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
1624P - Predictive factors for treatment success of second-line Nal-IRI/5-FU/FA in patients with metastatic pancreatic ductal adenocarcinoma (PDAC) (AIO-PAK-0216)
Presenter: Manfred Lutz
Session: Poster session 22
1626P - A novel endoscopic ultrasound guided extended-release siRNA implant targeting KRASG12D/V in localized pancreatic cancer
Presenter: Anna Varghese
Session: Poster session 22
1629P - Modified-FOLFIRINOX-losartan followed by chemoradiotherapy for locally advanced pancreatic cancer: A phase II study
Presenter: Alshaimaa Alhanafy
Session: Poster session 22
1630P - Phase I/Ib study of SHP2-ERK inhibition in KRASm pancreatic cancer (SHERPA trial) and preclinical identification of potential resistance markers
Presenter: Ashwini Cheryl Kanhailal
Session: Poster session 22
1631P - Phase I study of endoscopic ultrasound (EUS)-guided NBTXR3 delivery activated by radiotherapy (RT) for locally advanced or borderline resectable pancreatic cancer (LAPC or BRPC)
Presenter: Gabriela Fuentes
Session: Poster session 22
1632P - Organoids as tools for functional precision oncology in advanced pancreatic cancer
Presenter: Alice Boileve
Session: Poster session 22
1633P - Development and clinical validation of news transcriptomic tools for predicting the response to individual drug of the mfolfirinox regimen in patients with pancreatic ductal adenocarcinoma
Presenter: Nicolas Fraunhoffer
Session: Poster session 22