Abstract 7931: Distinct microbiota composition in anorectal mucosal melanoma is associated with resistance to immune checkpoint inhibition

Abstract Anorectal mucosal melanoma (AMM) is a rare and aggressive melanoma subtype characterized by poor responses to immune checkpoint inhibitor (ICI) therapy. While cutaneous melanoma metastases to gastrointestinal (GI) sites often retain strong ICI responses, the mechanisms underlying poor responses in AMM remain unclear. Given that AMM arises in microbial rich mucosal environments, we hypothesized that tumor-associated microbiota may contribute to local immune suppression. To investigate this, we performed 16S rRNA gene sequencing on primary AMM tumors and compared their microbial composition with cutaneous melanoma GI metastases (CM-GI-met) and normal mucosal reference samples, including nasal, rectal, and vaginal swabs. AMM tumors were enriched with Firmicutes Clostridia taxa, including Lactospiraceae and Ruminococcaceae, known butyrate producers associated with immunomodulation. In contrast, CM-GI-met tumors exhibited distinct microbial signatures, with a relatively higher abundance of Fusobacteriaceae and Bacteriodaceae. These patients notably had improved ICI responses compared to AMM primaries. Functional profiling suggested that AMM microbiomes had increased butyrate synthesis, known to create an immunosuppressive tumor microenvironment, which may contribute to poor ICI response. These findings are also seen in our orthotopic rectal mouse melanoma model, which showed reduced tumor growth rates, tumor burden, and overall survival in mice treated with combination vancomycin (Gram-positive selective antibiotic which targets Firmicutes Clostridia) and anti-PD-1 therapy compared to controls and monotherapy. Our findings demonstrate that AMM tumors contain a distinct butyrate-rich microbiome that may contribute to local tumor evasion whereas CM tumors contain a more ICI-permissive microbiome. Citation Format: Pritika Parmar, Morgan MacBeth, Mallory Karr, Nichole Nusbacher, Stacey M. Bagby, Phaedra Whitty, Kylie Michel, Richard P. Tobin, Martin McCarter, Theresa Medina, Catherine Lozupone, William A. Robinson, Kasey Couts. Distinct microbiota composition in anorectal mucosal melanoma is associated with resistance to immune checkpoint inhibition abstract. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 7931.