The GENTLENESS study is a prospective, multicenter, observational registry designed to evaluate the endoscopic management of patients with suspected biliopancreatic and periampullary neoplastic diseases within the Pancreas Units network of the Lombardy Region. Patients undergoing endoscopic ultrasound (EUS) for suspected pancreatic or periampullary malignancies, including pancreatic ductal adenocarcinoma, pancreatic neuroendocrine tumors, cystic pancreatic neoplasms requiring endoscopic, surgical, or oncological management, and periampullary tumors of the distal bile duct, ampulla, or duodenum, will be prospectively enrolled according to standard clinical practice. The study aims to assess the diagnostic accuracy of EUS-guided tissue acquisition, procedural safety, the need for repeat sampling, and organizational performance indicators, including time to definitive cyto-histological diagnosis and time to initiation of disease-specific treatment. No additional procedures beyond routine clinical care will be performed as a result of study participation.
Despite advances in oncological therapies, pancreatic cancer remains one of the leading causes of cancer-related mortality worldwide, with an increasing burden projected over the coming decades. The diagnostic and therapeutic pathway of biliopancreatic malignancies is complex and requires a high level of multidisciplinary expertise, particularly in high-volume referral centers organized as Pancreas Units. Endoscopic ultrasound (EUS) plays a central role in the diagnostic work-up of biliopancreatic and periampullary lesions, allowing high-resolution morphological assessment and, when indicated, tissue acquisition through fine-needle aspiration (FNA) or fine-needle biopsy (FNB). Accurate histological diagnosis is essential for therapeutic decision-making, including surgical planning, systemic therapy, and molecular profiling. The Lombardy Region has adopted a Hub-and-Spoke organizational model for Pancreas Units, defining minimum procedural volumes, expertise requirements, and performance benchmarks for referral centers. However, a centralized prospective system for monitoring endoscopic activity, diagnostic performance, and procedural outcomes across these centers is currently lacking. The GENTLENESS study has been designed to prospectively collect real-world data on EUS procedures performed in Lombardy Pancreas Unit Hub centers, with the primary objective of evaluating the diagnostic accuracy of EUS-guided biopsies. Secondary objectives include assessment of procedural volume, sampling techniques, need for repeat biopsies, complication rates, and time intervals from procedure to definitive diagnosis and initiation of treatment. The study is observational, does not introduce changes to clinical practice, and reflects routine patient management pathways. Any future analyses beyond the scope of the present registry will require separate Ethics Committee approval.
Study Type
OBSERVATIONAL
Enrollment
2,500
ASST Papa Giovanni XXIII - P.O. Papa Giovanni XXIII Bergamo
Bergamo, Italy
ASST Spedali Civili di Brescia - P.O. Spedali Civili Brescia
Brescia, Italy
Casa di Cura Poliambulanza di Brescia
Brescia, Italy
ASST di Cremona - P.O. Cremona
Cremona, Italy
ASST Ovest Milanese - P.O. Legnano
Legnano, Italy
ASST Mantova - P.O. Carlo Poma Mantova
Mantua, Italy
ASST Grande Ospedale Metropolitano Niguarda
Milan, Italy
ASST Santi Paolo e Carlo - Milano
Milan, Italy
Fondazione IRCCS Istituto Nazionale dei Tumori Milano
Milan, Italy
IRCCS Istituto Clinico Humanitas Milano
Milan, Italy
...and 3 more locations
Diagnostic Accuracy
Number of patients with a correct diagnosis obtained through EUS-guided cyto-histological sampling, confirmed by the final diagnosis
Time frame: 30 days
Procedural Volume
Number of EUS procedures performed for suspected biliopancreatic neoplasms
Time frame: 6 months
Need of Repeat Sampling
Need for additional EUS-guided sampling after an initial non-diagnostic procedure
Time frame: 30 days, 60 days
Sampling Technique
Type of tissue acquisition (FNA vs FNB; ROSE vs MOSE)
Time frame: Intraprocedural
Adverse Events
Intra- and post-procedural complications classified according to ASGE criteria
Time frame: Intraprocedural, 30 days
Time to Diagnosis
Time from EUS to availability of definitive cyto-histological report
Time frame: 30 days, 60 days
Time to Treatment
Time from diagnosis to initiation of disease-specific treatment
Time frame: 30 days, 60 days
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