Practicality of STAT3 Gene Polymorphisms and Sorafenib Trough Concentration as Biomarkers for Sorafenib-Induced Hand-Foot Skin Reaction in Hepatocellular Carcinoma

IF 2.1 4区 医学 Q3 PHARMACOLOGY & PHARMACY Journal of Clinical Pharmacy and Therapeutics Pub Date : 2023-08-19 DOI:10.1155/2023/6682459
Hirokazu Takatsuka, Takato Sugawara, M. Uchida, S. Yamazaki, Takaaki Suzuki, Naoya Kanogawa, S. Ogasawara, Y. Shiko, Yohei Kawasaki, Naoya Kato, I. Ishii
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Abstract

Introduction. The aim of this study was to evaluate the practicality of the signal transducer and activator of transcription (STAT) 3 polymorphisms as a predictive biomarker and sorafenib trough concentration as a monitoring biomarker for hand-foot skin reaction (HFSR) in patients with hepatocellular carcinoma (HCC). Methods. In total, 43 Japanese HCC patients were included. Sorafenib concentrations were measured, if possible, on days 8, 29, 35, and 57. The sorafenib concentration on day 8 (Cday8) was used for the analysis of HFSR occurring up to day 29. The median concentration for each patient (Cmedian) was used for HFSR occurring up to day 57 (study period). The STAT3 single nucleotide polymorphism (SNP) rs4796793 was determined using cell-free DNA extracted from plasma. Result. The Cday8 tended to be higher in the HFSR onset or grade ≥ 2 HFSR severity group than in the non-HFSR or grade ≤ 1 HFSR severity group. The Cmedian was significantly higher in the HFSR onset or grade ≥ 2 group than in the non-HFSR or grade ≤ 1 HFSR group. The Cmedian thresholds for predicting HFSR onset and severity were 3.62 μg/mL and 6.10 μg/mL, respectively. There was no association between STAT3 rs4796793 and HFSR onset or severity. In multivariate analysis, Cmedian values ≥ 3.62 μg/mL and >6.10 μg/mL were associated with the increased risk of HFSR onset (odds ratio: 16.6, p  < 0.01) and severity (odds ratio: 15.7, p  < 0.01), respectively. Conclusion. Monitoring of the sorafenib trough concentration may be practical for avoiding HFSR.
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STAT3基因多态性和索拉非尼谷浓度作为索拉非尼诱导肝癌手足皮肤反应生物标志物的实用性
介绍本研究的目的是评估信号转导子和转录激活子(STAT)3多态性作为预测生物标志物和索拉非尼谷浓度作为肝细胞癌(HCC)患者手足皮肤反应(HFSR)监测生物标志物的实用性。方法。总共包括43名日本HCC患者。如果可能的话,在第8、29、35和57天测量索拉非尼的浓度。索拉非尼在第8天的浓度(Cday8)用于分析直到第29天发生的HFSR。每位患者的中位浓度(Cmedian)用于第57天(研究期)发生的HFSR。使用从血浆中提取的无细胞DNA测定STAT3单核苷酸多态性(SNP)rs4796793。后果Cday8在HFSR发作或分级中往往更高 ≥ 2 HFSR严重程度组高于非HFSR或级别 ≤ 1 HFSR严重程度组。Cmedian在HFSR发作或分级中显著较高 ≥ 2组比非HFSR或年级 ≤ 1 HFSR组。预测HFSR发作和严重程度的Cmedian阈值为3.62 μg/mL和6.10 μg/mL。STAT3 rs4796793与HFSR的发作或严重程度之间没有关联。在多变量分析中,Cmedian值 ≥ 3.62 μg/mL且>6.10 μg/mL与HFSR发病风险增加相关(比值比:16.6,p < 0.01)和严重程度(比值比:15.7,p < 0.01)。结论监测索拉非尼的谷浓度对于避免HFSR可能是可行的。
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来源期刊
CiteScore
4.10
自引率
5.00%
发文量
226
审稿时长
6 months
期刊介绍: The Journal of Clinical Pharmacy and Therapeutics provides a forum for clinicians, pharmacists and pharmacologists to explore and report on issues of common interest. Reports and commentaries on current issues in medical and pharmaceutical practice are encouraged. Papers on evidence-based clinical practice and multidisciplinary collaborative work are particularly welcome. Regular sections in the journal include: editorials, commentaries, reviews (including systematic overviews and meta-analyses), original research and reports, and book reviews. Its scope embraces all aspects of clinical drug development and therapeutics, including: Rational therapeutics Evidence-based practice Safety, cost-effectiveness and clinical efficacy of drugs Drug interactions Clinical impact of drug formulations Pharmacogenetics Personalised, stratified and translational medicine Clinical pharmacokinetics.
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