1. Management of small subepithelial tumors by endoscopic banding without resection and single-incision needle-knife–assisted biopsy sampling: a prospective multicenter study.
- Author
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Bas-Cutrina, Francesc, Loras, Carme, Pardo, Albert, Ballester-Clau, Raquel, Huertas, Carlos, Guarner-Argente, Carlos, Colan-Hernandez, Juan, Consiglieri, Claudia F., Andujar, Xavi, Vilanova-Serra, Magdalena, González-Huix, Ferran, Pardo-Grau, Laura, Maisterra, Sandra, Ruiz-Ramírez, Pablo, Garcia-Sumalla, Albert, Tebé, Cristian, Videla, Sebastià, and Gornals, Joan B.
- Abstract
Endoscopic band ligation (EBL) without resection combined with single-incision needle-knife (SINK) biopsy sampling may have a positive impact on small GI subepithelial tumor (SET) management, but the method needs to be tested. The aim was to evaluate the feasibility of this strategy in small-sized SETs. This prospective multicenter observational cohort study in 7 centers included patients with SETs ≤15 mm (confirmed by EUS) between March 2017 and March 2020. The primary outcome was clinical success at 4 weeks, defined as complete SET disappearance on EUS. Secondary outcomes were long-term (1-year) clinical success, technical difficulty level, clinical impact, yield pathology, and safety. Of 273 patients screened, 122 (62.3% women; mean age, 60.9 ± 13.2 years) were included with SETs (mean size, 9 ± 2.8 mm; gastric location, 77%; superficial layer dependence, 63%). The primary endpoint was achieved in 73.6% of patients (95% confidence interval [CI], 64.8-81.2). At the 1-year follow-up, the success rate was 68.4% (95% CI, 59.1-76.8). A favorable clinical impact was observed in 97 cases (79.5%; 95% CI, 71.3-86.3). Pathology diagnosis was known in 70%. Potentially malignant lesions were present in 24.7%. The related adverse events rate was 4.1% (95% CI, 1.3-9.3; all mild: 2 bleeding, 2 abdominal pain). On multivariable analysis, the ≤10-mm SET group was associated with a greater success rate (1 year, 87%; relative risk, 5.07; 95% CI, 2.63-9.8) and clinical impact rate (92.7%; relative risk, 6.15; 95% CI, 2.72-13.93). EBL plus SINK biopsy sampling seems to be feasible and safe, and it may offer a favorable clinical impact in small-sized SETs. In particular, SETs ≤10 mm are the best candidates. (Clinical trial registration number: NCT03247231.) [Display omitted] [ABSTRACT FROM AUTHOR]
- Published
- 2023
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