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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorTarantino, Paolo
dc.contributor.authorTayob, Nabihah
dc.contributor.authorDANG, CHAU
dc.contributor.authorYardley, Denise A.
dc.contributor.authorVillacampa Javierre, Guillermo
dc.contributor.authorIsakoff, Steven
dc.date.accessioned2024-11-19T09:41:53Z
dc.date.available2024-11-19T09:41:53Z
dc.date.issued2024-11-01
dc.identifier.citationTarantino P, Tayob N, Villacampa G, Dang C, Yardley DA, Isakoff SJ, et al. Adjuvant Trastuzumab Emtansine Versus Paclitaxel Plus Trastuzumab for Stage I Human Epidermal Growth Factor Receptor 2–Positive Breast Cancer: 5-Year Results and Correlative Analyses From ATEMPT. J Clin Oncol. 2024 Nov 1;42(31):3652–65.
dc.identifier.issn1527-7755
dc.identifier.urihttps://hdl.handle.net/11351/12237
dc.descriptionPaclitaxel; Breast cancer; Epidermal growth factor
dc.description.abstractPurpose Long-term outcomes of patients with stage I human epidermal growth factor receptor 2 (HER2)–positive breast cancer receiving adjuvant trastuzumab emtansine (T-DM1) remain undefined, and prognostic predictors represent an unmet need. Methods In the ATEMPT phase II trial, patients with stage I centrally confirmed HER2-positive breast cancer were randomly assigned 3:1 to adjuvant T-DM1 for 1 year or paclitaxel plus trastuzumab (TH). Coprimary objectives were to compare the incidence of clinically relevant toxicities between arms and to evaluate invasive disease-free survival (iDFS) with T-DM1. Correlative analyses included the HER2DX genomic tool, multiomic evaluations of HER2 heterogeneity, and predictors of thrombocytopenia. Results After a median follow-up of 5.8 years, 11 iDFS events were observed in the T-DM1 arm, consistent with a 5-year iDFS of 97.0% (95% CI, 95.2 to 98.7). At 5 years, the recurrence-free interval (RFI) was 98.3% (95% CI, 97.0 to 99.7), the overall survival was 97.8% (95% CI, 96.3 to 99.3), and the breast cancer-specific survival was 99.4% (95% CI, 98.6 to 100). Comparable iDFS was observed with T-DM1 irrespective of tumor size, hormone receptor status, centrally determined HER2 immunohistochemical score, and receipt of T-DM1 for more or less than 6 months. Although ATEMPT was not powered for this end point, the 5-year iDFS in the TH arm was 91.1%. Among patients with sufficient tissue for HER2DX testing (n = 187), 5-year outcomes significantly differed according to HER2DX risk score, with better RFI (98.1% v 81.8%, hazard ratio [HR], 0.10, P = .01) and iDFS (96.3% v 81.8%, HR, 0.20, P = .047) among patients with HER2DX low-risk versus high-risk tumors, respectively. Conclusion Adjuvant T-DM1 for 1 year leads to outstanding long-term outcomes for patients with stage I HER2-positive breast cancer. A high HER2DX risk score predicted a higher risk of recurrence in ATEMPT.
dc.language.isoeng
dc.publisherAmerican Society of Clinical Oncology
dc.relation.ispartofseriesJournal of Clinical Oncology;42(31)
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.subjectAvaluació de resultats (Assistència sanitària)
dc.subject.meshDisease-Free Survival
dc.subject.meshAntineoplastic Combined Chemotherapy Protocols
dc.subject.meshBreast Neoplasms
dc.subject.mesh/drug therapy
dc.titleAdjuvant Trastuzumab Emtansine Versus Paclitaxel Plus Trastuzumab for Stage I Human Epidermal Growth Factor Receptor 2–Positive Breast Cancer: 5-Year Results and Correlative Analyses From ATEMPT
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1200/JCO.23.02170
dc.subject.decssupervivencia sin enfermedad
dc.subject.decsprotocolos de quimioterapia antineoplásica combinada
dc.subject.decsneoplasias de la mama
dc.subject.decs/farmacoterapia
dc.relation.publishversionhttps://doi.org/10.1200/JCO.23.02170
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Tarantino P] Medical Oncology, Dana-Farber Cancer Institute, Boston, MA. Breast Oncology Program, Dana-Farber Brigham Cancer Center, Boston, MA. Harvard Medical School, Boston, MA. Department of Oncology and Hemato-Oncology, University of Milan, Milan, Italy. [Tayob N] Harvard Medical School, Boston, MA. Division of Data Science, Dana-Farber Cancer Institute, Boston, MA. [Villacampa G] SOLTI Breast Cancer Research Group, Barcelona, Spain. Oncology Data Science Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. [Dang C] Memorial Sloan Kettering Cancer Center, New York, NY. [Yardley DA] Sarah Cannon Research Institute and Tennessee Oncology, Nashville, TN. [Isakoff SJ] Harvard Medical School, Boston, MA. Massachusetts General Hospital, Boston, MA
dc.identifier.pmid38935923
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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