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Paper ยท 40627530

Phase Ib Trial of Fulvestrant, Palbociclib, and Erdafitinib, a pan-FGFR Tyrosine Kinase Inhibitor, in HR+/HER2- Metastatic Breast Cancer.

Gonzalez-Ericsson PI and 14 others. Clin Cancer Res, 2025. Cited by 10 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. Phase Ib Trial of Fulvestrant, Palbociclib, and Erdafitinib, a pan-FGFR Tyrosine Kinase Inhibitor, in HR+/HER2- Metastatic Breast Cancer. Papers, record 40627530. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/40627530

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Paper

PubMed's record of the paper, with iCite's citation figures. No abstract is shown.

Title
Phase Ib Trial of Fulvestrant, Palbociclib, and Erdafitinib, a pan-FGFR Tyrosine Kinase Inhibitor, in HR+/HER2- Metastatic Breast Cancer.
PubMed
Journal
Clin Cancer Res
PubMed
Year
2025
PubMed
Publication types
Clinical Trial, Phase I, Journal Article, Multicenter Study
PubMed
Citations, by iCite
10
iCite
Relative citation ratio, by iCite
2.41, provisional
iCite
Revised in PubMed
2026-03-07
PubMed

Authors15

The authors in the order PubMed's record lists them, with the ORCID iDs it states.

Topics20

NLM's MeSH indexing of the paper, its major topics first.

MeSH termMajor
Antineoplastic Combined Chemotherapy ProtocolsMajor topic
Breast NeoplasmsMajor topic
Adult
Aged
Female
Humans
Middle Aged
Fulvestrant
Maximum Tolerated Dose
Neoplasm Metastasis
Piperazines
Protein Kinase Inhibitors
Pyrazoles
Pyridines
Quinoxalines
Erb-b2 Receptor Tyrosine Kinases
Receptors, Estrogen
Receptors, Fibroblast Growth Factor
Receptors, Progesterone
Tyrosine Kinase Inhibitors

Source PubMed

Grants7

Each grant PubMed's record writes, matched to the NIH project NIH's grant and paper links name for this paper, and each of those links the record does not write.

Grant, as the record writes itAgencyCountryNIH projectStated bySource
R01 CA273246NCI NIH HHSUnited StatesR01CA273246PubMed and NIHNIH RePORTER
P30 CA013148NCI NIH HHSUnited StatesP30CA013148PubMedNIH RePORTER
P30 CA068485NCI NIH HHSUnited StatesP30CA068485PubMed and NIHNIH RePORTER
P30 CA008748NCI NIH HHSUnited StatesP30CA008748PubMedNIH RePORTER
P50 CA098131NCI NIH HHSUnited StatesP50CA098131PubMed and NIHNIH RePORTER
P30 CA142543NCI NIH HHSUnited StatesP30CA142543PubMed and NIHNIH RePORTER
P50CA098131Center for Cancer Research (CCR)P50CA098131PubMed and NIHNIH RePORTER

Trials1

The trials whose ClinicalTrials.gov record lists the paper, and the trial numbers the paper's PubMed record names.

TrialTitleThe trial lists it asNamed in the paper's record
NCT03238196Fulvestrant, Palbociclib and Erdafitinib in ER+/HER2-/FGFR-amplified Metastatic Breast CancerDerived from the trialYes

Comments and corrections0

PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.

None in this release.

References31

The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.

OrderPMIDTitleJournalYearIn PapersSource
129,846,104Human Epidermal Growth Factor Receptor 2 Testing in Breast Cancer: American Society of Clinical Oncology/College of American Pathologists Clinical Practice Guideline Focused Update.Arch Pathol Lab Med2018https://conductscience.org/library/papers/29846104PubMed
228,968,163MONARCH 3: Abemaciclib As Initial Therapy for Advanced Breast Cancer.J Clin Oncol2017https://conductscience.org/library/papers/28968163PubMed
335,688,802Results of the phase IIa RADICAL trial of the FGFR inhibitor AZD4547 in endocrine resistant breast cancer.Nat Commun2022https://conductscience.org/library/papers/35688802PubMed
434,102,253
Ribociclib plus fulvestrant for postmenopausal women with hormone receptor-positive, human epidermal growth factor receptor 2-negative advanced breast cancer in the phase III randomized MONALEESA-3 trial: updated overall survival.
Ann Oncol2021https://conductscience.org/library/papers/34102253PubMed
530,914,635Aberrant FGFR signaling mediates resistance to CDK4/6 inhibitors in ER+ breast cancer.Nat Commun2019https://conductscience.org/library/papers/30914635PubMed
638,603,651Phase II Study of Erdafitinib in Patients With Tumors With FGFR Amplifications: Results From the NCI-MATCH ECOG-ACRIN Trial (EAY131) Subprotocol K1.JCO Precis Oncol2024https://conductscience.org/library/papers/38603651PubMed
738,710,951Pemigatinib in previously treated solid tumors with activating FGFR1-FGFR3 alterations: phase 2 FIGHT-207 basket trial.Nat Med2024https://conductscience.org/library/papers/38710951PubMed
836,083,147FGFR1 Antibody Validation and Characterization of FGFR1 Protein Expression in ER+ Breast Cancer.Appl Immunohistochem Mol Morphol2022https://conductscience.org/library/papers/36083147PubMed
920,473,330Therapeutic CDK4/6 inhibition in breast cancer: key mechanisms of response and failure.Oncogene2010https://conductscience.org/library/papers/20473330PubMed
1026,947,331
Fulvestrant plus palbociclib versus fulvestrant plus placebo for treatment of hormone-receptor-positive, HER2-negative metastatic breast cancer that progressed on previous endocrine therapy (PALOMA-3): final analysis of the multicentre, double-blind, phase 3 randomised controlled trial.
Lancet Oncol2016https://conductscience.org/library/papers/26947331PubMed

Cited by11

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 10 citations.

