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Long-term Prognosis for Non-functional Neuroendocrine Tumors of the Pancreatic Body and Tail ≤ 3cm

Long-term Prognosis Comparison Between Parenchyma-sparing and Oncologic Resections for Non-functional Neuroendocrine Tumors of the Pancreatic Body and Tail ≤ 3cm: a Real-world Data Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05907824
Enrollment
800
Registered
2023-06-18
Start date
2023-05-01
Completion date
2023-12-31
Last updated
2023-09-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non Functioning Pancreatic Endocrine Tumor

Keywords

Non Functioning Pancreatic Endocrine Tumor, Body and Tail of the Pancreas, Parenchyma-sparing Resection, Oncologic Resection, Long-term Prognosis

Brief summary

This study aims to quantify the malignant potential of non-functional neuroendocrine tumors of the pancreatic body and tail ≤ 3 cm by collecting real-world data from large pancreatic centers across the country, and to evaluate the appropriateness of parenchyma-sparing resection and oncologic resection.

Detailed description

According to epidemiological investigations, the incidence of neuroendocrine tumors has increased 6.4-fold (6.98 per 100,000) . There is controversy in the latest guidelines regarding the management of sporadic non-functional pancreatic neuroendocrine tumors (pNETs) ≤ 2 cm, including follow-up and the choice between parenchyma-sparing resection (PSR) and oncologic resection (OR) . Although pNETs are generally considered indolent tumors, current experience suggests that 9.5%-12.3% of pNETs ≤ 2 cm may have lymph node metastasis, and nearly 20% of resected tumors exhibit one or more invasive features. Awareness of surgical treatment for these patients has been increasing gradually. However, there is no clear recommendation for the choice of surgical approach, and if OR is routinely performed, its prognostic value is unclear and there may be a risk of overtreatment. The advantages of PSR include preservation of both endocrine and exocrine pancreatic function. However, the main oncological limitations of these techniques are inadequate surgical margin clearance and the risk of lack of lymph node dissection. A recent retrospective analysis of prospective databases from four large pancreatic surgery centers showed that for ≤ 3 cm non-functional pNETs, PSR or lymph node-preserving resection had less blood loss, shorter operation time, lower complications rate, and similar long-term oncological outcomes compared to OR. However, this study did not differentiate the tumor locations, as pNETs in the pancreatic head and body/tail have different lymphatic drainage patterns and surgical approaches. Furthermore, the study also showed significant differences in the proportion of PSR and the rate of positive lymph nodes between tumors located in the pancreatic head and those in the body/tail. The ability of existing literature to provide reliable guidelines for pNETs is limited by the low incidence of the disease and short follow-up times. This study aims to quantify the malignant potential of pNETs of the pancreatic body and tail ≤ 3 cm by collecting real-world data from large pancreatic centers across the country, and to evaluate the appropriateness of PSR and OR.

Interventions

OTHERHistopathological review, long-term prognosis and quality of life follow-up

Histopathological review, long-term prognosis and quality of life follow-up

Sponsors

The Third Affiliated Hospital of Soochow University
CollaboratorOTHER
Qilu Hospital of Shandong University
CollaboratorOTHER
First Affiliated Hospital Xi'an Jiaotong University
CollaboratorOTHER
Southern Medical University, China
CollaboratorOTHER
Fudan University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Non-functional neuroendocrine tumors of the pancreatic body and tail ≤ 3 cm.

Exclusion criteria

* Presence of liver or distant metastasis. * Presence of concomitant malignancy. * Multifocal or recurrent disease. * Presence of hereditary syndrome (MEN1, VHL, NF). * Presence of symptoms (specific symptoms of clinical syndromes suspected to be related to excessive secretion of bioactive compounds). * History of preoperative antitumor therapy. * Loss to follow-up.

Design outcomes

Primary

MeasureTime frameDescription
Overall survival (OS)Through study completion, an average of 1 year.The time from the surgery to death from any cause.
Disease-free survival (DFS)Through study completion, an average of 1 year.The time of surgery to the time of tumor recurrence or death from any cause.

Secondary

MeasureTime frameDescription
G stagingFrom the date of surgery to 1 month after surgery.The G staging evaluated according to the 2019 WHO classification and grading criteria for digestive neuroendocrine tumors.
R0 resection rateFrom the date of surgery to 1 month after surgery.R0 margin rate on postoperative pathological assessment.
Perioperative complication rateWithin 90 days after surgery.Adverse events that occur during or after the surgery, including the incidence of postoperative complications reported according to the Clavien-Dindo classification, clinical relevant postoperative pancreatic fistula (POPF), postoperative pancreatic hemorrhage (PPH), delayed gastric emptying (DGE), reoperation rate and mortality rate within 90 days after surgery.
Life quality satisfaction evaluated according to a scale.Through study completion, an average of 1 year.The patient's health-related quality of life after surgical intervention. It includes physical, emotional, and social aspects of a patient's well-being. This study evaluated quality of life using a telephone survey.
Lymph node positivity rateFrom the date of surgery to 1 month after surgery.Lymph node positivity rate on postoperative pathological assessment.
Postoperative pathological stagingFrom the date of surgery to 1 month after surgery.The tumor staging according to the 8th edition of the AJCC TNM staging system.

Countries

China

Contacts

Primary ContactXianjun Yu, MD, PhD
yuxianjun@fudanpci.org+86-13801669875
Backup ContactZheng Li, MD
lizheng@fudanpci.org+86-18521097686

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026