Literature DB >> 28771999

Monitoring of plexiform neurofibroma in children and adolescents with neurofibromatosis type 1 by [18 F]FDG-PET imaging. Is it of value in asymptomatic patients?

Amedeo A Azizi1, Irene Slavc1, Benjamin Emile Theisen1, Ivo Rausch2, Michael Weber3, Wolfgang Happak4, Oskar Aszmann4, Azadeh Hojreh3, Andreas Peyrl1, Gabriele Amann5, Thomas M Benkoe4, Wolfgang Wadsak3, Gregor Kasprian3, Anton Staudenherz3, Marcus Hacker3, Tatjana Traub-Weidinger3.   

Abstract

PURPOSE: About 10% of patients with neurofibromatosis type 1 (NF-1) develop malignant peripheral nerve sheath tumours (MPNST) mostly arising in plexiform neurofibroma (PN); 15% of MPNST arise in children and adolescents. 2-[18 F]fluoro-2-deoxy-d-glucose ([18 F]FDG)-PET (where PET is positron emission tomography) is a sensitive method in differentiating PN and MPNST in symptomatic patients with NF-1. This study assesses the value of [18 F]FDG-PET imaging in detecting malignant transformation in symptomatic and asymptomatic children with PN.
METHODS: Forty-one patients with NF-1 and extensive PN underwent prospective [18 F]FDG imaging from 2003 to 2014. Thirty-two of the patients were asymptomatic. PET data, together with histological results and clinical course were re-evaluated retrospectively. Maximum standardised uptake values (SUVmax) and lesion-to-liver ratio were assessed.
RESULTS: A total of 104 examinations were performed. Mean age at first PET was 13.5 years (2.6-22.6). Eight patients had at least one malignant lesion; four of these patients were asymptomatic. Two of four symptomatic patients died, while all patients with asymptomatic malignant lesions are alive. All malignant tumours could be identified by PET imaging in both symptomatic and asymptomatic patients. All lesions judged as benign by [18 F]FDG imaging and clinical judgment were either histologically benign if removed or remained clinically silent during follow-up. SUVmax of malignant and benign lesions overlapped, but no malignant lesion showed FDG uptake ≤3.15. Asymptomatic malignant lesions were detected with a sensitivity of 100%, a negative predictive value of 100% and a specificity of 45.1%.
CONCLUSION: Malignant transformation of PN also occurs in asymptomatic children and adolescents. Detection of MPNST at early stages could increase the possibility of oncologically curative resections.
© 2017 Wiley Periodicals, Inc.

Entities:  

Keywords:  [18F]FDG-PET; children; malignant peripheral nerve sheath tumour; neurofibromatosis type 1; plexiform neurofibroma

Mesh:

Substances:

Year:  2017        PMID: 28771999     DOI: 10.1002/pbc.26733

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  8 in total

Review 1.  Current status and recommendations for imaging in neurofibromatosis type 1, neurofibromatosis type 2, and schwannomatosis.

Authors:  Shivani Ahlawat; Jaishri O Blakeley; Shannon Langmead; Allan J Belzberg; Laura M Fayad
Journal:  Skeletal Radiol       Date:  2019-08-08       Impact factor: 2.199

Review 2.  Image-Based Differentiation of Benign and Malignant Peripheral Nerve Sheath Tumors in Neurofibromatosis Type 1.

Authors:  Jun Liu; Jing-Ning Huang; Ming-Han Wang; Zhen-Yang Ni; Wei-Hao Jiang; Manhon Chung; Cheng-Jiang Wei; Zhi-Chao Wang
Journal:  Front Oncol       Date:  2022-05-23       Impact factor: 5.738

3.  Does elevated glucose metabolism correlate with higher cell density in Neurofibromatosis type 1 associated peripheral nerve sheath tumors?

Authors:  Dominik Berzaczy; Marius E Mayerhoefer; Amedeo A Azizi; Alexander R Haug; Daniela Senn; Dietrich Beitzke; Michael Weber; Tatjana Traub-Weidinger
Journal:  PLoS One       Date:  2017-12-05       Impact factor: 3.240

4.  A Bayesian approach for diagnostic accuracy of malignant peripheral nerve sheath tumors: a systematic review and meta-analysis.

Authors:  Enrico Martin; Ritchie T J Geitenbeek; J Henk Coert; David F Hanff; Laura H Graven; Dirk J Grünhagen; Cornelis Verhoef; Walter Taal
Journal:  Neuro Oncol       Date:  2021-04-12       Impact factor: 12.300

5.  Diagnostic value of 18F-FDG PET-CT in detecting malignant peripheral nerve sheath tumors among adult and pediatric neurofibromatosis type 1 patients.

Authors:  Ritch T J Geitenbeek; Enrico Martin; Laura H Graven; Martijn P G Broen; Monique H M E Anten; Jochem A J van der Pol; Cornelis Verhoef; Walter Taal
Journal:  J Neurooncol       Date:  2022-01-13       Impact factor: 4.130

6.  Detection of malignant peripheral nerve sheath tumors in patients with neurofibromatosis using aneuploidy and mutation identification in plasma.

Authors:  Austin K Mattox; Christopher Douville; Natalie Silliman; Janine Ptak; Lisa Dobbyn; Joy Schaefer; Maria Popoli; Cherie Blair; Kathy Judge; Kai Pollard; Christine Pratilas; Jaishri Blakeley; Fausto Rodriguez; Nickolas Papadopoulos; Allan Belzberg; Chetan Bettegowda
Journal:  Elife       Date:  2022-03-04       Impact factor: 8.713

Review 7.  Malignant Peripheral Nerve Sheath Tumors-A Comprehensive Review of Pathophysiology, Diagnosis, and Multidisciplinary Management.

Authors:  Samantha W E Knight; Tristan E Knight; Teresa Santiago; Andrew J Murphy; Abdelhafeez H Abdelhafeez
Journal:  Children (Basel)       Date:  2022-01-01

8.  SNMMI Procedure Standard/EANM Practice Guideline on Pediatric 18F-FDG PET/CT for Oncology 1.0.

Authors:  Reza Vali; Adam Alessio; Rene Balza; Lise Borgwardt; Zvi Bar-Sever; Michael Czachowski; Nina Jehanno; Lars Kurch; Neeta Pandit-Taskar; Marguerite Parisi; Arnoldo Piccardo; Victor Seghers; Barry L Shulkin; Pietro Zucchetta; Ruth Lim
Journal:  J Nucl Med       Date:  2021-01       Impact factor: 11.082

  8 in total

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