Nukatsuka Mamoru, Saito Hitoshi, Nakagawa Fumio, Tsujimoto Hiroaki, Sakamoto Kazuki, Tsukioka Sayaka, Uchida Junji, Kiniwa Mamoru, Kobunai Takashi, Takechi Teiji
Oncology Medical Affairs Division, Taiho Pharmaceutical Co., Ltd., Tokushima 771-0194;
Exp Ther Med. 2012 May;3(5):755-762. doi: 10.3892/etm.2012.484. Epub 2012 Feb 13.
In this study, combination therapies using the oral fluoropyrimidine tegafur-gimeracil-oteracil (S-1) with several targeted agents or antibodies, were evaluated. First, the effects of tyrosine kinase inhibitors (erlotinib hydrochloride, sorafenib tosilate and sunitinib malate) against human non-small cell lung cancer (NSCLC), breast cancer and colorectal cancer were evaluated in vivo. The effects of the combination of S-1 and targeted antibodies (bevacizumab and cetuximab) against human colorectal cancers was also evaluated in vivo. S-1 and the epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor, erlotinib, showed a significant inhibition of growth in human NSCLC (Lu-99 and PC-9 cell lines). The antitumor activity of the combination of S-1 and erlotinib against Lu-99 and PC-9 cancer cell lines was significantly superior to either monotherapy (P<0.05). Combination therapy using the multi-tyrosine kinase inhibitors, sorafenib or sunitinib, with S-1 against breast cancer (MX-1 cell line) and NSCLC (NCI-H460 cell line) was significantly superior to either monotherapy (P<0.01). The combination of the anti-vascular endothelial growth factor antibody bevacizumab or the anti-EGFR antibody, cetuximab, with S-1 against human colorectal cancer [Col-1, KM20C (bevacizumab) and DLD-1 (cetuximab) cell lines] and a 5-fluorouracil (5-FU)-resistant cell line (KM12C/5-FU) was significantly superior to either monotherapy (p<0.01). In particular, the growth of the Col-1 cells was completely inhibited by the combination of S-1 and bevacizumab. No toxic mortalities and no significant difference in the body weight changes of the animals treated with S-1 combined with the targeted agents or with the mono-therapies were observed; therefore, the treatments appeared to be well-tolerated. Our preclinical findings indicate that the combination therapies of S-1 and targeted agents are promising treatment options.
在本研究中,对使用口服氟嘧啶替吉奥(S-1)与多种靶向药物或抗体的联合疗法进行了评估。首先,在体内评估了酪氨酸激酶抑制剂(盐酸厄洛替尼、甲苯磺酸索拉非尼和苹果酸舒尼替尼)对人非小细胞肺癌(NSCLC)、乳腺癌和结直肠癌的作用。还在体内评估了S-1与靶向抗体(贝伐单抗和西妥昔单抗)联合使用对人结直肠癌的作用。S-1与表皮生长因子受体(EGFR)酪氨酸激酶抑制剂厄洛替尼对人NSCLC(Lu-99和PC-9细胞系)显示出显著的生长抑制作用。S-1与厄洛替尼联合使用对Lu-99和PC-9癌细胞系的抗肿瘤活性明显优于单一疗法(P<0.05)。使用多酪氨酸激酶抑制剂索拉非尼或舒尼替尼与S-1联合治疗乳腺癌(MX-1细胞系)和NSCLC(NCI-H460细胞系)明显优于单一疗法(P<0.01)。抗血管内皮生长因子抗体贝伐单抗或抗EGFR抗体西妥昔单抗与S-1联合用于人结直肠癌[Col-1、KM20C(贝伐单抗)和DLD-1(西妥昔单抗)细胞系]以及5-氟尿嘧啶(5-FU)耐药细胞系(KM12C/5-FU)明显优于单一疗法(p<0.01)。特别是,S-1与贝伐单抗联合使用完全抑制了Col-1细胞的生长。未观察到用S-1与靶向药物联合治疗或单一疗法治疗的动物出现毒性死亡,且动物体重变化无显著差异;因此,这些治疗似乎耐受性良好。我们的临床前研究结果表明,S-1与靶向药物的联合疗法是有前景的治疗选择。