Venous Resection During Pancreatoduodenectomy for Pancreatic Ductal Adenocarcinoma-A Multicentre Propensity Score Matching Analysis of the Recurrence After Whipple's (RAW) Study

  • Ruben Bellotti
  • , Somaiah Aroori
  • , Benno Cardini
  • , Florian Ponholzer
  • , Thomas B Russell
  • , Peter L Labib
  • , Stefan Schneeberger
  • , Fabio Ausania
  • , Elizabeth Pando
  • , Keith J Roberts
  • , Ambareen Kausar
  • , Vasileios K Mavroeidis
  • , Gabriele Marangoni
  • , Sarah C Thomasset
  • , Adam E Frampton
  • , Pavlos Lykoudis
  • , Nassir Alhaboob
  • , Hassaan Bari
  • , Andrew M Smith
  • , Duncan Spalding
  • Parthi Srinivasan, Brian R Davidson, Ricky H Bhogal, Daniel Croagh, Ismael Dominguez, Rohan Thakkar, Dhanny Gomez, Michael A Silva, Pierfrancesco Lapolla, Andrea Mingoli, Alberto Porcu, Nehal S Shah, Zaed Z R Hamady, Bilal Al-Sarrieh, Alejandro Serrablo, Raw Study Collaborators, Manuel Maglione

Research output: Contribution to journalArticlepeer-review

Abstract

Background: Pancreatoduodenectomy with venous resection (PDVR) may be performed to achieve tumour clearance in patients with a pancreatic ductal adenocarcinoma (PDAC) with venous involvement. This study aimed to evaluate the impact of PDVR on PDAC outcomes. Methods: In total, 435 PDAC patients with either R0 status (n = 322) or R1 status within the superior mesenteric vein groove (n = 113) were extracted from the Recurrence After Whipple's (RAW) study dataset. PDVR patients were matched in a 1:2 ratio with standard PD patients. Comparisons were then made between the two groups (surgical radicality and survival). Results: A total of 81 PDVRs were matched with 162 PDs. Neoadjuvant chemotherapy (5.7% vs. 13.6%, p = 0.032) and R1 resection rates (17.9% vs. 42%, p < 0.001) were higher in the PDVR group. Risk factors for R1 resection included venous resection (p < 0.001 for sleeve and p = 0.034 for segmental resection), pT3 (p = 0.007), and pN1 stage (p = 0.045). PDVR patients had lower median overall survival (OS, 21 vs. 30 months (m), p = 0.023) and disease-free survival (DFS, 17 m vs. 24 m, p = 0.043). Among PDVR patients, R status did not impact on OS (R0: 23 m, R1: 21 m, p = 0.928) or DFS (R0: 18 m, R1: 17 m, p = 0.558). Irrespective of R status, systemic recurrence was higher in the PDVR group (p = 0.034). Conclusions: Independent of R status, the PDVR group had lower overall survival and higher systemic recurrence rates.

Original languageEnglish
JournalCancers
Volume17
Issue number7
DOIs
Publication statusPublished - 4 Apr 2025
Externally publishedYes

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