Visual Abstract
Abstract
Surgery with curative intent can be offered to congenital hyperinsulinism (CHI) patients, provided that the lesion is focal. Radiolabeled exendin-4 specifically binds the glucagonlike peptide 1 receptor on pancreatic β-cells. In this study, we compared the performance of 18F-DOPA PET/CT, the current standard imaging method for CHI, and PET/CT with the new tracer 68Ga-NODAGA-exendin-4 in the preoperative detection of focal CHI. Methods: Nineteen CHI patients underwent both 18F-DOPA PET/CT and 68Ga-NODAGA-exendin-4 PET/CT before surgery. The images were evaluated in 3 settings: a standard clinical reading, a masked expert reading, and a joint reading. The target (lesion)-to-nontarget (normal pancreas) ratio was determined using SUVmax. Image quality was rated by pediatric surgeons in a questionnaire. Results: Fourteen of 19 patients having focal lesions underwent surgery. On the basis of clinical readings, the sensitivity of 68Ga-NODAGA-exendin-4 PET/CT (100%; 95% CI, 77%–100%) was higher than that of 18F-DOPA PET/CT (71%; 95% CI, 42%–92%). Interobserver agreement between readings was higher for 68Ga-NODAGA-exendin-4 than for 18F-DOPA PET/CT (Fleiss κ = 0.91 vs. 0.56). 68Ga-NODAGA-exendin-4 PET/CT provided significantly (P = 0.021) higher target-to-nontarget ratios (2.02 ± 0.65) than did 18F-DOPA PET/CT (1.40 ± 0.40). On a 5-point scale, pediatric surgeons rated 68Ga-NODAGA-exendin-4 PET/CT as superior to 18F-DOPA PET/CT. Conclusion: For the detection of focal CHI, 68Ga-NODAGA-exendin-4 PET/CT has higher clinical sensitivity and better interobserver correlation than 18F-DOPA PET/CT. Better contrast and image quality make 68Ga-NODAGA-exendin-4 PET/CT superior to 18F-DOPA PET/CT in surgeons’ intraoperative quest for lesion localization.
Congenital hyperinsulinism (CHI) is the most common cause of persistent and recurrent hypoglycemia in neonates. It occurs with an incidence of 1 in 35,000–40,000 births (1). CHI often presents in neonates as poor feeding, seizures, jitteriness, hypotonia, apnea, cyanosis, hypothermia, or a hypoglycemia-induced life-threatening event (2). CHI can also manifest in infancy or childhood and, in rare cases, even in adolescents or young adults (3). To avoid brain injury, early diagnosis and proper treatment of CHI are crucial. The diagnosis of CHI is based on clinical findings and hypoglycemic events, combined with inappropriately high insulin or C-peptide levels or low insulinlike growth factor– binding protein 1 levels (4,5). In diffuse CHI, which accounts for 60%–70% of all cases, there is diffuse involvement of the pancreatic β-cells, with enlarged hyperfunctioning cells that have abnormally large nuclei and abundant cytoplasm (6,7). This subform is caused by recessive or dominant mutations in the ABCC8 or KCNJ11 genes, encoding for the β-cell adenosine triphosphate– sensitive potassium channels. Diffuse CHI is treated primarily with medication, such as octreotide and diazoxide. However, many patients with recessive mutations in the ABCC8 and KCNJ11 genes are unresponsive to this therapy, and near-total pancreatectomy may then be the only option to avoid devastating hypoglycemia. Even after such an invasive procedure, some children present with recurring hypoglycemia, requiring further treatment with medication or even reoperation (8).
Focal CHI accounts for 30%–40% of all CHI cases associated with the adenosine triphosphate–sensitive potassium channel genes. This form is characterized by focal adenomatous islet cell hyperplasia caused by the concurrence of a paternal mutation in the ABCC8 or KCNJ11 gene and somatic loss of heterozygosity of the maternal chromosome 11p15 region within a limited pancreatic region (9,10). Because there is involvement of only a specific pancreatic area, focal CHI can be treated successfully by partial pancreatectomy or limited lesionectomy, which can cure the disease in cases of complete removal of the lesion (7). Since focal CHI can be treated with much less invasive surgery than diffuse CHI, correct differentiation between these subforms is of great importance. Also, precise presurgical localization of the focal lesion is important for correct surgical planning and optimization of surgical outcomes. If the lesion resides in the body or tail of the pancreas, a minimally invasive, laparoscopic, procedure may be performed (11).
