Cabozantinib sensitizes microsatellite stable colorectal cancer to immune checkpoint blockade by immune modulation in human immune system mouse models

• Published in: Frontiers in oncology Vol. 12; p. 877635
• Main Authors: Lang, Julie, Leal, Alexis D, Marín-Jiménez, Juan A, Hartman, Sarah J, Shulman, Jeremy, Navarro, Natalie M, Lewis, Matthew S, Capasso, Anna, Bagby, Stacey M, Yacob, Bethlehem W, MacBeth, Morgan, Freed, Brian M, Eckhardt, S Gail, Jordan, Kimberly, Blatchford, Patrick J, Pelanda, Roberta, Lieu, Christopher H, Messersmith, Wells A, Pitts, Todd M
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Media S.A 07.11.2022
• Subjects: colorectal cancer; humanized mouse model; immune checkpoint blockade; immunotherapy; Oncology; tumor immunology; tumor microenvironment; colorectal cancer; tumor immunology; nivolumab; humanized mouse model; immunotherapy; tumor microenvironment; cabozantinib; immune checkpoint blockade
• ISSN: 2234-943X; 2234-943X
• DOI: 10.3389/fonc.2022.877635

Immune checkpoint inhibitors have been found to be effective in metastatic MSI-high colorectal cancers (CRC), however, have no efficacy in microsatellite stable (MSS) cancers, which comprise the majority of mCRC cases. Cabozantinib is a small molecule multi-tyrosine kinase inhibitor that is FDA approved in advanced renal cell, medullary thyroid, and hepatocellular carcinoma. Using Human Immune System (HIS) mice, we tested the ability of cabozantinib to prime MSS-CRC tumors to enhance the potency of immune checkpoint inhibitor nivolumab. In four independent experiments, we implanted distinct MSS-CRC patient-derived xenografts (PDXs) into the flanks of humanized BALB/c-Rag2 Il2rγ Sirpα (BRGS) mice that had been engrafted with human hematopoietic stem cells at birth. For each PDX, HIS-mice cohorts were treated with vehicle, nivolumab, cabozantinib, or the combination. In three out of the four models, the combination had a lower tumor growth rate compared to vehicle or nivolumab-treated groups. Furthermore, interrogation of the HIS in immune organs and tumors by flow cytometry revealed increased Granzyme B+, TNFα+ and IFNγ+ CD4+ T cells among the human tumor infiltrating leukocytes (TIL) that correlated with reduced tumor growth in the combination-treated HIS-mice. Notably, slower growth correlated with increased expression of the CD4+ T cell ligand, HLA-DR, on the tumor cells themselves. Finally, the cabozantinib/nivolumab combination was tested in comparison to cobimetinib/atezolizumab. Although both combinations showed tumor growth inhibition, cabozantinib/nivolumab had enhanced cytotoxic IFNγ and TNFα+ T cells. This pre-clinical data warrants testing the combination in clinical trials for patients with MSS-CRC.