Department of Medical Oncology, The Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo 135-8550, Japan.
Department of Clinical Cancer Genomics, Hokkaido University Graduate School of Medicine, Sapporo 060-0814, Japan.
Endocr J. 2024 Apr 30;71(4):363-371. doi: 10.1507/endocrj.EJ23-0378. Epub 2024 Jan 31.
Proteinuria has been described as a major on-target adverse event of lenvatinib, although its long-term impact on renal function and clinical outcomes remains unclear. We conducted a retrospective observational study to assess renal function and prognosis in patients with radioiodine-refractory differentiated thyroid cancer (RR-DTC) receiving lenvatinib. Overall, 70 patients with RR-DTC treated with lenvatinib were enrolled. When proteinuria was observed, the dose and schedule of lenvatinib were adjusted to achieve a urine protein-to-creatinine ratio (UPCR) of less than 3.5 g/gCre according to the study protocols of recent pivotal trials. In total, 50 (71%) and 25 (36%) patients presented with any-grade and grade 3 proteinuria, respectively. Multivariate analysis revealed that age [>65; odds ratio (OR) 8.24, 95% confidence interval (CI) 1.74-39.00, p < 0.01], history of diabetes mellitus (OR 7.79, 95% CI 1.31-46.20, p = 0.02), and hypertension (OR 4.07, 95% CI 1.22-13.60, p = 0.02) were significantly associated with the development of grade 3 proteinuria. Overall, the median estimating glomerular filtration rate (eGFR) gradually decreased every 3 months during treatment. However, no significant deterioration in eGFR was observed in patients with grade 3 proteinuria compared with patients with grades 0-2 proteinuria until 48 months. Patients who developed proteinuria had better survival outcomes than those without proteinuria. In conclusion, the proteinuria grade was not significantly associated with decreased eGFR under UPCR monitoring in our study. Therefore, lenvatinib can carefully be continued targeting UPCR of less than 3.5 g/gCre.
蛋白尿已被描述为仑伐替尼的主要靶器官不良反应,但它对肾功能和临床结局的长期影响尚不清楚。我们进行了一项回顾性观察性研究,以评估接受仑伐替尼治疗的碘难治性分化型甲状腺癌(RR-DTC)患者的肾功能和预后。共有 70 名 RR-DTC 患者接受仑伐替尼治疗。当观察到蛋白尿时,根据最近的关键试验研究方案调整仑伐替尼的剂量和方案,以使尿蛋白与肌酐比值(UPCR)小于 3.5 g/gCre。总共有 50 名(71%)和 25 名(36%)患者分别出现任何级别和 3 级蛋白尿。多变量分析显示,年龄(>65 岁;优势比 [OR] 8.24,95%置信区间 [CI] 1.74-39.00,p < 0.01)、糖尿病史(OR 7.79,95% CI 1.31-46.20,p = 0.02)和高血压(OR 4.07,95% CI 1.22-13.60,p = 0.02)与 3 级蛋白尿的发生显著相关。总体而言,在治疗期间,每 3 个月估算肾小球滤过率(eGFR)中位数逐渐下降。然而,与 0-2 级蛋白尿患者相比,3 级蛋白尿患者在 48 个月内 eGFR 没有明显恶化。发生蛋白尿的患者比没有蛋白尿的患者生存结局更好。总之,在本研究中,根据 UPCR 监测,蛋白尿分级与 eGFR 下降无显著相关性。因此,仑伐替尼可以在靶向 UPCR 小于 3.5 g/gCre 的情况下谨慎继续使用。