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dc.contributor.authorDesmedt, C
dc.contributor.authorPingitore, J
dc.contributor.authorRothé, F
dc.contributor.authorMarchio, C
dc.contributor.authorClatot, F
dc.contributor.authorRouas, G
dc.contributor.authorRichard, F
dc.contributor.authorBertucci, F
dc.contributor.authorMariani, O
dc.contributor.authorGalant, C
dc.contributor.authorFribbens, C
dc.contributor.authorO'Leary, B
dc.contributor.authorvan den Eynden, G
dc.contributor.authorSalgado, R
dc.contributor.authorTurner, NC
dc.contributor.authorPiccart, M
dc.contributor.authorVincent-Salomon, A
dc.contributor.authorPruneri, G
dc.contributor.authorLarsimont, D
dc.contributor.authorSotiriou, C
dc.date.accessioned2019-03-18T10:04:27Z
dc.date.issued2019-01
dc.identifier.citationNPJ breast cancer, 2019, 5 pp. 9 - ?
dc.identifier.issn2374-4677
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/3155
dc.identifier.eissn2374-4677
dc.identifier.doi10.1038/s41523-019-0104-z
dc.description.abstractInvasive lobular breast cancer (ILC) represents the second most common histology of breast cancer after invasive ductal breast cancer (IDC), accounts for up to 15% of all invasive cases and generally express the estrogen receptor (ER, coded by the <i>ESR1</i> gene). <i>ESR1</i> mutations have been associated with resistance to endocrine therapy, however these have not been specifically evaluated in ILC. We assessed the frequency of <i>ESR1</i> mutations by droplet digital PCR in a retrospective multi-centric series of matched primary tumor and recurrence samples (<i>n</i> = 279) from 80 metastatic ER-positive ILC patients. We further compared <i>ESR1</i> mutations between IDC and ILC patients in metastatic samples from MSKCC-IMPACT (<i>n</i> = 595 IDC and 116 ILC) and in ctDNA from the SoFEA and PALOMA-3 trials (<i>n</i> = 416 IDC and 76 ILC). In the retrospective series, the metastases from seven patients (9%) harbored <i>ESR1</i> mutations, which were absent from the interrogated primary samples. Five patients (6%) had a mutation in the primary tumor or axillary metastasis, which could not be detected in the matched distant metastasis. In the MSKCC-IMPACT cohort, as well as in the SoFEA and PALOMA-3 trials, there were no differences in prevalence and distribution of the mutations between IDC and ILC, with D538G being the most frequent mutation in both histological subtypes. To conclude, no patient had an identical <i>ESR1</i> mutation in the early and metastatic disease in the retrospective ILC series. In the external series, there was no difference in terms of prevalence and type of ESR1 mutations between ILC and IDC.
dc.formatElectronic-eCollection
dc.format.extent9 - ?
dc.languageeng
dc.language.isoeng
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.title<i>ESR1</i> mutations in metastatic lobular breast cancer patients.
dc.typeJournal Article
dcterms.dateAccepted2018-11-27
rioxxterms.versionofrecord10.1038/s41523-019-0104-z
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2019-01
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfNPJ breast cancer
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research/Molecular Oncology
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research/Molecular Oncology
pubs.publication-statusPublished
pubs.volume5en_US
pubs.embargo.termsNot known
icr.researchteamMolecular Oncologyen_US
dc.contributor.icrauthorTurner, Nicholasen
dc.contributor.icrauthorO'Leary, Benjaminen


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