The Relationship Between IDH1 Mutation Status and Metabolic Imaging in Nonenhancing Supratentorial Diffuse Gliomas: A 11 C-MET PET Study

Abstract

Purpose:

We evaluated the relationship between isocitrate dehydrogenase 1 (IDH1) mutation status and metabolic imaging in patients with nonenhancing supratentorial diffuse gliomas using ¹¹C-methionine positron emission tomography (¹¹C-MET PET).

Materials and Methods:

Between June 2012 and November 2017, we enrolled 86 (38 women and 48 men; mean age, 41.9 ± 13.1 years [range, 8-67 years]) patients with newly diagnosed supratentorial diffuse gliomas. All patients underwent preoperative ¹¹C-MET PET. Tumor samples were obtained and immunohistochemically analyzed for IDH1 mutation status.

Results:

The mutant and wild-type IDH1 diffuse gliomas had significantly different mean maximum standardized uptake value values (2.73 [95% confidence interval, CI: 2.32-3.16] vs 3.85 [95% CI: 3.22-4.51], respectively; P = .004) and mean tumor-to-background ratio (1.90 [95% CI: 1.65-2.16] vs 2.59 [95% CI: 2.17-3.04], respectively; P = .007).

Conclusions:

¹¹C-methionine PET can noninvasively evaluate the IDH1 mutation status of patients with nonenhancing supratentorial diffuse gliomas.

Introduction

Cerebral gliomas are the most common primary malignant brain tumors, accounting for 29% of all primary and 81% of all malignant brain tumors. ¹ Previously, prognostic evaluations were based on the histological features of tumor tissues along with clinical variables, such as age and performance status. However, the clinical outcomes have greatly varied among patients regardless of having the same pathological classification. Although the histopathological classification of gliomas has a long history, it has high interobserver and intraobserver variability and does not adequately predict clinical outcomes.

Recently, several biomarkers have been discovered to play vital roles in tumor differentiation. Molecular characterizations have become even more relevant, with mutations of isocitrate dehydrogenase (IDH), tumor protein 53 (TP53), and α-thalassemia/mental retardation syndrome X-linked (ATRX); 1p/19q codeletion; and O ⁶ -methylguanine-DNA methyltransferase (MGMT) promoter methylation being the important diagnostic and prognostic markers for tumors with similar morphology. ² Consequently, clinicians now increasingly rely on genetic classification to guide clinical decision-making.

Currently, World Health Organization (WHO) grades II to III are considered diffuse gliomas because of their similar genetic characteristics. ³ Isocitrate dehydrogenase mutations are a characteristic of most diffuse gliomas and define a subtype associated with better prognosis. ⁴ Isocitrate dehydrogenase mutations can be found in up to 80% of grades II to III gliomas and secondary glioblastomas but rarely in primary glioblastomas. ^3,4 Furthermore, compared to IDH-mutated tumors, grades II to III gliomas with wild-type IDH more frequently show molecular genetic alterations, which resemble those in glioblastomas. ^3,5 The genetic similarities between IDH wild-type glioblastomas and IDH wild-type diffuse gliomas lead to the same aggressive clinical behaviors. ⁶ Compared to gliomas without IDH mutations, IDH-mutated gliomas progress slower over time and have better prognosis. ^4,7 Moreover, isocitrate dehydrogenase 1 (IDH1) mutation status can be used as a predictor of complete resection ⁸ and median survival time. ⁹ These associations have been justifiably accepted and have been shown to have a profound impact on the development of the new WHO Classification of central nervous system (CNS) tumors ¹⁰ and on the updates on the recent CNS guidelines of the National Comprehensive Cancer Network. Generally, these biomarkers are detected by immunohistochemical analysis or genetic sequencing of postoperative pathological specimens. Therefore, identification of complementary imaging markers for the aforementioned critical biomarkers would be greatly valuable in providing more information for preoperative decision-making and maximally safe resection.

