Centre de Recherches en Cancérologie de Toulouse, INSERM UMR-1037, CNRS ERL5294, Université Paul Sabatier.
Département d'hématologie, Institut Universitaire du Cancer de Toulouse-Oncopole.
Ther Drug Monit. 2021 Jun 1;43(3):408-415. doi: 10.1097/FTD.0000000000000813.
High-dose methotrexate is used for treating several types of cancer. However, it is associated with a high risk of acute kidney injury (AKI), especially in patients with high MTX concentrations. Although therapeutic drug monitoring is performed to monitor MTX concentrations, it is unclear what concentration should be considered critical, thus requiring rescue protocols to prevent nephrotoxicity.
Patients treated with high-dose methotrexate for lymphoma or acute lymphoblastic leukemia and those benefited from therapeutic drug monitoring were included. The relationship between MTX concentrations and the presence or absence of AKI was assessed. MTX concentrations were analyzed using a population pharmacokinetic approach. Specific attention was given to morphological covariates because MTX doses are individualized according to body surface area (BSA).
In total, 328 patients and 657 cycles of treatment were analyzed. Higher MTX concentrations were observed in the AKI+ group. For cycle 1, all patients showing an MTX concentration >6 µM at 36 hours or >2 µM at 48 hours after infusion developed nephrotoxicity. The final pharmacokinetic model had 2 compartments and included the effect of age on clearance (CL) and of body weight on peripheral distribution volume. None of the morphological covariates tested on CL led to significant improvement in the model. Higher MTX concentrations were observed in patients with extreme BSA values (≥2 m2) or body mass index (≥25 kg/m2). Patients with AKI who received at least 1 cycle had higher BSA and BMI.
The results from this study provide additional information on the relationship between MTX concentration and nephrotoxicity. Patients with a plasma MTX concentration >6 µM at 36 hours were more likely to manifest AKI. In addition, the results suggest that overweight patients have a high AKI risk and that BSA-based adjustment of MTX dose is not appropriate.
大剂量甲氨蝶呤用于治疗多种类型的癌症。然而,它与急性肾损伤(AKI)的风险很高相关,尤其是在 MTX 浓度高的患者中。尽管进行了治疗药物监测以监测 MTX 浓度,但尚不清楚应将哪个浓度视为临界值,因此需要制定挽救方案以防止肾毒性。
纳入接受大剂量甲氨蝶呤治疗淋巴瘤或急性淋巴细胞白血病且受益于治疗药物监测的患者。评估 MTX 浓度与 AKI 存在或不存在之间的关系。使用群体药代动力学方法分析 MTX 浓度。特别关注形态学协变量,因为 MTX 剂量根据体表面积(BSA)个体化。
共分析了 328 例患者和 657 个疗程。AKI+组观察到更高的 MTX 浓度。对于第 1 个周期,所有在输注后 36 小时 MTX 浓度>6 µM 或 48 小时 MTX 浓度>2 µM 的患者均出现肾毒性。最终的药代动力学模型有 2 个隔室,包括年龄对清除率(CL)的影响和体重对外周分布容积的影响。在 CL 上测试的所有形态学协变量均未导致模型显著改善。在 BSA 值(≥2 m2)或身体质量指数(BMI)(≥25 kg/m2)较大的患者中观察到更高的 MTX 浓度。发生 AKI 的患者至少接受了 1 个周期的治疗,BSA 和 BMI 更高。
本研究结果提供了关于 MTX 浓度与肾毒性之间关系的更多信息。在 36 小时时 MTX 血浆浓度>6 µM 的患者更有可能发生 AKI。此外,结果表明超重患者 AKI 风险较高,基于 BSA 的 MTX 剂量调整并不合适。