Abstract 1677P
Background
Pancreatic ductal adenocarcinoma (PDAC) is one of the big killers with a 5-year-survival rate of less than 2% in metastatic disease. Limited treatment options and early clinical deterioration often affect outcome. Exocrine pancreatic insufficiency (EPI) is often underestimated in patients with advanced PDAC and a large proportion of patients (60-80%) does not receive pancreatic enzyme replacement therapy (PERT). This study aims to optimize the clinical selection of patients with advanced PDAC treated with gemcitabine/nabpaclitaxel and to develop models to predict benefit from first-line therapy and duration of second-line therapy.
Methods
In this observational study we prospectively enrolled patients with advanced PDAC treated with gemcitabine/nabpaclitaxel as first-line therapy at the Medical Oncology Unit of Careggi University Hospital from 2015 to 2022. Clinical and laboratory data were collected and associated with survival outcomes, duration of second-line therapy and treatment exposure.
Results
A total of 107 patients were enrolled, 54 (50.5%) were women and 53 (49.5%) were men. Disease stage was classified as locally advanced in 42 (39.3%) and metastatic in 65 (60.7%). Median progression-free survival (PFS) was 5.6 months and median overall survival (OS) was 7.4 months. Among the baseline clinical variables, a trend towards a worse prognosis was observed in patients with a high tumor burden (OS p=0.065). Overall, 66.0% of patients received PERT at baseline or within 3 months from first-line treatment start. PERT-users had a significantly longer OS than non-PERT-users (9.5 months vs 5.5 months, respectively, HR 95%CI 2,1 [1,2-3,7], p=0.008). In addition, the probability to receive a second-line treatment for at least 2 months was higher in the PERT-user group than in the non-PERT-user group (X-squared=7.6558, p-value=0.005659).
Conclusions
The clinical management of patients with advanced PDAC is challenging and requires a multidisciplinary strategy to prevent EPI-related symptoms and optimize treatment adherence. PERT could play a crucial role in preventing weight loss, maintaining dose intensity and improving survival.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
1589P - Systemic treatment strategies and outcomes of patients with peritoneal metastases of gastric origin
Presenter: Niels Guchelaar
Session: Poster session 22
1590P - Real-world gastric cancer (GC) in Latin America (LATAM) and Europe (EU)
Presenter: Berenice Freile
Session: Poster session 22
1591P - Gastric cancer in young patients under 40 years: 5-year analyses of Georgian cancer registry
Presenter: Tamar Esakia
Session: Poster session 22
1617P - PRODIGE 29-UCGI 26 (NEOPAN): Quality of life results of a phase III randomised trial comparing chemotherapy with folfirinox (FFX) or gemcitabine (gem) in locally advanced pancreatic carcinoma (LAPC)
Presenter: Michel Ducreux
Session: Poster session 22
1618P - Durable efficacy of zenocutuzumab, a HER2 x HER3 bispecific antibody, in advanced NRG1 fusion positive (NRG1+) pancreatic ductal adenocarcinoma (PDAC)
Presenter: Alison Schram
Session: Poster session 22
1620P - A phase II study of perioperative nalirifox in patients with resectable pancreatic ductal adenocarcinoma (rPDAC): Survival update and biomarkers analysis of the NITRO trial
Presenter: Davide Melisi
Session: Poster session 22
1621P - Efficacy and safety of erdafitinib in adults with pancreatic cancer and prespecified fibroblast growth factor receptor alterations (FGFRalt) in the phase II open-label: Single-arm RAGNAR trial
Presenter: Shubham Pant
Session: Poster session 22
1622P - D-1553 in patients with KRAS G12C mutated advanced pancreatic cancer (pca)
Presenter: Shunsuke Kondo
Session: Poster session 22
1623P - Pelareorep (pela) + atezolizumab (atezo) and chemotherapy in first-line (1L) advanced or metastatic pancreatic ductal adenocarcinoma (PDAC) patients: Results from the GOBLET study
Presenter: Dirk Arnold
Session: Poster session 22