For decades, ¹¹C-methionine positron emission tomography (¹¹C-MET PET) has been applied for the diagnosis of gliomas; ¹¹ differentiation between tumor recurrence and radiation injury; ¹² and surgical ¹³ and radiotherapy ¹⁴ planning, owing to its strong contrast with background uptake in normal brain tissue. Moreover, the reported correlation of ¹¹C-MET uptake with cell proliferation, expressions of Ki-67 and proliferating cell nuclear antigen, and microvessel density ¹⁵ indicated its role as a marker of rapid tumor proliferation. Therefore, previous studies have applied ¹¹C-MET PET to explore the association of ¹¹C-MET uptake with preoperative tumor grading ¹⁶ and the prognosis of gliomas. ¹⁷

Although ¹¹C-MET PET has shown a possible association between ¹¹C-MET uptake and the molecular mechanisms of gliomas, the relationship between the key molecular biomarkers and ¹¹C-MET uptake has been rarely studied. Molecular biomarkers, which are used for diagnosis and prognostication, must be identified by surgery. However, preoperative diagnosis and prognostication can alter the medical treatment strategy. Given the value of noninvasive preoperative evaluation of molecular biomarkers for clinical applications, we evaluated the relationship between ¹¹C-MET PET uptake and IDH1 in patients with newly diagnosed diffuse supratentorial gliomas.

Material and Methods

Study Population

Between June 2012 and November 2017, we enrolled patients with newly diagnosed supratentorial diffuse glioma (WHO II and III) in this retrospective study. Patients who had previously undergone surgery, radiotherapy, or chemotherapy were excluded. Surgery was performed within a month of the latest diagnostic ¹¹C-MET PET. Histological diagnosis was based on biopsy or tumor resection, as available. The study was approved by the institutional review board, and informed consent was obtained from all individual participants included in the study.

¹¹C-Methionine Positron Emission Tomography and Computed Tomography

All patients underwent ¹¹C-MET PET using a 3-dimensional (3D) PET scanner (Biograph 64; Siemens, Munich, Germany). Data acquisition began 15 minutes after an intravenous bolus injection of 370 MBq (10 mCi) ¹¹C-MET. Special analysis and fasting were not required for ¹¹C-MET PET because no collateral effects were reported. Before PET, computed tomography (CT) was performed for attenuation correction and image fusion. ¹¹C-methionine PET images were obtained in a 15-minute static scan in 3D acquisition mode. The spatial resolution of the CT scanner in axial and tangential directions was 1.5 mm. Reconstructed imaging was achieved with filtered back projection and full width at a maximum of 3.5 mm using the manufacturer’s workstation and postreconstruction Gaussian 3D filter smoothing.

¹¹C-Methionine Positron Emission Tomography/CT Data Processing

Semiquantitative analysis was performed using the maximum standardized uptake value (SUVmax) and mean tumor-to-background ratio (TBRmean). For SUVmax, 3D spherical volume of interest that covered the entire tumor was drawn, and the workstation automatically detected tumor boundaries. Further manual adjustments were then made to allow region of interest (ROI) to cover the whole tumor shown on the magnetic resonance imaging (MRI), and the SUVmax value inside the ROI was calculated. If the tumor was hypometabolic on ¹¹C-MET PET, MRI only was used to delineate the tumor. For TBRmean, a circular ROI (7-mm diameter) was placed in the most intense area of the tumor in the center of the pixel with the maximum SUV, and in the unaffected corresponding contralateral region. ¹⁸ If the tumor affected the mirroring region, the ROI was placed on the intact region of the contralateral hemisphere. Mean tumor-to-background ratio was defined as the mean uptake of radioisotope in the lesion ROI divided by the mean uptake in the reference ROI.

Histopathological and Immunohistochemical Examinations

Samples obtained by biopsy and tumor resection were fixed in 10% formalin and embedded in paraffin. The hematoxylin and eosin-stained sections of all samples were reviewed by 2 blinded neuropathologists and were categorized according to the WHO Classification of Tumors of the CNS. The IDH1R132H protein expression was evaluated to determine the IDH1 mutation status because antibodies against IDH1-mutated proteins are routinely used to detect IDH mutation. ¹⁹ The histological definition was updated according to the WHO 2016 Classification of Tumors of the CNS, when all necessary data were available.

Statistical Analysis

Descriptive statistics were presented as mean with 95% confidence interval (CI) or mean with standard deviation. The relationships between ¹¹C-MET PET parameters and IDH mutation status were assessed. Student t test was performed for 2-group comparisons, with adjustments for cases with unequal variances, as analyzed by Levene test. Value of P < .05 was considered statistically significant. SPSS software (version 21, IBM, Armonk, New York) was used for data analysis.

