机构地区:[1]中国科学技术大学附属第一医院/安徽省立医院药剂科,安徽合肥230001 [2]中国科学技术大学附属第一医院西区骨科,安徽合肥230031
出 处:《中国医院药学杂志》2022年第19期2040-2045,共6页Chinese Journal of Hospital Pharmacy
基 金:国家自然科学基金项目(编号:82174031);安徽省高等学校省级质量工程教学研究项目(编号:2020jyxm2328)。
摘 要:目的:探讨甲氨蝶呤(MTX)代谢产物7-羟基甲氨蝶呤(7-OHMTX)血药浓度监测在接受大剂量甲氨蝶呤化疗(HD-MTX)的骨肉瘤患者肝功能损伤预测中的应用。方法:采用自建的高效液相色谱法同时测定患者不同时间点MTX及7-OHMTX血药浓度,收集患者相关信息,利用SPSS 22.0软件,考察性别、年龄、体质量、身高、体表面积、MTX剂量以及化疗后不同时间点MTX血药浓度、7-OHMTX血药浓度、7-OHMTX/MTX浓度比值与化疗所致急性肝功能损伤相关性。结果:在不干涉原治疗方案的情况下,有24例患者47例次行大剂量甲氨蝶呤化疗数据纳入分析。单因素分析结果显示,化疗引起的急性中重度肝功能损伤与7-OHMTX_(5 h)、7-OHMTX_(12 h)、7-OHMTX_(24 h)、7-OHMTX_(48 h)、7-OHMTX/MTX_(5 h)、7-OHMTX/MTX_(12 h)、7-OHMTX/MTX_(24 h)、7-OHMTX/MTX_(48 h)这8个指标正相关(P<0.05);经过标准方案解救治疗的骨肉瘤患者,急性肝功能损伤与延迟排泄无显著相关性(P>0.05)。多因素Logistic回归分析显示,仅MTX化疗剂量及7-OHMTX血药浓度分别纳入5,12,24,48 h这4个时间点的回归方程,与中重度肝功能损伤呈正相关(P<0.01),肝功能损伤预测模型受试者工作曲线(ROC)曲线下面积(AUC)分别为0.795,0.861,0.780,0.789。结论:高剂量的MTX、高浓度7-OHMTX是HD-MTX肝功能损伤的独立危险因素,通过测定不同时间点(5,12,24,48 h)7-OHMTX浓度,均可以较好地预测中重度肝功能损伤。在其他指标不变的情况下,MTX剂量每增加1 g·m^(-2),肝功能损伤风险增加2倍左右,7-OHMTX_(5 h)、7-OHMTX_(12 h)、7-OHMTX_(24 h)、7-OHMTX_(48 h)每增加1μmol·L^(-1),肝功能损伤风险分别增加1.070,1.058,1.131,1.866倍。5 h预测模型预警时间最早,12 h预测模型为最佳模型,7-OHMTX血药浓度5,12,24,48 h肝功能损伤预警值分别为20.36,33.37,4.54,0.47μmol·L^(-1)。OBJECTIVE To investigate the application of serum concentration monitoring of 7-hydroxymethotrexate(7-OHMTX),a metabolite of methotrexate(MTX),in predicting liver damage in osteosarcoma patients treated with high-dose methotrexate chemotherapy(HD-MTX).METHODS The serum concentrations of MTX and 7-OHMTX at different timepoints were determined simultaneously by a self-built high performance liquid chromatography method.The relevant information of patients was collected,and the correlations between gender,age,weight,height,body surface area,MTX dose,serum concentration of MTX,serum concentration of 7-OHMTX,7-OHMTX/MTX ratio and acute liver damage induced by HD-MTX were analyzed by SPSS 22.0 software.RESULTS The data from 47 cases of 24 patients who received HD-MTX were analyzed.Univariate analysis showed that acute moderate to severe liver damage caused by chemotherapy was positively correlated with 7-OHMTX_(5 h),7-OHMTX_(12 h),7-OHMTX_(24 h),7-OHMTX_(48 h),7-OHMTX/MTX_(5 h),7-OHMTX/MTX_(12 h),7-OHMTX/MTX_(24 h) and 7-OHMTX/MTX_(48 h)(P<0.05).There was no significant correlation between acute liver damage and delayed excretion in osteosarcoma patients rescued by regular treatment(P>0.05).Multivariate logistic regression analysis showed that only MTX dose and 7-OHMTX serum concentration were included in the regression equations at the time of 5,12,24 and 48 h,respectively,and were positively correlated with moderate to severe liver damage(P<0.01).The areas under receiver operator characteristic curve(ROC)of the liver damage prediction model were 0.795,0.861,0.780 and 0.789,respectively.CONCLUSION High-dose MTX and high-concentration 7-OHMTX are independent risk factors for liver damage caused by HD-MTX.Liver damage can be well predicted by measuring the concentration of 7-OHMTX at different time(5,12,24,48 h after chemotherapy).The risk of liver damage increases about 2 times for each increase of 1 g·m^(-2)MTX dose.The risk of liver damage increases 1.070,1.058,1.131 and 1.866 times for each increase of 1μmol·L^(-
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...