Vol 28, No 3 (2023)
Clinical vignette
Published online: 2023-06-14

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clinical vignette

Reports of Practical Oncology and Radiotherapy

2023, Volume 28, Number 3, pages: 433–434

DOI: 10.5603/RPOR.a2023.0038

Submitted: 13.01.2023

Accepted: 05.06.2023

© 2023 Greater Poland Cancer Centre.

Published by Via Medica.

All rights reserved.

e-ISSN 2083–4640

ISSN 1507–1367

Potential use of [18F]FDG heterogeneity in discrimination of two different synchronous primary tumors

Paulina Cegla1Anna Filipczuk1Witold Cholewinski12
1Department of Nuclear Medicine, Greater Poland Cancer Centre, Poznan, Poland
2Department of Electroradiology, Poznan University of Medical Science, Poznan, Poland

Address for correspondence: Paulina Cegla PhD, Department of Nuclear Medicine, Greater Poland Cancer Centre, Garbary 15 Street, 61–866 Poznan, Poland; fax: +48 61 8850 785; e-mail: paulina.cegla@gmail.com

This article is available in open access under Creative Common Attribution-Non-Commercial-No Derivatives 4.0 International (CC BY-NC-ND 4.0) license, allowing to download articles and share them with others as long as they credit the authors and the publisher, but without permission to change them in any way or use them commercially

Key words: heterogeneity; positron emission tomography/computed tomography; fluorodeoxyglucose
Rep Pract Oncol Radiother 2023;28(3):433–434

Nuclear medicine techniques include positron emission tomography/computed tomography (PET/CT) or single photon emission tomography (SPECT) which allow a non-invasive way to measure specific processes based on the radiotracer accumulation. Over 80% of PET/CT studies are performed in oncology and this modality is better than conventional imaging modalities like magnetic resonance imaging (MRI) or computed tomography (CT), because it allows the severity of the disease to be assessed by one examination [1]. It was shown that [18F]FDG PET/CT is helpful in detection of primary tumor including head and neck cancer patients [2].

An 71-year-old female with diagnosed planoepitheliale cancer of the nasal cavity underwent a standard [18F]FDG PET/CT examination (1h post injection of 348MBq) and delayed one (2h post injection) because of suspected dissemination of the disease. Examination was performed on a Gemini TOF PET/CT scanner with area from the vertex to the mid-tight according to the standard EANM protocols [3]. Metabolic parameter: maximum standardized uptake value (SUVmax), as well as heterogeneity parameters: kurtosis and skewness were extracted and evaluated in both (standard and delayed images) on the dedicated workstation.

The scan revealed a focal uptake into a nasal cavity with SUVmax up to 10.11 (a) increased uptake on the right temporal site of the skin with SUVmax up to 3.96 (b) and a hypermetabolic mass in the upper right lobe of the lung with SUVmax up to 11.27 (c). Delayed [18F]FDG PET/CT study which showed an increase of the activity in the nasal cavity (SUVmax up to 13.87), on the right temporal site of the skin (SUVmax up to 4.78) and in the right upper lobe of the lung (SUVmax up to 17.36). After histopathological examination of the mass in the right lobe anaplastic carcinoma: CK(AE1/AE3)+, TTF1+, SYN+, Ki67 > 90% was confirmed. Standard and delayed [18F]FDG PET/CT examination showed that the increase of [18F]FDG uptake in planoepitheliale cancer was 37%, while in anaplastic lung cancer it was 54%. Almost 50% difference was noted between planoepitheliale cancer and anaplastic lung cancer in kurtosis (–0.51 vs. –0.96 and –0.47 vs. –0.81) in standard and delayed images, respectively. Slight differences were shown in skewness (0.11 vs. –0.18 and 0.09 vs. –0.06) in standard and delayed images, respectively.

