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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.
Tarantino, Paolo; Tayob, Nabihah; Villacampa, Guillermo; Dang, Chau; Yardley, Denise A; Isakoff, Steven J; Valero, Vicente; Faggen, Meredith; Mulvey, Therese; Bose, Ron; Weckstein, Douglas; Wolff, Antonio C; Reeder-Hayes, Katherine; Rugo, Hope S; Ramaswamy, Bhuvaneswari; Zuckerman, Dan; Hart, Lowell; Gadi, Vijayakrishna K; Constantine, Michael; Cheng, Kit; Garrett, Audrey Merrill; Marcom, P Kelly; Albain, Kathy; DeFusco, Patricia; Tung, Nadine; Ardman, Blair; Nanda, Rita; Jankowitz, Rachel C; Rimawi, Mothaffar; Abramson, Vandana; Pohlmann, Paula R; Van Poznak, Catherine; Forero-Torres, Andres; Liu, Minetta C; Ruddy, Kathryn J; Waks, Adrienne G; DeMeo, Michelle; Burstein, Harold J; Partridge, Ann H; Dell'Orto, Patrizia; Russo, Leila; Krause, Emma; Newhouse, Daniel J; Kurt, Busem Binboga; Mittendorf, Elizabeth A; Schneider, Bryan; Prat, Aleix; Winer, Eric P; Krop, Ian E; Tolaney, Sara M.
Afiliação
  • Tarantino P; Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
  • Tayob N; Breast Oncology Program, Dana-Farber Brigham Cancer Center, Boston, MA.
  • Villacampa G; Harvard Medical School, Boston, MA.
  • Dang C; Department of Oncology and Hemato-Oncology, University of Milan, Milan, Italy.
  • Yardley DA; Harvard Medical School, Boston, MA.
  • Isakoff SJ; Division of Data Science, Dana-Farber Cancer Institute, Boston, MA.
  • Valero V; SOLTI Breast Cancer Research Group, Barcelona, Spain.
  • Faggen M; Oncology Data Science Vall d'Hebron Institute of Oncology, Barcelona, Spain.
  • Mulvey T; Memorial Sloan Kettering Cancer Center, New York, NY.
  • Bose R; Sarah Cannon Research Institute and Tennessee Oncology, Nashville, TN.
  • Weckstein D; Harvard Medical School, Boston, MA.
  • Wolff AC; Massachusetts General Hospital, Boston, MA.
  • Reeder-Hayes K; MD Anderson Cancer Center, Houston, TX.
  • Rugo HS; Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
  • Ramaswamy B; Harvard Medical School, Boston, MA.
  • Zuckerman D; Massachusetts General Hospital, Boston, MA.
  • Hart L; Washington University School of Medicine, St Louis, MO.
  • Gadi VK; New Hampshire Oncology Hematology, Manchester, NH.
  • Constantine M; Johns Hopkins Sidney Kimmel Cancer Center, Washington, DC.
  • Cheng K; University of North Carolina Lineberger Comprehensive Cancer Center, Chapel Hill, NC.
  • Garrett AM; University of California, San Francisco, CA.
  • Marcom PK; Ohio State University Comprehensive Cancer Center, Columbus, OH.
  • Albain K; St Luke's Mountain States Tumor Institute, Boise, ID.
  • DeFusco P; Wake Forest Baptist Health, Winston-Salem, NC.
  • Tung N; University of Illinois Cancer Center, Chicago, IL.
  • Ardman B; Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
  • Nanda R; North Shore-LIJ Cancer Institute, Lake Success, NY.
  • Jankowitz RC; Northern Light Cancer Care, Brewer, ME.
  • Rimawi M; Duke University School of Medicine, Durham, NC.
  • Abramson V; Loyola University Medical Center, Maywood, IL.
  • Pohlmann PR; Hartford Healthcare Cancer Institute, Hartford, CT.
  • Van Poznak C; Harvard Medical School, Boston, MA.
  • Forero-Torres A; Beth Israel Deaconess Medical Center, Boston, MA.
  • Liu MC; Lowell General Hospital, Lowell, MA.
  • Ruddy KJ; UChicago Medicine, Chicago, IL.
  • Waks AG; Perelman Center for Advanced Medicine, Philadelphia, PA.
  • DeMeo M; Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX.
  • Burstein HJ; Vanderbilt-Ingram Cancer Center, Nashville, TN.
  • Partridge AH; MD Anderson Cancer Center, Houston, TX.
  • Dell'Orto P; Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, DC.
  • Russo L; Rogel Cancer Center, University of Michigan, Ann Arbor, MI.
  • Krause E; Kirklin UAB Hematology Oncology, Birmingham, AL.
  • Newhouse DJ; Natera, Inc, Austin, TX.
  • Kurt BB; Mayo Clinic, Rochester, NY.
  • Mittendorf EA; Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
  • Schneider B; Breast Oncology Program, Dana-Farber Brigham Cancer Center, Boston, MA.
  • Prat A; Harvard Medical School, Boston, MA.
  • Winer EP; Breast Oncology Program, Dana-Farber Brigham Cancer Center, Boston, MA.
  • Krop IE; Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
  • Tolaney SM; Breast Oncology Program, Dana-Farber Brigham Cancer Center, Boston, MA.
J Clin Oncol ; : JCO2302170, 2024 Jun 27.
Article em En | MEDLINE | ID: mdl-38935923
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 31 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.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article