Evidence map›Paper›PMID 30911166›Full record

ArticleNature nanotechnology2019

FDA-approved ferumoxytol displays anti-leukaemia efficacy against cells with low ferroportin levels.

Vicenta Trujillo-Alonso, Edwin C Pratt, Hongliang Zong, Andres Lara-Martinez, Charalambos Kaittanis, Mohamed O Rabie, Valerie Longo, Michael W Becker, Gail J Roboz, Jan Grimm and 1 more

Registry-linked trialAbstract read
In one paragraph

Article in Nature nanotechnology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06048367 (Carbon Nanoparticle-Loaded Iron [CNSI-Fe), which is not on this map. Cited by 148 papers.

0numbers the graph read from it
0cells of the map it votes in
148citing papers in PubMed
27.0field-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.

NCT06048367 phase1completednot on this mapstarted 2022, after this paper: background citation

Carbon Nanoparticle-Loaded Iron [CNSI-Fe(II)] Dose Escalation Study for the Treatment of Advanced Solid Tumors: Phase 1 Clinical Trial

TypeinterventionalSponsorSichuan Enray Pharmaceutical Sciences CompanyRan2022 to 2025Enrolled19ConditionsAdvanced Solid Tumor, Lung Cancer, Pancreas Cancer, Breast CancerArmsCNSI-Fe(II) 30 mg, CNSI-Fe(II) 60 mg, CNSI-Fe(II) 90 mg, CNSI-Fe(II) 120 mg, CNSI-Fe(II) 150 mg
3 · Its place in the literature

Who cites it

148 citing papers in PubMed, 311 citations in OpenAlex.

  1. Article
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  9. Effect of clinically relevant iron oxide nanoparticles on macrophage polarization, tumor growth and tumor microenvironment modulation.Journal of controlled release : official journal of the Controlled Release Society · 2026
    Article
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  11. Article
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88 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 1 country.

Vicenta Trujillo-AlonsoDivision of Hematology/Oncology, Department of Medicine, Weill Cornell Medical College, New York, NY, USA.
Edwin C PrattDepartment of Pharmacology, Weill Cornell Graduate School, New York, NY, USA.ORCID http://orcid.org/0000-0002-6054-6983
Hongliang ZongDivision of Hematology/Oncology, Department of Medicine, Weill Cornell Medical College, New York, NY, USA.
Andres Lara-MartinezDivision of Hematology/Oncology, Department of Medicine, Weill Cornell Medical College, New York, NY, USA.
Charalambos KaittanisMolecular Pharmacology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Mohamed O RabieDivision of Hematology/Oncology, Department of Medicine, Weill Cornell Medical College, New York, NY, USA.
Valerie LongoSmall-Animal Imaging Core Facility, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Michael W BeckerDepartment of Medicine, Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY, USA.
Gail J RobozDivision of Hematology/Oncology, Department of Medicine, Weill Cornell Medical College, New York, NY, USA.
Jan GrimmDepartment of Pharmacology, Weill Cornell Graduate School, New York, NY, USA. grimmj@mskcc.org.ORCID http://orcid.org/0000-0002-5282-9385
Monica L GuzmanDivision of Hematology/Oncology, Department of Medicine, Weill Cornell Medical College, New York, NY, USA. mlg2007@med.cornell.edu.ORCID http://orcid.org/0000-0002-9262-8246
Cornell University · USMemorial Sloan Kettering Cancer Center · USUniversity of Rochester Medical Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
PHARMACOLOGICAL MODULATION OF EPIGENETIC CHANTGES IN AMLR01CA102031 · NCI · OHIO STATE UNIVERSITY · PI GUZMAN, MONICA L, MARCUCCI, GUIDO · 2004 to 2017
$3.8M
Smart and self-reporting clinical nano carriers for drug deliveryR01CA215700 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI GRIMM, JAN · 2017 to 2021
$3.5M
Biomarkers for predicting response to Hsp90 therapyR01CA172546 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI CHIOSIS, GABRIELA, DUNPHY, MARK P. · 2013 to 2017
$2.9M
Exploiting ferroportin for cancer imaging and therapyR01CA218615 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI GRIMM, JAN · 2017 to 2021
$2.7M
NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA102031NCI NIH HHS R01 CA172546NCI NIH HHS R01 CA215700NCI NIH HHS R01 CA218615
6 · The paper itself

Abstract

Acute myeloid leukaemia is a fatal disease for most patients. We have found that ferumoxytol (Feraheme), an FDA-approved iron oxide nanoparticle for iron deficiency treatment, demonstrates an anti-leukaemia effect in vitro and in vivo. Using leukaemia cell lines and primary acute myeloid leukaemia patient samples, we show that low expression of the iron exporter ferroportin results in a susceptibility of these cells via an increase in intracellular iron from ferumoxytol. The reactive oxygen species produced by free ferrous iron lead to increased oxidative stress and cell death. Ferumoxytol treatment results in a significant reduction of disease burden in a murine leukaemia model and patient-derived xenotransplants bearing leukaemia cells with low ferroportin expression. Our findings show how a clinical nanoparticle previously considered largely biologically inert could be rapidly incorporated into clinical trials for patients with leukaemia with low ferroportin levels.

Indexed as

Ferrosoferric OxideLeukemia, Myeloid, AcuteNeoplasms, ExperimentalAnimalsCation Transport ProteinsCell Line, TumorDrug ApprovalFerroportinMiceNeoplasm ProteinsReactive Oxygen SpeciesUnited StatesUnited States Food and Drug AdministrationXenograft Model Antitumor AssaysCation Transport ProteinsFerroportinFerrosoferric OxideNeoplasm ProteinsReactive Oxygen Species

Identifiers

PMID30911166
PMCPMC6554053
OpenAlexW2924151995

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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.