Results

Study Population

A total of 86 patients with newly diagnosed supratentorial diffuse gliomas were enrolled in this study and their descriptive data are summarized in Table 1. Isocitrate dehydrogenase mutations accounted for 55.8% (48 of 86) of all patients. Of the 61 patients diagnosed as WHO grade II glioma, 68.9% (42 of 61) had IDH1 mutation. Of the remaining 25 patients who were diagnosed as WHO grade III glioma, 24% (9 of 25) had IDH mutations. Of the enrolled patients, 22.1% (19 of 86) had a negative ¹¹C-MET PET uptake. Eleven patients with photopenic defects could be identified among these 19 negative ¹¹C-MET PET scans.

Table 1.

Patient Characteristics, Clinical Data, Pathologic Findings.^a

Characteristics	Value
Age, year
Range	8-67
Mean	41.9 ± 13.1
Sex
Male	48 (55.8%)
Female	38 (44.2%)
Surgical procedure
Resection	62 (72.1%)
Biopsy	24 (27.9%)
WHO grade and histologic diagnosis
WHO II
Astrocytoma	44 (51.2%)
Oligodendroglioma	16 (18.6%)
Pleomorphic xanthoastrocytoma	1 (1.2%)
WHO III
Anaplastic astrocytoma	25 (29.1%)
IDH1 mutation status
IDH1 mutation	48 (55.8%)
IDH1 wild-type	38 (44.2%)

Abbreviations: IDH1, isocitrate dehydrogenase 1; WHO, World Health Organization.

^a Values are shown as the number of patients, unless otherwise indicated.

Relationship Between ¹¹C-MET Uptake and Glioma Grade

The ¹¹C-MET uptake values were compared between the tumor grades. As shown in Figure 1, the SUVmax was significantly higher for grade III gliomas than for grade II gliomas (4.16 [95% CI: 3.29-5.05] vs 2.85 [95% CI: 2.49-3.22]; P = .011), whereas the TBRmean values were not significantly different between grade II and grade III gliomas (2.04 [95% CI: 1.80-2.32] vs 2.59 [95% CI: 2.08-3.13], respectively; P = .078).

Figure 1.

Relationship between ¹¹C-MET uptake and glioma grade. The SUVmax of grade III gliomas is significantly higher than that of grade II gliomas (P = .011), whereas there was no significant difference in the TBR mean values of grades II and III gliomas (P = .078). ¹¹C-MET indicates ¹¹C-methionine; IDH1, isocitrate dehydrogenase 1; SUVmax, maximum standardized uptake value; TBRmean, mean tumor-to-background ratio.

Effect of the Oligodendroglial Component on the ¹¹C-MET Uptake

In this study, gliomas with oligodendroglial component accounted for 18.6% (16 of 86) of all cases and were all grade II gliomas. Gliomas with oligodendroglial component and those without oligodendroglial component had no significant differences in SUVmax (2.89 [95% CI: 2.38-3.41] vs 3.31 [95% CI: 2.87-3.41], respectively; P = .232) and TBRmean (2.02 [95% CI: 1.71-2.30] vs 2.25 [95% CI: 1.97-2.57], respectively; P = .268).

Separate analyses of grade II gliomas showed that those with oligodendroglial component accounted for 22.5% (16 of 71). Gliomas with oligodendroglial component and those without oligodendroglial component had no significant differences in SUVmax (2.89 [95% CI: 2.41-3.38] vs 2.83 [95% CI: 2.39-3.31]; P = .896) and TBRmean values (2.02 [95% CI: 1.73-2.30] vs 2.05 [95% CI: 1.75-2.41]; P = .900).

Relationship Between ¹¹C-MET Uptake and IDH1 Mutation Status

The IDH1 mutation status of the supratentorial diffuse gliomas and its relationships with the ¹¹C-MET parameters were analyzed. As shown in Figure 2, compared to tumors with IDH1 mutation, wild-type IDH1 tumors had significantly higher SUVmax values (2.73 [95% CI: 2.32-3.16] vs 3.85 [95% CI: 3.22-4.51]; P = .004) and TBRmean values (1.90 [95% CI: 1.65-2.16] vs 2.59 [95% CI: 2.17-3.04]; P = .007). Representative cases are shown in Figure 3.

Figure 2.

Relationship between ¹¹C-MET parameter values and IDH1 mutation status. Gliomas with mutant and wild-type IDH1 have significantly different SUVmax values (P = .007) and TBR mean values (P = .004). ¹¹C-MET indicates ¹¹C-methionine; IDH1, isocitrate dehydrogenase 1; SUVmax, maximum standardized uptake value; TBRmean, mean tumor-to-background ratio.

