普通外文研报
P3 MAPKeeper 301 in 1L PDAC Underway
研报英文原文证据摘录
P3 MAPKeeper 301 in 1L PDAC Underway
data from an expanded cohort of 55 1L PDAC patients treated
Price Performance - 1 Year
with atebimetinib + mGnP, where the combo demonstrated mOS of 17.3 months vs.
the 8.5 month historical benchmark for GnP in MPACT. We got a more complete look USD
at baseline characteristics, which included fewer patients with liver mets (51% vs 85% 109
in MPACT) but more with peritoneal mets (36% vs 4% in MPACT). Notably, 60% of 8
patients went on to receive 2L treatment, including 1 patient receiving a RAS inhibitor 7
in 2L, vs. 40% in MPACT. We think this last point may be related to the combination’s 6
tolerability/safety profile, which included limited Gr 3+ TRAEs (anemia at 16% and 5
neutropenia at 18%, both deemed chemo-related), no reported Gr 4 atebi-related or Gr 4
5 TRAEs. Additionally, 84% of participants maintained or gained weight at three months, 2
a meaningful metric in a disease where cachexia can drive functional decline. 1
Jun-25 Aug-25 Oct-25 Dec-25 Feb-26 Apr-26 Jun-26
• ASCO Q&A framed the investor debate. The ASCO panel Q&A featured multiple Source: Bloomberg
physicians who were impressed by the OS data, including one who called it an
“outstanding” result, especially in the context of the tolerability profile. There was
particular interest in the weight stability/cachexia signal, including whether it could
have contributed to OS, helped preserve performance status as patients initiated 2L
treatment, and whether it could enable combination with full-dose chemo (answer: not
in the P3, where atebi is being combined with modified GnP to preserve QoL). A key
question was the extent that patient selection may have contributed to the 17.3-mo mOS
(e.g., fewer liver mets vs. MPACT) and how to reconcile atebi’s more modest 36% ORR
本摘录由系统从所标注的 PDF 证据页直接提取并保留英文原文,不做批量翻译;登录后在阅读器切换中文时才按需翻译。
打开研报阅读器