WebIMpower133及CASPIAN研究在ES-SCLC患者一线治疗中均取得了总生存期(overall survival, OS)的突破性进展,由此FDA批准PD-L1单克隆抗体Atezolizumab(阿特珠单抗)[8]及Durvalumab(德瓦鲁单抗)[9]与卡铂和依托泊苷联合用于ES-SCLC患者的一线治疗。 ... CheckMate 057[10]、KEYNOTE-010[11]及 ... WebNov 8, 2024 · CheckMate -816 is the first Phase 3 trial with an immunotherapy-based combination to demonstrate improved event-free survival and pathologic complete response in the neoadjuvant setting of non-small cell lung cancer Positive results reinforce the improved efficacy seen with Opdivo-based treatments in four Phase 3 clinical trials in …
CheckMate 73L: A Phase 3 Study Comparing Nivolumab Plus
Web在晚期NSCLC一线治疗中,CheckMate 227 Part 1研究首次证实纳武利尤单抗+低剂量Ipilimumab(伊匹木单抗)的双免疫联合治疗与含铂化疗相比能显著延长患者总生存(OS),为EGFR及ALK阴性患者提供一个 “去化疗”的一线治疗方案。 WebJul 19, 2024 · De Ruysscher D, Ramalingam S, Urbanic J, Gerber DE, Tan DSW, Cai J, Li A, Peters S. CheckMate 73L: A Phase 3 Study Comparing Nivolumab Plus Concurrent Chemoradiotherapy Followed by Nivolumab With or Without Ipilimumab Versus Concurrent Chemoradiotherapy Followed by Durvalumab for Previously Untreated, Locally … ham shoppe detroit
A Neoadjuvant Study of Nivolumab Plus Ipilimumab or Nivolumab …
WebMar 1, 2024 · 在III期临床研究上,目前有多种单药及联合方案新辅助免疫治疗的III期实验正在进行中,但尚未有研究报告发表,且除CheckMate-816研究外未公布研究结果和数据。 1.1 新辅助免疫治疗研究临床终点的选择 选择合适的临床终点是新辅助免疫治疗相关研究的重点 … WebDec 20, 2016 · Event-free survival (EFS) is defined as the length of time from randomization to any of the following events: any progression of disease precluding surgery, progression or recurrence disease based on blinded independent central review (BICR) assessment per response evaluation criteria in solid tumors (RECIST) 1.1 after surgery, or death due to … WebMay 18, 2024 · Other currently ongoing phase III trials of perioperative treatment with chemoimmunotherapy in the neoadjuvant setting and immunotherapy alone in the … ham shop raleigh