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Gene

PDGFRB

PDGFRB is a gene biomarker in the evidence tier "FDA companion diagnostic". This page lists evidence by type: FDA companion diagnostic assertions (1), Assay-provider ledger (19), Trial mentions (176), and 6 more evidence types, each linked to its source.

Ensembl ENSG00000113721 UniProt P09619 Matched to Ensembl and UniProt
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FDA companion diagnostic assertions FDA companion diagnostic assertions 1 Assay-provider ledger Assay-provider ledger 19 Trial mentions Trial mentions 176 Target-disease associations Target-disease associations 1,089 Vendor sourcing Vendor sourcing 544 Trial-cited literature Trial-cited literature 814 Protein variant mentions Protein variant mentions 23 Literature-extracted relations Literature-extracted relations 148 FDA companion diagnostic assertions FDA companion diagnostic assertions 1 Assay-provider ledger Assay-provider ledger 19 Trial mentions Trial mentions 176 Target-disease associations Target-disease associations 1,089 Vendor sourcing Vendor sourcing 544 Trial-cited literature Trial-cited literature 814 Protein variant mentions Protein variant mentions 23 Literature-extracted relations Literature-extracted relations 148

Rows recorded per section (log scale)

1 more section with rows · 3 sections measured, none recorded

FDA companion diagnostic

An FDA-cleared or approved companion diagnostic names this biomarker.

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Evidence over time

Share of that year: what fraction of the trials and papers our biomarker dictionary matched in a year mention PDGFRB. The denominator is documents that mention any gene, not every registered document, so improving the matcher moves both halves and never rewrites history. Gene named in free-text trial records. A mention, not a validated biomarker. Actionable-biomarker and target-disease-association evidence carries no date in our sources, so it is not on this chart. Publication mentions cover only papers cited by a registered clinical trial, not all of PubMed.

Trial mentions: plotted from 1990 to 2026, the years our matched corpus covers. Not plotted: 1 with no date at all.

Publication mentions: plotted from 1990 to 2023, the years our matched corpus covers. Not plotted: 13 at the structurally incomplete recent edge.

The yearly numbers
PDGFRB per year, by evidence type, the most recent 10 years, newest first; the chart covers 1990 to 2026. The share is of the trials and papers our biomarker dictionary matched that year, not of the literature at large, and a blank year is one our matched corpus does not cover at all.
Year Trial mentions Share of that year Publication mentions Share of that year
2026 0 of 8,738 0.00% not measured
2025 5 of 8,875 0.06% not measured
2024 6 of 8,597 0.07% not measured
2023 11 of 8,275 0.13% 52 of 11,460 0.45%
2022 9 of 8,285 0.11% 52 of 13,598 0.38%
2021 4 of 8,692 0.05% 62 of 15,045 0.41%
2020 3 of 7,640 0.04% 70 of 14,459 0.48%
2019 7 of 7,300 0.10% 53 of 12,159 0.44%
2018 2 of 6,927 0.03% 50 of 11,854 0.42%
2017 6 of 6,558 0.09% 66 of 11,595 0.57%

FDA companion diagnostic assertions (1)

Shown in this order: most recent decision first.

FDA companion diagnostic assertions
Diagnostic Source biomarker wording Manufacturer Indication Decision date
PDGFRB FISH Assay PDGFRB ARUP Laboratories, Inc. Myelodysplastic Syndrome/Myeloproliferative Disease 2015-12-18

Assay-provider ledger (19)

Shown in this order: most recent publication first.

Assay-provider ledger
Company Provider class Validation Papers Most recent publication
BT LAB, Zhejiang, China Reagent supplier Clinical validation 1 July 17, 2025
Hangzhou Eastbiopharm Co., Ltd. Reagent supplier Clinical validation 1 December 01, 2020
Meso Scale Discovery Reagent supplier Clinical validationAnalytical validation 1 June 01, 2020
ThermoFisher Scientific Reagent supplier Clinical validation 1 May 01, 2019
Illumina Unclassified Analytical validation 1 March 25, 2019

Trial mentions (176)

Shown in this order: fixed catalogue order, not by date.

Trial mentions
Trial Source
NCT00504153 Trial eligibility (AACT)
NCT06194695 Trial eligibility (AACT)
NCT00314873 Trial eligibility (AACT)
NCT02109016 Trial eligibility (AACT)
NCT00436605 Trial eligibility (AACT)

Target-disease associations (1,089)

Shown in this order: fixed catalogue order, not ranked.

Target-disease associations
Disease Therapeutic area Source
14q24.1q24.3 microdeletion syndrome genetic, familial or congenital disease Mouse knockout (IMPC)
15q11.2 microdeletion syndrome genetic, familial or congenital disease Mouse knockout (IMPC)
16p13.11 microduplication syndrome genetic, familial or congenital disease Mouse knockout (IMPC)
22q11.2 deletion syndrome cardiovascular disease Mouse knockout (IMPC)
22q11.2 microduplication syndrome genetic, familial or congenital disease Mouse knockout (IMPC)

Vendor sourcing (544)

Shown in this order: alphabetical by organization.