The current standard imaging technique for noninvasive detection of focal CHI is 18F-DOPA PET/CT (12). Because this technique has a sensitivity of only 85%–89% for the detection of focal CHI (13), focal lesions are still missed in some cases. In this study, we used a new radiotracer based on the peptide exendin-4, which binds with high affinity specifically to the glucagonlike peptide 1 receptor expressed on pancreatic β-cells (14). 68Ga-labeled exendin has been shown to detect insulinomas with high sensitivity (15,16). The specific tracer used in the current study, 68Ga-NODAGA-exendin-4, is being assessed in a large prospective trial for insulinoma imaging (NCT03189953). We have analyzed the data of patients with CHI who underwent both 18F-DOPA PET/CT and 68Ga-NODAGA-exendin-4 PET/CT to compare the effectiveness of these 2 imaging techniques for the detection and localization of focal CHI.
MATERIALS AND METHODS
Study Design and Patients
This prospective multicenter study (NCT03768518) included consecutive eligible patients at the Great Ormond Street Hospital in the United Kingdom (7 patients) and at the Radboud University Medical Centre in The Netherlands (1 patient). Patients were recruited directly by these centers and by referral from several tertiary centers across Europe.
Patients were enrolled with biochemically proven, endogenous CHI who were unresponsive to medical treatment and qualified for 18F-DOPA PET/CT on the basis of mutation analysis (no genetically proven diffuse CHI based on a homozygous or compound heterozygous ABCC8/KCNJ11 mutation). Exclusion criteria were renal insufficiency (creatinine clearance < 40 mL/min) and evidence of malignancies other than insulin-producing lesions. The study was approved by the local institutional review board of both participating institutes. The parents of all included patients provided written informed consent in accordance with provisions of the Declaration of Helsinki.
In addition, real-world evidence data from CHI patients diagnosed and treated at the Charité University Hospital in Germany (11 patients) were analyzed in accordance with national drug regulations. Parents of these patients provided written informed consent to the use of the new radiotracer.
Procedures
In all patients, 18F-DOPA PET/CT was performed according to the local guidelines for focal-CHI detection. 18F-DOPA (3 MBq/kg; lower limit, 40 MBq) was injected as a slow bolus over 1 min. Patients had not fasted and were not pretreated with carbidopa. A PET/CT acquisition at 1 bed position for 10 min was started 20 min after tracer injection. Depending on the assessment of the first scan, additional PET acquisitions were performed at 40 or 60 min after tracer injection.
For 68Ga-NODAGA-exendin-4 PET/CT, a 1.6 ± 0.1 MBq/kg dose of the tracer (lower limit, 20 MBq), corresponding to a peptide dose of maximally 0.08–0.12 µg/kg (lower limit, 1.4 µg), was injected intravenously as a slow bolus over 5 min. Details on radiopharmaceutical preparation are provided in the supplemental materials. The patients had fasted for 1 h before tracer injection to reduce endogenous glucagonlike peptide 1 production. Blood glucose levels were monitored before tracer injection and at least at 5, 10, 15, 30, 60, 90, and 120 min after tracer injection. Since blood glucose levels may decrease after 68Ga-NODAGA-exendin-4 injection, they were closely monitored. Intravenous glucose injection with a case-specific infusion rate was given to all patients to manage glucose levels during the procedure.
