Institut Català de la Salut
[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
Vall d'Hebron Barcelona Hospital Campus
2024-11-19T09:41:53Z
2024-11-19T09:41:53Z
2024-11-01
Paclitaxel; Cáncer de mama; Factor de crecimiento epidérmico
Paclitaxel; Càncer de mama; Factor de creixement epidèrmic
Paclitaxel; Breast cancer; Epidermal growth factor
Purpose 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.
We are grateful for the funding support to the Translational Breast Cancer Research Consortium (TBCRC), from The Breast Cancer Research Foundation and Susan G. Komen for funding support for translational analyses from MLSC Women’s Health Collaboration. The funders had no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; and in the decision to submit the paper for publication.
Article
Published version
English
Quimioteràpia combinada; Mama - Càncer - Tractament; Avaluació de resultats (Assistència sanitària); ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT::Diagnosis::Prognosis::Treatment Outcome::Disease-Free Survival; ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT::Therapeutics::Therapeutics::Drug Therapy::Antineoplastic Protocols::Therapeutics::Drug Therapy::Antineoplastic Combined Chemotherapy Protocols; DISEASES::Neoplasms::Neoplasms by Site::Breast Neoplasms; Other subheadings::Other subheadings::Other subheadings::/drug therapy; TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS::diagnóstico::pronóstico::resultado del tratamiento::supervivencia sin enfermedad; TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS::terapéutica::terapéutica::farmacoterapia::protocolos antineoplásicos::terapéutica::farmacoterapia::protocolos de quimioterapia antineoplásica combinada; ENFERMEDADES::neoplasias::neoplasias por localización::neoplasias de la mama; Otros calificadores::Otros calificadores::Otros calificadores::/farmacoterapia
American Society of Clinical Oncology
Journal of Clinical Oncology;42(31)
https://doi.org/10.1200/JCO.23.02170
Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/