Micetich K C, Jensen-Akula M, Mandard J C, Fisher R I
Am J Med. 1981 Dec;71(6):967-72. doi: 10.1016/0002-9343(81)90315-6.
The nephrotoxicity of semustine (methyl-CCNU) has been studied in 45 adult patients with surgically resected Stage I or II malignant melanoma who received this drug as adjuvant chemotherapy. Abnormalities of renal function (including three cases of renal failure) were noted in seven of 45 patients (16 percent); all these patients received more than 1,400 mg/m2. This represents an incidence of 26 percent in patients receiving more than 1,400 mg/m2 of semustine. Two distinct patterns emerged. Abnormal serum creatinine levels developed in two patients while receiving semustine and later progressed to renal failure. Five patients had normal serum creatinine levels throughout their treatment courses but had abnormal creatinine values one month to two years following the completion of drug therapy. Renal failure developed in one of these patients, but the remaining four have had stable renal function for one to two years of additional follow-up. No clinical signs of renal insufficiency were detected in any patients receiving less than 1,400 mg/m2 of semustine. No changes unequivocally attributable to semustine were seen in eight patients at autopsy despite the fact that three had received greater than 1,900 mg/m2 of nitrosourea. This incidence of nephrotoxicity appears to be significantly lower than that previously reported in children. Guidelines for future therapy with semustine are described.
对45例接受司莫司汀(甲环亚硝脲)辅助化疗的I期或II期恶性黑色素瘤成年患者进行了手术切除,研究了该药的肾毒性。45例患者中有7例(16%)出现肾功能异常(包括3例肾衰竭);所有这些患者接受的司莫司汀剂量均超过1400mg/m²。这代表接受超过1400mg/m²司莫司汀的患者中肾毒性发生率为26%。出现了两种不同的模式。两名患者在接受司莫司汀治疗期间血清肌酐水平异常,随后进展为肾衰竭。五名患者在整个治疗过程中血清肌酐水平正常,但在药物治疗结束后1个月至2年肌酐值异常。其中一名患者发生了肾衰竭,但其余四名患者在额外随访的1至2年中肾功能稳定。接受低于1400mg/m²司莫司汀的患者均未检测到肾功能不全的临床体征。尽管有三名患者接受的亚硝基脲剂量超过1900mg/m²,但在八名尸检患者中未发现明确归因于司莫司汀的变化。这种肾毒性发生率似乎明显低于先前报道的儿童发生率。文中描述了司莫司汀未来治疗的指南。