Skip to main content
The British Journal of Surgery logoLink to The British Journal of Surgery
. 2022 Aug 20;109(12):1186–1190. doi: 10.1093/bjs/znac267

Management of asymptomatic sporadic non-functioning pancreatic neuroendocrine neoplasms no larger than 2 cm: interim analysis of prospective ASPEN trial

Stefano Partelli 1,2, Sara Massironi 3,4, Alessandro Zerbi 5,6, Patricia Niccoli 7, Wooil Kwon 8, Luca Landoni 9, Francesco Panzuto 10, Ales Tomazic 11, Alberto Bongiovanni 12, Gregory Kaltsas 13, Alain Sauvanet 14, Emilio Bertani 15, Vincenzo Mazzaferro 16, Martyn Caplin 17, Thomas Armstrong 18, Martin O Weickert 19, John Ramage 20, Eva Segelov 21, Giovanni Butturini 22, Stefan Staettner 23, Mauro Cives 24, Andrea Frilling 25, Carol Anne Moulton 26,27, Jin He 28, Florian Boesch 29, Andreas Selberheer 30, Orit Twito 31,32, Antonio Castaldi 33, Claudio G De Angelis 34, Sebastien Gaujoux 35, Katharina Holzer 36, Colin H Wilson 37, Hussein Almeamar 38, Emanuel Vigia 39, Francesca Muffatti 40,41, Martina Lucà 42,43, Andrea Lania 44,45, Jacques Ewald 46, Hongbeom Kim 47, Roberto Salvia 48, Maria Rinzivillo 49, Alojz Smid 50, Andrea Gardini 51, Marina Tsoli 52, Olivia Hentic 53, Samuele Colombo 54, Davide Citterio 55, Christos Toumpanakis 56, Emma Ramsey 57, Harpal S Randeva 58, Ray Srirajaskanthan 59, Daniel Croagh 60, Paolo Regi 61, Silvia Gasteiger 62, Pietro Invernizzi 63,64, Cristina Ridolfi 65, Marc Giovannini 66, Jin-Young Jang 67, Claudio Bassi 68, Massimo Falconi 69,70,
PMCID: PMC10364756  PMID: 35986682

Introduction

The incidence of non-functioning pancreatic neuroendocrine neoplasms (NF-PanNENs) has increased recently1. Traditionally, surgery has been the treatment of choice for localized NF-PanNENs, although evidence has emerged that active surveillance could be advocated for most asymptomatic tumours no larger than 2 cm2–7. However, the practice of active surveillance varies considerably and, contrary to current recommendations8–10, many patients still undergo surgical resection11–13.

Current evidence is limited by the retrospective design of studies and the small number of patients. The present study is the most extensive prospective investigation to date on small, asymptomatic NF-PanNENs. The aim was to define the optimal management of incidentally found, sporadic NF-PanNENs no larger than 2 cm.

Methods

This was a prospective, non-randomized, international, multicentre, cohort study (NCT03084770). This report describes the results of the prespecified interim analysis. Overall, 41 centres have been included. The study protocol was published previously14 (Appendix S1). Briefly, CT or MRI was mandatory for all patients. The diagnosis must have been proven by a positive fine-needle aspiration (biopsy) (FNA(B)) or positive 68Ga-labelled DOTA PET. The treatment—active surveillance or surgical resection—was decided by the referring centre. Because current guidelines8–10 suggest surveillance for asymptomatic NF-PanNENs 2 cm or smaller in size, treating physicians were asked to indicate the reason for choosing surgery. An aggressive feature was defined by one or more of the following features: Ki-67 over 20 per cent, perineural invasion, microvascular invasion, nodal metastases, or distant metastases.

Results

The study flow diagram is shown in Fig. 1. After initial screening, all the patients had at least positive 68Ga-labelled DOTA PET and/or a positive FNA(B) for NF-PanNEN.

Fig. 1.

Fig. 1

Study flow chart

NF-PanNEN, non-functioning pancreatic neuroendocrine neoplasm.

