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Influence of genetic polymorphisms in vascular endothelial-related genes on the clinical outcome of axitinib in patients with metastatic renal cell carcinoma.

AbstractOBJECTIVE:
Axitinib is an oral multi-target tyrosine kinase inhibitor used for the treatment of renal cell carcinoma (RCC). Because of the severe adverse events (AEs) associated with axitinib, patients often need dose reductions or discontinue its use, highlighting the need for effective biomarkers to assess efficacy and/or AEs. The aim of this study was to investigate the relationship between single nucleotide polymorphisms (SNPs) in genes involved in the pharmacodynamic action of axitinib and clinical prognosis and AEs in metastatic RCC (mRCC) patients.
METHODS:
This study included 80 mRCC patients treated with first-, second-, or third-line axitinib (5 mg orally twice daily). Clinical parameters and genetic polymorphisms were examined in 75 cases (53 males and 22 females). We assessed three SNPs in each of three candidate genes namely, angiotensin-converting enzyme (ACE), nitric oxide synthase 3 (NOS3), and angiotensin II receptor type 1 (AT1R), all of which are involved in axitinib effects on vascular endothelial function.
RESULTS:
Axitinib-treated patients carrying the ACE deletion allele suffered more frequently from hand-foot syndrome and a deterioration in kidney function (p  = .045 and p =  0.005, respectively) whereas those carrying the NOS3 G allele suffered more frequently from proteinuria and multiple AEs (p  = .025 and p =  0.036, respectively).
CONCLUSIONS:
Our study found that the ACE deletion allele and the NOS3 G allele are associated with increased AEs.
AuthorsKazuyuki Numakura, Ryoma Igarashi, Makoto Takahashi, Taketoshi Nara, Sohei Kanda, Mitsuru Saito, Shintaro Narita, Takamitsu Inoue, Takenori Niioka, Masatomo Miura, Tomonori Habuchi
JournalCancer biology & therapy (Cancer Biol Ther) Vol. 25 Issue 1 Pg. 2312602 (12 31 2024) ISSN: 1555-8576 [Electronic] United States
PMID38327067 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Axitinib
  • Indazoles
  • Antineoplastic Agents
Topics
  • Humans
  • Male
  • Female
  • Axitinib (adverse effects)
  • Carcinoma, Renal Cell (drug therapy, genetics)
  • Kidney Neoplasms (drug therapy, genetics, pathology)
  • Indazoles (adverse effects)
  • Polymorphism, Single Nucleotide
  • Antineoplastic Agents (therapeutic use)

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