⁶⁸Ga-DOTATATE PET-CT as a tool for radiation planning and evaluating treatment responses in the clinical management of meningiomas

Abstract

Background and purpose

Meningiomas express the somatostatin receptor (SSTR), which normal bone and brain lack. PET imaging with SSTR ligands such as ⁶⁸ Ga-DOTATATE have been recently shown to aid in the imaging and identification of menginiomas. We hypothesize that ⁶⁸ Ga-DOTATATE PET/CT in conjunction with MRI aids in radiation (RT) target volume delineation and evaluating treatment response.

Materials and methods

Nineteen patients with meningiomas underwent ⁶⁸ Ga-DOTATATE PET/CT and MRI for RT planning and/or post-treatment follow-up. Meningiomas were grade I (n = 9) or not biopsied (n = 8) and frequently involved base of skull (n = 10). Ten (53%) patients received post-operative RT and 9 (47%) received fractaionted RT. In the subgroup that underwent both pre- and post-RT ⁶⁸ Ga-DOTATATE PET as well as MRI (n = 10), ROVER (ABX GmbH, Radeberg, Germany) adaptive thresholding software was utilized to measure total lesion activity (mean and max) before and after treatment. Tumor volume based on MRI was calculated before and after treatment. Total lesion activity and tumor volume changes were compared using Wilcoxon signed rank test.

Results

⁶⁸ Ga-DOTATATE PET/CT identified intraosseous (n = 4, 22%), falcine (n = 5, 26%) and satellite lesions (n = 3, 19%) and clarified the diagnosis of meningioma, resulting in a change in management in three patients. Mean total lesion activity decreased 14.7% (median), from pre to post-RT ⁶⁸ Ga-DOTATATE PET [range 97–8.5% (25–75%),S = − 26.5, p = 0.0039]. Max total lesion activity decreased 36% (median) over the same period [range 105–15% (25–75%), S = − 26.5 p = 0.0039]. In contrast, meningioma volumes based on MRI measurements did not significantly change per RECIST criteria and Wilcoxon signed rank test (S = − 3, p = 0.7422).

Conclusion

⁶⁸ Ga-DOTATATE PET/CT helped confirm suspected diagnoses and delineate target volumes particularly when lesions involved osseous structures and the falx. Mean and max total tumor ⁶⁸ Ga-DOTATATE activity on PET/CT decreased at three months following RT despite stable tumor volumes on MRI. Future studies are warranted to (1) assess the sensitivity and specificity of ⁶⁸ Ga-DOTATATE PET/CT, (2) evaluate the impact of ⁶⁸ Ga-DOTATATE PET/CT-based planning on treatment outcomes, and (3) assess the prognostic significance of these post-treatment imaging changes.

Introduction

Meningiomas are the most common primary brain tumor with a reported incidence of 8.33 per 100,000 [1] Radiation therapy (RT) is the preferred treatment for symptomatic meningiomas not amenable to surgical resection and is delivered in the adjuvant setting following resection of WHO II and III meningiomas.

Advanced RT techniques, including pencil beam scanning proton therapy (PBSPT), stereotactic radiosurgery (SRS), and intensity modulated radiotherapy (IMRT) are utilized to deliver a highly conformal dose to tumor, while also reducing radiation dose to surrounding healthy brain tissue. The efficacy of these techniques is highly dependent on accurate target delineation, which is currently guided by contrast-enhanced MRI.

The majority of meningiomas are now known to highly express somatostatin receptor-2 (SSTR2) [2, 3]. SSTR2 receptors have been exploited to allow for precise diagnostic and functional imaging of meningiomas. Klutman et al. demonstrated that Indium111 octreotide SPECT better identified residual or recurrent tumor versus MRI in post-operative surveillance of meningiomas [4]. More recently, PET utilizing radiotracer ligands of SSTR2 with ⁶⁸ Ga-DOTA have gained traction and are now used frequently in Europe in the diagnosis and treatment planning for meningiomas.

