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Licensed Unlicensed Requires Authentication Published by De Gruyter November 12, 2020

The utility of 68Ga-DOTATATE PET/CT in localizing primary/metastatic pheochromocytoma and paraganglioma in children and adolescents – a single-center experience

  • Sanjeet Kumar Jaiswal ORCID logo , Vijaya Sarathi , Gaurav Malhotra , Priya Hira , Ravikumar Shah , Virendra A. Patil , Abhay Dalvi , Gagan Prakash , Anurag R. Lila , Nalini S. Shah and Tushar Bandgar ORCID logo EMAIL logo

Abstract

Objectives

Pediatric pheochromocytoma and paraganglioma (PPGL) are rare tumors with limited data on the diagnostic performance of 68Ga-DOTA(0)-Tyr(3)-octreotate positron emission tomography–computed tomography (68Ga-DOTATATE PET/CT). We have described our experience of 68Ga-DOTATATE PET/CT in overall and von Hippel Lindau (VHL)-associated pediatric PPGL and compared its sensitivity with that of 131I-meta-iodobenzyl-guanidine (131I-MIBG), 18F-fluorodeoxyglucose PET/CT (18F-FDG PET/CT), and contrast-enhanced CT (CECT).

Methods

Retrospective evaluation of consecutive PPGL patients (age: ≤20 years), who had undergone at least one functional imaging [131I-MIBG, 18F-FDG PET/CT, and/or 68Ga-DOTATATE PET/CT], was done. Composite of anatomical and all the performed functional imaging scans, image comparator (IC), was considered as the gold standard for sensitivity analysis.

Results

In a cohort of 32 patients (16 males, age at diagnosis: 16.4 ± 2.68 years), lesion-wise sensitivity of 68Ga-DOTATATE PET/CT (95%) was higher than that of both 18F-FDG-PET/CT (80%, p=0.027) and 131I-MIBG (65%, p=0.0004) for overall lesions, than that of 18F-FDG-PET/CT (100 vs. 67%, p=0.017) for primary PPG, and than that of 131I-MIBG (93 vs. 42%, p=0.0001) for metastases. In the VHL (n=14), subgroup, 68Ga-DOTATATE PET/CT had higher lesion-wise sensitivity (100%) compared to 18F-FDG PET/CT (74%, p=0.045) and 131I-MIBG (64%, p=0.0145).

Conclusions

In our pediatric PPGL cohort, overall lesion-wise sensitivity of 68Ga-DOTATATE PET/CT was higher than that of 18F–FDG PET/CT and 131I-MIBG scintigraphy. Hence, we recommend 68Ga-DOTATATE PET/CT as the preferred modality in pediatric PPGL. 68Ga-DOTATATE PET/CT may evolve as a preferred imaging modality for disease surveillance in VHL.


Corresponding author: Tushar Bandgar, MD, DM, Department of Endocrinology, Seth G.S. Medical College & KEM hospital, Parel, 4000012Mumbai, Maharashtra, India, Phone: (+91) 02224162917, Fax: (022) 24162883, E-mail:

Funding source: Scientific and Engineering Research Board

Award Identifier / Grant number: Grant# SB/SO/HS/041/2013

Acknowledgment

We acknowledge Vyankatesh Shivane, Neeta Doiphode, and Neelam Jaguste for administrative help in the conduct of the study.

  1. Research funding: This study was funded by the Scientific and Engineering Research Board (SERB), Department of Science and Technology, Government of India (Grant# SB/SO/HS/041/2013).

  2. Author contributions: Study design: Tushar Bandgar. Literature review, data collection, analysis, and drafting of the manuscript: Sanjeet Kumar Jaiswal and Ravikumar shah. Tushar Bandgar, Vijaya Sarathi, and other authors have reviewed, edited, and approved the final manuscript.

  3. Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication. The authors have no conflict of interest to disclose.

  4. Informed consent: Considering the retrospective nature of the study waiver of informed consent was obtained for all individuals included in this study.

  5. Ethical approval: All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standard.

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Supplementary Material

The online version of this article offers supplementary material (https://doi.org/10.1515/jpem-2020-0354).

Received: 2020-06-11
Accepted: 2020-10-15
Published Online: 2020-11-12
Published in Print: 2021-01-27

© 2020 Walter de Gruyter GmbH, Berlin/Boston

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