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Interobserver Agreement Rates on Fibroblast Activation Protein Inhibitor–Directed Molecular Imaging and Therapy

Fibroblast activation protein (FAP) has emerged as a novel target for FAP inhibitor (FAPI)–directed molecular imaging and endoradiotherapy (ERT). We aimed to assess the interobserver agreement rates for interpretation of (68)Ga-FAPI-4 PET/CT and decision for ERT. PATIENTS AND METHODS: A random order...

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Autores principales: Serfling, Sebastian E., Hartrampf, Philipp E., Zhi, Yingjun, Higuchi, Takahiro, Rowe, Steven P., Bundschuh, Lena, Essler, Markus, Buck, Andreas K., Bundschuh, Ralph Alexander, Werner, Rudolf A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9071032/
https://www.ncbi.nlm.nih.gov/pubmed/35439187
http://dx.doi.org/10.1097/RLU.0000000000004189
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author Serfling, Sebastian E.
Hartrampf, Philipp E.
Zhi, Yingjun
Higuchi, Takahiro
Rowe, Steven P.
Bundschuh, Lena
Essler, Markus
Buck, Andreas K.
Bundschuh, Ralph Alexander
Werner, Rudolf A.
author_facet Serfling, Sebastian E.
Hartrampf, Philipp E.
Zhi, Yingjun
Higuchi, Takahiro
Rowe, Steven P.
Bundschuh, Lena
Essler, Markus
Buck, Andreas K.
Bundschuh, Ralph Alexander
Werner, Rudolf A.
author_sort Serfling, Sebastian E.
collection PubMed
description Fibroblast activation protein (FAP) has emerged as a novel target for FAP inhibitor (FAPI)–directed molecular imaging and endoradiotherapy (ERT). We aimed to assess the interobserver agreement rates for interpretation of (68)Ga-FAPI-4 PET/CT and decision for ERT. PATIENTS AND METHODS: A random order of (68)Ga-FAPI-4 PET/CTs from 49 oncology patients were independently interpreted by 4 blinded readers. Per scan, visual assessment was performed, including overall scan impression, number of organ/lymph node (LN) metastases, and number of affected organs/LN regions. Moreover, a maximum of 3 target lesions, defined as largest in size and/or most intense, per organ compartment were identified, which allowed for an additional quantitative interobserver assessment of LN and organ lesions. To investigate potential reference tissues, quantification also included unaffected liver parenchyma and blood pool. Readers also had to indicate whether FAPI-directed ERT should be considered (based on intensity of uptake and widespread disease). Interobserver agreement rates were evaluated using intraclass correlation coefficients (ICCs) and interpreted according to Cicchetti (with 0.4–0.59 indicating fair, and 0.6–0.74 good, agreement). RESULTS: On a visual basis, the agreement rate for an overall scan impression was fair (ICC, 0.42; 95% confidence interval [CI], 0.27–0.57). The concordance rate for number of affected LN areas was also fair (ICC, 0.59; 95% CI, 0.45–0.72), whereas the number of LN metastases, number of affected organs, and number of organ metastases achieved good agreement rates (ICC, ≥0.63). In a quantitative analysis, concordance rates for LN were good (ICC, 0.70; 0.48–0.88), but only fair for organ lesions (ICC, 0.43; 0.26–0.60). In regards to background tissues, ICCs were good for unaffected liver parenchyma (0.68; 0.54–0.79) and fair for blood pool (0.43; 0.29–0.58). When readers should decide on ERT, concordance rates were also fair (ICC, 0.59; 95% CI, 0.46–0.73). CONCLUSIONS: For FAPI-directed molecular imaging and therapy, a fair to good interobserver agreement rate was achieved, supporting the adoption of this radiotracer for clinical routine and multicenter trials.
