Hannes Leupe, Niloefar Ahmadi Bidakhvidi, Karolien Goffin, Bliede Van den Broeck, Sander Jentjens, Annouschka Laenen, Elin Pauwels, Willem Lybaert, Eric Van Cutsem, Guy Bormans, Timon Vandamme, Frederik Cleeren, Jeroen Dekervel, Karen Geboes, Sigrid Stroobants, Chris Verslype, Christophe M Deroose
{"title":"Comparison of inter- and intraobserver agreement between [<sup>18</sup>F]AlF-NOTA-octreotide and [<sup>68</sup>Ga]Ga-DOTA-SSA PET/CT.","authors":"Hannes Leupe, Niloefar Ahmadi Bidakhvidi, Karolien Goffin, Bliede Van den Broeck, Sander Jentjens, Annouschka Laenen, Elin Pauwels, Willem Lybaert, Eric Van Cutsem, Guy Bormans, Timon Vandamme, Frederik Cleeren, Jeroen Dekervel, Karen Geboes, Sigrid Stroobants, Chris Verslype, Christophe M Deroose","doi":"10.1186/s41824-025-00250-y","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>This study compares inter- and intraobserver agreement between [<sup>18</sup>F]AlF-NOTA-octreotide ([<sup>18</sup>F]AlF-OC) and [<sup>68</sup>Ga]Ga-DOTA-somatostatin analogues (SSAs) in PET/CT imaging for neuroendocrine neoplasm (NEN) patients.</p><p><strong>Materials and methods: </strong>This is a secondary endpoint analysis from our multicenter trial (clin trial.gov identifier: NCT04552847) including 75 NEN patients who received both [<sup>68</sup>Ga]Ga-DOTATATE (n = 56) or [<sup>68</sup>Ga]Ga-DOTA-NOC (n = 19) and [<sup>18</sup>F]AlF-OC PET imaging. Five readers assessed lesion detection and characterization across multiple organs, scoring lesions by number and conspicuity using a 5-point Likert scale. Agreement was measured using Gwet's agreement coefficient.</p><p><strong>Results: </strong>Results demonstrated nearly perfect interobserver agreement for lesion characterization across all organs for both tracers (0.921 for [<sup>18</sup>F]AlF-OC; 0.934 for [<sup>68</sup>Ga]Ga-DOTA-SSA). Similar agreement was observed for the number of lesions across organs (0.736 for [<sup>18</sup>F]AlF-OC and 0.749 for [<sup>68</sup>Ga]Ga-DOTA-SSAs). Organ-specific analysis revealed strong agreement for bone and liver lesions, with slightly lower agreement for lymph nodes. Both tracers also showed excellent agreement in determining Krenning scores (0.925 for [<sup>18</sup>F]AlF-OC and 0.927 for [<sup>68</sup>Ga]Ga-DOTA-SSAs). While mean lesion conspicuity was similar between tracers, [<sup>18</sup>F]AlF-OC had a higher global image quality score (4.22 vs. 3.86, p < 0.0001). Intraobserver agreement was consistent between tracers for lesion characterization (> 0.95 for both readers) and lesion count (> 0.80 for both readers).</p><p><strong>Conclusion: </strong>[<sup>18</sup>F]AlF-OC and [<sup>68</sup>Ga]Ga-DOTA-SSAs demonstrate comparable and excellent inter- and intraobserver agreement, reinforcing the clinical interchangeability of [<sup>18</sup>F]AlF-OC PET/CT with [<sup>68</sup>Ga]Ga-DOTA-SSAs in routine practice.</p>","PeriodicalId":519909,"journal":{"name":"EJNMMI reports","volume":"9 1","pages":"17"},"PeriodicalIF":0.0000,"publicationDate":"2025-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12078903/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"EJNMMI reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1186/s41824-025-00250-y","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Purpose: This study compares inter- and intraobserver agreement between [18F]AlF-NOTA-octreotide ([18F]AlF-OC) and [68Ga]Ga-DOTA-somatostatin analogues (SSAs) in PET/CT imaging for neuroendocrine neoplasm (NEN) patients.
Materials and methods: This is a secondary endpoint analysis from our multicenter trial (clin trial.gov identifier: NCT04552847) including 75 NEN patients who received both [68Ga]Ga-DOTATATE (n = 56) or [68Ga]Ga-DOTA-NOC (n = 19) and [18F]AlF-OC PET imaging. Five readers assessed lesion detection and characterization across multiple organs, scoring lesions by number and conspicuity using a 5-point Likert scale. Agreement was measured using Gwet's agreement coefficient.
Results: Results demonstrated nearly perfect interobserver agreement for lesion characterization across all organs for both tracers (0.921 for [18F]AlF-OC; 0.934 for [68Ga]Ga-DOTA-SSA). Similar agreement was observed for the number of lesions across organs (0.736 for [18F]AlF-OC and 0.749 for [68Ga]Ga-DOTA-SSAs). Organ-specific analysis revealed strong agreement for bone and liver lesions, with slightly lower agreement for lymph nodes. Both tracers also showed excellent agreement in determining Krenning scores (0.925 for [18F]AlF-OC and 0.927 for [68Ga]Ga-DOTA-SSAs). While mean lesion conspicuity was similar between tracers, [18F]AlF-OC had a higher global image quality score (4.22 vs. 3.86, p < 0.0001). Intraobserver agreement was consistent between tracers for lesion characterization (> 0.95 for both readers) and lesion count (> 0.80 for both readers).
Conclusion: [18F]AlF-OC and [68Ga]Ga-DOTA-SSAs demonstrate comparable and excellent inter- and intraobserver agreement, reinforcing the clinical interchangeability of [18F]AlF-OC PET/CT with [68Ga]Ga-DOTA-SSAs in routine practice.