Response assessment of GBM during immunotherapy by delayed contrast treatment response assessment maps.
Autor: | Cuccarini V; Neuroradiology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy., Savoldi F; Neuroradiology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy., Mardor Y; Advanced Technology Center, Sheba Medical Center, Ramat Gan, Israel.; Tel Aviv University, Tel Aviv, Israel., Last D; Advanced Technology Center, Sheba Medical Center, Ramat Gan, Israel., Pellegatta S; Molecular Neuro-Oncology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy., Mazzi F; Neuroradiology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy., Bruzzone MG; Neuroradiology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy., Anghileri E; Molecular Neuro-Oncology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy., Pollo B; Neuro-Pathology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy., Maddaloni L; Molecular Neuro-Oncology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy., Russo C; Dipartimento di Ingegneria Elettrica e delle Tecnologie dell'Informazione (DIETI), Università Degli Studi di Napoli 'Federico II', Naples, Italy., Bocchi E; Neuroradiology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy., Pinzi V; Radiotherapy Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy., Eoli M; Molecular Neuro-Oncology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy., Aquino D; Neuroradiology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy. |
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Jazyk: | angličtina |
Zdroj: | Frontiers in neurology [Front Neurol] 2024 Apr 08; Vol. 15, pp. 1374737. Date of Electronic Publication: 2024 Apr 08 (Print Publication: 2024). |
DOI: | 10.3389/fneur.2024.1374737 |
Abstrakt: | Introduction: Assessing the treatment response of glioblastoma multiforme during immunotherapy (IT) is an open issue. Treatment response assessment maps (TRAMs) might help distinguish true tumor progression (TTP) and pseudoprogression (PsP) in this setting. Methods: We recruited 16 naïve glioblastoma patients enrolled in a phase II trial consisting of the Stupp protocol (a standardized treatment for glioblastoma involving combined radiotherapy and chemotherapy with temozolomide, followed by adjuvant temozolomide) plus IT with dendritic cells. Patients were followed up till progression or death; seven underwent a second surgery for suspected progression. Clinical, immunological, and MRI data were collected from all patients and histology in case of second surgery. Patients were classified as responders (progression-free survival, PFS > 12 months), and non-responders (PFS ≤ 12), HIGH-NK (natural killer cells, i.e., immunological responders), and LOW-NK (immunological non-responders) based on immune cell counts in peripheral blood. TRAMs differentiate contrast-enhancing lesions with different washout dynamics into hypothesized tumoral (conventionally blue-colored) vs. treatment-related (red-colored). Results: Using receiver operating characteristic (ROC) curves, a threshold of -0.066 in V Discussion: In conclusion, in our pilot study TRAMs support the discrimination between tumoral and treatment-related enhancing features in immunological responders vs. non-responders, the distinction between PsP and TTP, and might provide surrogate markers of immunological response. Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision. (Copyright © 2024 Cuccarini, Savoldi, Mardor, Last, Pellegatta, Mazzi, Bruzzone, Anghileri, Pollo, Maddaloni, Russo, Bocchi, Pinzi, Eoli and Aquino.) |
Databáze: | MEDLINE |
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