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18F-FDG PET/MRI in Children with Oncologic Diseases: Initial Experience
Hansel Javier Otero1, Carolina L Maya1, Sabah E Servaes2, Jeffrey P Schmall1, and Lisa J States1

1Radiology, Children's Hospital of Philadelphia, Philadelphia, PA, United States, 2Raidology, Children's Hospital of Philadelphia, Philadelphia, PA, United States

Synopsis

We describe our initial experience with integrated whole-body Fluor-18-Fluordesoxyglucose-PET/MR imaging in children in a retrospective study of all 18F-FDG-PET/MR at our institution. 51 studies were carried out in 41 children (34 girls, 17 boys) with a mean age of 10.16 years (10 months-24 years). Primary diagnosis included rhabdomyosarcoma (n=18) and Osteosarcoma (n=5). The majority of studies (n=29, 57.9%) were performed for treatment response/restaging. All studies were diagnostic (technical success rate 100%). The mean effective dose was 5.25 mSv (2.1-11.5 mSv). Mean total imaging time was 80 minutes (42-138 minutes). Thirty-eight (74.5%) cases had an average of 2.2 additional MR sequences. 18F-FDG PET/MR is technically feasible for the evaluation of oncologic processes in children at a fraction of the radiation dose.

Introduction

Pediatric oncologic imaging with whole-body positron emission tomography (PET)/magnetic resonance (MR) has been introduced to clinical practice relatively recently and offers several potential advantages including reduced radiation dose, increased soft tissue contrast detail, and increased confidence in diagnosing bone metastasis. The aim of this study is to describe our experience on clinical performance, image quality, patient characteristics and imaging time of integrated whole-body PET/MR hybrid imaging in children.

Methods

This is an IRB approved retrospective descriptive study of all patients that underwent single-injection, dual-imaging whole-body PET/MR hybrid imaging with Fluor-18-Fluordesoxyglucose at our institution during the first year of clinical use. Patient characteristics, study indication, use of sedation/anesthesia, effective radiation dose, time from injection to imaging, total MR imaging time (define as time from start of localizers to end of last protocoled sequence), number of additional MR sequences (ad hoc by supervising physician outside protocol) and added imaging time were also recorded. The whole body MRI protocol included coronal STIR, axial Dixon and axial Diffusion-Weighted Imaging (DWI).

Results

A total of 51 whole body 18F-FDG PET/MRI studies were carried out in 41 children (34 girls, 17 boys) between December 2016 and November 2017. The children’s ages ranged from 10 months to 24 years (mean age: 10 years 2 months). Primary oncologic indication included rhabdomyosarcoma (n =18), Osteosarcoma (n = 5), neuroblastoma (n = 3), Ewing sarcoma (n = 2), teratoma (n=2), as well as one of each of the following: Burkitt’s lymphoma, Adrenal Cortical Carcinoma, Cutaneous T-cell lymphoma, GIST Tumor, Medulloblastoma, Rhabdoid Tumor, Urothelial Carcinoma, Paraganglioma and Wilm's Tumor. Eight children were investigated for cancer predisposition syndromes (Li-Fraumeni-n=4, Neurofibromatosis 1-n=3, Ataxia-Telangiectasia-n=1); while 3 others had benign diseases (Castleman's disease-n=1, Gorham-Stout disease-n=1, Langerhans Cell Hitiocytosis-n=1) and one patient underwent PET/MR for the investigation of a paraneoplastic syndrome (autoimmune encephalitis). Sixteen (31.4%) studies were performed for initial investigation/staging of known lesions, 29 (57.9%) were performed for evaluation of treatment response/restaging. The remaining 6 (11.8%) studies were performed for suspected malignancy/surveillance.

All studies were diagnostic (technical success rate 100%). Thirty-two patients (62.7%) underwent general anesthesia, two (3.9%) patients receive deep sedation and 17 (33.3%) did not require either. The mean effective dose was 5.25 mSv (range: 2.1-11.5 mSv). Average time from injection to imaging was 70 minutes (range: 49-199 minutes).

Total imaging time range from 42 minutes to 138 minutes (mean: 80 minutes +/- 22 minutes). Thirty-eight (74.5%) cases had additional MR sequences requested by the radiologist averaging 2.2 additional sequences per case and with an average additional time of 15 minutes (range 5-50). The remaining 13 (25.5%) cases had no additional sequences.

Discussion

Our early experience shows perfect technical success in a wide variety of oncologic processes both for initial staging and treatment response/follow up with a major impact in effective dose between 58% and 71% lower than previously reported averages (12.5 mSv +/- 4.1 and 18.35 +/- 13.52 mSv) for 18F-FDG PET/CT[1,2].

We acknowledge that our protocol has more sequences than most previously published protocols because it will allow us to determine which sequences are necessary for localization and characterization of lesions. The additional goal of this detailed protocol is to create a one-stop-shop imaging test that eliminates the need for additional studies. Eliminating additional MR studies is of particular importance in younger patients to decrease anesthesia/sedation time and eliminate sedation visits. This preliminary series will be used to create new, focused protocols. For example, DWI adds time and may not be necessary in areas without disease. Additional out-of-protocol sequences, present in a majority (74.5%) of cases and contributing to an average of 15 minutes per case, must also be addressed to eliminate uncertainty of exact study duration. As we transition more patients from PET/CT to PET/MRI, specifically tailored protocols that allow us to maintain reasonable table times and patient throughput.

Conclusion

18F-FDG PET/MR is technically feasible for the evaluation of oncologic processes in children with equivalent examination times at a fraction of the radiation dose. Hence, PET/MR is a promising modality for work-up of pediatric malignancies.

Acknowledgements

No acknowledgement found.

References

1. Klenk C, Gawande R, Uslu L, Khurana A, Qiu D, Quon A, Donig J, Rosenberg J, Luna-Fineman S, Moseley M, Daldrup-Link HE. Ionising radiation-free whole-body MRI versus (18)F-fluorodeoxyglucose PET/CT scans for children and young adults with cancer: a prospective, non-randomised, single-centre study. Lancet Oncol. 2014; 15(3):275-85.

2. Kim YY, Shin HJ, Kim MJ, Lee MJ. Comparison of effective radiation doses from X-ray, CT, and PET/CT in pediatric patients with neuroblastoma using a dose monitoring program. Diagn Interv Radiol. 2016; 22(4):390-4

Proc. Intl. Soc. Mag. Reson. Med. 26 (2018)
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