⁶⁸ Ga-DOTATATE PET/CT provides high contrast images of meningiomas, given that the surrounding normal brain and bone tissues lack the SSTR2. Furthermore, it has been shown to be more sensitive than MRI in detecting meningiomas [5, 6]. ⁶⁸ Ga-DOTATATE PET/CT is a particularly useful diagnostic tool when the risk of biopsy is prohibitive, as in the case of suspected optic nerve meningiomas [7]. Previous studies have also examined the utility of ⁶⁸ Ga-DOTATATE PET/CT for contouring and RT target delineation and demonstrated that it often results in modified treatment volumes compared to those created based upon CT and MRI [8,9,10,11,12]. However, post-treatment changes with ⁶⁸ Ga -DOTATATE PET/CT following radiation therapy have not been previously described.

In this series we report our experience incorporating ⁶⁸ Ga -DOTATATE PET/CT alongside conventional imaging in the workup, planning and post-treatment follow-up imaging assessment of patients with meningiomas treated with conventionally fractionated radiotherapy. Additionally, for those patients with both pre and post-treatment ⁶⁸ Ga -DOTATATE PET/CT we quantify the change in mean and max total tumor ⁶⁸ Ga-DOTATATE activity as compared to the change in tumor volume on pre and post-treatment MRI.

Methods and materials

Patients

We conducted an institutional review board approved retrospective evaluation of nineteen patients with clinically symptomatic meningiomas treated with radiation therapy at a single academic institution from 2017 to 2019. Patients underwent PET/CT with ⁶⁸ Ga-DOTATATE radiotracer, CT and brain MRI for radiation planning (n = 18, 95%) and/or post-treatment follow-up (n = 10, 53%). Inability to secure insurance authorization was a primary reason a portion of our population did not receive both pre and post treatment follow up ⁶⁸ Ga-DOTATATE PET/CT. Intracranial meningiomas were diagnosed by biopsy or based on classic imaging findings and multi-disciplinary tumor-board consensus opinion. Ten patients (53%) underwent a prior sub-total resection followed by adjuvant radiation, nine patients (47%) received radiation treatment alone. Medical records were reviewed and key clinical attributes were recorded.

Imaging

Conventional CT simulation with MRI fusion

Patients were immobilized in the RT treatment position using a three-point thermoplastic mask and thin-sliced CT scans were performed for RT treatment planning. Brain MRIs were performed within a week of treatment planning, and were fused to the RT CT-simulation images for target delineation.

68GA-DOTATATE PET/CT image acquisition

Brain ⁶⁸ Ga-DOTATATE PET/CT images were acquired on an integrated PET/CT scanner (Biograph mCT, Siemens) 60 min after intravenous administration of approximate 5 mCi of ⁶⁸ Ga-DOTATATE. Images were reconstructed in the sagittal, transverse and coronal axes for evaluation. A low dose CT scan was performed for attenuation correction.

Radiotherapy details

Initially, gross tumor volume (GTV) was delineated based on both the MRI and CT dataset. ⁶⁸ Ga-DOTATATE PET/CT was subsequently fused with CT simulation images, and the GTV was modified if there were PET-avid regions identified on PET imaging that were not previously identified on the MRI, but were felt to represent meningioma after review by the radiation oncologist and neuroradiologist. In accordance with our institutional clinical practice guidelines, a 3–5 mm clinical target volume expansion was added to the GTV for WHO grade I tumors. This margin was reduced to 0 mm around natural barriers and expanded at physician discretion when tumor infiltration into surrounding brain structures was less certain. The majority of patients were treated with fractionated PBSPT (n = 12, 63%) to a median dose of 5220 cGy in 29 fractions (range 4500–5940 cGy). Seven patients (37%) were treated with fractionated volumetric arc modulated radiotherapy to a median dose of 5220 cGy in 29 fractions (range 5220–5400 cGy).

Follow-up 68GA-DOTATATE PET/CT

A subgroup of ten patients received a follow-up ⁶⁸ Ga-DOTATATE PET/CT and independent MRI (n = 10) or PET-MR (n = 2) 3 months following completion of radiotherapy.

