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甲氨蝶呤曲线下面积是原发性中枢神经系统淋巴瘤患者的重要预后预测指标:来自 IELSG no. 20 试验的药代动力学-药效学分析。

Methotrexate area under the curve is an important outcome predictor in patients with primary CNS lymphoma: A pharmacokinetic-pharmacodynamic analysis from the IELSG no. 20 trial.

机构信息

Department of Oncology and Hematology, Cantonal Hospital, Switzerland.

出版信息

Br J Cancer. 2010 Feb 16;102(4):673-7. doi: 10.1038/sj.bjc.6605559. Epub 2010 Feb 2.

Abstract

BACKGROUND

This analysis was initiated to define the predictive value of the area under the curve of high-dose methotrexate (AUC(HD-MTX)) in patients with primary central nervous system lymphoma (PCNSL).

PATIENTS AND METHODS

We included 55 patients with PCNSL and available pharmacokinetic (PK) data from the International Extranodal Lymphoma Study Group (IELSG) no. 20 trial, randomised to HD-MTX (n=30) or HD-MTX and high-dose cytarabine (HD-AraC) (n=25). Individual AUC(HD-MTX) from population PK analysis was tested on drug toxicity and clinical outcome using multivariate logistic regression analysis and Cox hazards modelling.

RESULTS

AUC(HD-MTX), the IELSG score and treatment group were significant predictors for treatment response (complete or partial) in the adjusted model. The AUC(HD-MTX) did not predict toxicity, with the exception of liver toxicity and neutropaenia. A high AUC(HD-MTX) was associated with better event-free survival (EFS) (P=0.01) and overall survival (OAS) (P=0.02). Both the AUC(HD-MTX) and the IELSG score were significant predictors of EFS and OAS in the adjusted model, with a hazard ratio of 0.82 and 0.73, respectively, per 100 micromol l(-1) h(-1) increase in AUC(HD-MTX).

CONCLUSIONS

Individualised dosing of HD-MTX might have the potential to improve clinical outcome in patients with PCNSL, even when administered concurrently with HD-AraC. In the future, this could be carried out by using first-cycle PK modelling with determination of potential dose adaptations for later cycles using Bayesian analysis.

摘要

背景

本分析旨在定义高剂量甲氨蝶呤(HD-MTX)曲线下面积(AUC(HD-MTX))在原发性中枢神经系统淋巴瘤(PCNSL)患者中的预测价值。

患者和方法

我们纳入了 55 例 PCNSL 患者,这些患者来自国际结外淋巴瘤研究组(IELSG)第 20 项试验,且具有可供分析的药代动力学(PK)数据,这些患者被随机分配到 HD-MTX(n=30)或 HD-MTX 和高剂量阿糖胞苷(HD-AraC)组(n=25)。采用多变量逻辑回归分析和 Cox 风险模型,从群体 PK 分析中检测个体 AUC(HD-MTX)与药物毒性和临床结局的关系。

结果

AUC(HD-MTX)、IELSG 评分和治疗组是调整模型中治疗反应(完全或部分)的显著预测因素。AUC(HD-MTX) 除了与肝毒性和中性粒细胞减少有关外,不能预测毒性。高 AUC(HD-MTX)与无事件生存(EFS)(P=0.01)和总生存(OAS)(P=0.02)相关。AUC(HD-MTX) 和 IELSG 评分在调整模型中都是 EFS 和 OAS 的显著预测因素,AUC(HD-MTX) 每增加 100 μmol l(-1) h(-1),EFS 和 OAS 的风险比分别为 0.82 和 0.73。

结论

即使与 HD-AraC 同时给药,对 PCNSL 患者进行个体化 HD-MTX 给药也可能具有改善临床结局的潜力。未来,可以通过首次周期 PK 建模,并使用贝叶斯分析确定后续周期的潜在剂量调整来实现这一点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9401/2837574/94fcc7ebc4fe/6605559f1.jpg

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