PET acquisition methods varied because of differences in the institutional standard of care for CHI patients. Details on 68Ga-NODAGA-exendin-4 PET/CT and PET/MRI acquisition procedures for all centers and reconstruction parameters are given in Supplemental Table 1 (supplemental materials are available at http://jnm.snmjournals.org). At the Great Ormond Street Hospital, a protocol has been developed for 18F-DOPA PET/CT/CT to be performed under oral sedation with chloral hydrate in children with CHI to avoid general anesthesia (Sarah Kiff et al., unpublished data, 2021). This protocol was adopted for 68Ga-NODAGA-exendin-4 PET/CT acquisitions at the Great Ormond Street Hospital.
At the Radboud University Medical Centre, 1 patient was included. Scans there were performed without anesthesia with a vacuum mattress.
Real-world evidence from an institutional database of 11 CHI patients who underwent 68Ga-NODAGA-exendin-4 PET/CT for diagnostic purposes at the Charité University Hospital were included retrospectively. Younger children were imaged while receiving inhalation anesthesia with isoflurane under the supervision of an anesthesiologist; older children were able to undergo the procedure without sedation.
Evaluation
Histologic evaluation and clinical outcome (normalization of blood glucose levels after surgery) were used as a reference standard. 18F-DOPA PET/CT and 68Ga-NODAGA-exendin-4 PET/CT scans were clinically read at the site of patient inclusion by nonmasked observers. The clinical reading was performed by a pediatric endocrinologist (hyperinsulinism expert) together with a nuclear medicine physician and a pediatric surgeon at the site of the PET scan. After completion of data collection, all 18F-DOPA and 68Ga-NODAGA-exendin-4 PET/CT images were reevaluated by 1 masked 68Ga-NODAGA-exendin-4–experienced nuclear medicine physician (expert reading). Additionally, a joint reevaluation of all images was performed by this nuclear medicine physician together with a pediatric endocrinologist highly experienced in 18F-DOPA PET/CT reading. All images were evaluated in terms of disease subform and, if detected, the size and location of the focal lesion. For exact localization of the focal lesion, the pancreas was divided into 6 areas based on anatomic relation to the pancreatic duct and portal vein (Supplemental Fig. 1). Images from all time points were used for interpretation.
Quantitative analysis of the 18F-DOPA PET/CT and 68Ga-NODAGA-exendin-4 PET/CT or PET/MRI scans in which focal lesions had been confirmed by histopathology was performed by a nonmasked expert. Volumes of interest (VOIs) were drawn to determine tracer uptake, expressed as SUVmax, in different parts of the pancreas and visible focal lesions. The SUVmax ratios of the focal lesion or area with the highest tracer uptake (for 18F-DOPA PET/CT scans in which the focal lesion was not detected) and the area with the next highest tracer uptake were determined. VOIs were drawn over the head, body, and tail of the pancreas. Within these VOIs, isocontour VOIs were created consisting of the voxels with the 30% highest intensity (examples of resulting VOIs are depicted in Supplemental Fig. 2). For quantification of the dynamic PET scans, reconstructed images of the time frames from 30 to 40 min (Charité University Hospital) and from 40 to 45 min (University College London) after injection were used.
To estimate the optimal imaging time point for 68Ga-NODAGA-exendin-4 PET/CT, SUVmax ratios in reconstructed images of 5-min intervals over the imaging period from 0 to 45 min after tracer injection were determined in 4 patients with focal disease.
To evaluate image quality and correlation of imaging results with the intraoperative findings, 18F-DOPA PET/CT and 68Ga-NODAGA-exendin-4 PET/CT images of 13 patients with a detected focal lesion were rated by the involved pediatric surgeon using a questionnaire based on the Leiden surgical rating scale (supplemental materials).
Statistical Analysis
Imaging results confirmed by histopathology were regarded as true-positives or true-negatives. Imaging results with competing histopathology results were regarded as false-positives or false-negatives. Ninety-five percent CIs for sensitivity were calculated using the Clopper–Pearson method. Interobserver variation was calculated using the Fleiss κ. SUVmax ratios in 18F-DOPA PET/CT and 68Ga-NODAGA-exendin-4 PET/CT scans were compared using paired-sample t tests. Surgeon scores of image quality were compared using Wilcoxon signed-rank tests. Statistical analyses were performed using SPSS (version 22; IBM).
