The Impact of Rapid On-site Evaluation on Diagnostic Performance of Computed Tomography-Guided Core Needle Biopsy in Lung Cancer.


Journal

Journal of computer assisted tomography
ISSN: 1532-3145
Titre abrégé: J Comput Assist Tomogr
Pays: United States
ID NLM: 7703942

Informations de publication

Date de publication:
22 Mar 2024
Historique:
medline: 23 3 2024
pubmed: 23 3 2024
entrez: 22 3 2024
Statut: aheadofprint

Résumé

Rapid on-site-evaluation (ROSE) is a technique aimed at improving the diagnostic performance of computed tomography (CT)-guided core needle biopsy (CNB) in lung cancer. The aim of this retrospective study was to investigate the impact of ROSE on the rate of nondiagnostic specimens and on accuracy computed on diagnostic specimens. During a 3-year period, 417 CT-guided CNBs were performed at our center. The biopsies were retrospectively classified into 2 groups: 141 procedures were assisted by ROSE and 276 were not. All of them were reviewed for clinical, procedural, and pathological data. Pathology results were classified as diagnostic (positive or negative for malignancy) or nondiagnostic. The results were compared with the final diagnosis after surgery or clinical follow-up. Nondiagnostic rate, sensitivity/specificity/negative predictive value/positive predictive value for the ROSE and non-ROSE groups were calculated. Finally, procedural complications and the adequacy of the specimens for the molecular analysis were recorded. The study evaluated 417 CNBs (mean patients' age 71 years, 278 men). Nondiagnostic rates with and without ROSE were 4% (6/142) and 11% (29/276), respectively (P = 0.028). Sensitivity/specificity/negative predictive value/positive predictive value with and without ROSE did not show statistically significant differences, and no difference in major/minor complication rates was observed between the 2 groups. The adequacy of specimen for subsequent molecular analysis was 100% with (42/42) and 82% without ROSE (51/62). Rapid on-site-evaluation reduced the rate of nondiagnostic specimens by 50% with no change in complication rates or accuracy and increased by 20% the chances of a successful subsequent molecular analysis.

Identifiants

pubmed: 38518357
doi: 10.1097/RCT.0000000000001606
pii: 00004728-990000000-00297
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 The Author(s). Published by Wolters Kluwer Health, Inc.

Déclaration de conflit d'intérêts

The authors declare no conflict of interest.

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Auteurs

Andrea Magnini (A)

From the Departments of Experimental and Clinical Biomedical Sciences.

Chiara Lorini (C)

Health Science, University of Florence.

Linda Calistri (L)

From the Departments of Experimental and Clinical Biomedical Sciences.

Francesca Calcagni (F)

S.O.C. Interventional Radiology, Department of Diagnostic Imaging, Azienda Sanitaria Toscana Centro.

Federico Giuntoli (F)

S.O.C. Interventional Radiology, Department of Diagnostic Imaging, Azienda Sanitaria Toscana Centro.

Prassede Foxi (P)

S.O.C. Anatomical Pathology and Citodiagnostic, Department of Oncology, Azienda Sanitaria Toscana Centro, Florence, Italy.

Cosimo Nardi (C)

From the Departments of Experimental and Clinical Biomedical Sciences.

Stefano Colagrande (S)

From the Departments of Experimental and Clinical Biomedical Sciences.

Classifications MeSH