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Intraoperative Photodiagnosis for Malignant Glioma Using Photosensitizer Talaporfin Sodium

Objective: The aim of this study was to demonstrate the clinical feasibility of intraoperative photodiagnosis (PD) of malignant brain tumor using talaporfin sodium (TPS), which is an agent used in photodynamic therapy (PDT) for cancers. Methods: Forty-seven patients diagnosed with malignant gliomas...

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Autores principales: Akimoto, Jiro, Fukami, Shinjiro, Ichikawa, Megumi, Mohamed, Awad, Kohno, Michihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6438081/
https://www.ncbi.nlm.nih.gov/pubmed/30949484
http://dx.doi.org/10.3389/fsurg.2019.00012
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author Akimoto, Jiro
Fukami, Shinjiro
Ichikawa, Megumi
Mohamed, Awad
Kohno, Michihiro
author_facet Akimoto, Jiro
Fukami, Shinjiro
Ichikawa, Megumi
Mohamed, Awad
Kohno, Michihiro
author_sort Akimoto, Jiro
collection PubMed
description Objective: The aim of this study was to demonstrate the clinical feasibility of intraoperative photodiagnosis (PD) of malignant brain tumor using talaporfin sodium (TPS), which is an agent used in photodynamic therapy (PDT) for cancers. Methods: Forty-seven patients diagnosed with malignant gliomas by preoperative imaging (42 patients with gliomas and 5 patients with other brain tumors) received an intravenous injection of TPS at 40 mg/m(2) 24 h before resection. During surgery, these patients were irradiated with diode laser light at 664 nm, and tumor fluorescence was observed. The fluorescence intensity was visually rated on a 3-point rating scale [strong fluorescence, weak fluorescence and no fluorescence]. TPS concentrations in 124 samples from 47 cases were measured by HPLC (High performance liquid chromatography). Results: The fluorescence intensity was confirmed to be weak in all patients with Grade II gliomas and strong in almost all patients with Grade III or IV gliomas, reflecting the histological grade of malignancy. In patients with non-glioma brain tumors except for 1 patient with a metastatic brain tumor, the fluorescence intensity was strong. The mean TPS concentration in tissues was 1.62 μg/g for strong fluorescence areas, 0.67 μg/g for weak fluorescence areas and 0.19 μg/g for no fluorescence areas. Conclusions: Establishment of an appropriate fluorescence observation system enabled fluorescence-guided resection of malignant brain tumors using TPS, and the fluorescence intensity of tumors correlated with the TPS concentrations in tissues. These results suggest that TPS is a useful photosensitizer for both intraoperative fluorescence diagnosis and photodynamic therapy.
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spelling pubmed-64380812019-04-04 Intraoperative Photodiagnosis for Malignant Glioma Using Photosensitizer Talaporfin Sodium Akimoto, Jiro Fukami, Shinjiro Ichikawa, Megumi Mohamed, Awad Kohno, Michihiro Front Surg Surgery Objective: The aim of this study was to demonstrate the clinical feasibility of intraoperative photodiagnosis (PD) of malignant brain tumor using talaporfin sodium (TPS), which is an agent used in photodynamic therapy (PDT) for cancers. Methods: Forty-seven patients diagnosed with malignant gliomas by preoperative imaging (42 patients with gliomas and 5 patients with other brain tumors) received an intravenous injection of TPS at 40 mg/m(2) 24 h before resection. During surgery, these patients were irradiated with diode laser light at 664 nm, and tumor fluorescence was observed. The fluorescence intensity was visually rated on a 3-point rating scale [strong fluorescence, weak fluorescence and no fluorescence]. TPS concentrations in 124 samples from 47 cases were measured by HPLC (High performance liquid chromatography). Results: The fluorescence intensity was confirmed to be weak in all patients with Grade II gliomas and strong in almost all patients with Grade III or IV gliomas, reflecting the histological grade of malignancy. In patients with non-glioma brain tumors except for 1 patient with a metastatic brain tumor, the fluorescence intensity was strong. The mean TPS concentration in tissues was 1.62 μg/g for strong fluorescence areas, 0.67 μg/g for weak fluorescence areas and 0.19 μg/g for no fluorescence areas. Conclusions: Establishment of an appropriate fluorescence observation system enabled fluorescence-guided resection of malignant brain tumors using TPS, and the fluorescence intensity of tumors correlated with the TPS concentrations in tissues. These results suggest that TPS is a useful photosensitizer for both intraoperative fluorescence diagnosis and photodynamic therapy. Frontiers Media S.A. 2019-03-21 /pmc/articles/PMC6438081/ /pubmed/30949484 http://dx.doi.org/10.3389/fsurg.2019.00012 Text en Copyright © 2019 Akimoto, Fukami, Ichikawa, Mohamed and Kohno. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Surgery
Akimoto, Jiro
Fukami, Shinjiro
Ichikawa, Megumi
Mohamed, Awad
Kohno, Michihiro
Intraoperative Photodiagnosis for Malignant Glioma Using Photosensitizer Talaporfin Sodium
title Intraoperative Photodiagnosis for Malignant Glioma Using Photosensitizer Talaporfin Sodium
title_full Intraoperative Photodiagnosis for Malignant Glioma Using Photosensitizer Talaporfin Sodium
title_fullStr Intraoperative Photodiagnosis for Malignant Glioma Using Photosensitizer Talaporfin Sodium
title_full_unstemmed Intraoperative Photodiagnosis for Malignant Glioma Using Photosensitizer Talaporfin Sodium
title_short Intraoperative Photodiagnosis for Malignant Glioma Using Photosensitizer Talaporfin Sodium
title_sort intraoperative photodiagnosis for malignant glioma using photosensitizer talaporfin sodium
topic Surgery
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6438081/
https://www.ncbi.nlm.nih.gov/pubmed/30949484
http://dx.doi.org/10.3389/fsurg.2019.00012
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