Background: Glioblastoma (GBM) is the most common and aggressive primary brain tumor in adults, characterized by poor prognosis and limited treatment options. Liquid biopsy offers a minimally invasive approach for molecular profiling and disease monitoring, potentially overcoming tissue sampling and neuroimaging limitations. This prospective, single-center study aimed to establish and evaluate the feasibility of a standardized clinical liquid biopsy protocol for GBM, integrating circulating tumor DNA (ctDNA) and microRNA (miRNA) analyses across multiple biological matrices. Methods: Between 2022 and 2024, 26 patients were enrolled, including 14 with histologically confirmed IDH-wildtype GBM, 6 with other intracranial tumors, and 6 with hydrocephalus. Peripheral blood, lumbar cerebrospinal fluid (CSF-L), intraoperative sulcal CSF (CSF-S), and tumor tissue were collected when available. ctDNA was analyzed using a targeted amplicon-based sequencing panel, assessing variant allele frequency and fragmentation index. A panel of GBM-associated miRNAs was quantified by RT-qPCR. Tumor, necrotic, and edema volumes were measured by manual segmentation on contrast-enhanced T1-weighted and T2-FLAIR MRI. Results: ctDNA analysis was feasible across all matrices but showed higher rates of suboptimal samples compared with miRNA analysis. Plasma and CSF-L provided comparable ctDNA concentrations, with plasma emerging as the most consistently available matrix. miRNA profiling was robust across matrices, with consistent detectability between CSF-L and CSF-S. Conclusions: This study demonstrates the feasibility of integrating multimodal liquid biopsy and volumetric imaging into routine neurosurgical practice for GBM. The proposed workflow provides a reproducible foundation for larger studies aimed at advancing clinical implementation of liquid biopsy strategies.
Implementing Multimodal Liquid Biopsy in Glioblastoma: A Prospective Feasibility Study of a Standardized Clinical Workflow / Chiapponi, M., Cappella, F., Andreacchio, L., Antonini¹, R., Liverotti, V., Carelli, E., Goteri, G., Sabbatinelli, J., Bartoli, E., Filosa, A., Giuliani, A., Sbriscia, M., Procopio, A.D., Dobran, M.. - In: NEURO ONCOLOGY PRACTICE. - ISSN 2054-2585. - 13:5(2026), pp. 939-949. [10.1093/nop/npag034]
Implementing Multimodal Liquid Biopsy in Glioblastoma: A Prospective Feasibility Study of a Standardized Clinical Workflow
Chiapponi, Mario
Primo
;Cappella, Fabiola;Andreacchio, Laura;Antonini¹, Ruggero;Liverotti, Valentina;Goteri, Gaia;Sabbatinelli, Jacopo;Bartoli, Elisa;Filosa, Alessandra;Giuliani, Angelica;Sbriscia, Matilde;Procopio, Antonio Domenico;Dobran, MauroUltimo
2026-01-01
Abstract
Background: Glioblastoma (GBM) is the most common and aggressive primary brain tumor in adults, characterized by poor prognosis and limited treatment options. Liquid biopsy offers a minimally invasive approach for molecular profiling and disease monitoring, potentially overcoming tissue sampling and neuroimaging limitations. This prospective, single-center study aimed to establish and evaluate the feasibility of a standardized clinical liquid biopsy protocol for GBM, integrating circulating tumor DNA (ctDNA) and microRNA (miRNA) analyses across multiple biological matrices. Methods: Between 2022 and 2024, 26 patients were enrolled, including 14 with histologically confirmed IDH-wildtype GBM, 6 with other intracranial tumors, and 6 with hydrocephalus. Peripheral blood, lumbar cerebrospinal fluid (CSF-L), intraoperative sulcal CSF (CSF-S), and tumor tissue were collected when available. ctDNA was analyzed using a targeted amplicon-based sequencing panel, assessing variant allele frequency and fragmentation index. A panel of GBM-associated miRNAs was quantified by RT-qPCR. Tumor, necrotic, and edema volumes were measured by manual segmentation on contrast-enhanced T1-weighted and T2-FLAIR MRI. Results: ctDNA analysis was feasible across all matrices but showed higher rates of suboptimal samples compared with miRNA analysis. Plasma and CSF-L provided comparable ctDNA concentrations, with plasma emerging as the most consistently available matrix. miRNA profiling was robust across matrices, with consistent detectability between CSF-L and CSF-S. Conclusions: This study demonstrates the feasibility of integrating multimodal liquid biopsy and volumetric imaging into routine neurosurgical practice for GBM. The proposed workflow provides a reproducible foundation for larger studies aimed at advancing clinical implementation of liquid biopsy strategies.| File | Dimensione | Formato | |
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