Double dose of 5-aminolevulinic acid and its effect on protoporphyrin IX accumulation in low-grade glioma
Open accessAbstract
OBJECTIVE: Administration of 5-aminolevulinic acid (5-ALA) does not regularly elicit fluorescence in low-grade glioma (LGG) at currently established doses and timing of administration. One explanation may be differences in blood-brain barrier (BBB) integrity compared to high-grade glioma. The authors hypothesized that for a BBB semipermeable to 5-ALA there might be a relationship between plasma 5-ALA concentration and its movement into the brain. A higher dose would elicit more 5-ALA conversion into protoporphyrin IX (PPIX). The authors present a case series of patients harboring LGG who received higher doses of 5-ALA. METHODS: Patients undergoing surgery for indeterminate glioma later diagnosed as LGG were included in this study. 5-ALA was administered at a standard dose of 20 mg/kg body weight (bw) 4 hours prior to induction of anesthesia. A subgroup of patients received a higher dose of 40 mg/kg bw. Fluorescence was evaluated visually and PPIX concentration (cPPIX) was determined ex vivo by hyperspectral measurements in freshly extracted tissue. All adverse events were recorded. RESULTS: A total of 23 patients harboring diffuse low-grade astrocytomas (n = 19) and oligodendrogliomas (n = 4) were analyzed. Thirteen patients received 20 mg/kg bw, and 10 patients received 40 mg/kg bw of 5-ALA. In the 20 mg/kg group, 30.8% (4 of 13) of tumors harbored areas of visible fluorescence, compared to 60% of cases (n = 6 of 10) with 40 mg/kg bw. The threshold to visibility was 1 μg/ml in both groups. Measured over all biopsies, the mean cPPIX was significantly higher in the double-dose group (1.8 vs 0.45 μg/ml; p < 0.001). In non-visibly fluorescent tissue the mean cPPIX was 0.146 μg/ml in the 20 mg/kg and 0.347 μg/ml in the 40 mg/kg group, indicating an increase of 138% (p < 0.001). CONCLUSIONS: These observations demonstrate different regions with different levels of PPIX accumulation in LGG. With higher 5-ALA doses cPPIX increases, leading to more regions surpassing the visibility threshold of 1 μg/ml. These observations can be explained by the fact that the BBB in LGG is semipermeable to 5-ALA. Higher 5-ALA doses result in more PPIX conversion, an observation with implications for future dosing in LGG.
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Doubling the dose of ALA to 40 mg/kg or delaying the examination time to 7 and 8 h after ALA administration increases PpIX fluorescence in low-grade gliomas.
“There are studies showing that either doubling the dose of ALA to 40 mg/kg [55] or delaying the examination time to 7 and 8 h after ALA administration [53] increases the PpIX fluorescence in low-grade gliomas.”
From 5-Aminolevulinic Acid as a Theranostic Agent for Tumor Fluorescence Imaging and Photodynamic Therapy (2023) · cites this paper as [55]
Doubling the dose of ALA from 20 to 40 mg/kg significantly increases tumor PpIX fluorescence and doubles the rate of tumor detection in low-grade glioma patients.
“This notion is supported by the finding that doubling the dose of ALA from 20 to 40 mg/kg not only significantly increases tumor PpIX fluorescence but also doubles the rate of tumor detection in low-grade glioma patients [55].”
From 5-Aminolevulinic Acid as a Theranostic Agent for Tumor Fluorescence Imaging and Photodynamic Therapy (2023) · cites this paper as [55]
Cites
Teng, L., Nakada, M., Zhao, S.-G., Endo, Y., Furuyama, N., Nambu, E., Pyko, I. V., Hayashi, Y., & Hamada, J.-I. (2011) · British Journal of Cancer · doi:10.1038/bjc.2011.12 · Cited by 172 · see citing works
Transport of 5-aminolevulinic acid between blood and brain
Ennis, S. R., Novotny, A., Xiang, J., Shakui, P., Masada, T., Stummer, W., Smith, D. E., & Keep, R. F. (2003) · Brain Research · doi:10.1016/s0006-8993(02)03749-6 · Cited by 146 · see citing works
Self-citationJaber, M., Ewelt, C., Wölfer, J., Brokinkel, B., Thomas, C., Hasselblatt, M., Grauer, O., & Stummer, W. (2019) · Neurosurgery · doi:10.1093/neuros/nyy365 · Cited by 66 · see citing works
Self-citationKaneko, S., Suero Molina, E., Ewelt, C., Warneke, N., & Stummer, W. (2019) · Neurosurgery · doi:10.1093/neuros/nyz129 · Cited by 56 · see citing works
Self-citationBlack, D., Kaneko, S., Walke, A., König, S., Stummer, W., & Suero Molina, E. (2021) · Scientific Reports · doi:10.1038/s41598-021-99228-6 · Cited by 46 · see citing works
Self-citationFluorescence real-time kinetics of protoporphyrin IX after 5-ALA administration in low-grade glioma
Kaneko, S., Suero Molina, E., Sporns, P., Schipmann, S., Black, D., & Stummer, W. (2022) · Journal of Neurosurgery · doi:10.3171/2020.10.jns202881 · Cited by 28 · see citing works
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5-Aminolevulinic Acid as a Theranostic Agent for Tumor Fluorescence Imaging and Photodynamic Therapy
Howley, R., Chandratre, S., & Chen, B. (2023) · Bioengineering · doi:10.3390/bioengineering10040496 · Cited by 33 · see citing works
- Authors
- Suero Molina, E., Black, D., Kaneko, S., Müther, M., & Stummer, W.
- Affiliations
- Department of Neurosurgery, University Hospital of Münster;
- Carl Zeiss (Germany) (DE)
- Hokkaido University (JP)
- University Hospital Münster (DE)
- ORCID
- Müther, Michael
- Venue
- Journal of Neurosurgery
- Published
- 2022-10-01
- Volume
- 137
- Issue
- 4
- Pages
- 943-952
- ISSN
- 0022-3085 (ISSN-L)
- 1933-0693
- OpenAlex
- W4214569527
- Cited by
- 28
- References
- 6
- Citations by year
- 2026: 5 · 2025: 3 · 2024: 13 · 2023: 5 · 2022: 2
- FWCI
- 3.57
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of neurosurgery (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Carl Zeiss Meditec AG
- Topics
- Health Sciences › Medicine › Genetics › Glioma Diagnosis and Treatment
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Photodynamic Therapy Research Studies
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Optical Imaging and Spectroscopy Techniques
- Keywords
- 5-aminolevulinic acid, low-grade glioma, protoporphyrin IX, fluorescence-guided surgery, blood-brain barrier permeability, diffuse astrocytoma, oligodendroglioma, tumor fluorescence, hyperspectral imaging, glioma grading
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