Figure 3.

Representative cases. A, T1-weighted MRI shows a low-intensity lesion in the right frontal lobe. B, Fluid-attenuated inversion-recovery MRI outlines the margin of the lesion. C, ¹¹C-methionine PET shows weak accumulation in the lesion with SUVmax of 1.25 and TBRmean of 0.77. D, Surgery confirms the diagnosis of IDH1 mutated astrocytoma was confirmed. E, T1-weighted MRI shows a low-intensity lesion in the right frontal lobe. F, Fluid-attenuated inversion-recovery MRI outlines the margin of the lesion. G, ¹¹C-MET PET shows strong accumulation in the lesion, with SUVmax of 8.45 and TBRmean of 3.25. H, Surgery confirms the diagnosis of IDH1 wild-type anaplastic astrocytoma was confirmed. ¹¹C-MET PET indicates ¹¹C-methionine positron emission tomography; IDH1, isocitrate dehydrogenase 1; MRI, magnetic resonance imaging; SUVmax, maximum standardized uptake; TBRmean, mean tumor-to-background ratio.

Separate analyses of grade II gliomas showed that, compared to tumors with IDH1 mutation, wild-type IDH1 tumors had significantly higher SUVmax values (2.58 [95% CI: 2.21-2.96] vs 3.44 [95% CI: 2.78-4.21]; P = .025) and TBRmean values (1.84 [95% CI: 1.60-2.11] vs 2.50 [95% CI: 1.98-3.08]; P = .017; Figure 4).

Figure 4.

Relationship between ¹¹C-MET parameter values and IDH1 mutation status in WHO II gliomas. Gliomas with mutant and wild-type IDH1 have significantly different SUVmax values (P = .025) and TBRmean values (P = .017). ¹¹C-MET indicates ¹¹C-methionine; IDH1, isocitrate dehydrogenase 1; SUVmax, maximum standardized uptake value; TBRmean, mean tumor-to-background ratio; WHO, World Health Organization.

On the other hand, separate analyses of grade III supratentorial gliomas showed no such relationships between the ¹¹C-MET parameters and IDH1 mutation status. Compared with tumors with IDH1 mutation, wild-type IDH1 tumors had similar SUVmax values (3.86 [95% CI: 2.13-5.65] vs 4.26 [95% CI: 3.26-5.27], respectively; P = .718) and TBRmean values (2.32 [95% CI: 1.28-3.42] vs 2.68 [95% CI: 2.09-3.27], respectively; P = .587; Figure 5).

Figure 5.

Relationship between ¹¹C-MET parameter values and IDH1 mutation status in WHO III gliomas. Gliomas with mutant and wild-type IDH1 have no statistically significant difference in SUVmax values (P = .718) and TBRmean values (P = .587). ¹¹C-MET indicates ¹¹C-methionine; IDH1, isocitrate dehydrogenase 1; SUVmax, maximum standardized uptake value; TBRmean, mean tumor-to-background ratio; WHO, World Health Organization.

Discussion

The diagnosis and prognosis of diffuse gliomas had been primarily determined based on histopathological characteristics. However, the pathological classification of gliomas had been limited by sample heterogeneity. Because genomic analyses have dramatically increased our understanding of gliomas, we have been pursuing the trend of biomarker-driven glioma classification, which has been consistently proven to play a significant role in revealing the molecular characteristics and in the prognostication of gliomas. In particular, the mutation status of IDH, ATRX, TP53, and 1p/19q had been employed for the diagnosis and prognostication of diffuse gliomas, and MGMT promoter methylation status was reported to alter the chemotherapy plan. ²⁰

