Abstract 1643P
Background
Neoadjuvant (m)FOLFIRINOX has been established as one of standard therapy for borderline resectable (BRPC) and locally advanced pancreatic cancer (LAPC). Recently, its use has been expanded to resectable pancreatic cancer (RPC), but large pragmatic studies, particularly in Asia, to show the implication of localized pancreatic adenocarcinoma are still lacking.
Methods
This retrospective study included 781 patients with localized pancreatic adenocarcinoma who received (m)FOLFIRINOX as initial therapy in Asan Medical Center, Seoul, Korea, between DEC 2017 and DEC 2020.
Results
The median age was 62 years, and 341 (43.8%) patients were female. According to the NCCN criteria, 131 (16.8%), 326 (41.9%), and 321 (41.3%) patients had RPC, BRPC and LAPC, respectively. The objective response rates were 22.1%, 16.3%, and 15.0%, respectively. The curative-intent resection (R0 or R1) was performed in 94 (71.8%) patients of the RPC group, 137 (42.0%) patients of the BRPC group, and 40 (12.5%) patients of the LAPC group; patients who underwent curative resection, the R0 resection rates were similar among three groups (86.2%, 86.1%, and 80.0%, respectively). There were 11 patients who achieved surgery following salvage chemotherapy after progression on initial (m)FOLFIRINOX. The median overall survival (OS) was 28.1 months (95% CI, 22.7–33.5) for RPC, 22.0 months (95% CI, 19.8–24.1) for BRPC, and 20.3 months (95% CI, 18.7–21.9) for LAPC (p<0.001). In each resectability group, median OS was significantly better in patients with surgical resection (RPC, 41.6 vs 14.5 months, p<0.001; BRPC, 37.3 vs 14.7, p<0.001; LAPC, 51.4 vs 18.5 months, p<0.001). In multivariate analysis, female gender, RPC, baseline CA 19-9 < median (118.7 U/mL), objective response (CR or PR), and curative-intent surgery were significantly associated with better OS.
Conclusions
This large retrospective cohort study provides the realistic key clinical outcome data such as resection rates, survival outcomes and prognostic factors in RPC, BRPC and LAPC treated with front-line (m)FOLFIRINOX.
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
1644P - The mutation landscape and evolution pattern of liver or peritoneal metastasis in pancreatic cancer
Presenter: Guoliang Yao
Session: Poster session 22