Evidence map›Paper›PMID 35121932›Full record

Trial reportNature cancer2020

Flt3 ligand augments immune responses to anti-DEC-205-NY-ESO-1 vaccine through expansion of dendritic cell subsets.

Nina Bhardwaj, Philip A Friedlander, Anna C Pavlick, Marc S Ernstoff, Brian R Gastman, Brent A Hanks, Brendan D Curti, Mark R Albertini, Jason J Luke, Ana B Blazquez and 24 more

Registry-linked trialAbstract readClinical Trial, Phase IIRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Nature cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02129075 (A Phase II, Open-Label, Multicenter, Randomized Study of CDX-1401, a Dendritic Cell Targeting NY-ESO-1 Vaccine, in Patients With Malignant Melanoma Pre-Treated With Recombinant CDX-301, a Recombinant Human Flt3 Ligand), which is not on this map. Cited by 87 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
87citing papers in PubMed, 1 pooled it
4.6field-weighted citation impact, top 4% 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.

NCT02129075 phase2completednot on this map

A Phase II, Open-Label, Multicenter, Randomized Study of CDX-1401, a Dendritic Cell Targeting NY-ESO-1 Vaccine, in Patients With Malignant Melanoma Pre-Treated With Recombinant CDX-301, a Recombinant Human Flt3 Ligand

TypeinterventionalSponsorNational Cancer Institute (NCI)Ran2014 to 2018Enrolled60ConditionsCutaneous Melanoma, Melanoma, Melanoma of Unknown Primary, Mucosal MelanomaArmsDEC-205/NY-ESO-1 Fusion Protein CDX-1401, Poly ICLC, Recombinant Flt3 Ligand
3 · Its place in the literature

Who cites it

87 citing papers in PubMed, 1 synthesis or guideline pooled it, 119 citations in OpenAlex.

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  11. Tim-3-targeted vaccines overcome tumor immunosuppression and reduce cDC1 dependence to elicit potent anti-tumor immunity.Proceedings of the National Academy of Sciences of the United States of America · 2026
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27 more citing papers are in PubMed but not listed here.

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

34 authors at 18 institutions in 2 countries.

Nina BhardwajTisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA. nina.bhardwaj@mssm.edu.ORCID http://orcid.org/0000-0003-1865-4187
Philip A FriedlanderTisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Anna C PavlickNYU Perlmutter Cancer Center, New York, NY, USA.
Marc S ErnstoffRoswell Park Comprehensive Cancer Center, Buffalo, NY, USA.ORCID http://orcid.org/0000-0002-8132-7069
Brian R GastmanCleveland Clinic, Cleveland, OH, USA.
Brent A HanksDuke University Medical Center, Durham, NC, USA.
Brendan D CurtiProvidence Portland Medical Center, Portland, OR, USA.
Mark R AlbertiniUniversity of Wisconsin, Madison, WI, USA.
Jason J LukeUniversity of Chicago Comprehensive Cancer Center, Chicago, IL, USA.
Ana B BlazquezTisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Sreekumar BalanTisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.ORCID http://orcid.org/0000-0002-2092-5145
Davide BedognettiSidra Medicine, Doha, Qatar.
Joseph M BeechemNanoString Technologies, Seattle, WA, USA.
Andrea S CrockerCelldex Therapeutics, Hampton, NJ, USA.
Leonard D'AmicoCancer Immunotherapy Trials Network, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
Patrick DanaherNanoString Technologies, Seattle, WA, USA.ORCID http://orcid.org/0000-0002-2844-5883
Thomas A DavisGenocea Biosciences, Cambridge, MA, USA.
Thomas HawthorneCelldex Therapeutics, Hampton, NJ, USA.
Bruce W HessCancer Immunotherapy Trials Network, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
Tibor KelerCelldex Therapeutics, Hampton, NJ, USA.
Lisa LundgrenCancer Immunotherapy Trials Network, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
Chihiro MorishimaUniversity of Washington, Seattle, WA, USA.
Nirasha RamchurrenCancer Immunotherapy Trials Network, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
Darawan RinchaiSidra Medicine, Doha, Qatar.ORCID http://orcid.org/0000-0001-8851-7730
Andres M SalazarOncovir, Inc., Washington, DC, USA.
Bob A SalimAxio Research, Seattle, WA, USA.
Elad SharonNational Institutes of Health, Bethesda, MD, USA.
Laura A VitaleCelldex Therapeutics, Hampton, NJ, USA.
Ena WangSidra Medicine, Doha, Qatar.
Sarah WarrenNanoString Technologies, Seattle, WA, USA.
Michael J YellinCelldex Therapeutics, Hampton, NJ, USA.
Mary L DisisUniversity of Washington, Seattle, WA, USA.
Martin A CheeverCancer Immunotherapy Trials Network, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
Steven P FlingCancer Immunotherapy Trials Network, Fred Hutchinson Cancer Research Center, Seattle, WA, USA. sfling@fredhutch.org.ORCID http://orcid.org/0000-0001-6263-0153
Celldex Therapeutics (United States) · USFred Hutch Cancer Center · USIcahn School of Medicine at Mount Sinai · USNanostring Technologies (United States) · USUniversity of Washington · USAptevo Therapeutics (United states) · USCape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa · ZACleveland Clinic · USDuke Medical Center · USGenocea (United States) · USNational Institutes of Health · USNYU Langone’s Laura and Isaac Perlmutter Cancer CenterOncovir (United States) · USProvidence Portland Medical Center · USRoswell Park Comprehensive Cancer Center · USTisch Hospital · USUniversity of Chicago · USUniversity of Wisconsin–Madison · US

