Pre-operative dual-time-point [18F]FET PET differentiates CDKN2A/B loss and PIK3CA mutation status in adult-type diffuse glioma: a single-center prospective study

Dong Yun Lee; Jungsu S Oh; Jeong Won Kim; Minyoung Oh; Seung Jun Oh; Seungjoo Lee; Young-Hoon Kim; Jeong Hoon Kim; Soo Jeong Nam; Sang Woo Song; Jae Seung Kim

doi:10.1007/s00259-024-06935-z

Pre-operative dual-time-point [¹⁸F]FET PET differentiates CDKN2A/B loss and PIK3CA mutation status in adult-type diffuse glioma: a single-center prospective study

Eur J Nucl Med Mol Imaging. 2024 Oct 4. doi: 10.1007/s00259-024-06935-z. Online ahead of print.

Authors

Affiliations

¹ Department of Nuclear Medicine, Asan Medical Center, University of Ulsan College of Medicine, 88 Olympic-ro 43-gil, Songpa-gu, Seoul, 05505, Korea.
² Department of Neurosurgery, Asan Medical Center, University of Ulsan College of Medicine, 88 Olympic-ro 43-gil, Songpa-gu, Seoul, 05505, Korea.
³ Department of Pathology, Asan Medical Center, University of Ulsan College of Medicine, 88 Olympic-ro 43-gil, Songpa-gu, Seoul, 05505, Korea.
⁴ Department of Neurosurgery, Asan Medical Center, University of Ulsan College of Medicine, 88 Olympic-ro 43-gil, Songpa-gu, Seoul, 05505, Korea. [email protected].
⁵ Department of Nuclear Medicine, Asan Medical Center, University of Ulsan College of Medicine, 88 Olympic-ro 43-gil, Songpa-gu, Seoul, 05505, Korea. [email protected].

PMID: 39365462
DOI: 10.1007/s00259-024-06935-z

Abstract

Purpose: While [¹⁸F]FET PET plays a complementary role in glioma imaging, it needs to be more comprehensively understood for improved characterization of glioma prior to surgery given the evolving landscape of molecular neuropathology. Thus, we investigated the utility of pre-operative dual-time-point [¹⁸F]FET PET in correlation with next-generation sequencing (NGS) data in patients with adult-type diffuse glioma (ADG).

Methods: Adult patients who were suspected to have primary glioma were prospectively recruited between June 2021 and January 2024. They underwent pre-operative dual-time-point static PET/CT at 20 min (early) and 80 min (delay) after [¹⁸F]FET injection. Semi-quantitative parameters of the hottest lesion (SUV_max) of tumour and the hottest lesion-to-normal brain ratio (TBR_max) were assessed from each summed image. Furthermore, the percentage changes (△) of SUV_max and TBR_max between two images were calculated. Histopathology of glioma was determined according to the 2021 WHO classification and NGS data.

Results: This study investigated a dozen genes in 76 patients, of whom 51 had isocitrate dehydrogenase (IDH)-wild-type glioblastoma, 13 had IDH-mutant astrocytoma, and 12 had IDH-mutant oligodendroglioma. Every tumour was [¹⁸F]FET-avid having TBR_max more than 1.6. Patients with CDKN2A/B loss had significantly higher values of SUV_max (5.7 ± 1.6 vs. 4.7 ± 1.3, p = 0.004; 5.0 ± 1.4 vs. 4.4 ± 1.2, p = 0.026) and TBR_max (6.5 ± 1.8 vs. 5.1 ± 1.7, p = 0.001; 5.3 ± 1.5 vs. 4.3 ± 1.3, p = 0.004) in both scans than patients without CDKN2A/B loss, even after adjustment for age, MRI enhancement, tumor grade and type of pathology. Furthermore, patients with PIK3CA mutation (16.2 ± 11.8 vs. 6.7 ± 11.6, p = 0.007) had significantly higher △SUV_max than patients without PIK3CA mutation, even after adjustment for age, MRI enhancement, tumor grade, and type of pathology.

Conclusion: Among the dozen genes investigated in this prospective study in patients with ADG, we found out that CDKN2A/B loss and PIK3CA mutation status could be differentiated by pre-operative dual-time-point [¹⁸F]FET PET/CT.

Keywords: Adult-type diffuse glioma; CDKN2A/B loss; Dual-time-point [18F]FET PET; NGS data; PIK3CA mutation.

Abstract

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