Predictive value of De Ritis ratio in metastatic renal cell carcinoma treated with tyrosine-kinase inhibitors
Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu časopisecké články
PubMed
33649869
PubMed Central
PMC8405478
DOI
10.1007/s00345-021-03628-2
PII: 10.1007/s00345-021-03628-2
Knihovny.cz E-zdroje
- Klíčová slova
- De ritis ratio, Metastatic renal cell carcinoma, Prognostic marker, Tumor markers, Tyrosine-kinase inhibitors,
- MeSH
- alanintransaminasa analýza krev MeSH
- analýza přežití MeSH
- aspartátaminotransferasy analýza krev MeSH
- cytoredukční chirurgie metody MeSH
- indazoly * aplikace a dávkování škodlivé účinky MeSH
- inhibitory proteinkinas aplikace a dávkování škodlivé účinky MeSH
- karcinom z renálních buněk * krev farmakoterapie patologie chirurgie MeSH
- Karnofského skóre MeSH
- lidé středního věku MeSH
- lidé MeSH
- nádory ledvin * krev farmakoterapie patologie chirurgie MeSH
- nefrektomie metody MeSH
- prediktivní hodnota testů MeSH
- prognóza MeSH
- pyrimidiny * aplikace a dávkování škodlivé účinky MeSH
- sorafenib aplikace a dávkování škodlivé účinky MeSH
- staging nádorů MeSH
- stupeň nádoru MeSH
- sulfonamidy * aplikace a dávkování škodlivé účinky MeSH
- sunitinib * aplikace a dávkování škodlivé účinky MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- alanintransaminasa MeSH
- aspartátaminotransferasy MeSH
- indazoly * MeSH
- inhibitory proteinkinas MeSH
- pazopanib MeSH Prohlížeč
- pyrimidiny * MeSH
- sorafenib MeSH
- sulfonamidy * MeSH
- sunitinib * MeSH
BACKGROUND: Predictive markers can help tailor treatment to the individual in metastatic renal cell carcinoma (mRCC). De Ritis ratio (DRR) is associated with oncologic outcomes in various solid tumors. OBJECTIVE: To assess the value of DRR in prognosticating survival in mRCC patients treated with tyrosine-kinase inhibitors (TKI). METHODS: Overall, 220 mRCC patients treated with TKI first-line therapy were analyzed. An optimal cut-off point for DRR was determined with Youden's J. We used multiple strata for DRR, performed descriptive, Kaplan-Meier and multivariable Cox-regression analyses to assess associations of DRR with progression-free (PFS) and overall survival (OS). RESULTS: Patients above the optimal cut-off point for DRR of ≥ 1.58 had fewer liver metastases (p = 0.01). There was no difference in PFS (p > 0.05) between DRR groups. DRR above the median of 1.08 (HR 1.42; p = 0.03), DRR ≥ 1.1(HR 1.44; p = 0.02), ≥ 1.8 (HR 1.56; p = 0.03), ≥ 1.9 (HR 1.59; p = 0.02) and ≥ 2.0 (HR 1.63; p = 0.047) were associated with worse OS. These associations did not remain after multivariable adjustment. In the intermediate MSKCC group, DRR was associated with inferior OS at cut-offs ≥ 1.0 (HR 1.78; p = 0.02), ≥ 1.1 (HR 1.81; p = 0.01) and above median (HR 1.88; p = 0.007) in multivariable analyses. In patients with clear-cell histology, DRR above median (HR 1.54; p = 0.029) and DRR ≥ 1.1 (HR 1.53; p = 0.029) were associated with OS in multivariable analyses. CONCLUSION: There was no independent association between DRR and survival of mRCC patients treated with TKI in the entire cohort. However, OS of patients with intermediate risk and clear-cell histology were affected by DRR. DRR could be used for tailored decision-making in these subgroups.
Department of Urology 2nd Faculty of Medicine Charles University Prague Czech Republic
Department of Urology Jikei University School of Medicine Tokyo Japan
Department of Urology Medical University of Vienna Vienna Austria
Department of Urology Tabriz University of Medical Sciences Tabriz Iran
Department of Urology University of Texas Southwestern Medical Center Dallas TX USA
Department of Urology Weill Cornell Medical School New York NY USA
Institute for Urology and Reproductive Health Sechenov University Moscow Russia
Karl Landsteiner Institute of Urology and Andrology Vienna Austria
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