Table 1 summarizes demographics and clinical characteristics by the type of management. Younger age, larger tumour size, lower BMI, dilated main pancreatic duct (MPD), and enrolment of the patient in a surgical centre were associated more frequently with surgery. Global quality of life at diagnosis was similar in the two groups (Fig. S1). Overall, distant metastases were present in 4 patients (0.08 per cent), all of whom underwent surgery. On multivariable analysis, factors associated with surgery were: age 64 years or less (OR 2.5; P < 0.001), radiological size larger than 10 mm (OR 1.9; P = 0.030), MPD: over 3 mm (OR 3.4; P < 0.001), surgical centre (OR 2.0; P = 0.012), and Hospital Anxiety and Depression Scale—anxiety score above 3 and no more than 6 (OR 2.0; P = 0.029) (Table S1). Indication for surgery was attributed to patient’s preference in 42 instances (45 per cent), centre’s preference in 37 (39 per cent), MPD dilatation in 11 (12 per cent), and distant metastases in 4 (4 per cent).

Table 1.

Characteristics of patients in ASPEN study

Overall
(n = 500)
Active surveillance
(n = 406)
Surgical resection
(n = 94)
P§
Sex 0.529
 F 238 (47.6) 196 (48.3) 42 (45)
 M 262 (52.4) 210 (51.7) 52 (55)
Age (years), median (i.q.r.) 64 (54–71) 65 (56–71) 59 (51–68) <0.001¶
BMI (kg/m2) 0.052
 ≤ 25 175 (35.0) 134 (33.0) 41 (44)
 > 25 325 (65.0) 272 (67.0) 53 (56)
Diabetes 0.268
 No 417 (83.4) 335 (82.5) 82 (87)
 Yes 83 (16.6) 71 (17.5) 12 (13)
ECOG PS score 0.305
 0 436 (87.2) 349 (86.0) 87 (93)
 1 52 (10.4) 45 (11.1) 7 (7)
 ≥ 2 12 (2.4) 12 (2.9) 0 (0)
Year of diagnosis 0.059
 2017–2018 271 (54.2) 212 (52.2) 59 (63)
 2019–2020 229 (45.8) 194 (47.8) 35 (37)
Site of lesion 0.323
 Head 121 (24.2) 101 (24.9) 20 (21)
 Uncinate process 55 (11.0) 48 (11.8) 7 (8)
 Body 167 (33.4) 136 (33.5) 31 (33)
 Tail 157 (31.4) 121 (29.8) 36 (38)
Radiological tumour size (mm), mean(s.d.)* 13.2 (4.1) 12.9 (3.9) 14.8 (4.5) <0.010#
rN status 1.000
 rN0 499 (99.8) 406 (100) 93 (99)
 rN1 1 (0.02) 0 (0) 1 (1)
rM status 0.671
 rM0 496 (99.2) 406 (100) 90 (96)
 rM1 4 (0.08) 0 (0) 4 (4)
MPD diameter (mm), mean(s.d.) 2.9 (3.4) 2.5 (3.1) 4.3 (4.0) 0.001#
CgA (ng/ml), median (i.q.r.) 61 (30–36) 60 (25–106) 63 (44–123) 0.259¶
[18F]FDG PET 0.454
 Not performed 427 (85.4) 344 (84.7) 83 (88)
 Negative 55 (11.0) 48 (11.8) 7 (8)
 Positive 18 (3.6) 14 (3.4) 4 (4)
FNA(B) 0.001
 Not performed 170 (34.0) 124 (30.5) 46 (49)
 Negative 45 (9.0) 34 (8.4) 11 (12)
 Positive 285 (57.0) 248 (61.1) 37 (39)
Tumour grade† <0.001
 PanNET-G1 195 (68.4) 179 (72.2) 16 (43)
 PanNET-G2 22 (7.7) 12 (4.8) 10 (27)
 Not evaluable 68 (23.9) 57 (23.0) 11 (30)
Surgical centre 0.006
 No 178 (35.6) 156 (38.4) 22 (23)
 Yes 322 (64.4) 250 (61.6) 72 (77)
HADS score‡ 0.295
 ≤ 5 167 (33.4) 142 (35.0) 25 (27)
 6–12 172 (34.4) 137 (33.7) 35 (37)
 > 12 161 (32.2) 127 (31.3) 34 (36)
HADS—anxiety score‡ 0.108
 ≤ 3 148 (29.6) 126 (31.0) 22 (23)
 4–6 178 (35.6) 136 (33.5) 42 (45)
 > 6 174 (34.8) 144 (35.5) 30 (32)
HADS—depression score‡
 ≤ 2 114 (22.8) 95 (23.4) 19 (20) 0.563
 3–4 207 (41.4) 170 (41.9) 37 (39)
 > 4 179 (35.8) 141 (34.7) 38 (41)