Prominent evidence has indicated that IDH mutations are early events in glioma formation before molecular distinctions drive specific differentiation and frequently occur in astrocytic and oligodendroglial lineages; examples of such mutations are 1p/19q codeletions in oligodendrogliomas and TP53 and ATRX mutations in astrocytomas. ³ Isocitrate dehydrogenase mutations can be found in up to 80% of grades II to III gliomas and secondary glioblastomas but rarely in primary glioblastomas. ^3,4 Furthermore, compared with IDH-mutated grade II to III gliomas, those with wild-type IDH more frequently show molecular genetic alterations, such as epidermal growth factor receptor (EGFR), telomerase reverse transcriptase (TERT), Phosphatase And Tensin Homolog (PTEN), Cyclin Dependent Kinase Inhibitor 2A (CDKN2A), neurofibromatosis type 1 (NF1), and RB Transcriptional Corepressor 1 (RB1) alterations, which resemble the mutations in glioblastomas. ^3,5 Genetic similarities between IDH wild-type glioblastomas and IDH wild-type diffuse gliomas lead to the same aggressive clinical behaviors. ⁶ Compared to gliomas without IDH mutations, IDH-mutated gliomas progress slower over time and have better prognosis. ^4,7 Meanwhile, gliomas that have relatively high ¹¹C-MET uptake have been reported to have poor prognosis. ²¹ This may explain the significantly higher ¹¹C-MET uptake in gliomas with IDH1 wild-type than in those with mutants in our study.

Previously, ¹¹C-MET PET had been used to predict the status of 1p/19q codeletion ^{22 -24} and MGMT promoter methylation, ^24,25 although the correlations remain controversial. Moreover, the correlation between IDH mutation status and ¹¹C-MET uptake had been rarely studied. In this study, patients with newly diagnosed nonenhancing supratentorial diffuse gliomas were demonstrated to have higher SUVmax and TBRmean values when IDH1 mutation was present than when there was no IDH1 mutation. A prior study investigated the association between IDH1 mutation status in diffuse gliomas and ¹⁸F-fluorodeoxyglucose (¹⁸F-FDG) uptake, but the result showed that IDH1 mutation status did not correlate with ¹⁸F-FDG uptake. ²⁶ A possible explanation for this result was that the necrosis and blood–brain barrier (BBB) disruption in more aggressive gliomas resulted in a nonlinear increase in ¹⁸F-FDG uptake. A study using dynamic ¹⁸F-fluoroethyltyrosine (¹⁸F-FET) PET demonstrated that IDH mutations were more frequent in tumors with homogeneous increasing and focal decreasing time-activity curve but were rare in those exhibiting homogeneous decreasing time-activity curve. ²⁷ Verger et al ²⁸ have shown that ¹⁸F-FET PET had considerable diagnostic value for discriminating between astrocytomas and glioblastomas with mutant and wild-type IDH, suggesting that ¹⁸F-FET PET may be useful for noninvasive identification of IDH mutation status. However, another study that used static ¹⁸F-FET PET found no association between IDH mutation status and ¹⁸F-FET uptake in low-grade glioma patients. ²⁹ Using 3,4-dihydroxy-6-¹⁸F-fluoro-L-phynel-alanine (¹⁸F-FDOPA) PET, one study illustrated higher ¹⁸F-FDOPA uptake in gliomas with IDH mutation than in IDH wild-type gliomas. ³⁰ Previously, a study on ¹¹C-MET PET indicated that IDH-mutated gliomas showed lower ¹¹C-MET uptake, compared to that of IDH wild-type gliomas. ²⁴ This finding was contradictory to the findings of the previous study on ¹⁸F-FDOPA. The apparent discrepancy in the uptake patterns between ¹¹C-MET and ¹⁸F-FDOPA may be associated with the metabolic profile of IDH-mutated gliomas. Isocitrate dehydrogenase mutation status is associated with elevated intracellular free amino acids, which can reduce efflux rate constant from the tumor tissue and affect the uptake of ¹⁸F-FDOPA via amino acid transporters that act as exchangers. ^31,32 In a previous study on ¹¹C-MET, the samples included high-grade and recurrent gliomas with disrupted BBBs, the ¹¹C-MET uptake in gliomas was influenced by passive diffusion in areas with BBB. ³³ In our study, all gliomas had intact BBBs and were shown as nonenhancing supratentorial diffuse gliomas on MRI. Therefore, methionine uptake was relatively less influenced by BBB disruption and only reflected the metabolic tumor. After ruling out the aforementioned factor, our findings consistently confirmed that ¹¹C-MET uptake was significantly correlated with IDH1 mutation status in supratentorial diffuse glioma patients. However, the results were not significant in the subgroup of WHO III gliomas alone; this may be accounted for by the relatively few supratentorial WHO III gliomas in our study population.

