# Vascular Resection, Reconstruction, and Divestment in Pancreatoduodenectomy: Expanding Boundaries in Pancreatic Cancer Surgery

**Authors:** Dimitrios Moris, Brian M. Nguyen, Alexander Kroemer, Benjamin Weinberg, Keith R. Unger, Nadim G. Haddad, Thomas M. Fishbein, Yuri S. Genyk

PMC · DOI: 10.3390/cancers18040577 · Cancers · 2026-02-10

## TL;DR

Surgical techniques for pancreatic cancer have advanced, allowing safe removal and reconstruction of blood vessels in select patients, improving outcomes.

## Contribution

The paper highlights the evolution and current standards of vascular resection and reconstruction in pancreatic cancer surgery.

## Key findings

- Venous resection is now standard with acceptable safety and survival rates in high-volume centers.
- Arterial resection and divestment are selectively used in patients with favorable responses to neoadjuvant therapy.
- Arterial divestment offers comparable oncologic outcomes with reduced surgical risks in selected cases.

## Abstract

Pancreatic ductal adenocarcinoma is an aggressive cancer that often involves major blood vessels, limiting surgical options. Advances in surgical techniques now allow safe vascular resection and reconstruction in selected patients undergoing pancreaticoduodenectomy. Venous resection has become standardized in experienced centers, offering acceptable complication rates and meaningful survival when complete tumor removal is achieved. Arterial resection remains technically demanding and is associated with higher risks, but may benefit carefully selected patients who respond to neoadjuvant therapy. Emerging strategies such as arterial divestment aim to preserve arterial integrity while maintaining oncologic effectiveness. This review summarizes the evolution of vascular surgical approaches in pancreatic cancer, highlights clinical indications for venous and arterial interventions, and provides practical recommendations to guide multidisciplinary decision-making. Continued research is needed to refine patient selection, optimize perioperative management, and improve long-term outcomes.

Vascular resection and reconstruction during pancreatoduodenectomy (PD) have evolved from rare and controversial procedures into essential components of surgical management for selected patients with locally advanced pancreatic ductal adenocarcinoma (PDAC). Venous resection is now widely accepted and routinely performed in high-volume centers, whereas arterial resection and artery-sparing divestment remain selectively applied because of their technical demands and concerns regarding perioperative risk and oncologic benefit. Accumulating contemporary evidence indicates that venous resection can be performed with acceptable safety, with 30-day mortality rates generally ranging from 3% to 5% and median overall survival of approximately 18–26 months when margin-negative (R0) resection is achieved. Arterial resections, most commonly involving the common hepatic, celiac, or superior mesenteric arteries, have been increasingly utilized in highly selected patients, particularly following neoadjuvant therapy, achieving R0 resection rates of approximately 65–75% and median overall survival of 20–28 months. Arterial divestment has emerged as a promising artery-sparing strategy, offering comparable oncologic outcomes with reduced surgical morbidity in appropriately selected cases. Collectively, these advances have expanded the boundaries of resectability in PDAC, enabling surgical intervention in patients previously deemed inoperable. Venous resection is now considered an oncologically sound extension of standard PD, whereas arterial resection and divestment should remain restricted to carefully selected patients demonstrating favorable biologic behavior and response to neoadjuvant therapy. Future progress in this field will likely depend on improved biologic stratification, enhanced intraoperative perfusion assessment, and the integration of hybrid open and endovascular techniques.

## Linked entities

- **Diseases:** pancreatic ductal adenocarcinoma (MONDO:0005184)

## Full-text entities

- **Diseases:** injury to (MESH:D014947), PDAC (MESH:D021441), fibrosis (MESH:D005355), CHA (MESH:D016893), Pancreatic Cancer (MESH:D010190), ischemic (MESH:D002545), cancer (MESH:D009369), pancreatic mass (MESH:D010195), hemorrhage (MESH:D006470), vascular complication (MESH:D003925), Re-thrombosis (MESH:D000084063), blood (MESH:D006402), infection (MESH:D007239), ischemic complications (MESH:D017202), Venous thrombosis (MESH:D020246), Portal vein stenosis (MESH:D000071078)
- **Chemicals:** PTFE (MESH:D011138), CA19 (-), FOLFIRINOX (MESH:C000627770), gemcitabine (MESH:D000093542)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12938771/full.md

## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12938771/full.md

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Source: https://tomesphere.com/paper/PMC12938771