info@biomedres.us   +1 (502) 904-2126   One Westbrook Corporate Center, Suite 300, Westchester, IL 60154, USA   Site Map
ISSN: 2574 -1241

Impact Factor : 0.548

  Submit Manuscript

Short CommunicationOpen Access

Endoscopic Ultrasound in Gastrointestinal Oncology: Expanding Diagnostic and Therapeutic Indications Volume 63- Issue 3

Porpora Danilo2, Mauro Maria2, Hajduk Julia Elzbieta3, D’apice Flavia2, Di Chiara Maria Rosaria2, Sglavo Nicola2, Della Rocca Antonella2, De Sena Gabriele1,2*

  • 1University of Ostrava, Czech Republic
  • 2University of Campania Luigi Vanvitelli, Italy
  • 3University of Rome La Sapienza, Italy

Received: September 12, 2025; Published: September 30, 2025

*Corresponding author: De Sena Gabriele, Faculty of Medicine, University of Ostrava, Dvořákova 7, 701 03 Ostrava, Czech Republic

DOI: 10.26717/BJSTR.2025.63.009888

Abstract PDF

ABSTRACT

Endoscopic ultrasound (EUS) has transitioned from a purely diagnostic imaging technique to a comprehensive platform integrating staging, tissue acquisition, and therapeutic interventions. In gastrointestinal oncology, EUS provides high accuracy in the staging of esophageal and rectal cancers [1,2], enables tissue acquisition in pancreatic masses with fine-needle biopsy (FNB) as the current standard [3-6], and refines the characerization of pancreatic cystic neoplasms [7,8]. EUS-guided biliary drainage (EUS-BD) is now recommended over percutaneous drainage after failed ERCP in expert centers [9-11], while lumen-apposing metal stents (LAMS) have revolutionized the management of pancreatic fluid collections [12-15]. Emerging technologies such as contrast-enhanced EUS (CE-EUS), elastography, and artificial intelligence (AI) are expanding diagnostic confidence [16-18]. This short communication reviews current evidence and highlights the evolving role of EUS in gastrointestinal oncology.

Keywords: Endoscopic Ultrasound; FNB; Pancreatic Cancer; Biliary Drainage; Pancreatic Fluid Collections; CEEUS; LAMS

Abbreviations: EUS: Endoscopic Ultrasound; FNB: Fine-Needle Biopsy; EUS-BD: EUS-Guided Biliary Drainage; LAMS: Lumen-Apposing Metal Stents; CE-EUS: Contrast-Enhanced EUS; AI: Artificial Intelligence; EUS-TA: EUS-Guided Tissue Acquisition; PNETs: Pancreatic NeuroEndocrine Tumors; CE-EUS: Contrast-Enhanced EUS; DPPS: Double-Pigtail Stents; NET: NeuroEndocrine Tumor; FNA: Fine-needle Aspiration

Introduction

Since its introduction, EUS has provided unmatched resolution for gastrointestinal wall layers and peri-digestive structures. It rapidly became essential for staging esophageal and rectal cancer [1,2], with accuracy superior to CT and MRI for early T and N staging. The development of EUS-guided tissue acquisition (EUS-TA) allowed cytological and histological confirmation, transforming EUS into a diagnostic and therapeutic hub. Modern guidelines by the ASGE (2024) [3] and ESGE (2025) [4] have refined its role, recommending FNB needles for solid pancreatic lesions and recognizing EUS-BD as an evidence- based intervention after failed ERCP [9] (Figure 1).

Figure 1

biomedres-openaccess-journal-bjstr

Diagnostic Indications

EUS remains highly accurate in differentiating T1 from T2 esophageal cancer [1] and in guiding neoadjuvant therapy for rectal cancer [2]. For pancreatic adenocarcinoma, EUS detects small lesions often missed by CT, with pooled sensitivities around 95% and specificities >90% [3,4]. Meta-analyses confirm that FNB outperforms FNA in sample adequacy and diagnostic accuracy [5,6]. EUS-FNB also allows immunohistochemistry and Ki-67 index assessment in pancreatic neuroendocrine tumors (PNETs), achieving concordance >85% with surgical specimens [19]. For pancreatic cystic neoplasms, EUS identifies mural nodules, septa, and ductal communication [7,8]. Fluid aspiration for CEA and cytology, and increasingly molecular analysis, improves differentiation between mucinous and non-mucinous cysts [7,8]. Contrast-enhanced EUS (CE-EUS) and elastography further enhance lesion characterization [16], while AI-assisted CH-EUS systems are emerging [17,18] (Figure 2).

