TY - JOUR
T1 - Adjuvant Trastuzumab Emtansine Versus Paclitaxel Plus Trastuzumab for Stage i Human Epidermal Growth Factor Receptor 2-Positive Breast Cancer
T2 - 5-Year Results and Correlative Analyses from ATEMPT
AU - Consortium of the TBCRC Translational Investigators
AU - Tarantino, Paolo
AU - Tayob, Nabihah
AU - Villacampa, Guillermo
AU - Dang, Chau
AU - Yardley, Denise A.
AU - Isakoff, Steven J.
AU - Valero, Vicente
AU - Faggen, Meredith
AU - Mulvey, Therese
AU - Bose, Ron
AU - Weckstein, Douglas
AU - Wolff, Antonio C.
AU - Reeder-Hayes, Katherine
AU - Rugo, Hope S.
AU - Ramaswamy, Bhuvaneswari
AU - Zuckerman, Dan
AU - Hart, Lowell
AU - Gadi, Vijayakrishna K.
AU - Constantine, Michael
AU - Cheng, Kit
AU - Garrett, Audrey Merrill
AU - Marcom, P. Kelly
AU - Albain, Kathy
AU - Defusco, Patricia
AU - Tung, Nadine
AU - Ardman, Blair
AU - Nanda, Rita
AU - Jankowitz, Rachel C.
AU - Rimawi, Mothaffar
AU - Abramson, Vandana
AU - Pohlmann, Paula R.
AU - Van Poznak, Catherine
AU - Forero-Torres, Andres
AU - Liu, Minetta C.
AU - Ruddy, Kathryn J.
AU - Waks, Adrienne G.
AU - Demeo, Michelle
AU - Burstein, Harold J.
AU - Partridge, Ann H.
AU - Dell'orto, Patrizia
AU - Russo, Leila
AU - Krause, Emma
AU - Newhouse, Daniel J.
AU - Kurt, Busem Binboǧa
AU - Mittendorf, Elizabeth A.
AU - Schneider, Bryan
AU - Prat, Aleix
AU - Winer, Eric P.
AU - Krop, Ian E.
AU - Tolaney, Sara M.
AU - Barroso-Sousa, Romualdo
AU - Curigliano, Giuseppe
AU - Dilullo, Molly
AU - Hui, Winnie
AU - Kirkup, Christian
AU - Viale, Giuseppe
AU - Zheng, Yue
N1 - Publisher Copyright:
© 2024 American Society of Clinical Oncology.
PY - 2024/11/1
Y1 - 2024/11/1
N2 - PURPOSELong-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.METHODSIn 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.RESULTSAfter 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.CONCLUSIONAdjuvant 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.
AB - PURPOSELong-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.METHODSIn 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.RESULTSAfter 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.CONCLUSIONAdjuvant 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.
UR - http://www.scopus.com/inward/record.url?scp=85206951390&partnerID=8YFLogxK
U2 - 10.1200/JCO.23.02170
DO - 10.1200/JCO.23.02170
M3 - Article
C2 - 38935923
AN - SCOPUS:85206951390
SN - 0732-183X
VL - 42
SP - 3652
EP - 3665
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 31
ER -