结直肠癌
生物
免疫系统
免疫疗法
微卫星不稳定性
新辅助治疗
癌症研究
肿瘤科
化疗
癌症
免疫学
内科学
医学
乳腺癌
微卫星
等位基因
生物化学
遗传学
基因
作者
Pashtoon Murtaza Kasi,Manuel Hidalgo,Mehraneh D. Jafari,Heather Yeo,Lea Lowenfeld,Uqba Khan,Alana T. H. Nguyen,Despina Siolas,Brandon Swed,Jini Hyun,Sahrish Khan,Madeleine Wood,Benjamin Samstein,Juan P. Rocca,Allyson J. Ocean,E Popa,Daniel H. Hunt,Nikhil Uppal,Kelly A. Garrett,Alessio Pigazzi
出处
期刊:Oncogene
[Springer Nature]
日期:2023-09-21
卷期号:42 (44): 3252-3259
被引量:23
标识
DOI:10.1038/s41388-023-02835-y
摘要
In patients with locally advanced cancer without distant metastases, the neoadjuvant setting presents a platform to evaluate new drugs. For mismatch repair proficient/microsatellite stable (pMMR/MSS) colon and rectal cancer, immunotherapy has shown limited efficacy. Herein, we report exceptional responses observed with neoadjuvant botensilimab (BOT), an Fc-enhanced next-generation anti-CTLA-4 antibody, alongside balstilimab (BAL; an anti-PD-1 antibody) in two patients with pMMR/MSS colon and rectal cancer. The histological pattern of rapid immune response observed ("inside-out" (serosa-to-mucosa) tumor regression) has not been described previously in this setting. Spatial biology analyses (RareCyte Inc.) reveal mechanisms of actions of BOT, a novel innate-adaptive immune activator. These observations have downstream implications for clinical trial designs using neoadjuvant immunotherapy and potentially sparing patients chemotherapy.
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