Values are n (%) unless otherwise indicated. *Maximum size on radiological imaging or endoscopic ultrasonography. †Evaluated for patients with positive fine-needle aspiration (biopsy) (FNA(B) specimen. ‡Categorized by tertiles of Hospital Anxiety and Depression Scale (HADS) distribution. ECOG PS, Eastern Cooperative Oncology Group performance status; MPD, main pancreatic duct; CgA, chromogranin A; FDG, fluorodeoxyglucose. §Pearson χ2 test, except ¶Wilcoxon Mann–Whitney test and #t test.

Surgical outcomes are summarized in Table S2. Minimally invasive, either laparoscopic or robot-assisted, was the preferred approach in 55 per cent of patients. Severe complications (defined as those with a Clavien–Dindo grade15 of more than III) occurred in 13 per cent of patients whereas the mortality rate was zero. Final pathological examination characteristics are listed in Table S3. The choice of standard pancreatectomy over an atypical resection was justified by the need to perform an adequate lymphadenectomy in 52 patients (54 per cent) and the proximity of the nodule to the MPD in 23 (25 per cent). One or more aggressive histological features were observed in 19 patients (20 per cent). Of these 19 patients, 17 had a radiological tumour size larger than 10 mm. The remaining 2 patients with radiological tumour size less than 10 mm had a dilated MPD on preoperative imaging. In 5 of the 19 patients with aggressive features, the radiological MPD was larger than 3 mm.

After a median follow-up of 25 (i.q.r. 16–35) months, all patients were alive apart from 3 who died from causes unrelated to NF-PanNENs. Only 1 patient in the surgical group, who had liver metastases at diagnosis, eventually developed liver recurrence.

In the surveillance group, 9 patients (2 per cent) underwent surgery during follow-up. The reason for surgery was increasing tumour size in 4 patients, increased MPD dilatation in 3, and patient’s preference in 2.

Discussion

A non-operative strategy seems safe as only a negligible fraction of patients had an increase in tumour size and no patient developed distant metastases during follow-up. These results are consistent with the preliminary findings of a recent prospective study6, although the present series included a five-fold larger number of patients and compared the two types of management of asymptomatic small NF-PanNENs, leaving the therapeutic decision (surveillance versus surgery) to the treating centres.

Other factors that contributed to the decision to resect a NF-PanNEN of 2 cm or smaller were younger age, tumour size over 1 cm, and the presence of MPD dilatation. Furthermore, patient’s preference was the main reason for choosing surgery in many instances. This attitude might be explained by patients’ anxiety and by the ongoing debate in the scientific community about the optimal management of these lesions. Moreover, the current guidelines8–10 suggest that surveillance is recommended, especially for older patients, and this may explain why young age was an important factor in deciding on a surgical approach more frequently. In the present experience, it was found that nearly 20 per cent of resected tumours had one or more aggressive features. Notably, nearly all the lesions that presented at least one aggressive feature were also larger than 1 cm.