In this study, the significant correlation of the ¹¹C-MET PET parameters with IDH1 mutation status indicated the potential value of ¹¹C-MET PET for noninvasive evaluation of IDH1 mutation status. Although IDH1 detection mainly relies on postoperative pathological examination, preoperative noninvasive detection methods can enable the development of more personalized treatment plans. Beiko et al ⁸ found that IDH1 mutation was an independent predictor of complete resection and that IDH1-mutated gliomas were more frontally located. Kawaguchi et al ³⁴ suggested that IDH1-mutated grade III tumors without 1p/19q codeletion require a greater extent of resection. Maarten et al ³⁵ demonstrated that even very small postoperative volumes can have a strong negative effect on the overall survival of patients with IDH-mutated astrocytoma. A previous study on patients with IDH wild-type glioma reported that the median survival of patients with totally resected tumors was 2.86 years, whereas that for patients with partially resected tumors was 1.55 years. ⁹ Moreover, compared to IDH wild-type tumors, IDH-mutated tumors were suggested to have higher response rate to chemotherapy and longer progression-free survival after radiation therapy or chemotherapy. ³⁶ Moreover, IDH mutations in low grade gliomas were shown to predict longer survival and response to temozolomide. ³³ Therefore, the IDH1 mutation status of gliomas can enable individualized treatment strategies and make preoperative noninvasive detection essential.

Because the treatment regimens and strategies vary among different tumor classes, noninvasive imaging methods that predict tumor grade can provide clinicians the directions for treatment before surgery. Relevant studies on ¹¹C-MET PET have drawn different conclusions. Some studies have shown that ¹¹C-MET PET had certain significance in tumor classification, ^16,37,38 whereas other studies have shown opposite results. ^{39 -41} In our study, the SUVmax of grade III gliomas was significantly higher than that of the grade II gliomas, whereas the results on TBRmean showed only a certain trend but did not reach a statistically significant difference. The differences among the studies may be due to the different sample compositions because different gliomas have some differences in ¹¹C-MET uptake. Some literatures reported that ¹¹C-MET uptake may be higher in oligodendrogliomas than in astrocytomas. ^17,42,43 However, in our study, the SUVmax and TBRmean did not significantly differ according to the presence of an oligodendroglial component. Perhaps, this was because gliomas with oligodendroglial component accounted for a small proportion of our samples, and all of them were WHO II gliomas.

Recently, Galldiks et al ⁴⁴ reported that within 100 patients with ⁸F-FET negative gliomas, a subgroup of patients who exhibit photopenic defects in ⁸F-FET uptake had an unfavorable outcome compared to patients with isometabolic ⁸F-FET uptake, and the multivariate survival analysis indicated that photopenic defects predict an unfavorable progression-free survival (PFS). Further follow-up imaging changes showed that photopenic IDH-mutant WHO II astrocytomas turned into ⁸F-FET positive faster than isometabolic IDH-mutant WHO II astrocytomas. ⁴⁵ The survival discrepancy could be explained with an inverted U-shaped curve, showing isometabolic gliomas with the most favorable PFS and both photopenic gliomas and ⁸F-FET positive gliomas on the adverse end of the PFS spectrum; however, the hypothesis remains to be confirmed by the overall survival analysis. ⁴⁶ Moreover, a study using ¹⁸F-FDOPA PET demonstrated patients with photopenic defects showed a tendency for a shorter PFS in comparison to patients with isometabolic ¹⁸F-FDOPA uptake. ⁴⁵ In our study, 11 patients were identified as photopenic defects among the 19 patients who had negative ¹¹C-MET PET uptake. However, due to the small sample size and the lack of survival time data, further analysis was not feasible. Whether the relationship between ¹¹C-MET uptake and survival time also has the same U-shaped curve as ⁸F-FET PET is worth further exploration.

Some limitations of our study should be noted. First, the study was retrospective with a relatively small sample size. Therefore, the prognostic value of ¹¹C-MET PET must be validated in a larger prospective study. Second, the IDH1 mutations in our study were detected by immunohistochemistry. Although immunohistochemistry can detect most IDH1 mutations and is widely applied in clinical practice, genetic sequencing is needed to further improve the diagnostic accuracy. ^47,44

Conclusions

The ¹¹C-MET uptake was significantly related with IDH1 mutation status in patients with supratentorial diffuse glioma. From a clinical perspective, ¹¹C-MET PET can be used as an additional tool for noninvasive preoperative evaluation of the IDH1 mutation status of nonenhancing supratentorial diffuse gliomas.