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Validation of the PANAMA Score for Survival and Benefit of Adjuvant Therapy in Patients With Resected Pancreatic Cancer after Neoadjuvant FOLFIRINOX

Ingmar F. Rompen, Thomas F. Stoop, Stijn van Roessel, Eran van Veldhuisen, Quisette P. Janssen, Adnan Alseidi, Alberto Balduzzi, Gianpaolo Balzano, Frederik Berrevoet, Morgan Bonds, Olivier R. Busch, Giovanni Butturini, Ammar A. Javed, Marco Del Chiaro, Kevin C. Conlon, Massimo Falconi, Isabella Frigerio, Giuseppe K. Fusai, Johan Gagnière, Oonagh GriffinThilo Hackert, Ernesto Sparrelid, Asif Halimi, Knut J. Labori, Giuseppe Malleo, Marco V. Marino, Michael B. Mortensen, Andrej Nikov, Mickaël Lesurtel, Tobias Keck, Jörg Kleeff, Rupaly Pandé, Per Pfeiffer, Daniel Pietrasz, Keith J. Roberts, Antonio Sa Cunha, Roberto Salvia, Oliver Strobel, Timo Tarvainen, Hanneke W.M. van Laarhoven, Bas Groot Koerkamp, Martin Loos, Christoph W. Michalski, Marc G. Besselink, Thomas Hank*

*Korrespondierende/r Autor/-in für diese Arbeit

Abstract

Objective: To validate the prognostic value of the PAncreatic NeoAdjuvant MAssachusetts (PANAMA) score and to determine its predictive ability for survival benefit derived from adjuvant treatment in patients after resection of pancreatic ductal adenocarcinoma (PDAC) following neoadjuvant FOLFIRINOX. Background: The PANAMA score was developed to guide prognostication in patients after neoadjuvant therapy and resection for PDAC. As this score focuses on the risk for residual disease after resection, it might also be able to select patients who benefit from adjuvant after neoadjuvant therapy. Methods: This retrospective international multicenter study is endorsed by the European-African Hepato-Pancreato-Biliary Association. Patients with PDAC who underwent resection after neoadjuvant FOLFIRINOX were included. Mantel-Cox regression with interaction analysis was performed to assess the impact of adjuvant chemotherapy. Results: Overall, 383 patients after resection of PDAC following neoadjuvant FOLFIRINOX were included of whom 187 (49%), 137 (36%), and 59 (15%) had a low-risk, intermediate-risk, and high-risk PANAMA-score, respectively. Discrimination in median overall survival (OS) was observed stratified by risk groups (48.5, 27.6, and 22.3 months, log-rank Plow-intermediate = 0.004, log-rank Pintermediate-high = 0.027). Adjuvant therapy was not associated with an OS difference in the low-risk group [hazard ratio (HR): 1.50, 95% CI: 0.92–2.50], whereas improved OS was observed in the intermediate (HR: 0.58, 95% CI: 0.34–0.97) and high-risk groups (HR: 0.47, 95% CI: 0.24–0.94; P interaction = 0.008). Conclusions: The PANAMA 3-tier risk groups (low-risk, intermediate-risk, and high-risk, available through pancreascalculator. com) correspond with differential survival in patients with resected PDAC following neoadjuvant FOLFIRINOX. The risk groups also differentiate between survival benefits associated with adjuvant treatment, with only the intermediate- and high-risk groups associated with improved OS.

OriginalspracheEnglisch
ZeitschriftAnnals of Surgery
Jahrgang281
Ausgabenummer5
Seiten (von - bis)852-860
Seitenumfang9
ISSN0003-4932
DOIs
PublikationsstatusVeröffentlicht - 01.05.2025

Fördermittel

M.D.C. has been awarded an industry grant (Haemonics, Inc.) to conduct a multicenter study to evaluate the prognostic implications of TEG in pancreatic caner. He is a co-principal investigator of a Boston Scientific sponsored international multicenter study on the use of intraoperative pancreatoscopy of patients with IPMN. I.F.R. received funding from the Swiss National Science Foundation. The remaining authors report no conflicts of interest.

TrägerTrägernummer
Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

    UN SDGs

    Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung

    1. SDG 3 – Gesundheit und Wohlergehen
      SDG 3 – Gesundheit und Wohlergehen

    Strategische Forschungsbereiche und Zentren

    • Profilbereich: Lübeck Integrated Oncology Network (LION)

    DFG-Fachsystematik

    • 2.22-14 Hämatologie, Onkologie
    • 2.22-09 Pharmakologie

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