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Resection of the Primary Tumor vs. Systemic Treatment Alone for Patients With Small Intestinal Neuroendocrine Tumors and Unresectable Metastases: a Europe-wide Study

Resection of the Primary Tumor vs. Systemic Treatment Alone for Patients With Small Intestinal Neuroendocrine Tumors and Unresectable Metastases: a Retrospective, Europe-wide, Pooled Cohort Study (ENETS-SurgSmInt)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06787014
Acronym
ENETSSurgSmInt
Enrollment
3200
Registered
2025-01-22
Start date
2026-03-09
Completion date
2028-12-31
Last updated
2026-03-18

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

Conditions

Bowel Obstruction, Metastasis, Neuroendocrine (NE) Tumors

Brief summary

When possible, surgery to completely remove small intestinal neuroendocrine tumors (siNETs) is always recommended. However, in cases where the tumor has spread and cannot be cured completely, it is unclear whether a surgical removal of the primary tumor only is reasonable. In this situation, current guidelines from the European Neuroendocrine Tumor Society (ENETS) recommend surgery only for patients who have symptoms like intestinal blockage or bleeding, or are at risk of such complications. For patients without symptoms, it is still unclear whether removing the main tumor improves overall outcomes and prevents future problems. Studies evaluating this type of surgery on survival show conflicting results. These studies often do not separate patients with symptoms from those without, and they overlook other important factors like the amount of cancer in the liver and nearby tissues. Due to these uncertainties, the rarity of siNETs and many factors that can affect outcomes, like age, overall health, or other current treatments, conducting a high-quality study to answer this question is challenging. To address this, the present Europe-wide study is being planned. This study aims to determine if resecting the main tumor improves the 10-year overall survival and reduces risks like intestinal blockages or blood flow issues compared to no surgery in patients without symptoms. The study will also assess other outcomes, such as how long patients stay free from disease progression, the risks of surgery, and prognostic factors for long-term survival. This international collaboration among neuroendocrine tumor referral centers will provide robust evidence to guide clinical practice and update treatment guidelines for siNETs.

Interventions

Histopathological review

Sponsors

Insel Gruppe AG, University Hospital Bern
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

\- All patients with siNET and non-curative metastatic disease between 01.01.2005 and 31.12.2021 will be included.

Exclusion criteria

\- All patients with siNET G3, resectable metastatic disease and/or non-resectable primary tumor at initial diagnosis will be excluded. Furthermore, symptomatic patients (small intestinal obstruction, bleeding) or when imaging suggests that obstruction will probably occur (bowel dilatation, mesenteric fibrosis) at initial diagnosis will be excluded. Patients with diarrhea, flushing, or abdominal pain will not be excluded. Patients with a documented rejection for a further use of their data for scientific purposes will also be excluded.

Design outcomes

Primary

MeasureTime frameDescription
To evaluate the 10-year overall survival of non-curative metastatic siNET with or without primary tumor resection at initial diagnosis in asymptomatic patients.10 years follow-upFor the survival analysis, Kaplan-Meier method will be used to estimate overall survival at 10 years for patients with and without primary tumor resection.

Secondary

MeasureTime frameDescription
To evaluate the progression-free survival of non-curative metastatic siNET with or without primary tumor resection at initial diagnosis in asymptomatic patients.10 years follow-upFor the survival analysis, Kaplan-Meier method will be used to estimate overall survival at 10 years for patients with and without primary tumor resection.
To examine the risk of small intestinal obstruction with or without palliative primary tumor resection10 years follow-upTo account for additional established prognostic information, univariable and multivariable Cox proportional hazards regression will be used.
To examine the risk of small intestinal hypoperfusion with or without palliative primary tumor resection10 years follow-upTo account for additional established prognostic information, univariable and multivariable Cox proportional hazards regression will be used.
To evaluate the morbidity of palliative primary tumor resection10 years follow-upTo account for additional established prognostic information, univariable and multivariable Cox proportional hazards regression will be used.
To evaluate the mortality of palliative primary tumor resection10 years follow-upTo account for additional established prognostic information, univariable and multivariable Cox proportional hazards regression will be used.
To assess prognostic factors for long-term survival10 years follow-upThe following prognostic information will be taken into account: age, sex, ECOG, presence of second malignancy, and adjusted for characteristics of the siNET (Ki-67 index, number of siNETs, lymph node metastases, TBS, extrahepatic metastases, CgA level, 5-HIAA level, carcinoid heart disease, and use of other treatments), with results presented as adjusted hazard ratios (HRs) and 95% CI.

Countries

Switzerland

Contacts

CONTACTEliane Dohner
eliane.dohner@insel.ch0041 31 664 28 31
PRINCIPAL_INVESTIGATORReto M. Kaderli

Insel Gruppe AG, University Hospital Bern

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 19, 2026