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Oncological Safety of Spleen Preservation in Left Pancreatectomy for Pancreatic Ductal Adenocarcinoma (SPLENDID)

Oncological Safety of Spleen Preservation in Left Pancreatectomy for Pancreatic Ductal Adenocarcinoma (SPLENDID): Study Protocol for a Prospective Observational International Multicenter Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07157605
Acronym
SPLENDID
Enrollment
94
Registered
2025-09-05
Start date
2024-11-28
Completion date
2031-01-01
Last updated
2026-07-22

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

Conditions

Pancreatectomy, Pancreatic Cancer Resectable

Keywords

pancreatic adenocarcinoma, PDAC, left pancreatectomy, distal pancreatectomy, splenectomy, splenic hilum

Brief summary

The goal of this observational study is to determine how often lymph node metastases occur in the splenic hilum and surrounding fat in patients with left-sided pancreatic cancer. The main question the study aims to answer is: Is spleen removal necessary in all cases, or is the risk of lymph node metastases in the fat around the spleen low enough to reconsider this standard practice? Currently, spleen removal is part of the standard treatment for patients with left-sided pancreatic cancer to ensure that any potential lymph node metastases in the surrounding fat are also removed. However, the likelihood of metastases in this area is low, and spleen removal carries risks. This study is a first step toward changing the treatment approach. If the findings show that metastases in the fat around the spleen are rare, the next step will be a randomized trial to further investigate whether spleen removal is necessary.

Detailed description

Splenectomy is routinely performed during surgical resection of left-sided pancreatic ductal adenocarcinoma (PDAC) with the primary aim to facilitate adequate lymphadenectomy. However, asplenia is associated with several risks, including overwhelming post-splenectomy sepsis, and an increased risk of the development of cancer. Until several years ago, splenectomy was also routine practice in the surgical treatment of gastric cancer. Recently, several studies have shown that spleen-preservation in patients with gastric cancer is safe and therefore current guidelines advise against splenectomy. The rate of involved lymph nodes (LNs) in the splenic hilum (LN station 10) described in literature differs from 0 to 10% of patients. In these studies, the definition of the splenic hilum is often unclear and therefore these outcomes are difficult to interpret. Spleen-preservation in left-sided pancreatectomy for PDAC is currently not common practice in The Netherlands and goes against treatment guidelines. Two retrospective studies have suggested that spleenpreservation did not impair oncological outcomes and that postoperative complications occurred less after spleen preservation. However, these studies were retrospective, single-center and only included a very small number of patients and are therefore not providing enough evidence to change current practice. The SPLENDID-project focuses on evaluating the oncological safety of spleen-preservation in patients with left-sided PDAC. A prospective cohort study will be performed including all patients who undergo a left-sided pancreatectomy with splenectomy. The specimens will be transected at the precise level were spleen preservation (with resection of splenic vessels) would be performed (after removal of the specimen). Ratio of LN involvement will be collected for both specimen parts. Additionally, oncological patient outcomes, including survival, will be collected. When the pathological assessment confirms a \<9% LN involvement rate in the perihilar space, the next step will be to assess spleen preservation in an international, multicenter randomized controlled trial.

Interventions

None listed

Sponsors

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* All consecutive adult patients (≥ 18 years) who undergo an open or minimally invasive (i.e., robot-assisted or laparoscopic) left-sided pancreatectomy with concomitant splenectomy for primary resectable, borderline resectable, and locally advanced left-sided PDAC

Exclusion criteria

* Tumor involvement or abutment of the spleen

Design outcomes

Primary

MeasureTime frame
Lymph node metastasis in spleen-part1 month

Secondary

MeasureTime frameDescription
Predictors for the occurrence of lymph node metastasis in the spleen-part1 monthA regression analysis will be performed to determine the predictors for the lymph node metastasis in the spleen part
Overall and disease-free survival1 year, 2 years, 5 yearsOverall survival was defined as the time interval from surgery to death from any cause, and disease-free survival was defined as the time between surgery to either recurrence or death from any cause. 1-year, 2-year, and 5-year survival rates will be determined. Also the cause of death will be described.
Predictors for overall and disease-free survival1-year, 2-year, and 5-yearA multivariable regression analysis will determine independent prognostic factors for overall and disease-free survival (including whether lymph node metastases in the spleen part are an independent prognostic factor).
Recurrence1 year, 2 years, 5 years
Recurrence-free survival1 year, 2 years, 5 yearsdefined as the interval between surgery and recurrence, will be determined.
Lymph node metastasis (in pancreas-part and overall)1 monthin pathological assessment
Identification of left gastroepiploic vessels in spleen-part1 monthin pathological assessment
Identification of pancreatic tissue in spleen-part1 monthin pathological assessment
Distance from transection plane to tumor1 monthin pathological assessement
Tumor deposits1 monthin pathological assessment
Radical (R0) resection rate1 monthin pathological assessment
Histopathological diagnosis1 monthin pathological assessment
Postoperative complications90 days
Length of hospital stay90 days

Countries

China, Greece, Italy, Japan, Netherlands, Norway, Spain, Sweden

Contacts

PRINCIPAL_INVESTIGATORJony van Hilst, MD, PhD

Amsterdam UMC, location University of Amsterdam, Department of Surgery, Amsterdam, The Netherlands

PRINCIPAL_INVESTIGATORMarc G Besselink, MD, PhD, professor

Amsterdam UMC, location University of Amsterdam, Department of Surgery, Amsterdam, The Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 23, 2026