Clinical outcomes of FOLFIRINOX in locally advanced pancreatic cancer: A single center experience

dc.contributor.authorLee, Jongchan
dc.contributor.authorLee, Jong-chan
dc.contributor.authorGromski, Mark A.
dc.contributor.authorKim, Hyoung Woo
dc.contributor.authorKim, Jinwon
dc.contributor.authorKim, Jaihwan
dc.contributor.authorHwang, Jin-Hyeok
dc.contributor.departmentMedicine, School of Medicineen_US
dc.date.accessioned2019-07-02T16:58:34Z
dc.date.available2019-07-02T16:58:34Z
dc.date.issued2018-12
dc.description.abstractSystemic chemotherapy or chemoradiotherapy is the initial primary option for patients with locally advanced pancreatic cancer (LAPC). This study analyzed the effect of FOLFIRINOX and assessed the factors influencing conversion to surgical resectability for LAPC.Sixty-four patients with LAPC who received FOLFIRINOX as initial chemotherapy were enrolled retrospectively. Demographic characteristics, tumor status, interval/dosage/cumulative relative dose intensity (cRDI) of FOLFIRINOX, conversion to resection, and clinical outcomes were reviewed and factors associated with conversion to resectability after FOLFIRINOX were analyzed.After administration of FOLFIRINOX (median 9 cycles, 70% of cRDI), the median patient overall survival (OS) was 17.0 months. Fifteen of 64 patients underwent surgery and R0 resection was achieved in 11 patients. During a median follow-up time of 9.4 months after resection, cumulative recurrence rate was 28.5% at 18 months after resection. The estimated median OS was significantly longer for the resected group (>40 months vs 13 months). There were no statistical differences between the resected and non-resected groups in terms of baseline characteristics, tumor status and hematologic adverse effects. The patients who received standard dose of FOLFIRINOX had higher probability of subsequent resection compared with patients who received reduced dose, although cRDIs did not differ between groups.FOLFIRINOX is an active regimen in patients with LAPC, given acceptable resection rates and promising R0 resection rates. Additionally, our data demonstrate it is advantageous for obtaining resectability to administer FOLFIRINOX without dose reduction.en_US
dc.identifier.citationLee, J., Lee, J. C., Gromski, M. A., Kim, H. W., Kim, J., Kim, J., & Hwang, J. H. (). Clinical outcomes of FOLFIRINOX in locally advanced pancreatic cancer: A single center experience. Medicine, 97(50), e13592. doi:10.1097/MD.0000000000013592en_US
dc.identifier.urihttps://hdl.handle.net/1805/19807
dc.language.isoen_USen_US
dc.publisherWolters Kluweren_US
dc.relation.isversionof10.1097/MD.0000000000013592en_US
dc.relation.journalMedicineen_US
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
dc.sourcePMCen_US
dc.subjectDose intensityen_US
dc.subjectFOLFIRINOXen_US
dc.subjectLocally advanced pancreatic canceren_US
dc.subjectR0 resectionen_US
dc.subjectToxicityen_US
dc.titleClinical outcomes of FOLFIRINOX in locally advanced pancreatic cancer: A single center experienceen_US
dc.typeArticleen_US
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