Evidence map›Paper›PMID 30545915›Full record

Trial reportProceedings of the National Academy of Sciences of the United States of America2019

Blocking IL-1β reverses the immunosuppression in mouse breast cancer and synergizes with anti-PD-1 for tumor abrogation.

Irena Kaplanov, Yaron Carmi, Rachel Kornetsky, Avishai Shemesh, Galina V Shurin, Michael R Shurin, Charles A Dinarello, Elena Voronov, Ron N Apte

Registry-linked trialOpen access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04581343 (A Phase 1B Study to Determine the Safety and Tolerability and Confirm the Dose of Canakinumab and Spartalizumab in Combination With Nab-paclitaxel and Gemcitabine for Patients With Metastatic Pancreatic Cancer), which is not on this map. Cited by 273 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
273citing papers in PubMed, 3 pooled it
13.0field-weighted citation impact, top 1% of its field
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.

NCT04581343 phase1completednot on this mapstarted 2020, after this paper: background citation

A Phase 1B Study to Determine the Safety and Tolerability and Confirm the Dose of Canakinumab and Spartalizumab in Combination With Nab-paclitaxel and Gemcitabine for Patients With Metastatic Pancreatic Cancer

TypeinterventionalSponsorPancreatic Cancer Action NetworkRan2020 to 2023Enrolled10ConditionsMetastatic Pancreatic Ductal AdenocarcinomaArmsCanakinumab injection, spartalizumab, nab-paclitaxel, gemcitabine
3 · Its place in the literature

Who cites it

273 citing papers in PubMed, 3 syntheses or guidelines pooled it, 427 citations in OpenAlex.

  1. Pooled it
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  8. Enhanced efficacy of a next-generation EEEV self-replicating RNA platform for combination cancer immunotherapies.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
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  15. Progress in Designing Cytokine Antagonist Antibodies for Cancer Therapy.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2026
    Review
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213 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 3 countries.

Irena KaplanovThe Shraga Segal Department of Microbiology, Immunology and Genetics, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva 84105, Israel.
Yaron CarmiThe Shraga Segal Department of Microbiology, Immunology and Genetics, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva 84105, Israel.ORCID 0000-0002-0972-0616
Rachel KornetskyThe Shraga Segal Department of Microbiology, Immunology and Genetics, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva 84105, Israel.
Avishai ShemeshThe Shraga Segal Department of Microbiology, Immunology and Genetics, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva 84105, Israel.
Galina V ShurinDepartment of Pathology, University of Pittsburgh Medical Center, Pittsburgh, PA 15261.
Michael R ShurinDepartment of Pathology, University of Pittsburgh Medical Center, Pittsburgh, PA 15261.
Charles A DinarelloDepartment of Medicine, University of Colorado, Aurora, CO 80045; rapte@bgu.ac.il cdinare333@aol.com.ORCID 0000-0002-5073-8316
Elena VoronovThe Shraga Segal Department of Microbiology, Immunology and Genetics, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva 84105, Israel.
Ron N ApteThe Shraga Segal Department of Microbiology, Immunology and Genetics, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva 84105, Israel; rapte@bgu.ac.il cdinare333@aol.com.
Ben-Gurion University of the Negev · ILUniversity of Pittsburgh Medical Center · USRadboud University Nijmegen · NL

Funding

Yeast-based HTS Assay Technologies for ProteasesR01AI015614 · NIAID · UNIVERSITY OF COLORADO DENVER · PI DINARELLO, CHARLES ANTHONY · 1985 to 2025
$8.5M
Pathogenesis of Fever in ManR56AI015614 · NIAID · UNIVERSITY OF COLORADO DENVER · PI DINARELLO, CHARLES ANTHONY · 2016 to 2016
$311k
NIAID NIH HHS R01 AI015614NIAID NIH HHS R56 AI015614
6 · The paper itself

Abstract

Interleukin-1β (IL-1β) is abundant in the tumor microenvironment, where this cytokine can promote tumor growth, but also antitumor activities. We studied IL-1β during early tumor progression using a model of orthotopically introduced 4T1 breast cancer cells. Whereas there is tumor progression and spontaneous metastasis in wild-type (WT) mice, in IL-1β-deficient mice, tumors begin to grow but subsequently regress. This change is due to recruitment and differentiation of inflammatory monocytes in the tumor microenvironment. In WT mice, macrophages heavily infiltrate tumors, but in IL-1β-deficient mice, low levels of the chemokine CCL2 hamper recruitment of monocytes and, together with low levels of colony-stimulating factor-1 (CSF-1), inhibit their differentiation into macrophages. The low levels of macrophages in IL-1β-deficient mice result in a relatively high percentage of CD11b

Indexed as

AnimalsAntibodies, MonoclonalAntineoplastic AgentsBreast NeoplasmsCD11b AntigenCD8-Positive T-LymphocytesCell DifferentiationCell Line, TumorColony-Stimulating FactorsDendritic CellsFemaleGranzymesHumansImmunosuppression TherapyInflammationInterferon-gammaAntibodies, MonoclonalAntineoplastic AgentsCD11b AntigenColony-Stimulating FactorsGranzymesIL1B protein, mouseInterferon-gammaInterleukin-1betaPdcd1 protein, mouseProgrammed Cell Death 1 ReceptorTumor Necrosis Factor-alphaanti–PD-1antitumor immunitybreast cancerIL-1βimmunotherapy

Identifiers

PMID30545915
PMCPMC6347724
OpenAlexW2904125616

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.