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Eric Collisson · 1985 to 2026
$296.4M
Cancer Immunotherapy Trials Network Central Operations and Statistical CenterUM1CA154967 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI DAVIDSON, NANCY ELLEN · 2017 to 2022
$20.7M
Cancer Immunotherapy Trials Network Central Operations and Statistical CenterU01CA154967 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI CHEEVER, MARTIN ALEXANDER · 2010 to 2017
$16.8M
Modulating anti-HIV immunity by plasmacytoid dendritic cellsR01AI081848 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BHARDWAJ, NINA · 2010 to 2021
$4.5M
NK cell exhaustion in metastatic melanomaR01CA201189 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BHARDWAJ, NINA · 2016 to 2020
$2.1M
Matrix metalloproteinase-2 modulates inflammation via TLR2R01CA180913 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BHARDWAJ, NINA · 2014 to 2018
$1.8M
Melanoma-mediated Dendritic Cell Tolerization and Immune EvasionK08CA191063 · NCI · DUKE UNIVERSITY · PI HANKS, BRENT ALLEN · 2015 to 2019
$826k
NCI NIH HHS K08 CA191063NCI NIH HHS P30 CA015704NCI NIH HHS R01 CA180913NCI NIH HHS R01 CA201189NCI NIH HHS U01 CA154967NCI NIH HHS UM1 CA154967NIAID NIH HHS R01 AI081848
6 · The paper itself

Abstract

Generating responses to tumor antigens poses a challenge for immunotherapy. This phase II trial (NCT02129075) tested fms-like tyrosine kinase 3 (Flt3) ligand pre-treatment enhancement of responses to dendritic cell (DC)-targeting vaccines. We evaluated a regimen of Flt3L (CDX-301) to increase DCs and other antigen-presenting cells, poly-ICLC (TLR3 agonist that activates DCs) and a vaccine comprising anti-DEC-205-NY-ESO-1, a fusion antibody targeting CD205, linked to NY-ESO-1. High-risk melanoma patients were randomized to vaccine, with and without CDX-301. The end point was immune response to NY-ESO-1. Flt3L increased peripheral monocytes and conventional DCs (cDCs), including cross-presenting cDC1 and cDC2 and plasmacytoid DCs. Significant increases in humoral and T-cell responses and activation of DCs, natural killer cells and T cells were elicited. Transcriptional analyses revealed gene signatures associated with CDX-301 induction of an early, durable immune response. This study reveals in vivo effects of Flt3L on innate immune cells in the setting of vaccination, leading to an immunogenic vaccine regimen.

Indexed as

Cancer VaccinesMelanomaDendritic Cellsfms-Like Tyrosine Kinase 3HumansImmunityMembrane ProteinsCancer Vaccinesflt3 ligand proteinFLT3 protein, humanfms-Like Tyrosine Kinase 3Membrane Proteins

Identifiers

PMID35121932
OpenAlexW3100153578

What OpenQuestion holds

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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.