RESULTS
Patients
We included the data of 19 CHI patients. Baseline characteristics of the patients are given in Table 1, and clinical details are in Supplemental Table 2. All patients underwent 18F-DOPA PET/CT and 68Ga-NODAGA-exendin-4 PET/CT, with a median time of 13 d (range, 4–72 d) between the procedures. On clinical reading, 18F-DOPA PET/CT revealed focal areas of high tracer uptake suggestive of focal lesions in 10 patients (53%), and 68Ga-NODAGA-exendin-4 PET/CT revealed such areas in 14 patients (74%) (Table 2). The study profile is depicted in Supplemental Figure 3.
Patient Characteristics
Sensitivity of 18F-DOPA PET/CT and 68Ga-NODAGA-Exendin-4 PET/CT Based on Clinical and Study Readings
Tolerability
One patient (5%) experienced vomiting after injection of 68Ga-NODAGA-exendin-4. In 2 patients (11%), episodes of mild hypoglycemia requiring increased glucose infusion occurred after injection of 68Ga-NODAGA-exendin-4. In the other patients, glucose levels were stable (>3.5 mmol/L) under regular monitoring and intravenous glucose infusion. No other adverse events occurred in any of the patients.
Surgery
The results of both imaging procedures were used for surgical planning. Suggestive lesions were detected by clinical reading of the PET images in 14 patients. These patients underwent surgery, and the presence of focal lesions was confirmed by histopathologic evaluation. All surgically treated patients with focal lesions were cured after surgery (normalization of blood glucose levels in long-term follow-up).
Of the remaining 5 patients, in whom no focal lesion was detected by clinical reading (diffuse tracer uptake on both 18F-DOPA and 68Ga-NODAGA-exendin-4 PET/CT), 1 patient underwent near-total pancreatectomy because of an insufficient response to medication. In line with the imaging results, histopathology indicated diffuse disease in this patient. The 4 patients who did not undergo surgery (aged 10, 18, 68, and 125 mo) could be sufficiently managed with diet and medication.
Since histopathology and clinical follow-up were the reference standard, patients who did not undergo surgery were excluded from analysis.
Diagnostic Performance
Imaging results are summarized in Table 2. In this patient population, 68Ga-NODAGA-exendin-4 PET/CT had a sensitivity of 100% (95% CI, 77%–100%) for detection of focal lesions, compared with a sensitivity of 71% (95% CI, 42%–92%) for 18F-DOPA PET/CT, based on clinical readings of the images. In 4 of 15 patients (27%), focal lesions were identified only using 68Ga-NODAGA-exendin-4 PET/CT. In these patients, the surgery planning was based solely on the results of the 68Ga-NODAGA-exendin-4 PET/CT. 18F-DOPA PET/CT and 68Ga-NODAGA-exendin-4 PET/CT images of these 4 patients are shown in Figure 1. On the basis of the clinical readings, 68Ga-NODAGA-exendin-4 PET/CT performed better for detection of focal lesions.
68Ga-NODAGA-exendin-4 PET/CT and 18F-DOPA PET/CT images of patients 2 (A), 4 (B), 6 (C), and 9 (D), for whom 68Ga-NODAGA-exendin-4 PET/CT scans were reported as focal in clinical readings whereas 18F-DOPA PET/CT scans were reported as diffuse. Locations of focal lesions (for 18F-DOPA PET/CT detected during joint readings) are indicated with green arrows. In D, focal lesion in head is indicated with green arrows, and for comparison, red arrows indicate areas with the next highest tracer uptake in all images. Presence of focal lesions was confirmed by histopathology in all 4 patients.
