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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorGuerrero-Zotano, Angel
dc.contributor.authorPérez-García, José Manuel
dc.contributor.authorRuiz-Borrego, Manuel
dc.contributor.authorBERMEJO, BEGOÑA
dc.contributor.authorHaba Rodríguez, Juan Rafael de la
dc.contributor.authorBellet Ezquerra, Meritxell
dc.contributor.authorGil Gil, Miguel J.
dc.date.accessioned2024-11-14T13:51:17Z
dc.date.available2024-11-14T13:51:17Z
dc.date.issued2024-10
dc.identifier.citationGuerrero-Zotano Á, Pérez-García JM, Ruiz-Borrego M, Bermejo B, Gil-Gil M, de la Haba J, et al. Neoadjuvant letrozole and palbociclib in patients with HR-positive/HER2-negative early breast cancer and Oncotype DX Recurrence Score ≥18: DxCARTES study. ESMO Open. 2024 Oct;9(10):103733.
dc.identifier.issn2059-7029
dc.identifier.urihttps://hdl.handle.net/11351/12226
dc.descriptionEarly breast cancer; Hormone-receptor-positive; Letrozole
dc.description.abstractBackground The effect of the addition of cyclin-dependent kinases 4 and 6 inhibitors to endocrine therapy in terms of molecular downstaging remains undetermined. Switching from a high-risk to a low risk Recurrence Score (RS) group could provide useful information to identify patients who might not require chemotherapy. The purpose of this study was to assess the biological and clinical activity of letrozole plus palbociclib as neoadjuvant treatment for patients with hormone receptor (HR)-positive/human epidermal growth factor receptor 2 (HER2)-negative early breast cancer with an initial Oncotype DX RS ≥18. Patients and methods Participants were women aged ≥18 years with HR-positive/HER2-negative, Ki67 ≥ 20%, stage II-IIIB early breast cancer with a baseline RS ≥18. Eligible patients with a pretreatment RS 18-25 (cohort A) and 26-100 (cohort B) received six 28-day cycles of letrozole (2.5 mg per day; plus goserelin if pre- or perimenopausal) plus palbociclib (125 mg per day; 3/1 schedule) before surgery. The primary endpoint for both cohorts was the proportion of patients who achieved an RS ≤25 at surgery or a pathological complete response (pCR). Results A total of 67 patients were enrolled, among which 65 were assessable for the primary endpoint (32 patients in cohort A and 33 in cohort B). At surgery, 22 (68.8%) patients in cohort A and 18 (54.5%) patients in cohort B had an RS ≤25 or a pCR [only 1 (3.0%) patient in cohort B], meeting the primary endpoint in cohort B (P < 0.01), but not in cohort A (P = 0.98). No new safety signals were identified. Conclusions The efficacy of neoadjuvant treatment with letrozole plus palbociclib does not seem to depend on pretreatment RS for patients with RS ≥18. However, around half of patients with HR-positive/HER2-negative early breast cancer with an RS 26-100 at baseline achieved molecular downstaging with this regimen.
dc.language.isoeng
dc.publisherElsevier
dc.relation.ispartofseriesESMO Open;9(10)
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceScientia
dc.subjectQuimioteràpia combinada
dc.subjectMama - Càncer - Tractament
dc.subjectMedicaments antineoplàstics - Ús terapèutic
dc.subject.meshAntineoplastic Combined Chemotherapy Protocols
dc.subject.meshBreast Neoplasms
dc.subject.mesh/drug therapy
dc.subject.meshNeoadjuvant Therapy
dc.titleNeoadjuvant letrozole and palbociclib in patients with HR-positive/HER2-negative early breast cancer and Oncotype DX Recurrence Score ≥18: DxCARTES study
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1016/j.esmoop.2024.103733
dc.subject.decsprotocolos de quimioterapia antineoplásica combinada
dc.subject.decsneoplasias de la mama
dc.subject.decs/farmacoterapia
dc.subject.decstratamiento neoadyuvante
dc.relation.publishversionhttps://doi.org/10.1016/j.esmoop.2024.103733
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Guerrero-Zotano Á] lnstituto Valenciano de Oncología, Valencia. [Pérez-García JM] International Breast Cancer Center (IBCC), Pangaea Oncology, Quiron Group, Barcelona, Spain. Medica Scientia Innovation Research (MEDSIR) - Oncoclínicas&Co, Jersey City (New Jersey, USA), Sao Paulo, Brazil. [Ruiz-Borrego M] Hospital For Universitario Virgen del Rocío, Sevilla, Spain. [Bermejo B] Hospital Clínico Universitario de Valencia, Valencia, Spain. Biomedical Research Institute INCLIVA, Valencia, Spain. [Gil-Gil M] Institut Català d’Oncologia L’Hospitalet, Hospitalet de Llobregat, Barcelona, Spain. [de la Haba J] Hospital Universitario Reina Sofía, Cordoba, Spain. [Bellet M] Vall d’Hebron Hospital Universitari, Barcelona, Spain. Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain
dc.identifier.pmid39353215
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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