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Paper · 39265124

Datopotamab Deruxtecan Versus Chemotherapy in Previously Treated Inoperable/Metastatic Hormone Receptor-Positive Human Epidermal Growth Factor Receptor 2-Negative Breast Cancer: Primary Results From TROPION-Breast01.

Bardia A and 23 others. J Clin Oncol, 2025. Cited by 178 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. Datopotamab Deruxtecan Versus Chemotherapy in Previously Treated Inoperable/Metastatic Hormone Receptor-Positive Human Epidermal Growth Factor Receptor 2-Negative Breast Cancer: Primary Results From TROPION-Breast01. Papers, record 39265124. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/39265124

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Paper

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

Title
Datopotamab Deruxtecan Versus Chemotherapy in Previously Treated Inoperable/Metastatic Hormone Receptor-Positive Human Epidermal Growth Factor Receptor 2-Negative Breast Cancer: Primary Results From TROPION-Breast01.
PubMed
Journal
J Clin Oncol
PubMed
Year
2025
PubMed
Publication types
Journal Article, Randomized Controlled Trial, Clinical Trial, Phase III, Multicenter Study, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't
PubMed
Citations, by iCite
178
iCite
Relative citation ratio, by iCite
45.36, provisional
iCite
Revised in PubMed
2026-09-23
PubMed

Authors24

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

OrderAuthorForenameKindORCID iD
1Bardia AAdityahttps://orcid.org/0000-0003-4885-1157
2Jhaveri KKomalhttps://orcid.org/0000-0003-0472-1254
3Im SASeock-Ahhttps://orcid.org/0000-0002-5396-6533
4Pernas SSoniahttps://orcid.org/0000-0002-1485-5080
5De Laurentiis MMichelinohttps://orcid.org/0000-0001-9009-1572
6Wang SShusenhttps://orcid.org/0000-0003-0139-5780
7Martínez Jañez NNoelia
8Borges GGiuliano
9Cescon DWDavid Whttps://orcid.org/0000-0002-1080-0998
10Hattori MMasayahttps://orcid.org/0000-0002-0935-9269

1 to 10 of 24Source PubMed

See all 24 authors

Topics16

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

MeSH termMajor
Breast NeoplasmsMajor topic
Erb-b2 Receptor Tyrosine KinasesMajor topic
Antineoplastic Combined Chemotherapy ProtocolsMajor topic
ImmunoconjugatesMajor topic
Humans
Female
Middle Aged
Adult
Aged
Receptors, Estrogen
Receptors, Progesterone
Vinorelbine
Capecitabine
Gemcitabine
Progression-Free Survival
Deoxycytidine

Source PubMed

Grants2

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
P30 CA008748NCI NIH HHSUnited StatesP30CA008748PubMed and NIHNIH RePORTER
P30 CA016042NCI NIH HHSUnited StatesP30CA016042PubMedNIH 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
NCT05104866
A Phase-3, Open-Label, Randomized Study of Dato-DXd Versus Investigator's Choice of Chemotherapy (ICC) in Participants With Inoperable or Metastatic HR-Positive, HER2-Negative Breast Cancer Who Have Been Treated With One or Two Prior Lines of Systemic Chemotherapy (TROPION-Breast01)
Derived 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.