PMIDTitleJournalYearIn PapersSource
42,948,694Post CDK4/6 inhibitors: Novel targeted combinations based on SERDs in HR+/HER2- advanced breast cancer.Acta Pharm Sin B2026https://conductscience.org/library/papers/42948694PubMed
42,811,335Targeting cancer-associated fibroblasts: therapeutic strategies, translational challenges, and future perspectives.J Hematol Oncol2026https://conductscience.org/library/papers/42811335PubMed
42,633,326Advances in FGF/FGFR Signaling: Implications for Disease and Therapy.MedComm (2020)2026https://conductscience.org/library/papers/42633326PubMed
42,351,448Post-CDK4/6 Inhibitor Therapeutic Approaches in Hormone Receptor-Positive, HER2-Negative Metastatic Breast Cancer: Current Evidence and Emerging Strategies-A Narrative Review.Diagnostics (Basel)2026https://conductscience.org/library/papers/42351448PubMed
42,351,126
Integrative multi-omics and single-cell analysis identifies EGFR pathway activation and metabolic reprogramming as potential synthetic lethal vulnerabilities in resistance to the FGFR inhibitor AZD4547.
J Transl Med2026https://conductscience.org/library/papers/42351126PubMed
42,196,611CAFs and Endocrine Therapy Resistance in Hormone Receptor-Positive Breast Cancer.Int J Mol Sci2026https://conductscience.org/library/papers/42196611PubMed
42,083,272Artesunate Induces G0/G1 Phase Arrest in Tumor Cells and Associates With Cyclin-Dependent Kinase 4 (CDK4).Cancer Med2026https://conductscience.org/library/papers/42083272PubMed
42,013,308Covalent FAPI Imaging-Guided Precision Surgery in Patients with Medullary Thyroid Carcinoma: A Phase II Clinical Trial.Clin Cancer Res2026https://conductscience.org/library/papers/42013308PubMed
41,675,006
Biomarkers of primary and secondary resistance to cyclin dependent kinases 4 and 6 inhibitors in metastatic estrogen receptor-positive/human epidermal growth factor receptor 2-negative breast cancer: a narrative review.
Transl Breast Cancer Res2026https://conductscience.org/library/papers/41675006PubMed
41,499,130Defective DNA Damage Response Is a Targetable Therapeutic Vulnerability in ESR1-Mutant Breast Cancer.Cancer Res2026https://conductscience.org/library/papers/41499130PubMed

1 to 10 of 11

See all 11 cited by

Genes2

The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.

GeneNCBI Gene IDLinked byIn GenesSource
ERBB22,064PubTator's text mininghttps://conductscience.org/library/genes/2064NCBI Gene
FGFR12,260PubTator's text mininghttps://conductscience.org/library/genes/2260NCBI Gene

Drugs3

The drugs whose trials, in the Pipelines release, list the paper.

DrugChEMBL IDThe trials list it asTrialsIn Drugs and targetsSource
FULVESTRANTCHEMBL1358Derived from the trial1https://conductscience.org/library/drugs/CHEMBL1358ChEMBL
PALBOCICLIBCHEMBL189963Derived from the trial1https://conductscience.org/library/drugs/CHEMBL189963ChEMBL
ERDAFITINIBCHEMBL3545376Derived from the trial1https://conductscience.org/library/drugs/CHEMBL3545376ChEMBL

Data0

The data bank entries PubMed's record names. Trial numbers are under Trials.

None in this release.

Data dates

The date of each source this release read.

PubMed
2026-11-06
PubMed
iCite
2026-11-05
iCite
PMC's ID file
2026-11-05
PMC's ID file
NIH RePORTER's grant and paper links
2026-11-01
NIH RePORTER's grant and paper links
Trials
2026-11-12
Gene search
2026-11-11
Pipelines
2026-09-18

Sources 11

  • ChEMBL, through Open TargetsCC BY-SA 3.0
  • ClinicalTrials.govNo license stated
  • HGNCCC0
  • iCiteCC BY 4.0
  • NCBI GenePublic domain (US government)
  • NIH RePORTER's grant and paper linksPublic domain
  • Open TargetsCC0 1.0
  • PMC's ID filePublic domain (US government)
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0
Each source's terms
  • ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • ClinicalTrials.govnone stated
  • HGNCCC0: https://www.genenames.org/about/license/
  • iCiteCC BY 4.0
  • NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
  • Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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