The benefit of adjuvant chemotherapy following pancreaticoduodenectomy for pancreatic adenocarcinoma depends on response to neoadjuvant therapy

Author:

Carpenter Elizabeth L.1,Van Decar Spencer G.1ORCID,McCarthy Patrick M.1,Valdera Franklin A.1,Adams Alexandra M.1,O'Shea Anne E.1,Smolinsky Todd1ORCID,Thomas Katryna1,Clifton Guy T.1,Newhook Timothy E.2ORCID,Peoples George E.3,Nelson Daniel W.4,Vreeland Timothy J.1

Affiliation:

1. Brooke Army Medical Center San Antonio Texas USA

2. The University of Texas MD Anderson Cancer Center Houston Texas USA

3. Cancer Vaccine Development Program San Antonio Texas USA

4. William Beaumont Army Medical Center El Paso Texas USA

Abstract

AbstractBackgroundThe benefit of adjuvant therapy (AT) remains unclear in pancreatic ductal adenocarcinoma (PDAC) after neoadjuvant therapy (NAT) and surgical resection.MethodsThe 2019 National Cancer Database was queried for patients with non‐metastatic PDAC who received NAT followed by pancreaticoduodenectomy. Only patients with data regarding receipt of AT were included. Patients were classified if they had nodal down‐staging specifically, or any downstaging (Tumor, Nodal, or overall). Propensity score matching (PSM) adjusted for pretreatment covariate imbalance between groups. The weighted Kaplan–Meier method and log‐rank test were used to estimate the cumulative survival.ResultsAfter exclusion criteria and PSM, a total of 2784 patients remained; 1689 (60.7%) received AT and 1095 (39.3%) did not receive AT. Among all, those with additional AT had a significantly improved overall survival (OS) (p < 0.001). Upon evaluation of patients without downstaging after NAT, those who received AT had improved OS (no nodal downstaging or any downstaging; p = 0.002; p = 0.001). When evaluating patients with downstaging after NAT, those receiving AT did not have improved OS (nodal downstaging or any downstaging: p = 0.352; p = 0.99).ConclusionResponse to NAT appears to correlate with the benefit of AT following pancreaticoduodenectomy; patients who have a favorable response to NAT may not benefit from AT.

Publisher

Wiley

Reference25 articles.

1. Cancer Statistics, 2021

2. Pancreatic Adenocarcinoma, Version 2.2021, NCCN Clinical Practice Guidelines in Oncology

3. Potentially Curable Pancreatic Cancer: American Society of Clinical Oncology Clinical Practice Guideline

4. An update on treatment options for pancreatic adenocarcinoma

5. National Comprehensive Cancer Network Clinical Practice Guidelines in Oncology: Pancreatic Adenocarcinoma.2024.https://www.nccn.org/professionals/physician_gls/pdf/pancreatic.pdf

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