The optimal cut-off for considering NF-PanNENs as low-risk lesions is a matter of ongoing controversy. The European Neuroendocrine Tumor Society8 and National Comprehensive Cancer Network10 guidelines consider observation for lesions no larger than 2 cm. On the other hand, North American Neuroendocrine Tumor Society9 guidelines suggest that the treatment of asymptomatic NF-PanNENs between 1 and 2 cm in size should be individualized. The present findings seem to support these latter recommendations. The presence of MPD dilatation should be promptly recognized and always considered as a major sign of concern because of the strong correlation with aggressive features, as described previously16. Another possible role in predicting the biological behaviour of these small nodules may be played by novel promising biomarkers such as NETest17. Finally, another important result was the detection of synchronous liver metastases in four patients, which demonstrates a real, although rare, potential for distant spread also among NF-PanNENs of 2 cm or smaller.

In conclusion, active surveillance is the preferred approach for sporadic, asymptomatic, NF-PanNENs no larger than 2 cm. An active surveillance strategy seems safe, but the measurable risk of distant metastases, as well as the presence of histological characteristics of aggressiveness in almost one-fifth of operated tumours, necessitates personalized management for lesions larger than 1 cm as well as for young patients and in the presence of measurable growth of the nodule. Moreover, surgery is always mandatory for small NF-PanNENs with a dilated MPD. According to the protocol, the study will be concluded 1 year after the enrolment of the last patient. Nevertheless, as these preliminary results showed only a very low rate of patients with tumour growth after a median follow-up of 2 years, longer follow-up is probably needed for definitive conclusions to be reached.

Supplementary Material

znac267_Supplementary_Data

Acknowledgements

The authors thank F. di Salvo (Division of Pancreatic Surgery, Vita-Salute San Raffaele University, IRCCS Ospedale San Raffaele, Milan, Italy) for her contribution with acquisition and analysis of data; and the following people for their involvement in the acquisition of data: D. Horsch (Department of Gastroenterology/Endocrinology, Zentralklinik Bad Berka, Bad Berka, Germany), J. C. Percovich (Hospital Universitario Gregorio Maranon, Madrid, Spain), S. Jamdar (Manchester University NHS Foundation Trust, Manchester, UK), M. S. Khan (University Hospital of Wales, Cardiff and Vale University Health Board, Cardiff, UK), E. N. van Dijkum (Amsterdam Medical Centre, Amsterdam, the Netherlands), E. Martin Perez (University Hospital La Princesa, Madrid, Spain), and G. Donatini (Poitiers University Hospital, Poitiers, France).

Contributor Information

Stefano Partelli, School of Medicine, Vita-Salute San Raffaele University, Milan, Italy; Pancreas Translational and Clinical Research Centre, Pancreatic Surgery Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.

Sara Massironi, Division of Gastroenterology and Centre for Autoimmune Liver Diseases, San Gerardo Hospital, Monza, Italy; Department of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy.

Alessandro Zerbi, Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, Italy; IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.

Patricia Niccoli, Department of Medical Oncology, Paoli-Calmettes Institute, Marseille, France.

Wooil Kwon, Department of Surgery and Cancer Research Institute, Seoul National University College of Medicine, Seoul, Korea.

Luca Landoni, General and Pancreatic Surgery Unit, Pancreas Institute, University of Verona Hospital Trust, Verona, Italy.

Francesco Panzuto, Digestive Disease Unit, ENETS Centre of Excellence, Sant’ Andrea University Hospital, Rome, Italy.

Ales Tomazic, Department of Abdominal Surgery, University Medical Centre, Ljubijana, Slovenia.

Alberto Bongiovanni, Osteoncology and Rare Tumours Centre (CDO-TR), IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) ‘Dino Amadori’, Meldola, Italy.

Gregory Kaltsas, First Propaedeutic Department of Internal Medicine, National and Kapodistrian University of Athens, Athens, Greece.

Alain Sauvanet, Department of Pancreatology, Hôpital Beaujon, University of Paris, Paris, France.

Emilio Bertani, Division of Gastrointestinal Surgery, IEO, European Institute of Oncology IRCCS, Milan, Italy.

Vincenzo Mazzaferro, Gastrointestinal and Hepato-Pancreatic Surgery and Liver Transplantation Unit, Fondazione, IRCCS Istituto Nazionale Tumori (INT, National Cancer Institute) and Università degli Studi di Milano, Milan, Italy.