Interobserver Correlation
On reevaluation of the 18F-DOPA PET/CT images by an expert nuclear medicine physician, 2 additional focal lesions were identified, increasing the sensitivity to 86% (range, 57%–98%). In the expert readings of the 68Ga-NODAGA-exendin-4 PET/CT images, 1 focal lesion was missed, decreasing the sensitivity to 93% (range, 66%–100%). Through joint reading of the images by an expert nuclear medicine physician and a pediatric endocrinologist, all focal lesions were detected on both 68Ga-NODAGA-exendin-4 PET/CT and 18F-DOPA PET/CT. Although the sensitivity of both techniques reached 100%, the interobserver agreement was higher for 68Ga-NODAGA-exendin-4 PET/CT than for 18F-DOPA PET/CT (Fleiss κ = 0.91 vs. 0.56). For 68Ga-NODAGA-exendin-4 PET/CT, there was almost perfect agreement, whereas for 18F-DOPA PET/CT, the level of agreement between the readings was only moderate. The increased sensitivity of 18F-DOPA PET/CT on only reevaluation of the images, together with the higher interobserver agreement in evaluation of the 68Ga-NODAGA-exendin-4 PET/CT images, clearly indicates a facilitated and more reliable interpretation of the 68Ga-NODAGA-exendin-4 PET/CT images, resulting in less equivocal results.
Semiquantitative Analysis
In patients with histopathologically proven focal CHI, the SUVmax ratios of the focal lesion to the area of the pancreas with the next highest tracer uptake are significantly higher in 68Ga-NODAGA-exendin-4 PET/CT than in 18F-DOPA PET/CT (2.03 ± 0.63 and 1.03 ± 0.35, respectively; P = 0.0026) (Fig. 2). These quantitative data show that 68Ga-NODAGA-exendin-4 PET/CT provides better contrast to discriminate between focal and diffuse disease and thus explains the difference in interobserver agreement levels.
(A) SUVmax ratios between focal lesion and area with next highest tracer uptake. Data are given as mean ± SD, as well as individual datapoints. Scans with focal lesions identified during clinical reading are depicted in red. Scans reported to show diffuse disease are depicted in blue. (B and C) Rating scores of 68Ga-NODAGA-exendin-4 and 18F-DOPA PET/CT images by pediatric surgeons. Scores are on preoperative image quality for decision to perform surgery (B) and correlation of imaging results with intraoperative findings (C). *P < 0.05.
Quantification of reconstructed images of 5-min intervals over the imaging period shows some variability between patients in the time point of the highest SUVmax ratio. SUVmax ratios over time are depicted in Supplemental Figure 4. For all 4 patients, the highest SUVmax ratio was between 30 and 45 min after tracer injection. This therefore seems to be the best time frame for 68Ga-NODAGA-exendin-4 PET/CT imaging.
Surgical Ease
The influence of PET image quality on surgical ease was measured by rating of the DOPA and 68Ga-NODAGA-exendin-4 PET/CT images by the involved pediatric surgeons. These were all experienced surgeons who had performed more than 10 CHI surgeries during their career and more than 5 during the last 3 y. The surgeons’ rating of PET image quality showed significantly higher scores for 68Ga-NODAGA-exendin-4 PET/CT than for 18F-DOPA PET/CT regarding the decision to perform surgery (4.5 vs. 3.8, respectively; P = 0.025; Fig. 2B), as well as regarding correlation of the imaging results with intraoperative findings (4.4 vs. 3.7, respectively; P = 0.0083; Fig. 2C). Of 13 cases, the surgeons reported preferring 68Ga-NODAGA-exendin-4 PET/CT imaging for future CHI patients in 9 cases, versus 18F-DOPA PET/CT in only 1 case and no preference in 3 cases. This finding implies a better image quality for 68Ga-NODAGA-exendin-4 PET/CT than for 18F-DOPA PET/CT and a possible benefit for the surgical treatment of CHI patients.
DISCUSSION
The results of the present study indicate that 68Ga-NODAGA-exendin-4 PET/CT is a promising tool for detection and localization of focal CHI, providing a high sensitivity and diagnostic accuracy. The higher interreader agreement of 68Ga-NODAGA-exendin-4 PET/CT than of 18F-DOPA PET/CT indicates superior performance of 68Ga-NODAGA-exendin-4 PET/CT in some patients by providing less equivocal results.
