[<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.
Authors
- Shaunak Navalkissoor (ORCID: https://orcid.org/0000-0003-2886-9691)
- Christos Toumpanakis (ORCID: https://orcid.org/0000-0002-1152-7727)
- Martyn Caplin (ORCID: https://orcid.org/0000-0003-0177-1352)
- Ioannis Karfis (ORCID: https://orcid.org/0000-0003-2158-3981)
- Aimee R. Hayes (ORCID: https://orcid.org/0000-0003-4417-7716)
- Magdalena Mileva (ORCID: https://orcid.org/0000-0002-9929-4576)
- David Chan
- Alice Conner (ORCID: https://orcid.org/0000-0002-1313-1582)
- Stephen John Clarke (ORCID: https://orcid.org/0000-0001-5817-1222)
- Patrick Flamen (ORCID: https://orcid.org/0000-0003-2193-6599)
- PAUL J. ROACH (ORCID: https://orcid.org/0000-0003-2504-0474)
- Dale L. Bailey (ORCID: https://orcid.org/0000-0001-9154-7957)
- Nick Pavlakis (ORCID: https://orcid.org/0000-0002-1738-0316)
- Gopinath Gnanasekaran
- Elizabeth J. Bernard
Institutions
- The University of Sydney (AU)
- Royal North Shore Hospital (AU)
- The Royal Free Hospital (GB)
- University College London (GB)
Publication Details
- 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
- Type
- article
- Field-Weighted Citation Impact
- 1.35