Sleijfer D T, Smit E F, Meijer S, Mulder N H, Postmus P E
Department of Internal Medicine, University Hospital, Groningen, The Netherlands.
Br J Cancer. 1989 Jul;60(1):116-20. doi: 10.1038/bjc.1989.233.
Carboplatin, a cisplatinum analogue, has no reported nephrotoxicity in phase I/II studies, assessed by creatinine clearance. We prospectively determined renal function in 10 untreated lung cancer patients with normal baseline renal function, treated with carboplatin 400 mg m-2 day 1 and vincristine 2 mg day 1 and 8 every 4 weeks (max. five cycles) by means of clearance studies with 125I-sodium thalamate and 131I-hippurate to determine GFR and ERPF respectively. Tubular damage was monitored by excretion of tubular enzymes and relative beta 2-microglobulin clearance. During the first course no changes in renal function were seen. After the second course a significant fall in GFR and ERPF started, ultimately leading to a median decrease in GFR of 19.0% (range 6.8-38.7%) and in ERPF of 14% (range 0-38.9%). No increases in the excretion of tubular enzymes or changes in the relative beta 2-microglobulin clearances were seen. We conclude from our data that carboplatin causes considerable loss of renal function. Monitoring renal function in patients treated with multiple courses of carboplatin is warranted.
卡铂是顺铂的类似物,在I/II期研究中,通过肌酐清除率评估,未报告有肾毒性。我们前瞻性地测定了10例基线肾功能正常的未经治疗的肺癌患者的肾功能,这些患者接受卡铂400mg/m²第1天和长春新碱2mg第1天及每4周第8天(最多5个周期)治疗,通过分别用125I-碘肽酸钠和131I-马尿酸盐清除率研究来测定肾小球滤过率(GFR)和有效肾血浆流量(ERPF)。通过肾小管酶排泄和相对β2-微球蛋白清除率监测肾小管损伤。在第一个疗程期间,未观察到肾功能变化。第二个疗程后,GFR和ERPF开始显著下降,最终导致GFR中位数下降19.0%(范围6.8 - 38.7%),ERPF下降14%(范围0 - 38.9%)。未观察到肾小管酶排泄增加或相对β2-微球蛋白清除率变化。我们从数据中得出结论,卡铂会导致相当程度的肾功能丧失。对接受多个疗程卡铂治疗的患者进行肾功能监测是必要的。