Post-RT analysis

PET/CT image analysis

Two nuclear medicine physicians, blinded to the patients’ medical history, independently evaluated pre and post radiation PET/CT images using an adaptive threshholding system (ROVER software; ABX GmbH, Radeberg, Germany). DICOM images were obtained, spherical or cylindrical masks were placed over an active lesion and the adaptive threshholding algorithm of ROVER auto segmented each lesion’s boundaries. The software utilized a threshold of 50% SUV max. ROVER automatically determined the lesion volume and quantitative PET parameters including SUVmax, SUVmean, and partial volume corrected (PVC) SUVmax and SUVmean for the treated lesions. Total lesion activity (TLA) was calculated by multiplying the PVC SUV (mean or max) and the dotatate volume determined by ROVER.

MRI image analysis

MRIs were reviewed by a neuroradiologist and the treating radiation oncologist to document imaging indications of response to radiotherapy. RECIST criteria was utilized to objectify treatment response on 3 month follow-up MRI. The longest diameter of the lesion was measured on pre- and post-treatment MRI, and the percent change from pre-treatment was calculated. Threshholds for response were consistent with RECIST criteria and designated as follows: 1. Complete response was indicated with resolution of all enhancing tumor at 3 months; 2. Partial response was noted if ≥ 30% decrease in maximal diameter at 3 months; 3. Progressive disease was noted if ≥ 20% increase in the sum of max diameter at 3 months; 4. Stable disease was noted for all other responses [13].

Clinical analysis

Patients were seen in follow-up 3 months after treatment by the treating radiation oncologist. Clinical improvement was recorded if patients reported reduction in their presenting symptoms or the physician assessed improved neurologic function on physical exam.

Statistics

A wilcoxon signed-rank test was performed to determine the difference in total lesion activity between each patient’s pre- and post-treatment ⁶⁸ Ga -DOTATATE PET/CT and the difference in volume between their pre- and post-treatment MRIs at the same timepoints. Signed-rank test was utilized because the two groups are dependent (pre- and post- radiotherapy imaging assessment of the same sample) and do not follow a normal distribution.

Results

The median age of the population was 65 years and most patients were female (n = 16, 84%). For the subset of patients who underwent pre- and post-treatment ⁶⁸ Ga-DOTATATE PET/CT. Treated meningiomas were located at the base of skull (n = 4, 40%), falx (n = 3, 30%), frontoparietal cerebral convexities (n = 1, 10%), cerebellar tentorium (n = 1, 10%) and optic nerve sheath (n = 1, 10%). Two patients had recurrent tumors. One patient received prior radiosurgery (17 Gy). Six patients underwent biopsy for WHO grade 1 (n = 5, 50%) or WHO grade 2 (n = 1, 10%) tumors. Patient and tumor characteristics are summarized in Table 1.

Table 1 Patient characteristics

Pre-treament imaging

⁶⁸ Ga -DOTATATE PET/CT showed additional osseous involvement not well appreciated on MRI in four patients with base of skull tumors and in one patient with a parietal calvarial lesion (Fig. 1). ⁶⁸ Ga -DOTATATE PET/CT better emphasized the extent of falx involvement in five patients (26%). ⁶⁸ Ga-DOTATATE PET/CT supported a diagnosis of meningioma in one patient who presented with headaches and was found to have diffuse enhancement and thickening of the superior sagittal sinus and falx on MRI, but had previously undergone a non-diagnostic biopsy. This lesion was avid on ⁶⁸ Ga-DOTATATE PET/CT (Fig. 2). In the setting of prior resection, ⁶⁸ Ga-DOTATATE PET/CT identified residual tumor after surgical resection to include in radiation target volumes (Fig. 3). Additionally, ⁶⁸ Ga-DOTATATE PET/CT showed clinically asymptomatic satellite lesions in three patients (18%) that had not been previously identified based on MRI.

Fig. 1

Left parietal meningioma with calvarial involvement. A Pre-treatment MRI, B Pre-treatment CT-scan, C. Pre-treatment 68 Ga-DOTATATE PET, D image from ROVER adaptive thresholding software

Fig. 2.

68 Ga-DOTATATE PET highlighting a meningioma with falx involvement. A Sagittal and axial CT-scans, B Sagittal and axial 68 Ga-DOTATATE PET images. C Images from ROVER adaptive thresholding software

Fig. 3.

