Characteristics and clinical influence factors of arsenic species in plasma and their role of arsenic species as predictors for clinical efficacy in acute promyelocytic leukemia (APL) patients treated with arsenic trioxide.
Meihua GuoJin ZhouShengjin FanLimin LiHongzhu ChenLiwang LinQilei ZhaoXinyu WangWensheng LiuZhiqiang WuXin HaiPublished in: Expert review of clinical pharmacology (2021)
Background: Arsenic trioxide (ATO) is successfully applied to treat acute promyelocytic leukemia (APL). Arsenic species levels in blood are critical to reveal metabolic mechanism and relationship between arsenic species and clinical response. Characteristics and influence factors of arsenic species in APL patients have not been studied.Methods: 305 plasma samples from APL patients treated with ATO were analyzed using HPLC-HG-AFS. Trough concentration (Ctrough), distribution, methylation levels of arsenic species were evaluated. The influence factors on arsenic species levels of plasma and association between arsenic concentrations and clinical efficacy were explored.Results: Ctrough of arsenic in effective treatment groups provide basis for defining the target range of arsenic plasma concentrations in APL patients treated with ATO. Distribution trends: DMAV > AsIII, MMAV> AsV (p < 0.0001) for continuous slow-rate (CS) infusion and DMAV > MMAV > AsIII > AsV (p < 0.0001) for conventional infusion. Infusion methods and combined medication may affect arsenic metabolism. There was a weak correlation between ATO dose and plasma Ctrough of arsenic species. Ctrough of plasma arsenic species had predictive value for treatment efficacy.Conclusion: Arsenic concentration monitoring in APL patients treated with ATO is required. These findings are critical to optimize treatment outcomes of ATO therapy.
Keyphrases
- drinking water
- heavy metals
- healthcare
- end stage renal disease
- acute myeloid leukemia
- chronic kidney disease
- low dose
- stem cells
- intensive care unit
- mesenchymal stem cells
- high resolution
- ejection fraction
- hepatitis b virus
- genetic diversity
- single cell
- cell therapy
- prognostic factors
- tandem mass spectrometry
- peritoneal dialysis
- replacement therapy
- single molecule