Neoadjuvant botensilimab plus balstilimab response pattern in locally advanced mismatch repair proficient colorectal cancer

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,Elizabeta C. Popa, Daniel H. Hunt, Nikhil P. Uppal, Kelly A. Garrett, Alessio Pigazzi,Xi Kathy Zhou,Manish A. Shah,Erika Hissong

Oncogene(2023)

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Abstract
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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Key words
neoadjuvant botensilimab,colorectal cancer,advanced mismatch repair,balstilimab response pattern
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