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Role of surgical resection in the era of FOLFIRINOX for advanced pancreatic cancer

Cited 33 time in Web of Science Cited 37 time in Scopus
Authors

Byun, Yoonhyeong; Han, Youngmin; Kang, Jae Seung; Choi, Yoo Jin; Kim, Hongbeom; Kwon, Wooil; Kim, Sun-Whe; Oh, Do-Youn; Lee, Sang Hyub; Ryu, Ji Kon; Kim, Yong-Tae; Jang, Jin-Young

Issue Date
2019-09
Publisher
Springer Verlag
Citation
Journal of Hepato-Biliary-Pancreatic Sciences, Vol.26 No.9, pp.416-425
Abstract
Background The introduction of FOLFIRINOX regimen greatly changed the treatment for advanced pancreatic cancers. However, detailed studies on the clinical effects and factors affecting the prognosis are insufficient. We performed this study to evaluate the effects of FOLFIRINOX and the surgical resection in advanced pancreatic cancer. Methods Three hundred and thirty-seven patients with advanced pancreatic cancer who initially received FOLFIRINOX, from January 2011 to December 2017, were retrospectively reviewed. Patients were evaluated according to the National Comprehensive Cancer Network guideline, responses after four to six cycles of FOLFIRINOX were re-evaluated according to the response evaluation criteria in solid tumors, and further treatment was decided in the multidisciplinary meeting. Results Sixty-seven (19.9%) patients had borderline resectable pancreatic cancer, 135 (40.1%) locally advanced pancreatic cancer, and 135 (40.1%) metastatic pancreatic cancer. The median survival period was significantly longer in the surgical group than in the nonsurgical group in each clinical stage, even in metastatic pancreatic cancer (32 vs. 14, P = 0.012). In multivariate analysis, metastatic status at diagnosis, progressive disease after FOLFIRINOX, surgical resection, and declined CA19-9 after FOLFIRINOX were significant prognostic factors. Conclusions Surgical treatment greatly affects survival outcomes in advanced pancreatic cancer treated with FOLFIRINOX. Further studies on the optimal indication of operation and the protocol are needed.
ISSN
1868-6974
URI
https://hdl.handle.net/10371/212788
DOI
https://doi.org/10.1002/jhbp.648
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  • Department of Medicine
Research Area DNA 손상 반응 타겟 물질의 면역조절 효과, Effect of DNA damage response target substances on immunomodulatory action, Efficacy and biomarker validation studies of targeted therapeutics, Resistance mechanisms according to targeted therapeutics, 표적 항암제 내성 기전 연구, 표적 항암제의 효과 검증 및 바이오마커 규명

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