Quantitative analysis of scans of patients with histopathologically confirmed focal CHI showed significantly higher SUVmax ratios on 68Ga-NODAGA-exendin-4 PET/CT than on 18F-DOPA PET/CT. The higher contrast between uptake in the focal lesion and in the remainder of the pancreas on 68Ga-NODAGA-exendin-4 PET/CT scans enables easier detection of focal lesions. This finding explains the increased sensitivity of 68Ga-NODAGA-exendin-4 PET/CT based on the initial clinical reading, and the increased rate of agreement in readings of 68Ga-NODAGA-exendin-4 PET/CT images between clinical and expert readers, in comparison to 18F-DOPA PET/CT images. This increased sensitivity and agreement are of importance, especially in cases with a heterogeneous pattern of tracer uptake in the pancreas—cases that are usually difficult to diagnose (13).
The superior image quality of 68Ga-NODAGA-exendin-4 PET/CT is important for both the scan reading and the surgical procedure, since successful surgery depends on precise presurgical detection of focal CHI and the subsequent discovery and complete removal of the focal lesion intraoperatively, as reflected by pediatric surgeons’ image ratings. 68Ga-NODAGA-exendin-4 PET/CT could benefit the surgical treatment of CHI patients by facilitating the decision to perform surgery, as well as the intraoperative localization of the focal lesion.
In our limited population of 19 CHI patients, 4 cases of focal CHI were clinically not identified using 18F-DOPA PET/CT. This is a high number compared with a previous large prospective study with 50 cases and retrospective reviews of 105 and 195 cases, which reported sensitivities of 88%, 85%, and 89%, respectively, for detection of focal CHI using 18F-DOPA PET/CT (13,17,18). This result is suggestive of a high complexity in the cases in this study. An overrepresentation of such difficult cases in our study population could stem from an increased incentive to refer patients with complex and equivocal 18F-DOPA PET/CT imaging results for an investigative diagnostic procedure. In this population, 68Ga-NODAGA-exendin-4 PET/CT outperformed 18F-DOPA PET/CT in the clinical nonexpert setting, facilitating curative surgery without the need for further medicinal treatment or near-total pancreatectomy in 4 additional patients. 68Ga-NODAGA-exendin-4 PET/CT therefore had a major positive impact on the clinical management of these patients.
A limitation of the current study was the inability to exclude the possibility of missed focal lesions. All focal lesions that were identified by 68Ga-NODAGA-exendin-4 PET/CT were confirmed by histopathology. However, 4 patients in whom diffuse disease was indicated on both 18F-DOPA PET/CT and 68Ga-NODAGA-exendin-4 PET/CT did not undergo surgery but instead received continued medical treatment. In these patients, diffuse disease was not confirmed.
Another possible limitation of this study was the inclusion of patients from 3 centers with differences in the 68Ga-NODAGA-exendin-4 PET/CT acquisition procedure (Supplemental Table 1). However, the high degree of diagnostic accuracy and interreader agreement for 68Ga-NODAGA-exendin-4 PET/CT in all included patients shows the robustness of this technique in clinical practice.
On the basis of the data in this study, the expected optimal time frame for 68Ga-NODAGA-exendin-4 PET/CT imaging is between 30 and 45 min after tracer injection. In the tail of the pancreas, focal lesions that overlap the contour of the left kidney pose a diagnostic challenge with 18F-DOPA PET/CT, as has been described previously (13). Because of the high renal accumulation of 68Ga-NODAGA-exendin-4 PET/CT, this issue also occurs with PET/CT using this tracer. In such cases, performing additional scans at later time points could be beneficial, since uptake of 68Ga-NODAGA-exendin-4 PET/CT in the kidneys was shown to decrease over time in adults (19).
The introduction of 18F-DOPA PET/CT to discriminate between focal and diffuse CHI has had a major impact on the clinical approach by obviating more invasive diagnostic procedures, such as selective arterial calcium stimulation with simultaneous venous sampling or transhepatic portal venous insulin sampling, and by optimizing surgical treatment because of increased diagnostic accuracy. This study showed that 68Ga-NODAGA-exendin-4 PET/CT has the potential to even further improve the treatment of patients with focal CHI by improving diagnostic accuracy and certainty. This improvement could enable curative surgery in more patients and could benefit surgical planning by providing more precise and reliable preoperative images.
