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

Author:

Tarantino Paolo1234ORCID,Tayob Nabihah35ORCID,Villacampa Guillermo67ORCID,Dang Chau8,Yardley Denise A.9,Isakoff Steven J.310ORCID,Valero Vicente11,Faggen Meredith1,Mulvey Therese310ORCID,Bose Ron12ORCID,Weckstein Douglas13,Wolff Antonio C.14ORCID,Reeder-Hayes Katherine15ORCID,Rugo Hope S.16ORCID,Ramaswamy Bhuvaneswari17,Zuckerman Dan18ORCID,Hart Lowell19,Gadi Vijayakrishna K.20ORCID,Constantine Michael1,Cheng Kit21ORCID,Garrett Audrey Merrill22,Marcom P. Kelly23ORCID,Albain Kathy24ORCID,DeFusco Patricia25,Tung Nadine326ORCID,Ardman Blair27,Nanda Rita28ORCID,Jankowitz Rachel C.29ORCID,Rimawi Mothaffar30ORCID,Abramson Vandana31ORCID,Pohlmann Paula R.1132,Van Poznak Catherine33ORCID,Forero-Torres Andres34ORCID,Liu Minetta C.35ORCID,Ruddy Kathryn J.36ORCID,Waks Adrienne G.123,DeMeo Michelle2,Burstein Harold J.123ORCID,Partridge Ann H.123ORCID,Dell'Orto Patrizia37,Russo Leila37,Krause Emma38ORCID,Newhouse Daniel J.39,Kurt Busem Binboğa2ORCID,Mittendorf Elizabeth A.2340ORCID,Schneider Bryan41ORCID,Prat Aleix64243ORCID,Winer Eric P.12344ORCID,Krop Ian E.12344ORCID,Tolaney Sara M.123ORCID, ,Barroso-Sousa Romualdo,Curigliano Giuseppe,DiLullo Molly,Hui Winnie,Kirkup Christian,Viale Giuseppe,Zheng Yue

Affiliation:

1. Medical Oncology, Dana-Farber Cancer Institute, Boston, MA

2. Breast Oncology Program, Dana-Farber Brigham Cancer Center, Boston, MA

3. Harvard Medical School, Boston, MA

4. Department of Oncology and Hemato-Oncology, University of Milan, Milan, Italy

5. Division of Data Science, Dana-Farber Cancer Institute, Boston, MA

6. SOLTI Breast Cancer Research Group, Barcelona, Spain

7. Oncology Data Science Vall d’Hebron Institute of Oncology, Barcelona, Spain

8. Memorial Sloan Kettering Cancer Center, New York, NY

9. Sarah Cannon Research Institute and Tennessee Oncology, Nashville, TN

10. Massachusetts General Hospital, Boston, MA

11. MD Anderson Cancer Center, Houston, TX

12. Washington University School of Medicine, St Louis, MO

13. New Hampshire Oncology Hematology, Manchester, NH

14. Johns Hopkins Sidney Kimmel Cancer Center, Washington, DC

15. University of North Carolina Lineberger Comprehensive Cancer Center, Chapel Hill, NC

16. University of California, San Francisco, CA

17. Ohio State University Comprehensive Cancer Center, Columbus, OH

18. St Luke's Mountain States Tumor Institute, Boise, ID

19. Wake Forest Baptist Health, Winston-Salem, NC

20. University of Illinois Cancer Center, Chicago, IL

21. North Shore-LIJ Cancer Institute, Lake Success, NY

22. Northern Light Cancer Care, Brewer, ME

23. Duke University School of Medicine, Durham, NC

24. Loyola University Medical Center, Maywood, IL

25. Hartford Healthcare Cancer Institute, Hartford, CT

26. Beth Israel Deaconess Medical Center, Boston, MA

27. Lowell General Hospital, Lowell, MA

28. UChicago Medicine, Chicago, IL

29. Perelman Center for Advanced Medicine, Philadelphia, PA

30. Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX

31. Vanderbilt-Ingram Cancer Center, Nashville, TN

32. Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, DC

33. Rogel Cancer Center, University of Michigan, Ann Arbor, MI

34. Kirklin UAB Hematology Oncology, Birmingham, AL

35. Natera, Inc, Austin, TX

36. Mayo Clinic, Rochester, NY

37. IEO European Institute of Oncology, IRCCS, Milan, Italy

38. PathAI, Boston, MA

39. NanoString Technologies, Inc, Boston, MA

40. Division of Breast Surgery, Department of Surgery, Brigham and Women's Hospital, Boston, MA

41. Indiana University School of Medicine, Indianapolis, IN

42. Translational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain

43. Department of Medical Oncology, Hospital Clinic of Barcelona, Barcelona, Spain

44. Yale Cancer Center, New Haven, CT

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.

Publisher

American Society of Clinical Oncology (ASCO)

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