Evidence map›Paper›PMID 33721151›Full record

ReviewCurrent oncology reports2021

Neurofibromatosis in the Era of Precision Medicine: Development of MEK Inhibitors and Recent Successes with Selumetinib.

Robert Galvin, Adrienne L Watson, David A Largaespada, Nancy Ratner, Sara Osum, Christopher L Moertel

Open access · greenAbstract readReview
In one paragraph

Review in Current oncology reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.6field-weighted citation impact, top 8% 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

14 citing papers in PubMed, 30 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Identifying Bone Matrix Impairments in a Mouse Model of Neurofibromatosis Type 1 (NF1) by Clinically Translatable Techniques.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2022
    Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Neuro-oncology advances
    Article
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

6 authors at 4 institutions in 1 country.

Robert GalvinDivisions of Pediatric Hematology & Oncology and Bone Marrow Transplant, University of Minnesota, Minneapolis, MN, USA.ORCID 0000-0001-7139-9707
Adrienne L WatsonRecombinetics, Inc., Saint Paul, MN, USA.
David A LargaespadaDivision of Pediatric Hematology & Oncology, Masonic Cancer Center, University of Minnesota, Minneapolis, MN, USA.
Nancy RatnerCincinnati Children's Hospital Division of Exp. Hematology and Cancer Biology, Department of Pediatrics, University of Cincinnati, Cincinnati, OH, USA.
Sara OsumDivision of Pediatric Hematology & Oncology, Masonic Cancer Center, University of Minnesota, Minneapolis, MN, USA.
Christopher L MoertelDivision of Pediatric Hematology & Oncology, University of Minnesota, Minneapolis, MN, USA. moert001@umn.edu.
University of Minnesota · USUniversity of Minnesota Medical Center · USCincinnati Children's Hospital Medical Center · USRecombinetics (United States) · US

Funding

VITAMIN K DEFICIENCY IN CHOLESTATIC LIVER DISEASEM01RR008084 · NCRR · CINCINNATI CHILDRENS HOSP MED CTR · PI STRAUSS, ARNOLD W · 1994 to 2009
$20.6M
MITOGENIC ACTIVITIES IN NEUROFIBROMATOSISR01NS028840 · NINDS · UNIVERSITY OF CINCINNATI · PI NANCY RATNER · 1990 to 2026
$10.1M
Translational Pediatric Cancer Epidemiology Research Training GrantT32CA099936 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Logan G. Spector · 2004 to 2026
$5.1M
Targeting Tumors with NF1 LossR01NS095411 · NINDS · DARTMOUTH COLLEGE · PI HOOPES, JACK, RATNER, NANCY · 2015 to 2019
$2.7M
Disordered Regulation of Wnt/beta-catenin Signaling in MPNST Development and MaintenanceR01NS086219 · NINDS · UNIVERSITY OF MINNESOTA · PI LARGAESPADA, DAVID ANDREW, RATNER, NANCY · 2014 to 2018
$2.4M
NCI NIH HHS T32 CA099936NCRR NIH HHS M01 RR008084NINDS NIH HHS R01 NS028840NINDS NIH HHS R01 NS086219NINDS NIH HHS R01 NS095411
6 · The paper itself

Abstract

purpose of reviewPatients with neurofibromatosis type 1 (NF1) are at increased risk for benign and malignant neoplasms. Recently, targeted therapy with the MEK inhibitor class has helped address these needs. We highlight recent successes with selumetinib while acknowledging ongoing challenges for NF1 patients and future directions. RECENT

findingsMEK inhibitors have demonstrated efficacy for NF1-related conditions, including plexiform neurofibromas and low-grade gliomas, two common causes of NF1-related morbidity. Active investigations for NF1-related neoplasms have benefited from advanced understanding of the genomic and cell signaling alterations in these conditions and development of sound preclinical animal models. Selumetinib has become the first FDA-approved targeted therapy for NF1 following its demonstrated efficacy for inoperable plexiform neurofibroma. Investigations of combination therapy and the development of a representative NF1 swine model hold promise for translating therapies for other NF1-associated pathology.

Indexed as

AnimalsBenzimidazolesClinical Trials as TopicDisease Models, AnimalHumansMitogen-Activated Protein Kinase KinasesNeurofibroma, PlexiformNeurofibromatosis 1Precision MedicineProtein Kinase InhibitorsSignal TransductionSwineAZD 6244BenzimidazolesMitogen-Activated Protein Kinase KinasesProtein Kinase InhibitorsCombination therapyLow-grade gliomaMalignant peripheral nerve sheath tumorMEK inhibitorNeurofibromatosisOptic pathway gliomaPlexiform neurofibromaSelumetinib

Identifiers

PMID33721151
PMCPMC10859964
OpenAlexW3138209901

What OpenQuestion holds

Textmetadata
LicenceTDM
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.