Management of small, asymptomatic, non-functioning pancreatic neuroendocrine tumours: follow-up, ablation, or surgery?

被引:4
作者
Dabkowski, Krzysztof [1 ,2 ]
Starzynska, Teresa [1 ]
机构
[1] Pomeranian Med Univ, Dept Gastroenterol, Szczecin, Poland
[2] Unii Lubelskiej 1, PL-71252 Szczecin, Poland
关键词
pancreatic neuroendocrine tumour; ablation; EUS;
D O I
10.5603/EP.a2022.0080
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Non-functioning pancreatic neuroendocrine tumours (NF-pNETs) are potentially malignant neoplasms that are detected with increasing frequency. The management of small (<= 2 cm) asymptomatic NF-pNETs remains an area of controversy and clinical dilemma. Follow-up seems to be a reasonable strategy because of the relatively limited metastatic potential of these tumours, the good clinical prognosis, and considering the high complication rate associated with surgery. However, some studies show metastatic potential of these tumours, fuelling an ongoing debate in the literature regarding their management. Making the decision to observe or perform surgery is thus not an easy task. New, promising therapeutic methods involving ablation under endoscopic ultrasound (EUS) guidance with ethanol or radiofrequency ablation have been applied for these lesions with good clinical outcomes but only with short-term follow-up data. In this review, we address the emerging question of when to follow-up and when to perform surgery for small asymptomatic pancreatic tumours, with consideration of the potential of ablative therapies. (Endokrynol Pol 2023; 74 (1): 25-30)
引用
收藏
页码:25 / 30
页数:6
相关论文
共 62 条
[1]  
Dasari A, Shen C, Halperin D, Et al., Trends in the Incidence, Prevalence, and Survival Outcomes in Patients With Neuroendocrine Tumors in the United States, JAMA Oncol, 3, 10, pp. 1335-1342, (2017)
[2]  
Koniusz J, Dabkowski K, Buczek K, Et al., Gastroenterological manifestations of von Hippel-Lindau disease, Pol Merkur Lekarski, 43, 254, pp. 53-55, (2017)
[3]  
Koniusz J, Dabkowski K, Buczek K, Et al., Gastroenterological manifestations of von Hippel-Lindau disease - a case report, Pol Merkur Lekarski, 43, 254, pp. 66-68, (2017)
[4]  
Dabkowski K, Kos-Kudla B, Andrysiak-Mamos E, Et al., Cystic pancreatic neuroendocrine tumours - a gastroenterologist’s point of view, Endokrynol Pol, 69, 3, pp. 320-325, (2018)
[5]  
Falconi M, Eriksson B, Kaltsas G, Et al., Vienna Consensus Conference participants. ENETS Consensus Guidelines Update for the Management of Patients with Functional Pancreatic Neuroendocrine Tumors and Non-Functional Pancreatic Neuroendocrine Tumors, Neuroendocrinology, 103, 2, pp. 153-171, (2016)
[6]  
Yao JC, Hassan M, Phan A, Et al., One hundred years after “carcinoid”: epidemiology of and prognostic factors for neuroendocrine tumors in 35,825 cases in the United States, J Clin Oncol, 26, 18, pp. 3063-3072, (2008)
[7]  
Saftoiu A, Hassan C, Areia M, Et al., Role of gastrointestinal endoscopy in the screening of digestive tract cancers in Europe: European Society of Gastrointestinal Endoscopy (ESGE) Position Statement, Endoscopy, 52, 4, pp. 293-304, (2020)
[8]  
Bettini R, Partelli S, Boninsegna L, Et al., Tumor size correlates with malignancy in nonfunctioning pancreatic endocrine tumor, Surgery, 150, 1, pp. 75-82, (2011)
[9]  
Scarpa A, Mantovani W, Capelli P, Et al., Pancreatic endocrine tumors: improved TNM staging and histopathological grading permit a clinically efficient prognostic stratification of patients, Mod Pathol, 23, 6, pp. 824-833, (2010)
[10]  
Gullo L, Migliori M, Falconi M, Et al., Nonfunctioning pancreatic endocrine tumors: a multicenter clinical study, Am J Gastroenterol, 98, 11, pp. 2435-2439, (2003)