⁶⁸ Ga-DOTATATE PET identifying residual meningioma in the setting of prior resection. A T1 post-contrast MRI, B ⁶⁸ Ga-DOTATATE PET, C. Image from ROVER adaptive thresholding software

⁶⁸ Ga-DOTATATE PET/CT findings changed clinical management of three patients. An 86 year old male presented with worsening vision and a progressing right temporal lobe/ medial sphenoid wing meningioma. Initially the patient was planned for five fractions of stereotactic RT, however conventional fractionation was pursued when planning ⁶⁸ Ga-DOTATATE PET/CT highlighted disease compressing the right optic nerve (Fig. 4A). Planning ⁶⁸ Ga-DOTATATE PET/CT excluded the diagnosis of meningioma in 46-year old female with a history of treated Stage 3A breast cancer who presented with subacute onset of ataxia and falls and was found to have a 2.6 cm homogenously enhancing, extra-axial, dural-based mass originating from the right cerebellar tentorium on MRI. ⁶⁸ Ga-DOTATATE PET/CT was performed and this lesion demonstrated mild dotatate uptake, SUVmax = 4.1 (Fig. 4B). In light of the patient’s history of breast cancer and less than expected dotatate uptake, multi-disciplinary consensus deemed the lesion more likely a brain metastasis than a meningioma. The patient was treated with radiosurgery in one fraction of 18 Gy. The patient developed radiation necrosis and underwent surgical biopsy prior to laser interstitial thermal therapy. Pathology revealed substantial reactive gliosis but no viable tumor, in support of the diagnosis of brain metastasis as it is uncommon for meningiomas to cause large areas of reactive gliosis in the absence of brain invasion.

Fig. 4

Select patient cases for which radiation planning 68 Ga-DOTATATE PET changed clinical management. A Imaging demonstrating proximity of right medial sphenoid wing meningioma to the optic nerve. MRI, 68 Ga-DOTATATE PET and image from ROVER adaptive thresholding software. B Imaging demonstrating cerebellar tentorial lesion with mild dotatate uptake (SUV max = 4.1) favoring diagnosis of brain metastasis and treatment with radiosurgery in patient with remote history of breast cancer. MRI, 68 Ga-DOTATATE PET and image from ROVER adaptive thresholding software

Planning ⁶⁸ Ga-DOTATATE PET/CT supported a diagnosis of suspected optic nerve sheath meningioma. The patient, a 22-year old female with a family history of sarcoidosis, presented with an 8-month history of progressive decreased vision in her right eye. Ophthalmologic exam revealed optic disc pallor. Post-contrast MRI demonstrated a T1 hyperintense and T2 isointense lesion involving the intraocular right optic nerve extending into the intracanalicular segment. Differential diagnoses included optic nerve sheath meningioma, lymphoma, sarcoidosis, infection, inflammatory process and orbital pseudotumor. CT without contrast did not display classic calcifications encasing the optic nerve [14]. Neurosurgical evaluation deemed biopsy unsafe. ⁶⁸ Ga-DOTATATE PET/CT established asymmetric increased dotatate avidity (SUV = 6.3) corresponding to the known lesion, supporting the diagnosis of optic nerve sheath meningioma. The patient was treated with definitive PBSPT to a dose of 50.4 Gy in 28 fractions. There was no detectable change on post-RT MRI, SUVmax on ⁶⁸ Ga-DOTATATE PET/CT decreased 40% from 6.3 to 3.8 after RT (Fig. 5). At three months the patient reported improved right sided vision and recent ophthalmologic exam documented visual improvement.

Fig. 5

Optic nerve sheath meningioma. A Pre-RT imaging: T1 post-contrast MRI, Pre-treatment 68 Ga-DOTATATE PET, SUV Max = 6.3, image from ROVER adaptive thresholding software. B Three month post-RT PET-MR imaging: T1 post-contrast MRI, 68 Ga-DOTATATE PET/CT, SUV Max = 3.8, image from ROVER adaptive thresholding software

Post-treatment imaging

In the subset of patients who underwent both planning and follow-up ⁶⁸ Ga-DOTATATE PET/CT (n = 10), mean total lesion activity decreased 14.7% (median), from pre to post-RT ⁶⁸ Ga-DOTATATE PET [range 97–8.5% (25–75%), S = − 26.5, p = 0.0039]. Max total lesion activity decreased 36% (median) over the same period [range 105–15% (25–75%), S = − 26.5 p = 0.0039]. Figure 6. This decrease in mean and max total lesion activity was observed in 9 of 10 patients (Table 2). Inability to detect the same relationship in the case of the optic nerve sheath meningioma is likely attributable to the lesion’s small size and background activity from pot-treatment changes. Total mean and max activity of the adjacent medial rectus (0.1, 0.2) and contralateral normal left optic nerve were (0.1, 0.1) when measured utilizing the ROVER software.

