Abstract 1679P
Background
In patients with unresectable locally advanced (LAPC) or metastatic pancreatic cancer (MPC) gemcitabine-nab-paclitaxel (GEM-NAB) and FOLFIRINOX are standard first-line treatments. Recently, other combinations have shown to be associated with a survival advantage.
Methods
PubMed, CENTRAL, Embase and oncology meetings websites were searched to March 1st, 2023. We included phase II and III randomized controlled trials (RCTs) enrolling patients with unresectable LAPC or MPC which investigated gemcitabine-based (GEM) regimens, FOLFIRINOX, NALIRIFOX, PAXG or other first-line combinations. Efficacy outcomes were progression-free survival (PFS) and overall survival (OS). Hazard ratios (HRs) and 95% confidence intervals (95% CI) were computed using a random effects model. A frequentist network meta-analysis was conducted, and P-scores were used to rank treatments.
Results
4412 records were screened, and 45 studies were included; 37 studies were evaluable for PFS and 43 for OS. Considering PFS, PAXG (P-score 0.9410), NALIRIFOX (P-score 0.8723) and FOLFIRINOX (P-score 0.8696) were among the top-ranked strategies, while GEM-NAB had a P-score of 0.6388. In terms of OS, PAXG (P-score 0.9585), GEM-NAB sequential strategies (GEM-NAB > FOLFOX, P-score 0.9350 and GEM-NAB > FOLFIRI, P-score 0.9117), FOLFIRINOX (P-score 0.8512) and NALIRIFOX (P-score 0.8461) were among the top-ranked strategies, while the P-score of GEM-NAB was 0.6998. No difference was observed between NALIRIFOX and FOLFIRINOX (PFS HR: 1.01, 95% CI 0.68-1.50; OS HR: 0.99, 95% CI 0.74-1.31). A significant difference was observed between FOLFIRINOX and GEM+NAB in terms of PFS (HR 0.71, 95% CI 0.53-0.95), while a non-significant trend was observed in OS (HR 0.82, 95% CI 0.66-1.04). No difference was observed between NALIRIFOX and PAXG (PFS HR 1.25, 95% CI 0.72-2.17; OS HR 1.40, 95% CI 0.87-2.24) and between FOLFIRINOX and PAXG (PFS HR: 1.26, 95% CI 0.72-2.22; OS HR: 1.38, 95% CI 0.84-2.27).
Conclusions
With the limitations of a network meta-analysis, our results suggest that combinations with three or four drugs, when feasible, could provide a greater survival benefit compared to GEM-NAB in unresectable LAPC or MPC.
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
1654P - Circulating tumor cells (CTCs) as prognostic factor for pancreatic cancer: Updated of a prospective study
Presenter: Natalia Gutierrez Alonso
Session: Poster session 22
1655P - Nampt inhibitors re-sensitize MAP17 expressing pancreas tumors
Presenter: Julia Martinez Perez
Session: Poster session 22
1656P - Targeting NPC1L1 rescues anti-tumor immunity and improves immunotherapeutic efficacy in pancreatic cancer
Presenter: Houjie Liang
Session: Poster session 22
1657P - Understanding the role of SAGA and mediator in the resistance to Pdk1 deletion in PDAC
Presenter: Katarina Ondrejkova
Session: Poster session 22
1658P - Molecular subtyping of familial pancreatic ductal adenocarcinoma identifies novel pathogenic germline variants
Presenter: Julie Earl
Session: Poster session 22
1659P - The use of liquid biopsy in patients with advanced pancreatic cancer (PDAC) to guide enrollment in phase I clinical trials
Presenter: Octave Letissier
Session: Poster session 22
1660P - Squalene epoxidase promotes pancreatic cancer growth by attenuating ER stress and activating lipid rafts-regulated Src/PI3K/Akt signalling pathway
Presenter: Ruiyuan Xu
Session: Poster session 22
1661P - Precision medicine for pancreatic cancer: A clinical study validating EUS biopsies
Presenter: Joanne Lundy
Session: Poster session 22
1662P - Targeting stress granule formation as a synthetic lethality strategy for kras-induced pancreatic cancer initiation
Presenter: Patricia Santofimia
Session: Poster session 22
1663P - Role of next-generation sequencing somatic assays in patients with advanced pancreatic cancer
Presenter: Rafaela Naves
Session: Poster session 22