Targeted Oncology provides news, videos, and reviews on the rapidly evolving world of targeted therapies and immunotherapy ...
Kisqali has been FDA-approved with an aromatase inhibitor as postsurgical treatment for some with early breast cancer at a ...
Ad hoc announcement pursuant to Art. 53 LR Broad indication in HR+/HER2- stage II and III early breast cancer (EBC) at high risk of recurrence approximately doubles population eligible for CDK4/6 ...
在2024年欧洲肿瘤内科学会 (ESMO) 大会上,来凯医药公布了其创新产品LAE002联合氟维司群(下简称“联合疗法”),用于标准治疗失败的局部晚期或转移性HR+/HER2-乳腺癌患者Ib期研究的最终数据。在18位 ...
During a Community Case Forum series, breast cancer experts discussed the importance of testing for ESR1 mutations, in ...
2024年欧洲肿瘤内科学会(ESMO)年会于9月13日~17日在西班牙巴塞罗那召开。在最新公布的NATALEE研究数据中,一项重要发现揭示了年龄对治疗效果的影响。结果显示,年龄<40岁的HR+/HER2-EBC患者,在接受瑞波西利联合非甾体类芳香化酶 ...
- 58.1%的受试者伴有PIK3CA/AKT1/PTEN通路改变,64.5%受试者既往接受过CDK4/6抑制剂治疗 - 确认的ORR为33.3%,临床获益率66.7%,PFS为7.3个月 - 已报道的CAPItello-291 III 期研究的中国桥接研究,在PIK3CA/AKT1/PTEN通路改变人群中,capivasertib/氟维司群联合治疗组PFS数据为5.7个月,氟维司群单药治疗的PF ...
Findings from the NATALEE trial show that the combination of Kisqali and an aromatase inhibitor resulted in disease-free ...
The Food and Drug Administration approved ribociclib plus an aromatase inhibitor for hormone receptor (HR)–positive, ...
来凯医药-B(02105)涨超6%,截至发稿,涨6.7%,报4.78港元,成交额516.23万港元。 消息面上,在2024年欧洲肿瘤内科学会(ESMO)大会上,来凯医药公布了其创新产品LAE002联合氟维司群(下简称“联合疗法”),用于标准治疗失败的局部晚期或转移性HR+/HER2-乳腺癌患者Ib期研究的最终数据。在18位PIK3CA/AKT1/PTEN变异的乳腺癌患者中,中位无进展生存期(PFS ...
Novartis’ Kisqali receives US FDA approval to reduce risk of recurrence in people with HR+/HER2- early breast cancer: Basel Thursday, September 19, 2024, 13:00 Hrs [IST] Novarti ...