Evidence map›Paper›PMID 42599167›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2026

A Phase II Trial of Pembrolizumab plus Granulocyte-Macrophage Colony-Stimulating Factor in Advanced Biliary Cancer.

Robin Kate Kelley, Paige Bracci, John D Gordan, Spencer C Behr, Zoe Quandt, Chloe E Atreya, Wesley A Kidder, Andrew H Ko, Huat Chye Lim, Katherine Van Loon and 4 more

Abstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Robin Kate KelleyUniversity of California, San Francisco San Francisco, CA United States.ORCID 0000-0002-1984-2430
Paige BracciUniversity of California, San Francisco San Francisco, CA United States.ORCID 0000-0001-9338-9307
John D GordanUniversity of California, San Francisco San Francisco, CA United States.ORCID 0000-0001-8997-5725
Spencer C BehrUniversity of California, San Francisco San Francisco, California United States.ORCID 0000-0001-9400-0543
Zoe QuandtUniversity of California, San Francisco San Francisco, CA United States.ORCID 0000-0002-4568-4368
Chloe E AtreyaUniversity of California, San Francisco San Francisco, CA United States.ORCID 0000-0003-2954-1727
Wesley A KidderUniversity of California, San Francisco United States.ORCID 0000-0001-8851-7853
Andrew H KoUniversity of California, San Francisco San Francisco United States.ORCID 0000-0003-0426-1753
Huat Chye LimUniversity of California, San Francisco San Francisco, CA United States.ORCID 0000-0001-8161-1847
Katherine Van LoonUCSF Helen Diller Family Comprehensive Cancer Center San Francisco, CA United States.ORCID 0000-0002-9705-4114
Nia AdenijiStanford University United States.ORCID 0000-0002-7957-5987
Alan P VenookUniversity of California, San Francisco San Francisco, CA United States.ORCID 0000-0001-9749-6548
Lawrence FongFred Hutch Cancer Center Seattle, WA United States.ORCID 0000-0002-6428-428X
Bridget P KeenanUniversity of California, San Francisco San Francisco, CA United States.ORCID 0000-0001-6075-489X

Funding

Tumor Molecular Profiling and Response to Immunotherapy in Advanced Biliary CancersR03CA212877 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KELLEY, ROBIN KATE · 2017 to 2018
$159k
NCI NIH HHS R03 CA212877
6 · The paper itself

Abstract

purposeImmune 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

designPembrolizumab 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.

resultsAmong 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.

conclusionsthe 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.

Identifiers

PMID42599167
PMCPMC13591631

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.