de Rouw Nikki, Otten Leila-Sophie, Kicken Mart P, Piet Berber, Biesma Bonne, van Veggel Bianca, Steendam Christi M J, van den Borne Ben, Hendriks Lizza E L, Croes Sander, Dingemans Anne-Marie C, Dumoulin Daphne W, Mathijssen Ron H J, Burgers Jacobus A, Huitema Alwin D R, Derijks Hieronymus J, Deenen Maarten J, van den Heuvel Michel M, Ter Heine Rob
Department of Clinical Pharmacy, Amphia Hospital, Breda, The Netherlands.
Department of Pharmacy, Pharmacology & Toxicology, Research Institute for Medical Innovation, Radboudumc, Nijmegen, The Netherlands.
Clin Pharmacol Ther. 2025 Sep;118(3):715-722. doi: 10.1002/cpt.3735. Epub 2025 May 27.
Pemetrexed is a cornerstone in chemo(immunotherapy) of non-small cell lung cancer and mesothelioma; however, it is contraindicated in patients with renal impairment due to severe toxicity concerns. Therefore, a large proportion of patients is withheld from effective chemo(immunotherapy). We performed an intra-patient 3 + 3 dose escalation renal impairment study (eGFR < 45 mL/min). The pemetrexed dose was calculated based on renal function to reach a target AUC, and patients received oral folinic acid prophylaxis 45 mg four times daily on Days 2-15 of each cycle. Endpoints included safety (incidence of hematological and non-hematological toxicity, treatment delays) and pharmacokinetics in line with regulatory guidance for renal impairment trials. Six patients with an estimated glomerular filtration rate (eGFR) between 26 and 41 mL/min were included. All patients were successfully escalated to the full dose. Adverse event patterns and pharmacokinetics were comparable to those in patients with normal renal function. Grade I/II anemia occurred in five patients (already present at baseline). One occurrence of grade IV neutropenia was observed, which resolved without intervention. Moreover, in three patients, a 1-week treatment delay occurred. Treatment resulted in a response in four patients (n = 1 complete response, n = 2 partial response, n = 1 stable disease). Pemetrexed can be safely administered in patients with impaired renal function when the dose is calculated based on renal function and folinic acid prophylaxis is administered, thereby enabling an effective treatment modality for patients that, thus far, could not be treated.
培美曲塞是非小细胞肺癌和间皮瘤化疗(免疫治疗)的基石;然而,由于严重的毒性问题,肾功能不全患者禁用。因此,很大一部分患者无法接受有效的化疗(免疫治疗)。我们进行了一项针对肾功能不全患者的3+3剂量递增研究(估算肾小球滤过率[eGFR]<45 mL/min)。培美曲塞剂量根据肾功能计算以达到目标曲线下面积(AUC),患者在每个周期的第2 - 15天每天口服4次45 mg亚叶酸进行预防。终点指标包括安全性(血液学和非血液学毒性发生率、治疗延迟情况)以及符合肾功能不全试验监管指南的药代动力学。纳入了6例估算肾小球滤过率(eGFR)在26至41 mL/min之间的患者。所有患者均成功递增至全剂量。不良事件模式和药代动力学与肾功能正常的患者相当。5例患者出现I/II级贫血(基线时已存在)。观察到1例IV级中性粒细胞减少,未经干预自行缓解。此外,3例患者出现1周的治疗延迟。治疗使4例患者产生反应(n = 1例完全缓解,n = 2例部分缓解,n = 1例疾病稳定)。当根据肾功能计算培美曲塞剂量并给予亚叶酸预防时,培美曲塞可安全用于肾功能不全患者,从而为迄今无法接受治疗的患者提供一种有效的治疗方式。