A new approach to cancer treatment became available shortly before Jimmy Carter needed it. Now it's a pillar of care.
刚刚,FDA 结束了为期 1 天的肿瘤药物咨询委员会(ODAC)会议,讨论了 PD-1 抑制剂在临床的适应症及应用情况。会议主要涉及 3 款已上市的 PD-1 抑制剂药物,分别是:默沙东的帕博利珠单抗(pembrolizumab,K ...
▎药明康德内容团队编辑默沙东(MSD)今日宣布,美国FDA已批准其重磅PD-1抑制剂Keytruda(pembrolizumab)与培美曲塞和铂类化疗联合,作为一线疗法治疗不可切除的晚期或转移性恶性胸膜间皮瘤(MPM)成年患者。恶性间皮瘤是一类起源于 ...
BMS和默沙东方面则是主张维持现有的“全人群”适应症的标签。BMS的会议简报提到,不同药物的各项研究的评分方法和截断值存在差异,实施任何截断值都有可能让一部分患者失去获益的机会。
Pembrolizumab (Keytruda, Merck) has picked up another indication — this time for the first-line treatment of unresectable ...
Patients with locally advanced cervical cancer were randomized to receive either pembrolizumab or placebo in combination with ...
In KEYNOTE-522, treatment with neoadjuvant pembrolizumab and chemotherapy, followed by adjuvant pembrolizumab, led to ...
Pembrolizumab plus chemoradiotherapy improved survival in patients with previously untreated, high-risk locally advanced ...
Dr. Patel:我是加州大学圣地亚哥分校肿瘤内科学教授Sandip Patel医学博士,担任WCLC ...
Discover the results from the phase 3 ENGOT-cx11/GOG-3047/KEYNOTE-A18 study, presented at ESMO 2024, Barcelona, Spain ...
药王K药的一举一动总是牵动人心。近日,安斯泰来宣布日本MHLW已经批准其旗下的ADC药物恩诺单抗PADCEV与默沙东K药作为一线治疗根本性不可切除的尿路上皮癌成人患者的联合疗法。凭借优异的数据,让此联合治疗方案暨9月4日默沙东宣布获得欧盟委员会(EC ...