Martyn Caplin, ENETS Centre of Excellence, Neuroendocrine Tumour Unit, Royal Free Hospital, London, UK.

Thomas Armstrong, Department of Hepatobiliary Surgery, Wessex NET Group ENETS Centre of Excellence, University Hospital Southampton, Southampton, UK.

Martin O Weickert, ARDEN NET Centre, ENETS Centre of Excellence, University Hospitals Coventry and Warwickshire NHS Trust and Warwick Medical School, University of Warwick, Coventry, UK.

John Ramage, Kings Health Partners NET Centre, Kings College Hospital London, London, UK.

Eva Segelov, Department of Oncology and Surgery (School of Clinical Sciences at Monash Health), Monash University, Clayton, Victoria, Australia.

Giovanni Butturini, Department of Surgery, Pederzoli Hospital, Peschiera del Garda, Italy.

Stefan Staettner, Department of General, Visceral and Vascular Surgery, Salzkammergutklinikum Vöcklabruck, Vöcklabruck, Austria.

Mauro Cives, Department of Biomedical Sciences and Human Oncology, University of Bari ‘Aldo Moro’, Bari, Italy.

Andrea Frilling, Department of Surgery and Cancer, Imperial College London, London, UK.

Carol Anne Moulton, Division of General Surgery, University of Toronto, Toronto, Ontario, Canada; Department of Surgery, University Health Network, Princess Margaret Cancer Centre, University of Toronto, Toronto, Ontario, Canada.

Jin He, Department of Surgery, Johns Hopkins University School of Medical, Baltimore, Maryland, USA.

Florian Boesch, Department of General, Visceral, and Transplant Surgery, Ludwig-Maximilians-University Munich, Munich, Germany.

Andreas Selberheer, Section Endocrine Surgery, Division of General Surgery, Department of Surgery, Medical University, Vienna, Austria.

Orit Twito, Endocrine Institute, Meir Medical Center, Kfar-Sava, Israel; Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.

Antonio Castaldi, Department of Clinical Medicine and Surgery, University of Naples Federico II, Naples, Italy.

Claudio G De Angelis, Gastroenterology Unit, Department of Medical Sciences, City of Health and Science Hospital, Turin, Italy.

Sebastien Gaujoux, Department of Digestive, Hepatobiliary and Endocrine Surgery, Paris Sorbonne University, Pitiè Salpétrière Hospital, Paris, France.

Katharina Holzer, Department of Visceral-, Thoracic- and Vascular Surgery, Section of Endocrine Surgery, University Hospital Marburg (UKGM), Marburg, Germany.

Colin H Wilson, Hepatopancreatobiliary and Transplant Unit, Freeman Hospital, Newcastle upon Tyne, UK.

Hussein Almeamar, National NET Centre and ENETS Centre of Excellence, St Vincent’s University Hospital, Dublin, Ireland.

Emanuel Vigia, Hepato-Biliary-Pancreatic and Transplantation Centre, Curry Cabral Hospital, CHULC, Lisbon, Portugal.

Francesca Muffatti, School of Medicine, Vita-Salute San Raffaele University, Milan, Italy; Pancreas Translational and Clinical Research Centre, Pancreatic Surgery Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.

Martina Lucà, Division of Gastroenterology and Centre for Autoimmune Liver Diseases, San Gerardo Hospital, Monza, Italy; Department of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy.

Andrea Lania, Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, Italy; IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.

Jacques Ewald, Department of Medical Oncology, Paoli-Calmettes Institute, Marseille, France.

Hongbeom Kim, Department of Surgery and Cancer Research Institute, Seoul National University College of Medicine, Seoul, Korea.

Roberto Salvia, General and Pancreatic Surgery Unit, Pancreas Institute, University of Verona Hospital Trust, Verona, Italy.

Maria Rinzivillo, Digestive Disease Unit, ENETS Centre of Excellence, Sant’ Andrea University Hospital, Rome, Italy.

Alojz Smid, Department of Gastroenterology and Hepatology, University Medical Centre Ljubijana, Ljubljana, Slovenia.

