Tyrosine kinase inhibitors in the treatment of metastatic renal cell cancer patients with early cytokine intolerance: TURCOS, a Turkish national, prospective observational study

dc.contributor.authorBenekli, Mustafa
dc.contributor.authorGumus, Mahmut
dc.contributor.authorOzkan, Metin
dc.contributor.authorDane, Faysal
dc.contributor.authorElkiran, Emin T.
dc.contributor.authorCicin, Irfan
dc.contributor.authorSevinc, Alper
dc.contributor.authorAliustaoglu, Mehmet
dc.contributor.authorIsikdogan, Abdurrahman
dc.contributor.authorMeydan, Nezih
dc.contributor.authorOksuzoglu, Berna
dc.contributor.authorOzyilkan, Ozgur
dc.contributor.authorArtac, Mehmet
dc.contributor.authorOzdemir, Feyyaz
dc.contributor.authorKilickap, Sadettin
dc.contributor.orcID0000-0001-8825-4918en_US
dc.contributor.pubmedID33050804en_US
dc.contributor.researcherIDAAD-2817-2021en_US
dc.date.accessioned2021-04-28T06:09:10Z
dc.date.available2021-04-28T06:09:10Z
dc.date.issued2020
dc.description.abstractObjective Cytokines have been the mainstay of treatment in metastatic renal cell cancer (mRCC) for decades before the introduction of tyrosine kinase inhibitors (TKIs), which dramatically changed the therapeutic landscape in these patients. This observational study was designed to evaluate use of TKIs in the treatment of cytokine-intolerant mRCC patients. Methods A total of 151 cytokine-intolerant mRCC patients who were treated with TKIs (sunitinib, pazopanib and sorafenib) were enrolled in this prospective, non-interventional, multi-center observational study at 16 oncology centers across Turkey. Mean (SD) age was 61.3 (11.1) years and 74.8% were males. Data on duration of TKI treatment was the primary outcome measure. Additionally, overall response rate (ORR), progression free survival (PFS), overall survival (OS) and safety data were recorded. Results Median duration of treatment was 8.2 months at a median follow up of 17.9 months. ORR and disease control rate were 12.5% and 70.8%, respectively. Median PFS and OS were 7.5 months (95%CI: 6.4-10.4) and 27.3 months (95%CI: 17.6-27.3) with no significant difference among three TKI agents in terms of treatment duration, ORR, PFS and OS. The most common adverse events excluding progression-which was the protocol requirement were diarrhea (13.6%), asthenia (13.6%) and hand-foot syndrome (12.6%). Dose modifications were required in 30.5% of the patients and 15% discontinued TKIs because of toxicity. Conclusions Our findings confirm the efficacy and safety profile of TKIs in the first-line treatment of mRCC patients intolerant to cytokine treatment. There was no significant difference among three TKI agents in terms of treatment duration, ORR, PFS and OS.en_US
dc.identifier.issn1078-1552en_US
dc.identifier.scopus2-s2.0-85092561865en_US
dc.identifier.urihttp://hdl.handle.net/11727/5777
dc.identifier.wos000578499200001en_US
dc.language.isoengen_US
dc.relation.isversionof10.1177/1078155220963535en_US
dc.relation.journalJOURNAL OF ONCOLOGY PHARMACY PRACTICEen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergien_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectMetastatic renal cell carcinomaen_US
dc.subjecttyrosine kinase inhibitorsen_US
dc.subjectcytokine intoleranceen_US
dc.subjectprogression-free survivalen_US
dc.subjectoverall survivalen_US
dc.subjectsafetyen_US
dc.titleTyrosine kinase inhibitors in the treatment of metastatic renal cell cancer patients with early cytokine intolerance: TURCOS, a Turkish national, prospective observational studyen_US
dc.typearticleen_US

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