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
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