[<sup>18</sup>F]FDG Metabolic Tumor Volume as a Prognostic Marker in Neuroendocrine Neoplasm: A Multicenter Study

[<sup>18</sup>F]FDG PET/CT avidity predicts higher-grade disease and worse prognosis in patients with metastatic neuroendocrine neoplasm. However, there is less evidence regarding the role of [<sup>18</sup>F]FDG-avid tumor volume in predicting prognosis. We planned to determine whether metabolic tumor volume (MTV) on [<sup>18</sup>F]FDG PET/CT predicts prognosis in patients with advanced gastroenteropancreatic neuroendocrine neoplasm (GEPNEN). <b>Methods:</b> A multicenter retrospective study was performed on patients with advanced GEPNEN who underwent [<sup>18</sup>F]FDG PET/CT in a previously established cohort. Images were acquired across 3 centers using harmonized protocols and were contoured and verified at a flat SUV threshold of 4 using a semiautomated software workflow. The primary endpoint was overall survival. Patients were dichotomized into high- and low-MTV groups by the median value, with the overall survival of the 2 resulting cohorts compared by log-rank tests and multivariate analyses. <b>Results:</b> In total, 231 patients were included (49% male; median age, 60 y). In 45% of cases the primary was the pancreas, in 42% the small bowel, and in 13% another location. Regarding World Health Organization 2019 grade, 23% were grade 1, 52% grade 2, 21% grade 3, and 4% an unknown grade. The median follow-up was 27 mo (interquartile range, 11-49 mo), and median overall survival was 38.6 mo. Median overall survival was shorter in the high-MTV cohort than in the low-MTV cohort (cut point, 16.5 cm<sup>3</sup>; 23.8 mo vs. not reached; hazard ratio, 2.49; 95% CI, 1.69-3.66; <i>P</i> < 0.0001). Median time to treatment failure was also shorter in the high-MTV cohort (11.7 mo vs. 16.9 mo; hazard ratio, 1.52; 95% CI, 1.13-2.06; <i>P</i> = 0.005). Increasing histologic grade was associated with higher MTV (<i>P</i> = 0.0006, 1-way ANOVA). Multivariate analysis incorporating age, grade, sex, SUV<sub>max</sub>, and MTV showed that only grade (<i>P</i> = 0.001) and MTV (<i>P</i> < 0.001) were independently prognostic. <b>Conclusion:</b> MTV is a prognostic biomarker in advanced GEPNEN. Reports of [<sup>18</sup>F]FDG PET in GEPNEN may benefit from comments on MTV in addition to the degree of [<sup>18</sup>F]FDG avidity.

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Journal
Journal of Nuclear Medicine
Published
2025-05-22
DOI
https://doi.org/10.2967/jnumed.124.269031
Citations
1
Primary Topic
Neuroendocrine Tumor Research Advances
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article
Field-Weighted Citation Impact
1.35
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article

[18F]FDG Metabolic Tumor Volume as a Prognostic Marker in Neuroendocrine Neoplasm: A Multicenter Study

Shaunak Navalkissoor, Christos Toumpanakis, Martyn Caplin, Ioannis Karfis et al.
1 citations
Journal of Nuclear Medicine
Neuroendocrine Tumor Research Advances
1.35
article

[18F]FDG Metabolic Tumor Volume as a Prognostic Marker in Neuroendocrine Neoplasm: A Multicenter Study

Shaunak Navalkissoor, Christos Toumpanakis, Martyn Caplin, Ioannis Karfis, Aimee R. Hayes, Magdalena Mileva, David Chan, Alice Conner, Stephen John Clarke, Patrick Flamen, PAUL J. ROACH, Dale L. Bailey, Nick Pavlakis, Gopinath Gnanasekaran, Elizabeth J. Bernard
article en
1 citations

Abstract

[<sup>18</sup>F]FDG PET/CT avidity predicts higher-grade disease and worse prognosis in patients with metastatic neuroendocrine neoplasm. However, there is less evidence regarding the role of [<sup>18</sup>F]FDG-avid tumor volume in predicting prognosis. We planned to determine whether metabolic tumor volume (MTV) on [<sup>18</sup>F]FDG PET/CT predicts prognosis in patients with advanced gastroenteropancreatic neuroendocrine neoplasm (GEPNEN). <b>Methods:</b> A multicenter retrospective study was performed on patients with advanced GEPNEN who underwent [<sup>18</sup>F]FDG PET/CT in a previously established cohort. Images were acquired across 3 centers using harmonized protocols and were contoured and verified at a flat SUV threshold of 4 using a semiautomated software workflow. The primary endpoint was overall survival. Patients were dichotomized into high- and low-MTV groups by the median value, with the overall survival of the 2 resulting cohorts compared by log-rank tests and multivariate analyses. <b>Results:</b> In total, 231 patients were included (49% male; median age, 60 y). In 45% of cases the primary was the pancreas, in 42% the small bowel, and in 13% another location. Regarding World Health Organization 2019 grade, 23% were grade 1, 52% grade 2, 21% grade 3, and 4% an unknown grade. The median follow-up was 27 mo (interquartile range, 11-49 mo), and median overall survival was 38.6 mo. Median overall survival was shorter in the high-MTV cohort than in the low-MTV cohort (cut point, 16.5 cm<sup>3</sup>; 23.8 mo vs. not reached; hazard ratio, 2.49; 95% CI, 1.69-3.66; <i>P</i> < 0.0001). Median time to treatment failure was also shorter in the high-MTV cohort (11.7 mo vs. 16.9 mo; hazard ratio, 1.52; 95% CI, 1.13-2.06; <i>P</i> = 0.005). Increasing histologic grade was associated with higher MTV (<i>P</i> = 0.0006, 1-way ANOVA). Multivariate analysis incorporating age, grade, sex, SUV<sub>max</sub>, and MTV showed that only grade (<i>P</i> = 0.001) and MTV (<i>P</i> < 0.001) were independently prognostic. <b>Conclusion:</b> MTV is a prognostic biomarker in advanced GEPNEN. Reports of [<sup>18</sup>F]FDG PET in GEPNEN may benefit from comments on MTV in addition to the degree of [<sup>18</sup>F]FDG avidity.

Journal of Nuclear MedicineVol. 66(7)
The University of Sydney (AU), Royal North Shore Hospital (AU), The Royal Free Hospital (GB), University College London (GB)
Openalex Percentile: Top 20%
Neuroendocrine Tumor Research Advances
1.35
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