Impact of Neoadjuvant Therapy on Oncological Outcomes of Patients With Distal Pancreatic Adenocarcinoma.

chemotherapy distal neoadjuvant pancreatic adenocarcinoma survival

Journal

Journal of surgical oncology
ISSN: 1096-9098
Titre abrégé: J Surg Oncol
Pays: United States
ID NLM: 0222643

Informations de publication

Date de publication:
30 Sep 2024
Historique:
revised: 27 07 2024
received: 04 02 2024
accepted: 18 08 2024
medline: 30 9 2024
pubmed: 30 9 2024
entrez: 30 9 2024
Statut: aheadofprint

Résumé

Distal pancreatic ductal adenocarcinoma (D-PDAC) often presents at an advanced stage. The efficacy of neoadjuvant therapy (NAT) in improving outcomes for D-PDAC is not well-established. This study evaluates the impact of NAT on the oncological outcomes of patients with D-PDAC. A retrospective cohort study of consecutive patients with resectable and borderline-resectable D-PDAC treated at a single center from 2012 to 2020 was performed. Stratification was based on initial treatment-NAT or surgery first (SF). Survival analysis, following intention-to-treat framework, used Kaplan-Meier and Cox regression to assess NAT's impact on progression-free survival (PFS) and overall survival (OS) of D-PDAC. Among 141 patients (median age 69.8 years, 51.8% females) included in the study, 71 (50.4%) received NAT and 70 (49.6%) were planned for SF. Patients receiving NAT were younger (65.9 vs. 72.6 years) and had higher incidence of borderline-resectable disease (31% vs. 4.3%) (both p < 0.05) than those undergoing SF. Thirteen patients (18.3%) undergoing NAT and five (7.1%) in SF group, failed to undergo resection. Univariate comparison showed no difference in the PFS (SF:13.97 vs. NAT:17.00 months, p = 0.6), and OS (SF:23.73 vs. NAT:32.53 months, p = 0.35). Multivariate Cox regression analysis noted significantly improved PFS (HR = 0.64, 95%CI = 0.42-0.96, p = 0.031) and OS (HR = 0.60, 95%CI = 0.39-0.93, p = 0.021) with NAT. NAT is associated with improved PFS and OS in patients with -D-PDAC. Further randomized controlled trials are warranted to confirm these findings.

Sections du résumé

BACKGROUND BACKGROUND
Distal pancreatic ductal adenocarcinoma (D-PDAC) often presents at an advanced stage. The efficacy of neoadjuvant therapy (NAT) in improving outcomes for D-PDAC is not well-established. This study evaluates the impact of NAT on the oncological outcomes of patients with D-PDAC.
METHODS METHODS
A retrospective cohort study of consecutive patients with resectable and borderline-resectable D-PDAC treated at a single center from 2012 to 2020 was performed. Stratification was based on initial treatment-NAT or surgery first (SF). Survival analysis, following intention-to-treat framework, used Kaplan-Meier and Cox regression to assess NAT's impact on progression-free survival (PFS) and overall survival (OS) of D-PDAC.
RESULTS RESULTS
Among 141 patients (median age 69.8 years, 51.8% females) included in the study, 71 (50.4%) received NAT and 70 (49.6%) were planned for SF. Patients receiving NAT were younger (65.9 vs. 72.6 years) and had higher incidence of borderline-resectable disease (31% vs. 4.3%) (both p < 0.05) than those undergoing SF. Thirteen patients (18.3%) undergoing NAT and five (7.1%) in SF group, failed to undergo resection. Univariate comparison showed no difference in the PFS (SF:13.97 vs. NAT:17.00 months, p = 0.6), and OS (SF:23.73 vs. NAT:32.53 months, p = 0.35). Multivariate Cox regression analysis noted significantly improved PFS (HR = 0.64, 95%CI = 0.42-0.96, p = 0.031) and OS (HR = 0.60, 95%CI = 0.39-0.93, p = 0.021) with NAT.
CONCLUSION CONCLUSIONS
NAT is associated with improved PFS and OS in patients with -D-PDAC. Further randomized controlled trials are warranted to confirm these findings.

Identifiants

pubmed: 39348461
doi: 10.1002/jso.27856
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : The authors received no specific funding for this work.

Informations de copyright

© 2024 Wiley Periodicals LLC.

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Auteurs

Asmita Chopra (A)

Department of Surgery, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.

Anthony Gebran (A)

Department of Surgery, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.

Hussein Khachfe (H)

Department of Surgery, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.

Rudy El Asmar (RE)

Department of Surgery, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.

Ibrahim Nassour (I)

Department of Surgery, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.

Sowmya Narayanan (S)

Department of Surgery, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.

Samer AlMasri (S)

Department of Surgery, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.

Aatur Singhi (A)

Department of Pathology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.

Kenneth Lee (K)

Department of Surgery, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.

Amer Zureikat (A)

Department of Surgery, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.

Alessandro Paniccia (A)

Department of Surgery, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.

Classifications MeSH