Fig. 6

Box plot: post-RT mean (A) and max (B) total lesion activity

Table 2 Mean and max total lesion activity pre and post radiation treatment measured by ROVER adaptive threshholding software

In contrast, meningioma volumes were stable on the corresponding pre and post-RT MRI images per RECIST criteria and corroborated by Wilcoxon signed rank test which showed no significant difference in mengingioma volume comparing these two timepoints (S = − 3, p = 0.7422). One patient was determined to have radiation necrosis on follow-up MRI and another was unable to undergo a follow-up MRI due to the presence of a pacemaker. Clinical improvement in presenting neurologic symptoms was observed in 7 patients (70%).

Discussion

In this study, we evaluated the potential role of ⁶⁸ Ga-DOTATATE PET/CT in addition to MRI for both radiation planning and post-treatment surveillance of meningiomas. This work provides novel findings characterizing the radiotherapeutic responses using ⁶⁸ Ga-DOTATATE PET/CT three months after completion of radiotherapy. Using PET-based assessments, the majority of patients in this series (90%) responded to RT, mean total lesion activity decreased by 15% and max total lesion activity decreased by 36% and most patients experienced improvement in their presenting neurologic symptoms. At the same time point, MRIs noted stable disease.

Importantly, ⁶⁸ Ga-DOTATATE PET/CT modified the clinical management of three patients. ⁶⁸ Ga-DOTATATE PET/CT supported a diagnosis of optic nerve sheath meningioma and conversely, in another case ruled out a diagnosis of meningioma in favor of a brain metastasis. In yet another patient, ⁶⁸ Ga-DOTATATE PET/CT illustrated the extent of optic nerve involvement, prompting treatment with conventional fractionation rather than SRS. When ⁶⁸ Ga-DOTATATE PET/CT images were incorporated alongside MRI and CT for contouring, we found our clinical target volumes to be slightly larger because ⁶⁸ Ga-DOTATATE PET/CT highlighted areas of involvement (base of skull, osseous structures, falx) not definitively visualized on conventional imaging. In the postoperative setting, ⁶⁸ Ga-DOTATATE PET/CT helped distinguish residual disease from post-operative changes. Additionally ⁶⁸ Ga-DOTATATE PET/CT can be helpful when patients have pacemarkers or ICDs that are not compatible with MRI.

Recently, the benefits of including PET in radiotherapy planning were supported in a study of 339 meningiomas by Kessel et al.. They utilized PET in planning and target volume definition for radiation post-operatively or at recurrence and demonstrated significantly improved local control [15]. They hypothesized that this resulted from PET’s ability to improve detection of tumor cells and better distinguish between healthy and meningioma tissue [15].

Prior studies evaluating alternative imaging for surveillance of meningiomas, highlighted in the RANO/PET Group’s recent report [16], utilized older techniques or radiotracers targeting different mechanisms. Gudjonsson and co-investigators assessed the utility of pre-and post-treatment ¹¹C-L-methionine PET in a series of nineteen patients undergoing fractionated stereotactic proton radiotherapy for meningiomas [17]. Thirty-six months after delivering 24 Gy in 4 consecutive daily fractions the investigators observed nearly a 20% reduction in the radioactivity ratio of tumor to normal brain from pre to post treatment PET but were unable to appreciate significant volume reductions on MRI and suggested that ¹¹C-L-methionine PET could provide an earlier assessment of treatment response than MRI [17]. ¹¹C-L-methionine PET utilizes a radiolabeled amino acid analogue for which meningiomas show increased uptake. However, ⁶⁸ Ga-DOTATATE PET/CT allows for even better contrast between tumor and background brain than ¹¹C-L-methionine PET [16].

