van Doorn Leni, Crombag Marie-Rose B S, Rier Hánah N, van Vugt Jeroen L A, van Kesteren Charlotte, Bins Sander, Mathijssen Ron H J, Levin Mark-David, Koolen Stijn L W
Department of Medical Oncology, Erasmus MC Cancer Institute, 3015 GD Rotterdam, The Netherlands.
Department of Hospital Pharmacy, Erasmus MC, University Medical Center Rotterdam, 3015 GD Rotterdam, The Netherlands.
Pharmaceuticals (Basel). 2021 Jan 9;14(1):47. doi: 10.3390/ph14010047.
Changes in body composition are associated with chemotherapy-related toxicities and effectiveness of treatment. It is hypothesized that the pharmacokinetics (PK) of chemotherapeutics may depend on body composition. The effects of body composition on the variability of paclitaxel PK were studied in patients with esophageal cancer. Skeletal muscle index (SMI), visceral adipose tissue (VAT), and skeletal muscle density (SMD) were measured at the third lumbar vertebra on computed tomography (CT) scans performed before treatment. Paclitaxel PK data were collected from a prospective study performed between May 2004 and January 2014. Non-linear mixed-effects modeling was used to fit paclitaxel PK profiles and evaluate the covariates body surface area (BSA), SMI, VAT, and SMD using a significance threshold of < 0.001. Paclitaxel was administered to 184 patients in a dose range of 50 to 175 mg/m. Median BSA was 1.98 m (range of 1.4 to 2.8 m). SMI, VAT, and SMD were not superior to BSA in predicting paclitaxel PK. The additive value of SMI, VAT, and SMD to BSA was also negligible. We did not find evidence that paclitaxel dosing could be further optimized by correcting for SMI, VAT, or SMD.
身体成分的变化与化疗相关毒性及治疗效果有关。据推测,化疗药物的药代动力学(PK)可能取决于身体成分。本研究在食管癌患者中探讨了身体成分对紫杉醇PK变异性的影响。在治疗前进行的计算机断层扫描(CT)上,于第三腰椎测量骨骼肌指数(SMI)、内脏脂肪组织(VAT)和骨骼肌密度(SMD)。紫杉醇PK数据来自于2004年5月至2014年1月进行的一项前瞻性研究。采用非线性混合效应模型拟合紫杉醇PK曲线,并以<0.001的显著性阈值评估协变量体表面积(BSA)、SMI、VAT和SMD。184例患者接受了剂量范围为50至175mg/m的紫杉醇治疗。中位BSA为1.98m²(范围为1.4至2.8m²)。在预测紫杉醇PK方面,SMI、VAT和SMD并不优于BSA。SMI、VAT和SMD对BSA的附加值也可忽略不计。我们没有发现证据表明通过校正SMI、VAT或SMD可以进一步优化紫杉醇给药剂量。