Dible S E, Siddik Z H, Boxall F E, Harrap K R
Drug Development Section, Institute of Cancer Research, Sutton, Surrey, U.K.
Eur J Cancer Clin Oncol. 1987 Jun;23(6):813-8. doi: 10.1016/0277-5379(87)90284-7.
Carboplatin has recently been established as an effective agent in cancer chemotherapy. The dose limiting toxicity of this platinum complex is myelosuppression and, in this study, we have shown that through the use of diethyldithiocarbamate (DDTC), a protective thiol compound, the toxicity in rodents can be ameliorated and lethality prevented. DDTC protected against carboplatin-induced leucopoenia and anaemia when administered as a single bolus or as a multiple schedule incorporating three injections. With the single bolus, the effectiveness of this protection decreased as the lag time between carboplatin and DDTC administrations increased. Thrombocytopoenia was unaffected by DDTC. The growth profile of ADJ/PC6A tumour in mice was dependent on the timing of DDTC administration when given in combination with the platinum complex. The tumour growth delay, however, was unaffected by DDTC at any schedule. Multiple injections of DDTC increased the ED90 for carboplatin from 5.0 to 7.5 mg/kg. The LD50 value was increased from 115 to 216 mg/kg with the same DDTC schedule. Thus, DDTC improved the therapeutic index of carboplatin by 25%. A clinical role for the use of DDTC as a protective agent for carboplatin-induced toxicities is suggested.
卡铂最近已被确立为癌症化疗中的一种有效药物。这种铂类复合物的剂量限制性毒性是骨髓抑制,在本研究中,我们已表明,通过使用二乙基二硫代氨基甲酸盐(DDTC),一种具有保护作用的硫醇化合物,可减轻啮齿动物的毒性并防止致死情况发生。当以单次推注或采用包含三次注射的多次给药方案给予DDTC时,它可预防卡铂诱导的白细胞减少和贫血。对于单次推注,随着卡铂与DDTC给药之间的间隔时间增加,这种保护作用的有效性会降低。血小板减少症不受DDTC影响。当与铂类复合物联合给药时,小鼠体内ADJ/PC6A肿瘤的生长情况取决于DDTC的给药时间。然而,在任何给药方案下,肿瘤生长延迟均不受DDTC影响。多次注射DDTC可使卡铂的ED90从5.0毫克/千克增加至7.5毫克/千克。在相同的DDTC给药方案下,LD50值从115毫克/千克增加至216毫克/千克。因此,DDTC使卡铂的治疗指数提高了25%。这表明DDTC作为卡铂诱导毒性的保护剂具有临床应用价值。