INCREASED PULMONARY TOXICITY WITH BLEOMYCIN AND CISPLATIN CHEMOTHERAPY COMBINATIONS

被引:22
|
作者
RABINOWITS, M
SOUHAMI, L
GIL, RA
ANDRADE, CAV
PAIVA, HC
机构
[1] INST NACL CANC,DEPT MED ONCOL,RIO DE JANEIRO,BRAZIL
[2] INST NACL CANC,DEPT RADIAT ONCOL,RIO DE JANEIRO,BRAZIL
[3] INST NACL CANC,DEPT PATHOL,RIO DE JANEIRO,BRAZIL
来源
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS | 1990年 / 13卷 / 02期
关键词
D O I
10.1097/00000421-199004000-00009
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Combination chemotherapy that included bleomycin and cisplatin was administered to 45 evaluable patients (30 with cervic 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. Rencal tubular damage was found in four kidneys available for examination. Five (71.5%) of the seven patients whose serum creatine 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.
引用
收藏
页码:132 / 138
页数:7
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