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Gene

FGFR1

FGFR1 is a gene biomarker in the evidence tier "Cancer actionable (CGI)". This page lists evidence by type: Assay-provider ledger (36), Actionable biomarkers (4), Trial mentions (95), and 7 more evidence types, each linked to its source.

Ensembl ENSG00000077782 UniProt P11362 Matched to Ensembl and UniProt
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Assay-provider ledger Assay-provider ledger 36 Actionable biomarkers Actionable biomarkers 4 Trial mentions Trial mentions 95 Target-disease associations Target-disease associations 1,221 Vendor sourcing Vendor sourcing 327 Trial-cited literature Trial-cited literature 504 Protein variant mentions Protein variant mentions 91 Human sample screening reference Human sample screening reference 4 Assay-provider ledger Assay-provider ledger 36 Actionable biomarkers Actionable biomarkers 4 Trial mentions Trial mentions 95 Target-disease associations Target-disease associations 1,221 Vendor sourcing Vendor sourcing 327 Trial-cited literature Trial-cited literature 504 Protein variant mentions Protein variant mentions 91 Human sample screening reference Human sample screening reference 4

Rows recorded per section (log scale)

2 more sections with rows · 2 sections measured, none recorded

Cancer actionable (CGI)

Curated as clinically actionable in cancer by the Cancer Genome Interpreter.

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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 FGFR1. 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.

Publication mentions: plotted from 1990 to 2023, the years our matched corpus covers. Not plotted: 12 at the structurally incomplete recent edge.

The yearly numbers
FGFR1 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 3 of 8,738 0.03% not measured
2025 6 of 8,875 0.07% not measured
2024 5 of 8,597 0.06% not measured
2023 4 of 8,275 0.05% 40 of 11,460 0.35%
2022 10 of 8,285 0.12% 44 of 13,598 0.32%
2021 12 of 8,692 0.14% 51 of 15,045 0.34%
2020 12 of 7,640 0.16% 45 of 14,459 0.31%
2019 11 of 7,300 0.15% 31 of 12,159 0.25%
2018 4 of 6,927 0.06% 30 of 11,854 0.25%
2017 3 of 6,558 0.05% 38 of 11,595 0.33%

Assay-provider ledger (36)

Shown in this order: most recent publication first.

Assay-provider ledger
Company Provider class Validation Papers Most recent publication
Agilent Technologies Reagent supplier Clinical validationAnalytical validation 3 March 01, 2025
DAKO Unclassified Clinical validation 1 March 01, 2025
Promega Reagent supplier Analytical validation 1 November 08, 2021
Thermo Fisher Reagent supplier Analytical validation 1 November 08, 2021
Inivata Diagnostic provider Clinical validationAnalytical validation 2 July 01, 2021 +1 undated

Actionable biomarkers (4)

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

Actionable biomarkers
Alteration Drug Response Disease Source
FGFR1 amplification Lucitanib response-associated breast adenocarcinoma Cancer Genome Interpreter
FGFR1 amplification Fgfr Inhibitors response-associated endometrial carcinoma Cancer Genome Interpreter
FGFR1 amplification Fgfr Inhibitors response-associated head and neck malignant neoplasia Cancer Genome Interpreter
FGFR1 amplification Fgfr Inhibitors response-associated squamous cell lung carcinoma Cancer Genome Interpreter

Trial mentions (95)

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

Trial mentions
Trial Source
NCT04295824 Trial biospecimen (AACT)
NCT02299141 Trial eligibility (AACT)
NCT04045613 Trial eligibility (AACT)
NCT04149691 Trial eligibility (AACT)
NCT05560334 Trial eligibility (AACT)

Target-disease associations (1,221)

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

Target-disease associations
Disease Therapeutic area Source
3-M syndrome genetic, familial or congenital disease Mouse knockout (IMPC)
3M syndrome genetic, familial or congenital disease Mouse knockout (IMPC)
5-methyluridine (ribothymidine) measurement measurement GWAS credible sets
6q16 deletion syndrome endocrine system disease Mouse knockout (IMPC)
Aase-Smith syndrome genetic, familial or congenital disease Mouse knockout (IMPC)

Vendor sourcing (327)

Shown in this order: alphabetical by organization.

Vendor sourcing
Organization Role Tier Evidence Citation
3D Medicines, Inc. (China) Trial sponsor Named in trial exclusion criteriaTrial eligibility criteria : Subjects who meet any of the following criteria should be excluded from the study: 1. Subjects who received other investigational products or devices in ... View trial NCT04221204
3D Medicines, Inc. (China) Trial sponsor Mentioned in trial textTrial free-text mention FGFR1 View trial NCT04221204
3billion, Inc. (South Korea) Testing lab / CRO (runs the assay) Clinical-testing interpretation submitted (ClinVar)ClinVar clinical-testing submission Stop-gained (nonsense): predicted to result in a loss or disruption of normal protein function through nonsense-mediated decay (NMD) or protein truncation. M... View ClinVar record SCV002058223.1
ARIAD Pharmaceuticals (United States) Trial collaborator Named in trial inclusion criteriaTrial eligibility criteria : * PART A: Patients must have histologically or cytologically confirmed locally advanced (after failure of local therapy) or metastatic lung cancer (any hi... View trial NCT01935336
ARIAD Pharmaceuticals (United States) Trial collaborator Mentioned in trial textTrial free-text mention FGFR1 View trial NCT01935336

Trial-cited literature (504)

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

Trial-cited literature
Publication Journal Year Citations
Pemigatinib for Myeloid/Lymphoid Neoplasms with <i>FGFR1</i> Rearrangement. NEJM evidence 2025 8
Phase Ib Trial of Fulvestrant, Palbociclib, and Erdafitinib, a pan-FGFR Tyrosine Kinase Inhibitor, in HR+/HER2- Metastatic Breast Cancer. Clinical cancer research : an official journal of the American Association for Cancer Research 2025 8
Circulating Tumor DNA Genotyping of Intrinsic and Acquired Gene Alterations in Patients With Advanced Breast Cancer Receiving Palbociclib: Biomarker Results From POLARIS Study. JCO precision oncology 2025 3
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
Extracellular vesicles in lung donor plasma: Potential indicators of donor organ quality. The Journal of thoracic and cardiovascular surgery 2025 2

Protein variant mentions (91)

Shown in this order: alphabetical by variant.

