tumor grading by correlating the specific hemodynamic patterns posed by diffuse glioma to molecular and pathophysiological alterations

Read more

Summary

Introduction

The traditional histopathological grading of diffuse gliomas has bee1n. cIonmtropdleumctieonnted by a more refined molecular analysis of tumor markers. A description of hemodynamic imaging modalities and relative assessed parameters is presented in Part A of the present review (see Tables 1 and 2 of Part A) [6] In this context, the inclusion of objective measurable glioma imaging features may have the potential to enhance the individualized care of diffuse glioma patients, which can better inform standard-of-care treatment efficacy and novel therapies, such as immunotherapies that are currently being increasingly investigated [7]. With the increasingly understood role of biology in correlating tumor aggressiveness and prognosis, the old histological entities are outdated and tumor classification depends on underlying molecular features [2] This information, which is crucial in patient management, is currently only available after the analysis of tumor specimens (biopsy/resection). We focus in particular on hemodynamic correlates of isocitrate dehydrogenase (IDH) mutation status, 1p19q codeletion, O6-methylguanine-DNA methyl-transferase (MGMT) promoter methylation, and epidermal growth factor receptor (EGFR) alterations

IDH Mutation Status
MGMT Promoter Methylation
EGFR Mutation
Other Markers
Differentiation between
Prognosis Prediction
Contrast-Enhanced Ultrasound (CEUS)
Intravoxel Incoherent Motion (IVIM)-MRI
Gas Modulation and BOLD Imaging
Machine-Learning and Radiomics
Findings
Conclusions
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.