TY - JOUR
T1 - Five-year clinical outcome and immune biomarkers of durable response from the MM1636 trial on IDO/PD-L1 vaccination and PD-1 blockade in first line metastatic melanoma
AU - Pedersen, Sidsel
AU - Byrdal, Mikkel
AU - Martinenaite, Evelina
AU - Lorentzen, Cathrine Lund
AU - Kjeldsen, Julie Westerlin
AU - Thorsen, Steffen Ullitz
AU - Kverneland, Anders
AU - Zocca, Mai-Britt
AU - Andersen, Mads Hald
AU - Svane, Inge Marie
N1 - © 2025. The Author(s).
PY - 2025/12/14
Y1 - 2025/12/14
N2 - We report long-term clinical and immunologic outcomes from the MM1636 trial (NCT03047928), which evaluated a peptide vaccine targeting IDO and PD-L1 in combination with nivolumab in patients with advanced melanoma. At a five-year follow-up, the combination demonstrated durable clinical efficacy, with a 25.5-month median progression-free survival. Serum proteomic profiling identified vaccine-specific immune signatures, with increase in CCL3, CCL4, and TNFα emerging as biomarkers of long progression-free survival. Increase in these markers were not observed in a matched anti-PD-1 monotherapy cohort, suggesting distinct immune modulation by the vaccine. Functional studies confirmed vaccine-induced targeting of myeloid cells and associated increase in these cytokines. These findings provide evidence for durable benefit from immune modulatory vaccination and nominate CCL3, CCL4, and TNFα as candidate biomarkers for response.
AB - We report long-term clinical and immunologic outcomes from the MM1636 trial (NCT03047928), which evaluated a peptide vaccine targeting IDO and PD-L1 in combination with nivolumab in patients with advanced melanoma. At a five-year follow-up, the combination demonstrated durable clinical efficacy, with a 25.5-month median progression-free survival. Serum proteomic profiling identified vaccine-specific immune signatures, with increase in CCL3, CCL4, and TNFα emerging as biomarkers of long progression-free survival. Increase in these markers were not observed in a matched anti-PD-1 monotherapy cohort, suggesting distinct immune modulation by the vaccine. Functional studies confirmed vaccine-induced targeting of myeloid cells and associated increase in these cytokines. These findings provide evidence for durable benefit from immune modulatory vaccination and nominate CCL3, CCL4, and TNFα as candidate biomarkers for response.
KW - Adult
KW - B7-H1 Antigen/immunology
KW - Biomarkers, Tumor/blood
KW - Cancer Vaccines/immunology
KW - Chemokine CCL3/blood
KW - Chemokine CCL4/blood
KW - Female
KW - Humans
KW - Immune Checkpoint Inhibitors/therapeutic use
KW - Indoleamine-Pyrrole 2,3,-Dioxygenase/immunology
KW - Male
KW - Melanoma/immunology
KW - Middle Aged
KW - Nivolumab/therapeutic use
KW - Programmed Cell Death 1 Receptor/antagonists & inhibitors
KW - Progression-Free Survival
KW - Proteomics
KW - Skin Neoplasms/immunology
KW - Treatment Outcome
KW - Tumor Necrosis Factor-alpha/blood
KW - Vaccination
KW - Vaccines, Subunit/immunology
U2 - 10.1038/s41467-025-67508-8
DO - 10.1038/s41467-025-67508-8
M3 - Journal article
C2 - 41392152
SN - 2041-1722
VL - 17
SP - 806
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 806
ER -