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
1634P - Extensive molecular profiling of KRAS wild-type versus KRAS mutant pancreatic ductal adenocarcinoma on 233 patients
Presenter: Jeanne Lena
Session: Poster session 22
1635P - Germline pathogenic variants of cancer predisposition genes in a multicentre Italian cohort of pancreatic ductal adenocarcinoma patients
Presenter: Giulia Orsi
Session: Poster session 22
1636P - Circulating tumor DNA (ctDNA) profile in patients (pts) with pancreatic cancer (PC): A multicenter experience and challenges for clinical application
Presenter: Francisco Muñoz i Carrillo
Session: Poster session 22
1637P - Early retention of KRAS mutations in cfDNA is an ominous sign for pancreatic cancer patients during chemotherapy: A prospective cohort study
Presenter: Chien-Jui Huang
Session: Poster session 22
1638P - The prognostic and predictive role of class III β-tubulin and hENT1 expression in patients with advanced pancreatic ductal adenocarcinoma
Presenter: Taha Koray Sahin
Session: Poster session 22
1639P - Feasibility of tumor genomic sequencing on tissue obtained from endoscopic ultrasound in patients with pancreatic cancer
Presenter: Vaia Florou
Session: Poster session 22
1640P - Response monitoring with ctDNA in metastatic pancreatic cancer
Presenter: Jinwoo Ahn
Session: Poster session 22
1642P - Prognostic impact of an immunomorphological signature integrating immune, fibroblastic and tumor markers in a series of 217 resected pancreatic adenocarcinoma patients
Presenter: Franck MONNIEN
Session: Poster session 22
1643P - Clinical outcomes of FOLFIRINOX as front-line therapy in patients with localized pancreatic adenocarcinoma: Asian retrospective study of 781 patients
Presenter: Kyunghye Bang
Session: Poster session 22