4.8 Article

Sotigalimab and/or nivolumab with chemotherapy in first-line metastatic pancreatic cancer: clinical and immunologic analyses from the randomized phase 2 PRINCE trial

Journal

NATURE MEDICINE
Volume 28, Issue 6, Pages 1167-+

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41591-022-01829-9

Keywords

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Funding

  1. Parker Institute for Cancer Immunotherapy (PICI)
  2. Cancer Research Institute
  3. Bristol Myers Squibb
  4. PICI

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Chemotherapy combined with immunotherapy has improved the treatment of certain solid tumors, however, finding effective regimens for pancreatic ductal adenocarcinoma (PDAC) remains a challenge. A randomized phase 2 trial evaluated the efficacy of nivolumab and sotigalimab with chemotherapy in metastatic PDAC patients. The primary endpoint of 1-year overall survival was met for nivo/chemo but not for sotiga/chemo or sotiga/nivo/chemo. Biomarker analyses identified immune signatures associated with survival for different treatment groups.
Chemotherapy combined with immunotherapy has improved the treatment of certain solid tumors, but effective regimens remain elusive for pancreatic ductal adenocarcinoma (PDAC). We conducted a randomized phase 2 trial evaluating the efficacy of nivolumab (nivo; anti-PD-1) and/or sotigalimab (sotiga; CD40 agonistic antibody) with gemcitabine/nab-paclitaxel (chemotherapy) in patients with first-line metastatic PDAC (NCT03214250). In 105 patients analyzed for efficacy, the primary endpoint of 1-year overall survival (OS) was met for nivo/chemo (57.7%, P = 0.006 compared to historical 1-year OS of 35%, n = 34) but was not met for sotiga/chemo (48.1%, P = 0.062, n = 36) or sotiga/nivo/chemo (41.3%, P = 0.223, n = 35). Secondary endpoints were progression-free survival, objective response rate, disease control rate, duration of response and safety. Treatment-related adverse event rates were similar across arms. Multi-omic circulating and tumor biomarker analyses identified distinct immune signatures associated with survival for nivo/chemo and sotiga/chemo. Survival after nivo/chemo correlated with a less suppressive tumor microenvironment and higher numbers of activated, antigen-experienced circulating T cells at baseline. Survival after sotiga/chemo correlated with greater intratumoral CD4 T cell infiltration and circulating differentiated CD4 T cells and antigen-presenting cells. A patient subset benefitting from sotiga/nivo/chemo was not identified. Collectively, these analyses suggest potential treatment-specific correlates of efficacy and may enable biomarker-selected patient populations in subsequent PDAC chemoimmunotherapy trials.

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