Uchida Naomi, Yamada Hajime, Maekawa Ryuji, Yoshioka Takayuki
Discovery Research Laboratory, Shionogi & Co., Ltd.
Gan To Kagaku Ryoho. 2002 Nov;29(11):1943-9.
The antitumor activity of a combination of paclitaxel (TXL) followed by nedaplatin (NDP) against SK-OV-3 human ovarian cancer was evaluated. We also compared the antitumor activity of TXL plus NDP with that of TXL plus carboplatin (CBDCA) or TXL plus cisplatin (CDDP). TXL was injected i.v. daily for four days and either NDP, CBDCA or CDDP was injected i.v. once after the TXL treatment, into tumor-bearing mice. The sequential administration of TXL prior to NDP resulted in enhanced inhibition of tumor growth in comparison with either TXL or NDP monotherapy. The combination in TXL plus NDP was synergistic and superior to that of TXL plus CDDP or TXL plus CBDCA therapy. Histological tests demonstrated that the fraction of BrdU-incorporated cells in tumor tissue was significantly inhibited by the combination of TXL with NDP. These results demonstrated the antitumor efficacy of TXL with NDP against human ovarian cancer and suggest the clinical effectiveness of combination of TXL with NDP.
评估了紫杉醇(TXL)后接奈达铂(NDP)联合用药对SK-OV-3人卵巢癌的抗肿瘤活性。我们还比较了TXL加NDP与TXL加卡铂(CBDCA)或TXL加顺铂(CDDP)的抗肿瘤活性。将TXL静脉注射,每日一次,共四天,在TXL治疗后,将NDP、CBDCA或CDDP静脉注射一次,注入荷瘤小鼠体内。与TXL或NDP单一疗法相比,NDP之前序贯给予TXL可增强对肿瘤生长的抑制作用。TXL加NDP联合用药具有协同作用,优于TXL加CDDP或TXL加CBDCA疗法。组织学检测表明,TXL与NDP联合用药可显著抑制肿瘤组织中掺入BrdU的细胞比例。这些结果证明了TXL与NDP联合用药对人卵巢癌的抗肿瘤疗效,并提示TXL与NDP联合用药的临床有效性。