References29

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
226,000,093Trop2 and its overexpression in cancers: regulation and clinical/therapeutic implications.Genes Cancer2015https://conductscience.org/library/papers/26000093PubMed
337,387,213TROPION-Breast01: Datopotamab deruxtecan vs chemotherapy in pre-treated inoperable or metastatic HR+/HER2- breast cancer.Future Oncol2024https://conductscience.org/library/papers/37387213PubMed
434,413,126Datopotamab Deruxtecan, a Novel TROP2-directed Antibody-drug Conjugate, Demonstrates Potent Antitumor Activity by Efficient Drug Delivery to Tumor Cells.Mol Cancer Ther2021https://conductscience.org/library/papers/34413126PubMed
537,526,149TROPION-Breast02: Datopotamab deruxtecan for locally recurrent inoperable or metastatic triple-negative breast cancer.Future Oncol2023https://conductscience.org/library/papers/37526149PubMed
636,027,558Sacituzumab Govitecan in Hormone Receptor-Positive/Human Epidermal Growth Factor Receptor 2-Negative Metastatic Breast Cancer.J Clin Oncol2022https://conductscience.org/library/papers/36027558PubMed
732,946,924Sacituzumab govitecan in previously treated hormone receptor-positive/HER2-negative metastatic breast cancer: final results from a phase I/II, single-arm, basket trial.Ann Oncol2020https://conductscience.org/library/papers/32946924PubMed
837,256,976Capivasertib in Hormone Receptor-Positive Advanced Breast Cancer.N Engl J Med2023https://conductscience.org/library/papers/37256976PubMed
921,376,385Eribulin monotherapy versus treatment of physician's choice in patients with metastatic breast cancer (EMBRACE): a phase 3 open-label randomised study.Lancet2011https://conductscience.org/library/papers/21376385PubMed
1034,324,367Endocrine Treatment and Targeted Therapy for Hormone Receptor-Positive, Human Epidermal Growth Factor Receptor 2-Negative Metastatic Breast Cancer: ASCO Guideline Update.J Clin Oncol2021https://conductscience.org/library/papers/34324367PubMed

Cited by137

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 178 citations.

PMIDTitleJournalYearIn PapersSource
42,988,817Antibody-drug conjugates: unpacking toxicity profiles and optimized designs for enhanced safety and antitumor efficacy.Signal Transduct Target Ther2026https://conductscience.org/library/papers/42988817PubMed
42,964,697Endocrine resistance in HR+/HER2- breast cancer: molecular mechanisms and emerging therapeutic strategies.Front Oncol2026https://conductscience.org/library/papers/42964697PubMed
42,943,283Discovery and Optimization of the Novel Immunotoxins Targeting TROP2 for Cancer Therapy.Pharmaceuticals (Basel)2026https://conductscience.org/library/papers/42943283PubMed
42,920,907Molecular and immune-mediated resistance to antibody-drug conjugates in breast cancer.Front Immunol2026https://conductscience.org/library/papers/42920907PubMed
42,900,402Antibody-drug conjugates and tumor immunity in breast cancer.Med Oncol2026https://conductscience.org/library/papers/42900402PubMed
42,882,921Choosing Between Anti-TROP2 ADCs in Advanced Breast Cancer Without Head-to-Head Evidence: A Practical Evidence-Informed Decision Framework Endorsed by the Polish Society of Clinical Oncology.Cancers (Basel)2026https://conductscience.org/library/papers/42882921PubMed
42,863,323Cell-resolved spatial mapping of antibody-drug conjugate targets in breast cancer.Transl Oncol2026https://conductscience.org/library/papers/42863323PubMed
42,835,399Antibody-Drug Conjugates in Breast Cancer: Therapeutic-Window Engineering, Tumor Heterogeneity, and Immunotherapy Combinations.Drug Des Devel Ther2026https://conductscience.org/library/papers/42835399PubMed
42,820,303Antibody-drug conjugates in breast cancer: redefining targeted therapy.J Clin Invest2026https://conductscience.org/library/papers/42820303PubMed
42,820,289Toward targeted therapeutics for lobular breast cancer.J Clin Invest2026https://conductscience.org/library/papers/42820289PubMed

1 to 10 of 137

See all 137 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
NR4A13,164PubTator's text mininghttps://conductscience.org/library/genes/3164NCBI Gene

Drugs1

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

DrugChEMBL IDThe trials list it asTrialsIn Drugs and targets
DATOPOTAMAB DERUXTECANCHEMBL4297939Derived from the trial1https://conductscience.org/library/drugs/CHEMBL4297939

Source ChEMBL

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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