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dc.contributor.authorTastekin, Didem
dc.contributor.authorOven, Basak Bala
dc.contributor.authorGÜMÜŞ, MAHMUT
dc.contributor.authorPaksoy, Nail
dc.contributor.authorAy, Seval
dc.contributor.authorAtci, Muhammed Mustafa
dc.contributor.authorArikan, Rukiye
dc.contributor.authorDulgar, Ozgecan
dc.contributor.authorOzyukseler, Deniz Tataroglu
dc.contributor.authorDOĞAN, İzzet
dc.contributor.authorÖZTOSUN, BUĞRA
dc.date.accessioned2022-02-18T09:05:08Z
dc.date.available2022-02-18T09:05:08Z
dc.identifier.citationAy S., Atci M. M. , Arikan R., Dulgar O., Ozyukseler D. T. , Paksoy N., DOĞAN İ., ÖZTOSUN B., Tastekin D., Oven B. B. , et al., "FOLFIRINOX versus gemcitabine plus nab-paclitaxel as the first-line chemotherapy in metastatic pancreatic cancer", JOURNAL OF CHEMOTHERAPY, 2022
dc.identifier.issn1120-009X
dc.identifier.othervv_1032021
dc.identifier.otherav_1713fffe-a3ab-475b-a19c-3ebc3f15798c
dc.identifier.urihttp://hdl.handle.net/20.500.12627/176475
dc.identifier.urihttps://doi.org/10.1080/1120009x.2022.2026125
dc.description.abstractPancreas cancer (PCa) is one of the mortal cancer types with ranking as fourth leading cancer death in both sexes together. FOLFIRINOX (FFX) and Gemcitabine plus nab-paclitaxel (GNP) are approved as first-line metastatic treatment in PCa. The aim of this study was to compare the clinical outcomes, treated with FFX and GNP as first-line metastatic PCa. Medical records of patients diagnosed with metastatic PCa, from January 2010 to December 2020 were analyzed. This study was a retrospective cohort, multi-institution analysis. The focus of the present study was to compare the efficiency of FFX and GNP chemotherapy combinations in the first-line treatment of PCa. Efficacy had been measured by progression-free survival (PFS) and overall survival (OS). 182 patients diagnosed with PCa receiving metastatic first-line treatment were retrospectively analyzed. Patients were divided into two groups one hundred and three (56.6%) patients treated with FFX and seventy-nine (43.4%) patients treated with GNP. Patients in the FFX group were younger and had a better ECOG performance status. Overall response rate (ORR) was 69.9% in FFX and 37.9% in GNP group (p: 0.000). Disease control rate (DCR) was 73.7% in patients treated with FFX and 39.2% in GNP group (p: 0.000). The median PFS was 8.3 months (FFX 9.1 vs. GNP 6.7, HR = 0.25, 95% CI: 0.16-0.38) the median OS was 12.2 months (FFX 14.1 vs. GNP 9.6, HR = 0.48, 95% CI: 0.31-0.72). Guidelines recommend both FFX and GNP regimens as a first-line treatment of metastatic PCa. In clinical routine, it is still unclear which regiment is more effective. The present study showed increased survival parameters with FFX versus GNP with similar toxicity profiles.
dc.language.isoeng
dc.subjectBULAŞICI HASTALIKLAR
dc.subjectİmmünoloji
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectPATOLOJİ
dc.subjectBiyoloji ve Biyokimya
dc.subjectFARMAKOLOJİ VE ECZACILIK
dc.subjectFarmakoloji ve Toksikoloji
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectTemel Tıp Bilimleri
dc.subjectBiyokimya
dc.subjectDahili Tıp Bilimleri
dc.subjectİç Hastalıkları
dc.subjectCerrahi Tıp Bilimleri
dc.subjectPatoloji
dc.subjectOnkoloji
dc.subjectEczacılık
dc.subjectTemel Eczacılık Bilimleri
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.subjectGeneral Immunology and Microbiology
dc.subjectPharmacology
dc.subjectImmunology
dc.subjectGeneral Pharmacology, Toxicology and Pharmaceutics
dc.subjectPharmacology, Toxicology and Pharmaceutics (miscellaneous)
dc.subjectHistology
dc.subjectPathology and Forensic Medicine
dc.subjectPharmacology (medical)
dc.subjectOncology
dc.subjectBiochemistry (medical)
dc.subjectPharmacy
dc.subjectDrug Guides
dc.subjectInfectious Diseases
dc.subjectLife Sciences
dc.subjectHealth Sciences
dc.subjectONKOLOJİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.titleFOLFIRINOX versus gemcitabine plus nab-paclitaxel as the first-line chemotherapy in metastatic pancreatic cancer
dc.typeMakale
dc.relation.journalJOURNAL OF CHEMOTHERAPY
dc.contributor.departmentİstanbul Medeniyet Üniversitesi , ,
dc.contributor.firstauthorID3134309


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