Evidence map›Paper›PMID 32459399›Full record

ArticlePediatric blood & cancer2020

Early administration of imatinib mesylate reduces plexiform neurofibroma tumor burden with durable results after drug discontinuation in a mouse model of neurofibromatosis type 1.

Amy E Armstrong, Steven D Rhodes, Abbi Smith, Shi Chen, Waylan Bessler, Michael J Ferguson, Li Jiang, Xiaohong Li, Jin Yuan, Xianlin Yang and 5 more

Open access · greenAbstract read
In one paragraph

Article in Pediatric blood & cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.2field-weighted citation impact, top 46% 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.

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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Trial
  2. TheCancers · 2024
    Review
  3. Combined CDK4/6 and ERK1/2 Inhibition Enhances Antitumor Activity in NF1-Associated Plexiform Neurofibroma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
    Article
  4. [Progress in diagnosis and treatment of neurofibromatosis in children].Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery · 2022
    Review
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

15 authors at 5 institutions in 1 country.

Amy E ArmstrongDivision of Pediatric Hematology/Oncology, Riley Hospital for Children, Indianapolis, Indiana.ORCID 0000-0002-7784-0476
Steven D RhodesDivision of Pediatric Hematology/Oncology, Riley Hospital for Children, Indianapolis, Indiana.
Abbi SmithDepartment of Pediatrics, Herman B. Wells Center for Pediatric Research, Indianapolis, Indiana.
Shi ChenDepartment of Pediatrics, Herman B. Wells Center for Pediatric Research, Indianapolis, Indiana.
Waylan BesslerDepartment of Pediatrics, Herman B. Wells Center for Pediatric Research, Indianapolis, Indiana.
Michael J FergusonDivision of Pediatric Hematology/Oncology, Riley Hospital for Children, Indianapolis, Indiana.
Li JiangDepartment of Pediatrics, Herman B. Wells Center for Pediatric Research, Indianapolis, Indiana.
Xiaohong LiDepartment of Pediatrics, Herman B. Wells Center for Pediatric Research, Indianapolis, Indiana.
Jin YuanDepartment of Pediatrics, Herman B. Wells Center for Pediatric Research, Indianapolis, Indiana.
Xianlin YangDepartment of Pediatrics, Herman B. Wells Center for Pediatric Research, Indianapolis, Indiana.
Feng-Chun YangDepartment of Pediatrics, Herman B. Wells Center for Pediatric Research, Indianapolis, Indiana.
Kent A RobertsonDivision of Pediatric Hematology/Oncology, Riley Hospital for Children, Indianapolis, Indiana.
David A IngramDepartment of Pediatrics, Herman B. Wells Center for Pediatric Research, Indianapolis, Indiana.
Jaishri O BlakeleyDepartment of Neurology, The Johns Hopkins University School of Medicine, Baltimore, Maryland.
D Wade ClappDepartment of Pediatrics, Herman B. Wells Center for Pediatric Research, Indianapolis, Indiana.
Indiana University · USRiley Hospital for Children · USIndiana University School of MedicineJohns Hopkins University · USWashington University in St. Louis · US

Funding

Pediatric Scientist Development Program (PSDP) [K12]K12HD000850 · NICHD · YALE UNIVERSITY · PI Sallie R. Permar · 1987 to 2026
$44.1M
Project 4: Secondary Cancers Among NF1 Cancer SurvivorsU54CA196519 · NCI · INDIANA UNIVERSITY INDIANAPOLIS · PI David W Clapp, KEVIN M. SHANNON · 2015 to 2026
$26.9M
Transgenic CoreP50NS052606 · NINDS · UT SOUTHWESTERN MEDICAL CENTER · PI CLAPP, DAVID W · 2005 to 2014
$12.6M
Neurofibromatosis Type 1 Gene Regulates MyelopoiesisR01CA074177 · NCI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI CLAPP, DAVID W · 2002 to 2012
$3.6M
Preclinical Testing of Targeted Therapies for NeurofibromasU01NS055849 · NINDS · INDIANA UNIVERSITY INDIANAPOLIS · PI CLAPP, DAVID W · 2008 to 2011
$2.4M
F-box ubiquitin ligases destabilize neurofibrominR01NS104489 · NINDS · INDIANA UNIVERSITY INDIANAPOLIS · PI CLAPP, DAVID W · 2018 to 2022
$1.7M
NCI NIH HHS R01 CA074177NCI NIH HHS U54 CA196519NICHD NIH HHS K12 HD000850NIH HHS P50NS052606-1 (DWC)NIH HHS R01NS104489-02 (DWC)NIH HHS SPORE U54-CA196519-05 NIH/NCI (DWC)NIH HHS U01NS055849-04 (DWC)NINDS NIH HHS P50 NS052606NINDS NIH HHS R01 NS104489NINDS NIH HHS U01 NS055849
6 · The paper itself

Abstract

backgroundNeurofibromatosis type 1 (NF1) is a common genetic disorder characterized by plexiform neurofibromas (pNF), which are thought to be congenital tumors that arise in utero and enlarge throughout life. Genetic studies in murine models delineated an indispensable role for the stem cell factor (SCF)/c-kit pathway in pNF initiation and progression. A subsequent phase 2 clinical trial using imatinib mesylate to inhibit SCF/c-kit demonstrated tumor shrinkage in a subset of preexisting pNF; however, imatinib's role on preventing pNF development has yet to be explored. PROCEDURE: We evaluated the effect of imatinib dosed at 10-100 mg/kg/day for 12 weeks to one-month-old Nf1

resultsImatinib administered preventatively led to a significant decrease in pNF number, even at doses as low as 10 mg/kg/day. Tumor development continued to be significantly inhibited after cessation of imatinib dosed at 50 and 100 mg/kg/day. In the cohort of treated mice that underwent prolonged follow-up, the size of residual tumors was significantly reduced as compared with age-matched littermates that received vehicle control.

conclusionsEarly administration of imatinib inhibits pNF genesis in vivo, and effects are sustained after discontinuation of therapy. These findings may guide clinical use of imatinib in young NF1 patients prior to the substantial development of pNF.

Indexed as

AnimalsDrug Screening Assays, AntitumorHumansImatinib MesylateMiceMice, TransgenicNeoplasms, ExperimentalNeurofibroma, PlexiformNeurofibromatosis 1Imatinib Mesylateimatinib mesylateNF1plexiform neurofibromapreventative therapy

Identifiers

PMID32459399
PMCPMC7516834
OpenAlexW3031215759

What OpenQuestion holds

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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.