Figure 2

biomedres-openaccess-journal-bjstr

Therapeutic Indications

EUS-guided biliary drainage (EUS-BD) is recommended over percutaneous drainage after failing ERCP by ESGE guidelines [9]. Meta- analyses confirm high technical (~97%) and clinical (~91%) success [10-12]. Comparative studies consolidate EUS-BD as the preferred rescue strategy [13,14]. For pancreatic fluid collections, EUS-guided drainage using LAMS is now standard, with success rates >90% [12,15]. Studies suggest that coaxial double-pigtail stents (DPPS) within LAMS may reduce bleeding and occlusion [13-15]. EUS-guided celiac plexus neurolysis provides effective pain relief in pancreatic cancer, while investigational approaches include brachytherapy, fiducial placement, and ablation techniques [20] (Figure 3).

Figure 3

biomedres-openaccess-journal-bjstr

Discussion

EUS has matured into a multipurpose platform: high-resolution imaging, reliable tissue acquisition, and therapeutic interventions. FNB-first strategies for pancreatic lesions improve diagnostic adequacy and facilitate advanced pathology [5,6,21]. CE-EUS and elastography enhance lesion targeting, while AI offers a glimpse of real-time decision support [16-18]. Therapeutically, EUS-BD has become an evidence- based alternative to percutaneous drainage [9-14], and LAMS have transformed outcomes for pancreatic fluid collections [12-15]. Challenges include operator dependence, procedure-related risks, and device availability outside expert centers. Nevertheless, EUS is increasingly indispensable in gastrointestinal oncology.

Conclusion

EUS is a cornerstone of modern gastrointestinal oncology. Its applications in cancer staging, tissue acquisition, and minimally invasive therapy are supported by strong evidence and international guidelines. Future perspectives include routine FNB, wider integration of CE-EUS and elastography, AI-assisted workflows, and expansion of therapeutic EUS in referral centers.

References

  1. Isenberg G, et al. (1998) Gastrointest Endosc 48: 158-163.
  2. Rosch T, et al. (2002) Scand J Gastroenterol 37: 856-862.
  3. (2024) ASGE Standards of Practice Committee. Guideline on EUS-guided tissue acquisition for solid pancreatic masses. Gastrointest Endosc.
  4. Polkowski M, et al. (2025) ESGE Guideline on EUS-guided tissue acquisition. Endoscopy.
  5. Bellocchi MC, Di Matteo F, Zanini N, et al. (2024) EUS-FNB vs FNA meta-analysis. Pancreatology 24(7): 678-686.
  6. Chalhoub JM, Baron TH, Topazian MD, et al. (2024) Diagnostic performance of EUS-FNB by number of passes. Gastrointest Endosc 99(2): 345-353.
  7. Iglesias Garcia J, et al. (2009) Role of EUS in pancreatic cystic lesions. Gastrointest Endosc 70: 1101-1108.
  8. Lee KH, Lee JK (2011) Clinical Endoscopy 44: 6-12.
  9. Teoh AY, et al. (2022) ESGE Guideline on therapeutic EUS (EUS-BD). Endoscopy 54: 222-232.
  10. Mazza S, Coppola A, Binda C, et al. (2024) EUS-HGS meta-analysis. Diagnostics 14(23): 2644.
  11. Peppas S, Karamanolis G, et al. (2025) EUS-BD vs PTBD meta-analysis. Clin Endosc.
  12. Fabbri C, et al. (2012) EUS drainage of pseudocysts. World J Gastrointest Endosc 4: 479-488.
  13. Rashmee P, et al. (2016) EUS-LAMS for PFC drainage. Ann Gastroenterol 29: 168-173.
  14. Ghoneem E, et al. (2024) EUS-BD multicenter study. Int J Gastrointest Interv.
  15. Marzioni M, Fabbri C, et al. (2024) Dedicated vs non-dedicated stents for EUS-HGS. Surg Endosc 38(4): 2050-2060.
  16. Esposto G, et al. (2024) CE-EUS meta-analysis in pancreatic lesions. Cancers 16(9): 1658.
  17. Kitano M, et al. (2023) Contrast harmonic EUS and AI systems. Dig Endosc.
  18. Minaga K, et al. (2024) AI-assisted CH-EUS for pancreatic cancer. Endosc Ultrasound.
  19. Chatzipantelis P, et al. (2008) EUS-FNA cytology of PNETs. Cancer Cytopathol 114: 255-262.
  20. Sun S, et al. (2006) EUS-guided brachytherapy and ablation. Endoscopy 38: 399-403.
  21. Ahn DW, Lee JH, Yun JY, et al. (2023) Practice patterns of EUS-FNA/FNB. Gut Liver 17(3): 425-435.