Trastuzumab Plus Anastrozole Versus Anastrozole Alone for the Treatment of Postmenopausal Women With Human Epidermal Growth Factor Receptor 2–Positive, Hormone Receptor–Positive Metastatic Breast Cancer: Results From the Randomized Phase III TAnDEM Study

Author:

Kaufman Bella1,Mackey John R.1,Clemens Michael R.1,Bapsy Poonamalle P.1,Vaid Ashok1,Wardley Andrew1,Tjulandin Sergei1,Jahn Michaela1,Lehle Michaela1,Feyereislova Andrea1,Révil Cédric1,Jones Alison1

Affiliation:

1. From the Chaim Sheba Medical Center, Tel Hashomer, Israel; Cross Cancer Institute, Edmonton, Alberta, Canada; Klinikum Mutterhaus der Borromäerinnen, Trier, Germany; Kidwai Memorial Institute of Oncology, Bangalore; Rajiv Gandhi Cancer Institute, New Delhi, India; Christie Hospital National Health Service Foundation Trust, Manchester; Royal Free Hospital, London, United Kingdom; Russian Cancer Research Center, Moscow, Russia; and F. Hoffmann-La Roche, Basel, Switzerland.

Abstract

Purpose TAnDEM is the first randomized phase III study to combine a hormonal agent and trastuzumab without chemotherapy as treatment for human epidermal growth factor receptor 2 (HER2)/hormone receptor–copositive metastatic breast cancer (MBC). Patients and Methods Postmenopausal women with HER2/hormone receptor–copositive MBC were randomly assigned to anastrozole (1 mg/d orally) with or without trastuzumab (4 mg/kg intravenous infusion on day 1, then 2 mg/kg every week) until progression. The primary end point was progression-free survival (PFS) in the intent-to-treat population. Results Overall, 103 patients received trastuzumab plus anastrozole; 104 received anastrozole alone. Patients in the trastuzumab plus anastrozole arm experienced significant improvements in PFS compared with patients receiving anastrozole alone (hazard ratio = 0.63; 95% CI, 0.47 to 0.84; median PFS, 4.8 v 2.4 months; log-rank P = .0016). In patients with centrally confirmed hormone receptor positivity (n = 150), median PFS was 5.6 and 3.8 months in the trastuzumab plus anastrozole and anastrozole alone arms, respectively (log-rank P = .006). Overall survival in the overall and centrally confirmed hormone receptor–positive populations showed no statistically significant treatment difference; however, 70% of patients in the anastrozole alone arm crossed over to receive trastuzumab after progression on anastrozole alone. Incidence of grade 3 and 4 adverse events was 23% and 5%, respectively, in the trastuzumab plus anastrozole arm, and 15% and 1%, respectively, in the anastrozole alone arm; one patient in the combination arm experienced New York Heart Association class II congestive heart failure. Conclusion Trastuzumab plus anastrozole improves outcomes for patients with HER2/hormone receptor–copositive MBC compared with anastrozole alone, although adverse events and serious adverse events were more frequent with the combination.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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