Endoscopic Ultrasound-guided Fine-needle Biopsy With or Without Rapid On-site Evaluation for Diagnosis of Solid Pancreatic Lesions: A Randomized Controlled Non-Inferiority Trial.

Crinò, Stefano Francesco;Di Mitri, Roberto;Nguyen, Nam Q;Tarantino, Ilaria;Larghi, Alberto;et.al.
(2021) Gastroenterology — Vol. 161, n° 3, p. 899-909 (2021)

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Authors
  • Crinò, Stefano Francesco
    Author
  • Di Mitri, Roberto
    Author
  • Nguyen, Nam Q
    Author
  • Tarantino, Ilaria
    Author
  • Author
  • Borbath, IvanUCLouvain
    Author
  • Komuta, MinaUCLouvain
    Author
  • Larghi, Alberto
    Author
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Abstract
(en) BACKGROUND AND AIMS: The benefit of rapid on-site evaluation (ROSE) on the diagnostic accuracy of endoscopic ultrasound-guided fine-needle biopsy (EUS-FNB) has never been evaluated in a randomized study. This trial aimed to test the hypothesis that in solid pancreatic lesions (SPLs), diagnostic accuracy of EUS-FNB without ROSE was not inferior to that of EUS-FNB with ROSE. METHODS: A noninferiority study (noninferiority margin, 5%) was conducted at 14 centers in 8 countries. Patients with SPLs requiring tissue sampling were randomly assigned (1:1) to undergo EUS-FNB with or without ROSE using new-generation FNB needles. The touch-imprint cytology technique was used to perform ROSE. The primary endpoint was diagnostic accuracy, and secondary endpoints were safety, tissue core procurement, specimen quality, and sampling procedural time. RESULTS: Eight hundred patients were randomized over an 18-month period, and 771 were analyzed (385 with ROSE and 386 without). Comparable diagnostic accuracies were obtained in both arms (96.4% with ROSE and 97.4% without ROSE, P = .396). Noninferiority of EUS-FNB without ROSE was confirmed with an absolute risk difference of 1.0% (1-sided 90% confidence interval, -1.1% to 3.1%; noninferiority P < .001). Safety and sample quality of histologic specimens were similar in both groups. A significantly higher tissue core rate was obtained by EUS-FNB without ROSE (70.7% vs. 78.0%, P = .021), with a significantly shorter mean sampling procedural time (17.9 ± 8.8 vs 11.7 ± 6.0 minutes, P < .0001). CONCLUSIONS: EUS-FNB demonstrated high diagnostic accuracy in evaluating SPLs independently on execution of ROSE. When new-generation FNB needles are used, ROSE should not be routinely recommended. (ClinicalTrial.gov number NCT03322592.).
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Citations

Crinò, S. F., Di Mitri, R., Nguyen, N. Q., Tarantino, I., de Nucci, G., Deprez, P., Carrara, S., Kitano, M., Shami, V. M., Fernández-Esparrach, G., Poley, J.-W., Baldaque-Silva, F., Itoi, T., Manfrin, E., Bernardoni, L., Gabbrielli, A., Conte, E., Unti, E., Naidu, J., et al. (2021). Endoscopic Ultrasound-guided Fine-needle Biopsy With or Without Rapid On-site Evaluation for Diagnosis of Solid Pancreatic Lesions: A Randomized Controlled Non-Inferiority Trial. Gastroenterology, 161(3), 899-909. https://doi.org/10.1053/j.gastro.2021.06.005 (Original work published 2021)