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spelling pubmed-90710322022-05-09 Interobserver Agreement Rates on Fibroblast Activation Protein Inhibitor–Directed Molecular Imaging and Therapy Serfling, Sebastian E. Hartrampf, Philipp E. Zhi, Yingjun Higuchi, Takahiro Rowe, Steven P. Bundschuh, Lena Essler, Markus Buck, Andreas K. Bundschuh, Ralph Alexander Werner, Rudolf A. Clin Nucl Med Original Articles Fibroblast activation protein (FAP) has emerged as a novel target for FAP inhibitor (FAPI)–directed molecular imaging and endoradiotherapy (ERT). We aimed to assess the interobserver agreement rates for interpretation of (68)Ga-FAPI-4 PET/CT and decision for ERT. PATIENTS AND METHODS: A random order of (68)Ga-FAPI-4 PET/CTs from 49 oncology patients were independently interpreted by 4 blinded readers. Per scan, visual assessment was performed, including overall scan impression, number of organ/lymph node (LN) metastases, and number of affected organs/LN regions. Moreover, a maximum of 3 target lesions, defined as largest in size and/or most intense, per organ compartment were identified, which allowed for an additional quantitative interobserver assessment of LN and organ lesions. To investigate potential reference tissues, quantification also included unaffected liver parenchyma and blood pool. Readers also had to indicate whether FAPI-directed ERT should be considered (based on intensity of uptake and widespread disease). Interobserver agreement rates were evaluated using intraclass correlation coefficients (ICCs) and interpreted according to Cicchetti (with 0.4–0.59 indicating fair, and 0.6–0.74 good, agreement). RESULTS: On a visual basis, the agreement rate for an overall scan impression was fair (ICC, 0.42; 95% confidence interval [CI], 0.27–0.57). The concordance rate for number of affected LN areas was also fair (ICC, 0.59; 95% CI, 0.45–0.72), whereas the number of LN metastases, number of affected organs, and number of organ metastases achieved good agreement rates (ICC, ≥0.63). In a quantitative analysis, concordance rates for LN were good (ICC, 0.70; 0.48–0.88), but only fair for organ lesions (ICC, 0.43; 0.26–0.60). In regards to background tissues, ICCs were good for unaffected liver parenchyma (0.68; 0.54–0.79) and fair for blood pool (0.43; 0.29–0.58). When readers should decide on ERT, concordance rates were also fair (ICC, 0.59; 95% CI, 0.46–0.73). CONCLUSIONS: For FAPI-directed molecular imaging and therapy, a fair to good interobserver agreement rate was achieved, supporting the adoption of this radiotracer for clinical routine and multicenter trials. Lippincott Williams & Wilkins 2022-06 2022-04-19 /pmc/articles/PMC9071032/ /pubmed/35439187 http://dx.doi.org/10.1097/RLU.0000000000004189 Text en Copyright © 2022 The Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Original Articles
Serfling, Sebastian E.
Hartrampf, Philipp E.
Zhi, Yingjun
Higuchi, Takahiro
Rowe, Steven P.
Bundschuh, Lena
Essler, Markus
Buck, Andreas K.
Bundschuh, Ralph Alexander
Werner, Rudolf A.
Interobserver Agreement Rates on Fibroblast Activation Protein Inhibitor–Directed Molecular Imaging and Therapy
title Interobserver Agreement Rates on Fibroblast Activation Protein Inhibitor–Directed Molecular Imaging and Therapy
title_full Interobserver Agreement Rates on Fibroblast Activation Protein Inhibitor–Directed Molecular Imaging and Therapy
title_fullStr Interobserver Agreement Rates on Fibroblast Activation Protein Inhibitor–Directed Molecular Imaging and Therapy
title_full_unstemmed Interobserver Agreement Rates on Fibroblast Activation Protein Inhibitor–Directed Molecular Imaging and Therapy
title_short Interobserver Agreement Rates on Fibroblast Activation Protein Inhibitor–Directed Molecular Imaging and Therapy
title_sort interobserver agreement rates on fibroblast activation protein inhibitor–directed molecular imaging and therapy
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9071032/
https://www.ncbi.nlm.nih.gov/pubmed/35439187
http://dx.doi.org/10.1097/RLU.0000000000004189
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