<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Rapizzi E</submitter><funding>Associazione Italiana per la Ricerca sul Cancro</funding><funding>Projects of Relevant National Interest (PRIN) 2022</funding><funding>Università degli Studi di Firenze</funding><pagination>33</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12484271</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>36(1)</volume><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Paragangliomas (PGLs) are rare malignant non-epithelial neuroendocrine neoplasms characterized by a strong genetic determinism and heterogeneous metastatic potential with no reliable histopathological predictors. In this retrospective study we investigated the role of serum succinate as a biomarker for metastatic risk and developed a novel preoperative scoring tool.&lt;h4>Matherials and methods&lt;/h4>Seventy patients with PGLs evaluated between 2006 and 2023 were analysed. Clinical, biochemical, imaging, and genetic data were collected. Germline genetic variants were analysed via Sanger sequencing or NGS through a targeted panel of susceptibility genes. Serum succinate concentrations were quantified by gas chromatography-mass spectrometry.&lt;h4>Results&lt;/h4>Succinate levels were significantly higher in patients with Cluster 1 genetic variants (p &lt; 0.001), extra-adrenal PGLs (p = 0.006), and metastatic disease (p = 0.024). We developed a novel preoperative risk assessment tool, the P-SMART (Preoperative Succinate MetAstatic Risk Tool), combining serum succinate levels, tumour size, and location. P-SMART assigns: 3 points for extra-adrenal localization, 3.5 points for serum succinate ≥ 8.95 µM, and 3 points for tumour size ≥ 7.0 cm. In our cohort a P-SMART score > 4.75 predicted metastatic disease with 72.7% sensitivity and 83% specificity, outperforming the ASES score (Age, Size, Extra-adrenal, Secretory type; AUC 0.891 vs 0.752, p = 0.005).&lt;h4>Conclusions&lt;/h4>Though limited by sample size and retrospective design, our findings suggest that succinate is a minimally invasive biomarker that could enhance preoperative metastatic risk stratification, especially when integrated into a multiparametric score such as P-SMART. Larger prospective studies are needed to validate its role, but P-SMART could optimize clinical decision-making, refine patient selection for whole-body imaging, reduce unnecessary radiation exposure, and inform surveillance strategies.</pubmed_abstract><journal>Endocrine pathology</journal><pubmed_title>Presurgical Succinate MetAstatic Risk Tool (P-SMART) in Paragangliomas.</pubmed_title><pmcid>PMC12484271</pmcid><funding_grant_id>CUP B53D23021440001</funding_grant_id><funding_grant_id>CUP B53D23021320001</funding_grant_id><funding_grant_id>IG 2020-ID 24820</funding_grant_id><pubmed_authors>Staderini F</pubmed_authors><pubmed_authors>Rapizzi E</pubmed_authors><pubmed_authors>Maggi M</pubmed_authors><pubmed_authors>Sparano C</pubmed_authors><pubmed_authors>Galeotti N</pubmed_authors><pubmed_authors>Ercolino T</pubmed_authors><pubmed_authors>Santi A</pubmed_authors><pubmed_authors>Amore F</pubmed_authors><pubmed_authors>Zanatta L</pubmed_authors><pubmed_authors>Canu L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Presurgical Succinate MetAstatic Risk Tool (P-SMART) in Paragangliomas.</name><description>&lt;h4>Introduction&lt;/h4>Paragangliomas (PGLs) are rare malignant non-epithelial neuroendocrine neoplasms characterized by a strong genetic determinism and heterogeneous metastatic potential with no reliable histopathological predictors. In this retrospective study we investigated the role of serum succinate as a biomarker for metastatic risk and developed a novel preoperative scoring tool.&lt;h4>Matherials and methods&lt;/h4>Seventy patients with PGLs evaluated between 2006 and 2023 were analysed. Clinical, biochemical, imaging, and genetic data were collected. Germline genetic variants were analysed via Sanger sequencing or NGS through a targeted panel of susceptibility genes. Serum succinate concentrations were quantified by gas chromatography-mass spectrometry.&lt;h4>Results&lt;/h4>Succinate levels were significantly higher in patients with Cluster 1 genetic variants (p &lt; 0.001), extra-adrenal PGLs (p = 0.006), and metastatic disease (p = 0.024). We developed a novel preoperative risk assessment tool, the P-SMART (Preoperative Succinate MetAstatic Risk Tool), combining serum succinate levels, tumour size, and location. P-SMART assigns: 3 points for extra-adrenal localization, 3.5 points for serum succinate ≥ 8.95 µM, and 3 points for tumour size ≥ 7.0 cm. In our cohort a P-SMART score > 4.75 predicted metastatic disease with 72.7% sensitivity and 83% specificity, outperforming the ASES score (Age, Size, Extra-adrenal, Secretory type; AUC 0.891 vs 0.752, p = 0.005).&lt;h4>Conclusions&lt;/h4>Though limited by sample size and retrospective design, our findings suggest that succinate is a minimally invasive biomarker that could enhance preoperative metastatic risk stratification, especially when integrated into a multiparametric score such as P-SMART. Larger prospective studies are needed to validate its role, but P-SMART could optimize clinical decision-making, refine patient selection for whole-body imaging, reduce unnecessary radiation exposure, and inform surveillance strategies.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-06-04T16:49:24.317Z</modification><creation>2026-05-13T14:24:30.962Z</creation></dates><accession>S-EPMC12484271</accession><cross_references><pubmed>41026309</pubmed><doi>10.1007/s12022-025-09878-9</doi></cross_references></HashMap>