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1.
J Cancer Res Ther ; 19(Supplement): S0, 2023 Apr.
Article in English | MEDLINE | ID: mdl-37147975

ABSTRACT

Aim: It is red cell distribution width (RDW) that has been reported to show an inflammatory response which has been studied recently. The aim of this study is to investigate whether the pre-treatment RDW in patients using first-line vascular endothelial growth factor tyrosine kinase inhibitor (VEGFR TKI) with the diagnosis of metastatic renal cell carcinoma (mRCC) predicts treatment response and is a prognostic factor or not. Methods: About 92 patients diagnosed with mRCC who were being treated with sunitinib or pazopanib in the first line between January 2015 and June 2021 were included in the study. The patients were divided into 2 groups, as being ≤15.3 and >15.3, according to the RDW cut-off value calculated by ROC analysis. Results: The mOS of patients with a RDW of ≤15.3% was 45.0 (30.0-59.9) months, and of 21.3 (10.4-32.2) in those with a RDW of >15.3%. This difference was statistically significant (p < 0.001). In the group of patients with a RDW of ≤15.3, median progression free survival (mPFS) (38.04 [16.3-59.7] months) was found to be significantly higher than those with a RDW of >15.3 (17.1 [11.8-22.5] months) (p = 0.04). In multivariate analysis, RDW level (≤15.3, >15.3), was determined to be prognostic markers (p = 0.022). Conclusion: In mRCC patients, the RDW value measured before first-line VEGFR TKI therapy is an independent prognostic marker.


Subject(s)
Carcinoma, Renal Cell , Kidney Neoplasms , Humans , Carcinoma, Renal Cell/pathology , Vascular Endothelial Growth Factor A , Kidney Neoplasms/pathology , Erythrocyte Indices , Protein Kinase Inhibitors , Prognosis , Angiogenesis Inhibitors/therapeutic use , Receptors, Vascular Endothelial Growth Factor , Erythrocytes , Retrospective Studies
2.
J Oncol Pharm Pract ; 23(5): 392-395, 2017 Jul.
Article in English | MEDLINE | ID: mdl-27105898

ABSTRACT

Bevacizumab is a humanized monoclonal antibody targeting vascular endothelial growth factor, and it has been shown to improve progression-free survival in patients with recurrent glioblastome multiforme when administered as second-line therapy. However, it has been associated with serious and fatal hemorrhagic events. Here, we present a 68-year-old male who developed severe periocular bleeding while on bevacizumab for recurrent temozolamide-resistant glioblastome multiforme.


Subject(s)
Antineoplastic Agents, Immunological/adverse effects , Bevacizumab/adverse effects , Brain Neoplasms/drug therapy , Glioblastoma/drug therapy , Hemorrhage/chemically induced , Neoplasm Recurrence, Local/drug therapy , Aged , Eye , Fatal Outcome , Humans , Male
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