Efficacy and safety of folfiri plus aflibercept in second-line treatment of metastatic colorectal cancer: Real-life data from Turkish oncology group

dc.authorid0000-0001-6397-8207
dc.authorid0000-0003-0411-8818
dc.authorid0000-0002-5823-1704
dc.authorid0000-0001-7182-6641
dc.authorid0000-0002-7197-211X
dc.authorid0000-0002-0499-8918
dc.authorid0000-0002-5328-6554
dc.contributor.authorErol, Cihan
dc.contributor.authorSendur, Mehmet Ali Nahit
dc.contributor.authorBilgetekin, Irem
dc.contributor.authorGarbioglu, Duygu Bayir
dc.contributor.authorHamdard, Jamshid
dc.contributor.authorAkbas, Sinem
dc.contributor.authorHizal, Mutlu
dc.date.accessioned2025-05-10T19:30:57Z
dc.date.issued2022
dc.departmentİstanbul Medeniyet Üniversitesi
dc.description.abstractAims: The addition of aflibercept to the fluorouracil and irinotecan (FOLFIRI) regimen significantly improved clinical outcomes in patients with metastatic colorectal cancer (CRC) previously treated with oxaliplatin. We aimed to investigate the efficacy and safety of second-line FOLFIRI and aflibercept combination in patients with metastatic CRC in real-life experience. Materials and Methods: Four hundred and thirty-three patients who treated with FOLFIRI and aflibercept in the second-line were included in the study. The clinical and pathological features of the patients were recorded retrospectively. Survival (overall and progression-free survival [PFS]), response rates, and safety data were analyzed. Results: The median age was 61. Majority of patients (87.5%) received first-line bevacizumab and 10.1% of patients received anti-epidermal growth factor receptor agents. About 80% of patients had KRAS, 18.6% of patients had NRAS, and 6.4% of patients had BRAF mutations. The median OS was 11.6 months (95% confidence interval [CI], 10.6-12.6) and the median PFS was 6 months (95% CI, 5.5-6.5). About 4.6% of patients had complete response and 30.6% of patients had partial response as best tumor response. Grade 1-2 toxicities were seen in 33.4% of patients, while grade 3-4 toxicities were recorded in 27% of patients. Eight patients (2%) died due to treatment toxicity. Conclusions: Overall and PFS were similar in routine clinical practice compared to phase III pivotal VELOUR trial. However, response rates were found to be higher. It was observed that there were fewer adverse events compared to the VELOUR trial.
dc.identifier.doi10.4103/jcrt.jcrt_1104_21
dc.identifier.endpageS353
dc.identifier.issn0973-1482
dc.identifier.issn1998-4138
dc.identifier.issue9
dc.identifier.pmid36510987
dc.identifier.scopus2-s2.0-85143994465
dc.identifier.scopusqualityQ3
dc.identifier.startpageS347
dc.identifier.urihttps://doi.org/10.4103/jcrt.jcrt_1104_21
dc.identifier.urihttps://hdl.handle.net/20.500.14730/7776
dc.identifier.volume18
dc.identifier.wosWOS:000908442000034
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherWolters Kluwer Medknow Publications
dc.relation.ispartofJournal of Cancer Research and Therapeutics
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WOS_20250302
dc.subjectAflibercept
dc.subjectclinical practice
dc.subjectcolorectal cancer
dc.subjectreal-life data
dc.subjectsecond-line
dc.titleEfficacy and safety of folfiri plus aflibercept in second-line treatment of metastatic colorectal cancer: Real-life data from Turkish oncology group
dc.typeArticle

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