Evidence map›Paper›PMID 34433663›Full record

ArticleMolecular cancer therapeutics2021

Vimseltinib: A Precision CSF1R Therapy for Tenosynovial Giant Cell Tumors and Diseases Promoted by Macrophages.

Bryan D Smith, Michael D Kaufman, Scott C Wise, Yu Mi Ahn, Timothy M Caldwell, Cynthia B Leary, Wei-Ping Lu, Gege Tan, Lakshminarayana Vogeti, Subha Vogeti and 5 more

Open access · bronzeAbstract readCase Reports
In one paragraph

Article in Molecular cancer therapeutics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
7.0field-weighted citation impact, top 2% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 65 citations in OpenAlex.

  1. Pooled it
  2. CSF1R Inhibition in Patients with Advanced Solid Tumors or Tenosynovial Giant Cell Tumor: A Phase I Study of Vimseltinib.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
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  4. Small-Molecule Drugs Approved by the FDA in 2025.Molecules (Basel, Switzerland) · 2026
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  12. Design and Synthesis of Pyridine-Based Pyrrolo[2,3-Pharmaceuticals (Basel, Switzerland) · 2025
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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 3 institutions in 1 country.

Bryan D SmithDeciphera Pharmaceuticals, LLC, Waltham, Massachusetts.
Michael D KaufmanDeciphera Pharmaceuticals, LLC, Waltham, Massachusetts.
Scott C WiseDeciphera Pharmaceuticals, LLC, Waltham, Massachusetts.ORCID 0000-0003-2078-8758
Yu Mi AhnDeciphera Pharmaceuticals, LLC, Waltham, Massachusetts.
Timothy M CaldwellDeciphera Pharmaceuticals, LLC, Waltham, Massachusetts.
Cynthia B LearyDeciphera Pharmaceuticals, LLC, Waltham, Massachusetts.
Wei-Ping LuDeciphera Pharmaceuticals, LLC, Waltham, Massachusetts.
Gege TanDeciphera Pharmaceuticals, LLC, Waltham, Massachusetts.
Lakshminarayana VogetiDeciphera Pharmaceuticals, LLC, Waltham, Massachusetts.
Subha VogetiDeciphera Pharmaceuticals, LLC, Waltham, Massachusetts.
Breelyn A WilkyUniversity of Colorado Cancer Center, Aurora, Colorado.
Lara E DavisOregon Health & Science University, Knight Cancer Institute, Portland, Oregon.ORCID 0000-0002-6480-1611
Maitreyi SharmaDeciphera Pharmaceuticals, LLC, Waltham, Massachusetts.
Rodrigo Ruiz-SotoDeciphera Pharmaceuticals, LLC, Waltham, Massachusetts.
Daniel L FlynnDeciphera Pharmaceuticals, LLC, Waltham, Massachusetts. dflynn@deciphera.com.
Deciphera Pharmaceuticals (United States) · USOregon Health & Science University · USUniversity of Colorado Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Macrophages can be co-opted to contribute to neoplastic, neurologic, and inflammatory diseases. Colony-stimulating factor 1 receptor (CSF1R)-dependent macrophages and other inflammatory cells can suppress the adaptive immune system in cancer and contribute to angiogenesis, tumor growth, and metastasis. CSF1R-expressing osteoclasts mediate bone degradation in osteolytic cancers and cancers that metastasize to bone. In the rare disease tenosynovial giant cell tumor (TGCT), aberrant CSF1 expression and production driven by a gene translocation leads to the recruitment and growth of tumors formed by CSF1R-dependent inflammatory cells. Small molecules and antibodies targeting the CSF1/CSF1R axis have shown promise in the treatment of TGCT and cancer, with pexidartinib recently receiving FDA approval for treatment of TGCT. Many small-molecule kinase inhibitors of CSF1R also inhibit the closely related kinases KIT, PDGFRA, PDGFRB, and FLT3, thus CSF1R suppression may be limited by off-target activity and associated adverse events. Vimseltinib (DCC-3014) is an oral, switch control tyrosine kinase inhibitor specifically designed to selectively and potently inhibit CSF1R by exploiting unique features of the switch control region that regulates kinase conformational activation. In preclinical studies, vimseltinib durably suppressed CSF1R activity

Indexed as

AdultAnimalsCell ProliferationCross-Over StudiesDisease Models, AnimalFemaleGiant Cell Tumor of Tendon SheathHumansMacrophagesMaleMiceMice, NudeMiddle AgedModels, MolecularProtein Kinase InhibitorsRatsProtein Kinase Inhibitors

Identifiers

PMID34433663
PMCPMC9398179
OpenAlexW3193545729

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.