癌症研究
细胞凋亡
拓扑异构酶
细胞培养
药理学
抗体
化学
作用机理
药品
细胞毒性
癌细胞
癌症
DNA损伤
体内
抗体-药物偶联物
细胞
单克隆抗体
前药
医学
抗原
细胞内
肺癌
转染
免疫疗法
程序性细胞死亡
作者
Daisuke Okajima,Satoru Yasuda,Takanori Maejima,Tsuyoshi Karibe,Ken Sakurai,Tetsuo Aida,Tadashi Toki,Junko Yamaguchi,Michiko Kitamura,Reiko Kamei,Tomomichi Fujitani,Tomoyo Honda,Tomoko Shibutani,Sumie Muramatsu,Takashi Nakada,Riki Goto,Shu Takahashi,Miki Yamaguchi,Hirofumi Hamada,Yutaka Noguchi
标识
DOI:10.1158/1535-7163.mct-21-0206
摘要
antitumor activity with DNA damage induced by the accumulated DXd in TROP2-expressing xenograft tumors, but neither isotype control IgG-ADC nor anti-TROP2 antibody had this effect. Dato-DXd also showed potent antitumor activity with tumor regression in several TROP2-expressing xenograft tumors including NSCLC PDX models. Safety profiles of Dato-DXd in rats and cynomolgus monkeys were acceptable.Dato-DXd demonstrated potent antitumor activity against TROP2-expressing tumors by efficient payload delivery into tumors and acceptable safety profiles in preclinical models. These results suggest Dato-DXd could be a valuable treatment option for patients with TROP2-expressing tumors in the clinical setting.
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