de Rouw N, Boosman R J, van de Bruinhorst H, Biesma B, van den Heuvel M M, Burger D M, Hilbrands L B, Ter Heine R, Derijks H J
Radboud University Medical Center, Radboud Institute for Health Sciences, Department of Pharmacy, Nijmegen, The Netherlands; Jeroen Bosch Hospital, Department of Pharmacy, 's-Hertogenbosch, The Netherlands.
Antoni van Leeuwenhoek - The Netherlands Cancer Institute, Department of Pharmacy & Pharmacology, Amsterdam, The Netherlands.
Lung Cancer. 2020 Aug;146:30-35. doi: 10.1016/j.lungcan.2020.05.022. Epub 2020 May 21.
Pemetrexed is a pharmacotherapeutic cornerstone in the treatment of non-small cell lung cancer. As it is primarily eliminated by renal excretion, adequate renal function is essential to prevent toxic exposure. There is growing evidence for the nephrotoxic potential of pemetrexed, which even becomes a greater issue now combined immuno-chemotherapy prolongs survival. Therefore, the aim of this study was to describe the incidence of nephrotoxicity and related treatment consequences during pemetrexed-based treatment.
A retrospective cohort study was conducted in the Jeroen Bosch Hospital, Den Bosch, the Netherlands. All patients that received at least 1 cycle of pemetrexed based therapy were included in the dataset. The primary outcome was defined as a ≥25 % reduction in eGFR. Additionally, the treatment consequences of decreased renal function were assessed. Logistic regression was used to identify risk factors for nephrotoxicity during treatment with pemetrexed.
Of the 359 patients included in this analysis, 21 % patients had a clinically relevant decline in renal function after treatment and 8.1 % of patients discontinued treatment due to nephrotoxicity. Cumulative dose (≥10 cycles of pemetrexed based therapy) was identified as a risk factor for the primary outcome measure (adjusted OR 5.66 (CI 1.73-18.54)).
This study shows that patients on pemetrexed-based treatment are at risk of developing renal impairment. Risk significantly increases with prolonged treatment. Renal impairment is expected to become an even greater issue now that pemetrexed-based immuno-chemotherapy results in longer survival and thus longer treatment duration.
培美曲塞是治疗非小细胞肺癌的药物治疗基石。由于其主要通过肾脏排泄消除,因此足够的肾功能对于预防毒性暴露至关重要。越来越多的证据表明培美曲塞具有肾毒性潜力,现在联合免疫化疗延长生存期,这一问题变得更加突出。因此,本研究的目的是描述基于培美曲塞治疗期间肾毒性的发生率及相关治疗后果。
在荷兰登博斯的耶罗恩·博世医院进行了一项回顾性队列研究。所有接受至少1个周期培美曲塞基础治疗的患者均纳入数据集。主要结局定义为估算肾小球滤过率(eGFR)降低≥25%。此外,评估了肾功能下降的治疗后果。采用逻辑回归分析确定培美曲塞治疗期间肾毒性的危险因素。
本分析纳入的359例患者中,21%的患者治疗后肾功能出现临床相关下降,8.1%的患者因肾毒性而停止治疗。累积剂量(基于培美曲塞的治疗≥10个周期)被确定为主要结局指标的危险因素(调整后的比值比为5.66(95%置信区间为1.73 - 18.54))。
本研究表明,接受培美曲塞基础治疗的患者有发生肾功能损害的风险。随着治疗时间延长,风险显著增加。鉴于基于培美曲塞的免疫化疗可延长生存期,从而延长治疗时间,肾功能损害预计将成为一个更严重的问题。