Nicolato and colleagues utilized somatostatin receptor imaging to evaluate treatment response in 20 patients with WHO grade I symptomatic cavernous sinus meningiomas. 7–12 months after SRS, cranial nerve deficits improved in the majority (75%) of patients, however MRI at this timepoint demonstrated decrease in tumor volume in only 15% of patients, similar to the pattern observed in our series. Utilizing SPECT with octreotide, neurologic responders demonstrated a more significant decrease in receptor activity at the same timepoint after SRS than nonresponders (p < 0.05) [18].

Meningiomas regress slowly after radiation and consequently follow-up of these tumors requires serial MRIs. This can be burdensome for patients and costly to the healthcare system. For the same reasons, shorter-term imaging endpoints in clinical trials with these tumors can be difficult to measure. Additionally, meningiomas are often located adjacent to cranial nerves and critical brain structures, therefore only a small volumetric increase could cause symptoms. For these reasons, an imaging modality like ⁶⁸ Ga-DOTATATE PET/CT may be an earlier indicator of positive treatment response and thus could be of considerable benefit.

The recently published NETTER-1 trial demonstrated dramatically improved progression free survival adding ¹⁷⁷Lu-Dotatate to octreotide therapy in patients with somatostatin-receptor-positive midgut neuroendocrine tumors [19]. These results revived interest in peptide receptor radionuclide therapy for refractory meningiomas. A single arm phase II investigation administering Lutathera (¹⁷⁷Lu-DOTATATE) to patients with refractory or high-risk meningiomas is currently being conducted. This study will assess tumor response 6 months post drug initiation with ⁶⁸ Ga-DOTATATE PET/MRI (ClinicalTrials.gov identifier: NCT03971461). High expression of SSTR2 has been shown to correlate with faster tumor growth rates on MRI in WHO grade I and II meningiomas [20]. Further investigation into the utility of ⁶⁸ Ga-DOTATATE PET/CT to identify non-responders to radiotherapy and potential candidates for peptide receptor radionuclide therapy is warranted. ⁶⁸ Ga-DOTATATE PET/CT could also prove useful in the setting of initial observation or surveillance of recurrent meningiomas. SUVmax could help distinguish active, recurrent meningioma from scar tissue and prior treatment induced changes, a distinction that can be challenging based on CT or MRI alone [16].

This series has inherent limitations. This was a single retrospective institution analysis with a limited sample size. Separate traditional MRI based CTV volumes and ⁶⁸ Ga-DOTATATE PET/CT based CTV volumes were not contoured precluding quantification of the difference in treatment volumes generated with each imaging modality. Histopathologic confirmation of the change in concentration of SSTR receptors after radiotherapy was not performed. The median follow-up (3 months) for the cohort was short. Prospective studies utilizing a systematic approach to measuring longer-term changes with ⁶⁸ Ga-DOTATATE PET/CT are needed to validate that decreased uptake of dotatate after radiotherapy is associated with high tumor control rates and the prognostic value of the degree and timing of response measured on ⁶⁸ Ga-DOTATATE PET/CT imaging. Functional imaging ⁶⁸ Ga-DOTATATE PET/CT has inherently inferior spacial resolution than MRI. Accurate assessment of response can be limited by the small size of the lesion as demonstrated in the case of the optic nerve lesion in our population. It’s ability to identify areas not well seen on MRI make it a useful adjunct rather than replacement imaging modality.

Conclusions

Taken together, our findings contribute to the growing body of evidence supporting the use ⁶⁸ Ga-DOTATATE PET/CT as an adjunctive imaging modality to help aid in the diagnosis and radiation treatment planning of meningiomas. This study represents one of the first series evaluating the response of meningiomas to radiotherapy utilizing ⁶⁸ Ga-DOTATATE PET/CT. In this population, meningioma uptake of the SSTR2 ligand ⁶⁸ Ga-DOTATATE decreased by three months after RT, even in absence of objective MRI response. Future prospective studies are necessary to determine the prognostic significance of ⁶⁸ Ga -DOTATATE PET/CT post-treatment imaging changes and to characterize molecular profiles of PET responders vs. non-responders.