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Figure 1. A. Focal uptake into a nasal cavity with SUVmax up to 10.11; B. Increased uptake on the right temporal site of the skin with SUVmax up to 3.96; C. A hypermetabolic mass in the upper right lobe of the lung with SUVmax up to 11.27

[18F]FDG PET/CT examination is a commonly used tool for staging, assessing therapy response, recurrence and prognosis in cancer patients [4]. Histopathological type of the cancer have been shown to have an impact on several [18F]FDG PET-derived parameters [5]. It has been reported that dual and multiple time point [18F]FDG PET imaging provides useful diagnostic and prognostic information [6]. That was also confirmed in our examination: both primary tumor values increased in delayed imaging; moreover, they differed depending on histopathology (SUVmax of 13.87 for planoepitheliale compared to 17.36 for anaplastic carcinoma) in delayed images. Moreover, some authors suggest that heterogeneity parameters provide incremental value over SUVmax in predicting response in some types of cancer [7]. Some studies also suggest that heterogeneity measured on initial [18F]FDG PET/CT provides information about outcome in oncological patients, including lung and head and neck cancer [7]. Even though we did not assess the outcome of this patient, we noticed almost 50% difference in terms of kurtosis parameter between the two distinct histopatholgical types of primary tumor. This indicates that not the only commonly known SUVmax, but, more importantly, also heterogeneity parameters obtained from [18F]FDG PET studies might serve as the first line differentiation (histopathological examination is still a gold standard) of different histopathology.

Performing standard and delayed examination with additional analysis of lesion kurtosis provides additional value in the discrimination of different histopathological primaries.

Conflict of interest

None declared.

Founding

None declared

References

  1. Lozano Ruiz FJ, Ileana Pérez Álvarez S, Poitevin Chacón MA, et al. The importance of image guided radiotherapy in small cell lung cancer: Case report and review of literature. Rep Pract Oncol Radiother. 2020; 25(1): 146–149, doi: 10.1016/j.rpor.2019.12.013, indexed in Pubmed: 31933543.
  2. Majchrzak E, Cholewiński W, Golusiński W. Carcinoma of unknown primary in the head and neck: The evaluation of the effectiveness of (18)F-FDG-PET/CT, own experience. Rep Pract Oncol Radiother. 2015; 20(5): 393–397, doi: 10.1016/j.rpor.2015.07.002, indexed in Pubmed: 26549998.
  3. Boellaard R, Delgado-Bolton R, Oyen WJG, et al. European Association of Nuclear Medicine (EANM). FDG PET/CT: EANM procedure guidelines for tumour imaging: version 2.0. Eur J Nucl Med Mol Imaging. 2015; 42(2): 328–354, doi: 10.1007/s00259-014-2961-x, indexed in Pubmed: 25452219.
  4. Colosimo C, Pasqualetti F, Aristei C, et al. Stereotactic radiotherapy for bone oligometastases. Rep Pract Oncol Radiother. 2022; 27(1): 40–45, doi: 10.5603/RPOR.a2022.0009, indexed in Pubmed: 35402030.
  5. Bitencourt AG, Lima EN, Chojniak R, et al. Correlation between PET/CT results and histological and immunohistochemical findings in breast carcinomas. Radiol Bras. 2014; 47(2): 67–73, doi: 10.1590/S0100-39842014000200006, indexed in Pubmed: 25741051.
  6. Baun C, Falch K, Gerke O, et al. Quantification of FDG-PET/CT with delayed imaging in patients with newly diagnosed recurrent breast cancer. BMC Med Imaging. 2018; 18(1): 11, doi: 10.1186/s12880-018-0254-8, indexed in Pubmed: 29743027.
  7. Azad GK, Cousin F, Siddique M, et al. Does Measurement of First-Order and Heterogeneity Parameters Improve Response Assessment of Bone Metastases in Breast Cancer Compared to SUV in [F]fluoride and [F]FDG PET? Mol Imaging Biol. 2019; 21(4): 781–789, doi: 10.1007/s11307-018-1262-3, indexed in Pubmed: 30250989.