Munshi N C, Loehrer P J, Williams S D, Langefeld C, Sledge G, Nichols C R, Roth B J, Neuman A, Walsh W B, Einhorn L H
Indiana University, Indianapolis.
Invest New Drugs. 1992 Aug;10(3):159-63. doi: 10.1007/BF00877240.
From January 1983 through August 1988, 318 consecutive patients with refractory germ cell neoplasms were treated with ifosfamide-containing combination chemotherapy. The patients received ifosfamide at 1.2 gm/m2/day with cis-platin 20 mg/m2/day for 5 days and etoposide 75 mg/m2/day for 5 days or vinblastine 0.11 mg/kg on days 1 and 2 for each cycle. Of 277 evaluable patients, NAC was used as an uroprotector in the initial 86 patients while the latter 191 consecutive patients received mesna to reduce urothelial toxicity. Dosages of NAC was 2.0 gm po q 6 hr and for mesna 120 mg/m2 IV push prior to ifosfamide and then 1200 mg/m2/day as continuous infusion of 5 consecutive days. All patients received 3.0 liters of normal saline per day. The number of courses of chemotherapy given in the two groups were similar. Twenty-four of the 86 patients (27.9%) receiving NAC developed hematuria (13 patients - grade 1, 4 patients - grade 2, and 7 patients - grade 3 toxicity). While 8 out of 191 (4.2%) mesna patients developed hematuria (6 - grade 1 and 2 - grade 3) (p < 0.0001). The incidence of severity of renal toxicity was similar in the two groups. Ifosfamide dosage was reduced solely for urothelial toxicity in 11 patients receiving NAC compared with none of the patients receiving mesna (p < 0.0001). Chemotherapy response was similar in the two groups. In conclusion, mesna provides better urothelial protection from ifosfamide-induced toxicity than NAC and allows better maintenance of the drug dosage.
从1983年1月至1988年8月,318例连续的难治性生殖细胞肿瘤患者接受了含异环磷酰胺的联合化疗。患者接受异环磷酰胺1.2 gm/m²/天,顺铂20 mg/m²/天,共5天,依托泊苷75 mg/m²/天,共5天,或长春花碱0.11 mg/kg,于每个周期的第1天和第2天使用。在277例可评估的患者中,最初的86例患者使用NAC作为尿路保护剂,而后191例连续患者接受美司钠以降低尿路毒性。NAC的剂量为口服2.0 gm,每6小时一次,美司钠的剂量为在异环磷酰胺之前静脉推注120 mg/m²,然后以1200 mg/m²/天连续输注5天。所有患者每天接受3.0升生理盐水。两组给予的化疗疗程数相似。接受NAC的86例患者中有24例(27.9%)出现血尿(13例为1级,4例为2级,7例为3级毒性)。而接受美司钠的191例患者中有8例(4.2%)出现血尿(6例为1级,2例为3级)(p < 0.0001)。两组肾毒性严重程度的发生率相似。接受NAC的11例患者仅因尿路毒性而降低了异环磷酰胺剂量,而接受美司钠的患者中无此情况(p < 0.0001)。两组化疗反应相似。总之,美司钠比NAC能更好地保护尿路免受异环磷酰胺诱导的毒性,并能更好地维持药物剂量。