Rabinowits M, Souhami L, Gil R A, Andrade C A, Paiva H C
Department of Medical Oncology, Instituto Nacional de Cancer, Rio de Janeiro, Brazil.
Am J Clin Oncol. 1990 Apr;13(2):132-8. doi: 10.1097/00000421-199004000-00009.
Combination chemotherapy that included bleomycin and cisplatin was administered to 45 evaluable patients (30 with cervix carcinoma and 15 with germ cell tumors). Bleomycin was given, following cisplatin infusion, either by intravenous continuous infusion over 72 h (germ cell tumor patients) or intramuscularly every 12 h for 4 days (cervix carcinoma patients). Total bleomycin doses ranged from 156 to 360 U. Nine patients with normal renal function and no previous pulmonary disease prior to chemotherapy developed serious pulmonary toxicity. Six patients died from irreversible respiratory failure. Postmortem lung studies were performed in all six patients and revealed findings compatible with bleomycin-induced lung toxicity. Renal tubular damage was found in four kidneys available for examination. Five (71.5%) of the seven patients whose serum creatinine increased after chemotherapy was initiated developed lung injury, whereas 10.5% of those without change in the serum creatinine level presented this complication (p = 0.001). Renal damage, following cisplatin administration, with subsequent accumulation of bleomycin was the likely cause of the high lung toxicity. Extreme caution is recommended in the administration of combined bleomycin-cisplatin chemotherapy. Whenever possible, bleomycin should precede cisplatin infusion to minimize the risk of lung toxicity.
45例可评估患者(30例宫颈癌患者和15例生殖细胞肿瘤患者)接受了包含博来霉素和顺铂的联合化疗。在输注顺铂后,博来霉素给药方式如下:生殖细胞肿瘤患者通过72小时静脉持续输注,宫颈癌患者每12小时肌肉注射一次,共4天。博来霉素总剂量范围为156至360单位。9例化疗前肾功能正常且无既往肺部疾病的患者发生了严重的肺部毒性。6例患者死于不可逆的呼吸衰竭。对所有6例患者进行了尸检肺研究,结果显示与博来霉素诱导的肺毒性相符。在4个可供检查的肾脏中发现了肾小管损伤。在化疗开始后血清肌酐升高的7例患者中,5例(71.5%)发生了肺损伤,而血清肌酐水平无变化的患者中10.5%出现了这种并发症(p = 0.001)。顺铂给药后肾脏受损,随后博来霉素蓄积,可能是导致高肺毒性的原因。建议在使用博来霉素 - 顺铂联合化疗时要格外谨慎。只要有可能,博来霉素应在输注顺铂之前使用,以尽量降低肺毒性风险。