No survival benefit with suboptimal CA19-9 response: defining effective neoadjuvant chemotherapy in resectable or borderline resectable pancreatic cancer.


Journal

HPB : the official journal of the International Hepato Pancreato Biliary Association
ISSN: 1477-2574
Titre abrégé: HPB (Oxford)
Pays: England
ID NLM: 100900921

Informations de publication

Date de publication:
05 2023
Historique:
received: 24 07 2022
revised: 14 11 2022
accepted: 30 01 2023
medline: 2 5 2023
pubmed: 23 2 2023
entrez: 22 2 2023
Statut: ppublish

Résumé

Neoadjuvant chemotherapy (NAC) is gaining popularity over a surgery-first (SF) approach in treating resectable and borderline resectable pancreatic ductal adenocarcinoma (PDAC). However, what constitutes effective neoadjuvant chemotherapy is unknown. We retrospectively analyzed resectable and borderline resectable PDAC patients who underwent pancreaticoduodenectomy (2010-2019) at a single institution. Optimal CA19-9 response was defined as normalization AND >50% reduction. We utilized Kaplan-Meier and multivariable-adjusted Cox models and competing risk subdistribution methods for statistical analysis. 586 patients were included in this study. The multivariable-adjusted analysis demonstrated OS benefit in the NAC group only when OS was calculated from diagnosis (HR = 0.72, p = 0.02), but not from surgery (HR = 0.81, p = 0.1). However, in 59 patients who achieved optimal CA19-9 response, OS is significantly longer than the 134 patients with suboptimal CA19-9 response (39.3 m vs. 21.5 m, p = 0.005) or the 117 SF patients (39.3 m vs. 19.5 m, p < 0.001). Notably, a suboptimal CA19-9 response conferred no OS advantage compared to SF patients. The accumulative incidence of liver metastases (but not other metastases) was significantly reduced only in patients with optimal CA19-9 response to NAC (multivariable-adjusted subdistribution HR = 0.26, p = 0.03). CA19-9 response to NAC may serve as the marker for effective NAC. These findings warrant validation in a multi-institutional study.

Sections du résumé

BACKGROUND/PURPOSE
Neoadjuvant chemotherapy (NAC) is gaining popularity over a surgery-first (SF) approach in treating resectable and borderline resectable pancreatic ductal adenocarcinoma (PDAC). However, what constitutes effective neoadjuvant chemotherapy is unknown.
METHODS
We retrospectively analyzed resectable and borderline resectable PDAC patients who underwent pancreaticoduodenectomy (2010-2019) at a single institution. Optimal CA19-9 response was defined as normalization AND >50% reduction. We utilized Kaplan-Meier and multivariable-adjusted Cox models and competing risk subdistribution methods for statistical analysis.
RESULTS
586 patients were included in this study. The multivariable-adjusted analysis demonstrated OS benefit in the NAC group only when OS was calculated from diagnosis (HR = 0.72, p = 0.02), but not from surgery (HR = 0.81, p = 0.1). However, in 59 patients who achieved optimal CA19-9 response, OS is significantly longer than the 134 patients with suboptimal CA19-9 response (39.3 m vs. 21.5 m, p = 0.005) or the 117 SF patients (39.3 m vs. 19.5 m, p < 0.001). Notably, a suboptimal CA19-9 response conferred no OS advantage compared to SF patients. The accumulative incidence of liver metastases (but not other metastases) was significantly reduced only in patients with optimal CA19-9 response to NAC (multivariable-adjusted subdistribution HR = 0.26, p = 0.03).
CONCLUSION
CA19-9 response to NAC may serve as the marker for effective NAC. These findings warrant validation in a multi-institutional study.

Identifiants

pubmed: 36804826
pii: S1365-182X(23)00029-1
doi: 10.1016/j.hpb.2023.01.016
pii:
doi:

Substances chimiques

CA-19-9 Antigen 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

521-532

Informations de copyright

Copyright © 2023 International Hepato-Pancreato-Biliary Association Inc. Published by Elsevier Ltd. All rights reserved.

Auteurs

Hao Liu (H)

Department of Surgery, University of Pittsburgh Medical Center (UPMC), United States.

Mark D'Alesio (M)

School of Medicine, University of Pittsburgh, United States.

Samer AlMasri (S)

Department of Surgery, University of Pittsburgh Medical Center (UPMC), United States.

Abdulrahman Hammad (A)

Department of Surgery, University of Pittsburgh Medical Center (UPMC), United States.

Annissa Desilva (A)

Department of Surgery, University of Pittsburgh Medical Center (UPMC), United States.

Steven Lebowitz (S)

School of Medicine, University of Pittsburgh, United States.

Caroline Rieser (C)

Department of Surgery, University of Pittsburgh Medical Center (UPMC), United States.

Eishan Ashwat (E)

School of Medicine, University of Pittsburgh, United States.

Erica Hampton (E)

School of Medicine, University of Pittsburgh, United States.

Hussein Khachfe (H)

Department of Surgery, University of Pittsburgh Medical Center (UPMC), United States.

Mckenna Laffey (M)

School of Medicine, University of Pittsburgh, United States.

Aatur Singhi (A)

Department of Pathology, University of Pittsburgh Medical Center, United States.

Nathan Bahary (N)

Department of Medicine, University of Pittsburgh Medical Center, United States.

Kenneth Lee (K)

Department of Surgery, University of Pittsburgh Medical Center (UPMC), United States.

Amer Zureikat (A)

Department of Surgery, University of Pittsburgh Medical Center (UPMC), United States.

Alessandro Paniccia (A)

Department of Surgery, University of Pittsburgh Medical Center (UPMC), United States. Electronic address: panicciaa2@upmc.edu.

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