In addition to the better image quality of 68Ga-NODAGA-exendin-4 PET/CT than of 18F-DOPA PET/CT, another important advantage to 68Ga-NODAGA-exendin-4 PET/CT is the production of 68Ga by a generator. Because of the short half-life of 68Ga (68 min), it cannot be transported between centers. However, production by a generator enables on-site production of the radiotracer even at PET centers without a cyclotron, thereby enabling broad availability. Since 18F-DOPA is often difficult to obtain, this capability could transform the care of focal-CHI patients at such centers. In addition, the equivocal results provided by 68Ga-NODAGA-exendin-4 PET/CT will also enable correct image interpretation at less experienced centers. An additional important advantage to 68Ga-NODAGA-exendin-4 is the very low PET radiation dose to the patients, which we previously calculated to be about 4-fold lower for newborn patients than the radiation dose from 18F-DOPA (19).
CONCLUSION
Through this study, we provided the first (to our knowledge) clinical evidence of detection and localization of focal CHI using 68Ga-NODAGA-exendin-4 PET/CT. These first results show that image quality is better for 68Ga-NODAGA-exendin-4 PET/CT than for the standard 18F-DOPA PET/CT, resulting in an excellent sensitivity and diagnostic accuracy, which changed the surgical management in 4 of 19 patients. Although the performance of 68Ga-NODAGA-exendin-4 PET/CT needs to be further assessed in a larger patient population, we believe that it has the potential to replace 18F-DOPA PET/CT as the primary imaging tool for detection and localization of focal CHI.
DISCLOSURE
This work was supported by BetaCure (FP7/2014-2018, grant 602812). PET/MRI use at Charité University Hospital was supported by Deutsche Forschungsgemeinschaft (INST 335/543-1 FUGG). Martin Gotthardt is an inventor on, and holder of, the patent “Invention Affecting GLP-1 and Exendin” (Philipps-Universität Marburg, June 17, 2009). Paolo De Coppi is supported by NIHR BRC Great Ormond Street Hospital. No other potential conflict of interest relevant to this article was reported.
KEY POINTS
QUESTION: Is 68Ga-NODAGA-exendin-4 PET/CT effective for preoperative detection and localization of focal CHI?
PERTINENT FINDINGS: 68Ga-NODAGA-exendin-4 PET/CT has higher clinical sensitivity and a better interobserver correlation for the detection of focal CHI than does 18F-DOPA PET/CT. 68Ga-NODAGA-exendin-4 PET/CT provided significantly higher target-to-nontarget ratios than did 18F-DOPA PET/CT, and pediatric surgeons rated 68Ga-NODAGA-exendin-4 PET/CT superior to 18F-DOPA PET/CT.
IMPLICATIONS FOR PATIENT CARE: 68Ga-NODAGA-exendin-4 PET/CT has the potential to benefit the treatment of patients with focal CHI by improving diagnostic accuracy and certainty. This advantage could enable curative surgery in more patients and benefit surgical planning by providing more precise and reliable preoperative images.
ACKNOWLEDGMENTS
We thank all patients and their parents or caretakers for participating in the study. We also thank the technical staff at the Radboud University Medical Centre, Charité University Hospital, and University College London for their support with radiochemical preparations and PET investigations.
Footnotes
Published online July 02, 2021.
- © 2022 by the Society of Nuclear Medicine and Molecular Imaging.
Immediate Open Access: Creative Commons Attribution 4.0 International License (CC BY) allows users to share and adapt with attribution, excluding materials credited to previous publications. License: https://creativecommons.org/licenses/by/4.0/. Details: http://jnm.snmjournals.org/site/misc/permission.xhtml.
REFERENCES
- Received for publication March 17, 2021.
- Revision received May 5, 2021.
