Gut microbiome is associated with recurrence-free survival in patients with resected high-risk melanoma receiving adjuvant immune checkpoint blockade
Summary
bioRxiv. 2024 Apr 20:2024.04.16.589761. doi: 10.1101/2024.04.16.589761. Patients with resected, high-risk melanoma receive adjuvant immune checkpoint blockade (ICB), yet clinical benefit remains unpredictable, with 25%-40% of patients experiencing recurrence. To evaluate whether pre-treatment gut microbiome (GMB) features predict recurrence, we analyzed stool samples from 674 patients enrolled in a phase 3 clinical trial, CheckMate 915, which investigated the combination of nivolumab plus i
Content
# Gut microbiome is associated with recurrence-free survival in patients with resected high-risk melanoma receiving adjuvant immune checkpoint blockade
*Published: 2026 Apr 17*
bioRxiv. 2024 Apr 20:2024.04.16.589761. doi: 10.1101/2024.04.16.589761.
Patients with resected, high-risk melanoma receive adjuvant immune checkpoint
blockade (ICB), yet clinical benefit remains unpredictable, with 25%-40% of
patients experiencing recurrence. To evaluate whether pre-treatment gut
microbiome (GMB) features predict recurrence, we analyzed stool samples from 674
patients enrolled in a phase 3 clinical trial, CheckMate 915, which investigated
the combination of nivolumab plus ipilimumab versus nivolumab as a single agent
across five geographic regions. Region-specific and cross-region meta-analyses
identified pre-treatment taxa associated with recurrence, including Eubacterium,
Ruminococcus, Firmicutes, and Clostridium. Recurrence prediction was strongest
when the validation cohort exhibited GMB profiles similar to those in the
discovery cohort. Among closely matched individuals (Jensen-Shannon divergence
[JSD] ≤ 0.11), the area under the curve (AUC) for recurrence prediction ranged
from 0.78 to 0.94 across regions. GMB composition remained largely stable
following treatment. These findings suggest that gut bacterial markers can
predict recurrence after adjuvant ICB treatment in melanoma, supporting their
potential as clinically actionable biomarkers to guide personalized therapy.
DOI: 10.1016/j.cell.2026.03.041