Protein variant mentions
Variant Distinct papers Year range Sample papers
p.A20N 1 2014 PMID 25056707
p.A640V 1 2015 PMID 25741868
p.A645V 1 2016 PMID 26467025
p.C736R 1 2015 PMID 25741868
p.D224H 1 2006 PMID 16764984

Human sample screening reference (4)

Shown in this order: alphabetical by variant.

Human sample screening reference
Variant GDC project Disease / site Affected cases Profiled cases Observed frequency 95% interval
p.G485R ALCHEMIST-ALCH Not Reported; Not Reported 1 1,170 0.09% 0.02% to 0.48%
p.R254Q TCGA-UCEC Not Reported; Epithelial Neoplasms, NOS; Adenomas and Adenocarcinomas; Cystic, Mucinous and Serous Neoplasms; Corpus uteri; Uterus, NOS 1 559 0.18% 0.03% to 1.01%
p.R78C TCGA-COAD Epithelial Neoplasms, NOS; Adenomas and Adenocarcinomas; Cystic, Mucinous and Serous Neoplasms; Complex Epithelial Neoplasms; Rectosigmoid junction; Colon 1 461 0.22% 0.04% to 1.22%
p.V561M CCDI-MCI Cystic, Mucinous and Serous Neoplasms; Granular Cell Tumors and Alveolar Soft Part Sarcomas; Specialized Gonadal Neoplasms; Neoplasms, NOS; Adenomas and Adenocarcinomas; Gliomas; Meningiomas; Acinar Cell Neoplasms; Odontogenic Tumors; Soft Tissue Tumors and Sarcomas, NOS; Nevi and Melanomas; Malignant Lymphomas, NOS or Diffuse; Epithelial Neoplasms, NOS; Thymic Epithelial Neoplasms; Other and unspecified parts of mouth; Rectosigmoid junction; Thyroid gland; Connective, subcutaneous and other soft tissues; Peripheral nerves and autonomic nervous system; Other endocrine glands and related structures; Retroperitoneum and peritoneum; Vagina; Other and ill-defined digestive organs; Pancreas; Renal pelvis; Bladder; Nasal cavity and middle ear; Meninges; Adrenal gland; Bones, joints and articular cartilage of limbs; Bones, joints and articular cartilage of other and unspecified sites; Breast; Skin; Thymus; Esophagus; Other and ill-defined sites in lip, oral cavity and pharynx; Larynx; Other and unspecified urinary organs; Brain; Testis; Heart, mediastinum, and pleura; Rectum; Nasopharynx; Palate; Prostate gland; Base of tongue; Accessory sinuses; Other and unspecified female genital organs; Lip; Spinal cord, cranial nerves, and other parts of central nervous system; Colon; Oropharynx; Other and ill-defined sites; Unknown; Other and ill-defined sites within respiratory system and intrathoracic organs; Other and unspecified male genital organs; Cervix uteri; Bronchus and lung; Eye and adnexa; Ovary; Small intestine; Lymph nodes; Stomach 3 3,033 0.10% 0.03% to 0.29%

Literature-extracted relations (112)

Shown in this order: chemicals, then diseases.

Literature-extracted relations
Related entity Kind Source relation label Paper Year
FULVESTRANT Chemical associate Phase Ib Trial of Fulvestrant, Palbociclib, and Erdafitinib, a pan-FGFR Tyrosine Kinase Inhibitor, in HR+/HER2- Metastatic Breast Cancer. 2025
Sorafenib Chemical negative_correlate The impact of FGFR1 and FRS2α expression on sorafenib treatment in metastatic renal cell carcinoma. 2015
Sorafenib Chemical negative_correlate Population pharmacokinetic analysis of sorafenib in patients with solid tumours. 2011
CISPLATIN Chemical associate Inhibition of FGFR2 and FGFR1 increases cisplatin sensitivity in ovarian cancer. 2010
ADENOSINE TRIPHOSPHATE Chemical negative_correlate The neural cell adhesion molecule binds to fibroblast growth factor receptor 2. 2006

Organizations publishing (519)

Shown in this order: most papers first.

Organizations publishing
Organization Type Papers Years
Memorial Sloan Kettering Cancer Center Hospital 28 2011 to 2025
Mass General Brigham Hospital 25 2005 to 2022
The University of Texas System Academic 24 2011 to 2024
Harvard Medical School Academic 23 2011 to 2025
Dana-Farber Cancer Institute Other 22 2011 to 2022

Where FGFR1 appears

  • animal disease
  • biological_process
  • cancer or benign tumor
  • cardiovascular disease
  • disorder of ear
  • 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
  • psychiatric disorder
  • reproductive system or breast disease
  • respiratory or thoracic disease
  • urinary system disease

1,044 diseases touched.

Not on this page

Checked, with nothing recorded for this biomarker: fda companion diagnostic assertions and fda biomarker qualification projects.

Browse all biomarker evidence pages