Tsukagoshi S
Cancer Chemotherapy Center, Cancer Institute.
Gan To Kagaku Ryoho. 1990 Sep;17(9):1949-58.
Carboplatin (CBDCA; commercial name: Paraplatin) is a platinum complex having 1-cyclobutanedicarboxylic acid group at the two chlorine positions of cisplatin (CDDP). In the preclinical studies, CBDCA was proved to be almost equally effective to various murine tumors compared to cisplatin. Compared to cisplatin, of which free platinum was not detected from 2 hr after administration, the free type of more than 85% of total platinum concentration remained in the blood even 8 hrs after administration. Total urine excretion at 2-4 hrs after administration of CBDCA was about 57-82%, indicating CBDCA's relative rapid urine excretion compared to CDDP. In the clinical trials in Japan, appreciable clinical responses were observed in head and neck, small cell lung, ovarian, uterine cervical cancers, testicular tumor and malignant lymphoma. The renal toxicity was considerably slight, resulting in almost no hydration during treatment. Nausea and vomiting were also slight and there were no hearing-loss and neurotoxicities. The dose-limiting factor (DLF) in the phase I study was myelosuppression. From these results, it was found that carboplatin's antitumor efficacies were almost identical with cisplatin and much less toxic than cisplatin. Carboplatin will serve as a useful antitumor drug in current cancer chemotherapy.
卡铂(CBDCA;商品名:顺铂)是一种在顺铂(CDDP)的两个氯原子位置带有1-环丁烷二羧酸基团的铂络合物。在临床前研究中,已证明CBDCA对各种鼠类肿瘤的疗效与顺铂几乎相同。与顺铂相比,顺铂给药后2小时就检测不到游离铂,而CBDCA给药后8小时,血液中仍有超过85%的总铂浓度以游离形式存在。CBDCA给药后2 - 4小时的总尿排泄量约为57 - 82%,表明与CDDP相比,CBDCA的尿排泄相对较快。在日本的临床试验中,在头颈部、小细胞肺癌、卵巢癌、子宫颈癌、睾丸肿瘤和恶性淋巴瘤中观察到了明显的临床反应。肾毒性相当轻微,治疗期间几乎无需水化。恶心和呕吐也很轻微,没有听力丧失和神经毒性。I期研究中的剂量限制因素(DLF)是骨髓抑制。从这些结果发现,卡铂的抗肿瘤疗效与顺铂几乎相同,但毒性比顺铂小得多。卡铂将成为当前癌症化疗中一种有用的抗肿瘤药物。