Vendor sourcing
Organization Role Tier Evidence Citation
3billion, Inc. (South Korea) Testing lab / CRO (runs the assay) Clinical-testing interpretation submitted (ClinVar)ClinVar clinical-testing submission The variant reported as a pathogenic variant (ClinVar ID: VCV000973199) but it has only been observed as a somatic variant for a different phenotype, infanti... View ClinVar record SCV002058431.1
AB Science (France) Trial sponsor Named in trial inclusion criteriaTrial eligibility criteria include: * Histologically proven, metastatic or locally advanced non resectable, or recurrent post-surgery GIST * Naïve patient or patient previously treate... View trial NCT00812240
AB Science (France) Trial sponsor Mentioned in trial textTrial free-text mention PDGFR View trial NCT00812240
ARIAD Pharmaceuticals (United States) Trial sponsor Named in trial inclusion criteriaTrial eligibility criteria : 1. Male or female participants \>=18 years old. 2. GIST with failure of prior TKI therapy defined as: 1. Histologically confirmed metastatic and/or un... View trial NCT01874665
ARIAD Pharmaceuticals (United States) Trial sponsor Mentioned in trial textTrial free-text mention PDGFR View trial NCT01874665

Trial-cited literature (814)

Shown in this order: newest first, then most cited.

Trial-cited literature
Publication Journal Year Citations
Reciprocal regulation of hMENA and TGF-β signaling in cancer-associated fibroblasts promotes EMT, immunosuppression, poor prognosis, and ICT resistance in NSCLC. Journal for immunotherapy of cancer 2026 1
Anlotinib in combination with docetaxel for advanced nonsmall cell lung cancer after failure of platinum-based treatment: A phase 1/2 trial. Cancer 2025 2
Anlotinib plus sintilimab as first-line treatment for patients with advanced colorectal cancer (APICAL-CRC): an open-label, single-arm, phase II trial. Signal transduction and targeted therapy 2025 1
Regorafenib versus local standard of care in patients with grade 2-3 meningioma no longer eligible for loco-regional treatments: a phase II randomized controlled trial (the MIRAGE study). Trials 2025 1
Targeting pancreatic cancer metabolic dependencies through glutamine antagonism. Nature cancer 2024 116

Protein variant mentions (23)

Shown in this order: alphabetical by variant.

Protein variant mentions
Variant Distinct papers Year range Sample papers
p.A513T 1 2018 PMID 30220708
p.A537D 1 2015 PMID 25741868
p.E1081K 1 2015 PMID 25741868
p.E460K 1 2015 PMID 25741868
p.E485K 1 2015 PMID 25741868

Literature-extracted relations (148)

Shown in this order: chemicals, then diseases.

Literature-extracted relations
Related entity Kind Source relation label Paper Year
THALIDOMIDE Chemical positive_correlate A phase 2 study of thalidomide for the treatment of radiation-induced blood-brain barrier injury. 2023
Imatinib Chemical associate World Health Organization-defined eosinophilic disorders: 2022 update on diagnosis, risk stratification, and management. 2022
Nicotinamide Mononucleotide Chemical positive_correlate Nicotinamide mononucleotide increases muscle insulin sensitivity in prediabetic women. 2021
Sorafenib Chemical negative_correlate Phase II trial of bevacizumab and sorafenib in recurrent ovarian cancer patients with or without prior-bevacizumab treatment. 2020
DOXORUBICIN Chemical associate First-Line Therapy for Metastatic Soft Tissue Sarcoma. 2019

Organizations publishing (584)

Shown in this order: most papers first.

Organizations publishing
Organization Type Papers Years
Government of the United States of America Government 39 2004 to 2023
Dana-Farber Cancer Institute Other 38 2001 to 2024
The University of Texas System Academic 36 2008 to 2023
Mayo Clinic Hospital 32 2009 to 2024
Harvard Medical School Academic 28 2001 to 2024

Where PDGFRB appears

  • animal disease
  • biological_process
  • cancer or benign tumor
  • cardiovascular disease
  • disorder of visual system
  • endocrine system disease
  • gastrointestinal disease
  • genetic, familial or congenital disease
  • hematologic disease
  • immune system disease
  • infectious disease
  • injury, poisoning or other complication
  • integumentary system disease
  • measurement
  • musculoskeletal or connective tissue disease
  • nervous system disease
  • nutritional or metabolic disease
  • phenotype
  • pregnancy or perinatal disease
  • respiratory or thoracic disease
  • urinary system disease

900 diseases touched.

Not on this page

Checked, with nothing recorded for this biomarker: fda biomarker qualification projects, actionable biomarkers, and human sample screening reference.

Browse all biomarker evidence pages