Survival benefit of neoadjuvant FOLFIRINOX for patients with borderline resectable pancreatic cancer.

CA-19-9 antigen Neoadjuvant therapy Pancreatic cancer Pancreatic neoplasms

Journal

Annals of hepato-biliary-pancreatic surgery
ISSN: 2508-5859
Titre abrégé: Ann Hepatobiliary Pancreat Surg
Pays: Korea (South)
ID NLM: 101698342

Informations de publication

Date de publication:
01 Feb 2024
Historique:
received: 14 09 2023
revised: 05 12 2023
accepted: 09 12 2023
medline: 1 2 2024
pubmed: 1 2 2024
entrez: 31 1 2024
Statut: aheadofprint

Résumé

While patients with borderline resectable pancreatic cancer (BRPC) are a target population for neoadjuvant chemotherapy (NAC), formal guidelines for neoadjuvant therapy are lacking. We assessed the perioperative and oncological outcomes in patients with BRPC undergoing NAC with FOLFIRINOX for patients undergoing upfront surgery (US). The AHPBA criteria for borderline resectability and/or a CA19-9 level > 100 μ/mL defined borderline resectable tumors retrieved from a prospectively populated institutional registry from 2007 to 2020. The primary outcome was overall survival (OS) at 1 and 3 years. A Cox Proportional Hazard model based on intention to treat was used. A receiver-operator characteristics (ROC) curve was constructed to assess the discriminatory capability of the use of CA19-9 > 100 μ/mL to predict resectability and mortality. Forty BRPC patients underwent NAC, while 46 underwent US. The median OS with NAC was 19.8 months (interquartile range [IQR] 10.3-44.24) vs. 10.6 months (IQR 6.37-17.6) with US. At 1 year, 70% of the NAC group and 41.3% of the US group survived ( We found a survival benefit of NAC with FOLFIRINOX for BRPC. Greater pre-treatment of CA19-9 and multivessel involvement on initial imaging were associated with progression of the disease following NAC.

Sections du résumé

Backgrounds/Aims UNASSIGNED
While patients with borderline resectable pancreatic cancer (BRPC) are a target population for neoadjuvant chemotherapy (NAC), formal guidelines for neoadjuvant therapy are lacking. We assessed the perioperative and oncological outcomes in patients with BRPC undergoing NAC with FOLFIRINOX for patients undergoing upfront surgery (US).
Methods UNASSIGNED
The AHPBA criteria for borderline resectability and/or a CA19-9 level > 100 μ/mL defined borderline resectable tumors retrieved from a prospectively populated institutional registry from 2007 to 2020. The primary outcome was overall survival (OS) at 1 and 3 years. A Cox Proportional Hazard model based on intention to treat was used. A receiver-operator characteristics (ROC) curve was constructed to assess the discriminatory capability of the use of CA19-9 > 100 μ/mL to predict resectability and mortality.
Results UNASSIGNED
Forty BRPC patients underwent NAC, while 46 underwent US. The median OS with NAC was 19.8 months (interquartile range [IQR] 10.3-44.24) vs. 10.6 months (IQR 6.37-17.6) with US. At 1 year, 70% of the NAC group and 41.3% of the US group survived (
Conclusions UNASSIGNED
We found a survival benefit of NAC with FOLFIRINOX for BRPC. Greater pre-treatment of CA19-9 and multivessel involvement on initial imaging were associated with progression of the disease following NAC.

Identifiants

pubmed: 38296221
pii: ahbps.23-107
doi: 10.14701/ahbps.23-107
doi:

Types de publication

Journal Article

Langues

eng

Auteurs

Evelyn Waugh (E)

Division of General Surgery, Department of Surgery, Western University, London, ON, Canada.

Juan Glinka (J)

Division of General Surgery, Department of Surgery, Western University, London, ON, Canada.

Daniel Breadner (D)

Division of Medical Oncology, Department of Oncology, Western University, London, ON, Canada.

Rachel Liu (R)

Division of General Surgery, Department of Surgery, Western University, London, ON, Canada.

Ephraim Tang (E)

Division of General Surgery, Department of Surgery, Western University, London, ON, Canada.

Laura Allen (L)

Division of General Surgery, Department of Surgery, Western University, London, ON, Canada.

Stephen Welch (S)

Division of Medical Oncology, Department of Oncology, Western University, London, ON, Canada.

Ken Leslie (K)

Division of General Surgery, Department of Surgery, Western University, London, ON, Canada.

Anton Skaro (A)

Division of General Surgery, Department of Surgery, Western University, London, ON, Canada.

Classifications MeSH