| dc.contributor | Vall d'Hebron Barcelona Hospital Campus |
| dc.contributor.author | Tarantino, Paolo |
| dc.contributor.author | Tayob, Nabihah |
| dc.contributor.author | DANG, CHAU |
| dc.contributor.author | Yardley, Denise A. |
| dc.contributor.author | Villacampa Javierre, Guillermo |
| dc.contributor.author | Isakoff, Steven |
| dc.date.accessioned | 2024-11-19T09:41:53Z |
| dc.date.available | 2024-11-19T09:41:53Z |
| dc.date.issued | 2024-11-01 |
| dc.identifier.citation | Tarantino 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.issn | 1527-7755 |
| dc.identifier.uri | https://hdl.handle.net/11351/12237 |
| dc.description | Paclitaxel; Breast cancer; Epidermal growth factor |
| dc.description.abstract | 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. |
| dc.language.iso | eng |
| dc.publisher | American Society of Clinical Oncology |
| dc.relation.ispartofseries | Journal of Clinical Oncology;42(31) |
| dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 International |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ |
| dc.source | Scientia |
| dc.subject | Quimioteràpia combinada |
| dc.subject | Mama - Càncer - Tractament |
| dc.subject | Avaluació de resultats (Assistència sanitària) |
| dc.subject.mesh | Disease-Free Survival |
| dc.subject.mesh | Antineoplastic Combined Chemotherapy Protocols |
| dc.subject.mesh | Breast Neoplasms |
| dc.subject.mesh | /drug therapy |
| dc.title | 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 |
| dc.type | info:eu-repo/semantics/article |
| dc.identifier.doi | 10.1200/JCO.23.02170 |
| dc.subject.decs | supervivencia sin enfermedad |
| dc.subject.decs | protocolos de quimioterapia antineoplásica combinada |
| dc.subject.decs | neoplasias de la mama |
| dc.subject.decs | /farmacoterapia |
| dc.relation.publishversion | https://doi.org/10.1200/JCO.23.02170 |
| dc.type.version | info:eu-repo/semantics/publishedVersion |
| dc.audience | Professionals |
| dc.contributor.organismes | Institut 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.pmid | 38935923 |
| dc.rights.accessrights | info:eu-repo/semantics/openAccess |