Andrea Gardini, General and Oncological Surgery Unit, Morgagni-Pierantoni Hospital, Forlì, Italy.

Marina Tsoli, First Propaedeutic Department of Internal Medicine, National and Kapodistrian University of Athens, Athens, Greece.

Olivia Hentic, Department of Pancreatology, Hôpital Beaujon, University of Paris, Paris, France.

Samuele Colombo, Division of Gastrointestinal Surgery, IEO, European Institute of Oncology IRCCS, Milan, Italy.

Davide Citterio, Gastrointestinal and Hepato-Pancreatic Surgery and Liver Transplantation Unit, Fondazione, IRCCS Istituto Nazionale Tumori (INT, National Cancer Institute) and Università degli Studi di Milano, Milan, Italy.

Christos Toumpanakis, ENETS Centre of Excellence, Neuroendocrine Tumour Unit, Royal Free Hospital, London, UK.

Emma Ramsey, Department of Hepatobiliary Surgery, Wessex NET Group ENETS Centre of Excellence, University Hospital Southampton, Southampton, UK.

Harpal S Randeva, Warwick Medical School, University of Warwick, Coventry, UK.

Ray Srirajaskanthan, Kings Health Partners NET Centre, Kings College Hospital London, London, UK.

Daniel Croagh, Department of Oncology and Surgery (School of Clinical Sciences at Monash Health), Monash University, Clayton, Victoria, Australia.

Paolo Regi, Department of Surgery, Pederzoli Hospital, Peschiera del Garda, Italy.

Silvia Gasteiger, Department of Visceral, Transplantation and Thoracic Surgery, Medical University of Innsbruck, Innsbruck, Austria.

Pietro Invernizzi, Division of Gastroenterology and Centre for Autoimmune Liver Diseases, San Gerardo Hospital, Monza, Italy; Department of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy.

Cristina Ridolfi, Pancreatic Surgery Unit, Humanitas Clinical and Research Hospital—IRCCS, Rozzano, Milan, Italy.

Marc Giovannini, Department of Medical Oncology, Paoli-Calmettes Institute, Marseille, France.

Jin-Young Jang, Department of Surgery and Cancer Research Institute, Seoul National University College of Medicine, Seoul, Korea.

Claudio Bassi, General and Pancreatic Surgery Unit, Pancreas Institute, University of Verona Hospital Trust, Verona, Italy.

Massimo Falconi, School of Medicine, Vita-Salute San Raffaele University, Milan, Italy; Pancreas Translational and Clinical Research Centre, Pancreatic Surgery Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.

Funding

This study was funded by European Neuroendocrine Tumor Society.

Disclosure

The authors declare no conflict of interest.

Supplementary material

Supplementary material is available at BJS online.

