A Phase II Trial of Pembrolizumab plus Granulocyte-Macrophage Colony-Stimulating Factor in Advanced Biliary Cancer
PURPOSE: Immune checkpoint inhibitors have limited activity as monotherapy in biliary cancers. Granulocyte-macrophage colony-stimulating factor (GM-CSF) is a pleiotropic immune cell growth factor which achieved prolonged survival when combined with ipilimumab in melanoma. We conducted a single-center, phase II trial to evaluate the efficacy and safety of combining GM-CSF with pembrolizumab in patients with advanced biliary cancers after prior chemotherapy but no prior immune checkpoint inhibitor. EXPERIMENTAL DESIGN: Pembrolizumab 200 mg was administered intravenously in 21-day cycles, along with two cycles of GM-CSF 250 µg subcutaneously days 1 through 14. The primary endpoint was objective response rate. RESULTS: Among 42 patients enrolled, the median age was 61 years, 67% had intrahepatic cholangiocarcinoma, 90% had stage IV disease, and 24% had underlying viral hepatitis. The confirmed objective response rate was 12% (95% confidence interval: 4, 26), including two patients with complete response, and 26% of patients had progression-free survival ongoing at 6 months. Treatment was well-tolerated with treatment-related grade 3-4 events in 7% and treatment-related serious adverse events in 10%. Tumor PD-L1 expression was present in 46% and was associated with a higher rate of 6-month progression-free survival. Paired tumor biopsies showed upregulation of CD8+ T cell populations and antigen processing pathways after the addition of GM-CSF. CONCLUSIONS: the addition of GM-CSF to pembrolizumab was well-tolerated but did not meet the pre-specified response rate for efficacy. A subset of patients experienced deep responses and prolonged stable disease. GM-CSF elicited changes in the tumor immune microenvironment that could guide future combination approaches.
Authors
- Bridget P. Keenan (ORCID: https://orcid.org/0000-0001-6075-489X)
- Katherine Van Loon (ORCID: https://orcid.org/0000-0002-9705-4114)
- Andrew Ko (ORCID: https://orcid.org/0000-0003-0426-1753)
- Robin Kate Kelley (ORCID: https://orcid.org/0000-0002-1984-2430)
- Zoe Quandt (ORCID: https://orcid.org/0000-0002-4568-4368)
- Spencer C. Behr (ORCID: https://orcid.org/0000-0001-9400-0543)
- Alan P. Venook (ORCID: https://orcid.org/0000-0001-9749-6548)
- John D. Gordan (ORCID: https://orcid.org/0000-0001-8997-5725)
- Paige M. Bracci (ORCID: https://orcid.org/0000-0001-9338-9307)
- Wesley A. Kidder (ORCID: https://orcid.org/0000-0001-8851-7853)
- Huat Chye Lim (ORCID: https://orcid.org/0000-0001-8161-1847)
- Chloé E. Atreya (ORCID: https://orcid.org/0000-0003-2954-1727)
- Lawrence H. Fong (ORCID: https://orcid.org/0000-0002-6428-428X)
- Nia Adeniji (ORCID: https://orcid.org/0000-0002-7957-5987)
Institutions
- Cape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa (ZA)
- University of California, San Francisco (US)
- Fred Hutch Cancer Center (US)
- UCSF Helen Diller Family Comprehensive Cancer Center (US)
- University of San Francisco (US)
- Stanford University (US)
Publication Details
- Journal
- Clinical Cancer Research
- Published
- 2026-08-14
- DOI
- https://doi.org/10.1158/1078-0432.ccr-25-3987
- Primary Topic
- Cholangiocarcinoma and Gallbladder Cancer Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00