References

  • 1. Dasari A, Shen C, Halperin D, Zhao B, Zhou S, Xu Yet al. . Trends in the incidence, prevalence, and survival outcomes in patients with neuroendocrine tumors in the United States. JAMA Oncol 2017;3:1335–1342 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2. Lee LC, Grant CS, Salomao DR, Fletcher JG, Takahashi N, Fidler JLet al. . Small, nonfunctioning, asymptomatic pancreatic neuroendocrine tumors (PNETs): role for nonoperative management. Surgery 2012;152:965–974 [DOI] [PubMed] [Google Scholar]
  • 3. Sadot E, Reidy-Lagunes DL, Tang LH, Do RKG, Gonen M, D’Angelica MIet al. . Observation versus resection for small asymptomatic pancreatic neuroendocrine tumors: a matched case–control study. Ann Surg Oncol 2016;23:1361–1370 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4. Barenboim A, Lahat G, Nachmany I, Nakache R, Goykhman Y, Geva Ret al. . Resection versus observation of small asymptomatic nonfunctioning pancreatic neuroendocrine tumors. J Gastrointest Surg 2019;24:1366–1374 [DOI] [PubMed] [Google Scholar]
  • 5. Partelli S, Cirocchi R, Crippa S, Cardinali L, Fendrich V, Bartsch DKet al. . Systematic review of active surveillance versus surgical management of asymptomatic small non-functioning pancreatic neuroendocrine neoplasms. Br J Surg 2017;104:34–41 [DOI] [PubMed] [Google Scholar]
  • 6. Heidsma CM, Engelsman AF, Van Dieren S, Stommel MWJ, de Hingh I, Vriens Met al. . Watchful waiting for small non-functional pancreatic neuroendocrine tumours: nationwide prospective cohort study (PANDORA). Br J Surg 2021;108:888–891 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7. Bettini R, Partelli S, Boninsegna L, Capelli P, Crippa S, Pederzoli Pet al. . Tumor size correlates with malignancy in nonfunctioning pancreatic endocrine tumor. Surgery 2011;150:75–82 [DOI] [PubMed] [Google Scholar]
  • 8. Partelli S, Bartsch DK, Capdevila J, Chen J, Knigge U, Niederle Bet al. . ENETS consensus guidelines for the standards of care in neuroendocrine tumours: surgery for small intestinal and pancreatic neuroendocrine tumours. Neuroendocrinology 2017;105:255–265 [DOI] [PubMed] [Google Scholar]
  • 9. Howe JR, Merchant NB, Conrad C, Keutgen XM, Hallet J, Drebin JAet al. . The North American Neuroendocrine Tumor Society consensus paper on the surgical management of pancreatic neuroendocrine tumors. Pancreas 2020;49:1–33 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10. Shah MH, Goldner WS, Halfdanarson TR, Bergsland E, Berlin JD, Halperin Det al. . NCCN guidelines insights: neuroendocrine and adrenal tumors, version 2.2018. J Natl Compr Canc Netw 2018;16:693–702 [DOI] [PubMed] [Google Scholar]
  • 11. Partelli S, Mazza M, Andreasi V, Muffatti F, Crippa S, Tamburrino Det al. . Management of small asymptomatic nonfunctioning pancreatic neuroendocrine tumors: limitations to apply guidelines into real life. Surgery 2019;166:157–163 [DOI] [PubMed] [Google Scholar]
  • 12. Mintziras I, Keck T, Werner J, Fichtner-Feigl S, Wittel U, Senninger Net al. . Implementation of current ENETS guidelines for surgery of small (≤ 2 cm) pancreatic neuroendocrine neoplasms in the German Surgical Community: an analysis of the prospective DGAV StuDoQ|Pancreas Registry. World J Surg 2018;43:175–182 [DOI] [PubMed] [Google Scholar]
  • 13. Chivukula SV, Tierney JF, Hertl M, Poirier J, Keutgen XM. Operative resection in early stage pancreatic neuroendocrine tumors in the United States: are we over- or undertreating patients? Surgery 2020;167:180–186 [DOI] [PubMed] [Google Scholar]
  • 14. Partelli S, Ramage JK, Massironi S, Zerbi A, Kim HB, Niccoli Pet al. . Management of asymptomatic sporadic nonfunctioning pancreatic neuroendocrine neoplasms (ASPEN) ≤ 2 cm: study protocol for a prospective observational study. Front Med 2020;7:1–8 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15. Dindo D, Demartines N, Clavien PA. Classification of surgical complications: a new proposal with evaluation in a cohort of 6336 patients and results of a survey. Ann Surg 2004;240:205–213 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16. Zhou B, Zhan C, Xiang J, Ding Y, Yan S. Clinical significance of the preoperative main pancreatic duct dilation and neutrophil-to-lymphocyte ratio in pancreatic neuroendocrine tumors (PNETs) of the head after curative resection. BMC Endocr Disord 2019;19:123. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17. Partelli S, Andreasi V, Muffatti F, Schiavo Lena M, Falconi M. Circulating neuroendocrine gene transcripts (NETest): a postoperative strategy for early identification of the efficacy of radical surgery for pancreatic neuroendocrine tumors. Ann Surg Oncol 2020;27:3928–3936 [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

znac267_Supplementary_Data

Articles from The British Journal of Surgery are provided here courtesy of Oxford University Press

RESOURCES