AVEREL: A Randomized Phase III Trial Evaluating Bevacizumab in Combination With Docetaxel and Trastuzumab As First-Line Therapy for HER2-Positive Locally Recurrent/Metastatic Breast Cancer

Author:

Gianni Luca1,Romieu Gilles H.1,Lichinitser Michail1,Serrano Sergio V.1,Mansutti Mauro1,Pivot Xavier1,Mariani Paola1,Andre Fabrice1,Chan Arlene1,Lipatov Oleg1,Chan Stephen1,Wardley Andrew1,Greil Richard1,Moore Nicola1,Prot Sylvie1,Pallaud Celine1,Semiglazov Vladimir1

Affiliation:

1. Luca Gianni, Ospedale San Raffaele; Paola Mariani, Fondazione Istituto Di Ricovero e Cura a Carattere Scientifico, Istituto Nazionale Tumori, Milan; Mauro Mansutti, University Hospital of Udine, Udine, Italy; Gilles H. Romieu, Centre Régionale de Lutte contre le Cancer, Val d'Aurelle, Montpellier; Xavier Pivot, University Hospital Jean Minjoz, Besançon; Fabrice Andre, Gustave Roussy Institute, Villejuif, France; Michail Lichinitser, N.N. Blokhin Russian Oncology Research Center, Moscow; Oleg Lipatov,...

Abstract

Purpose The AVEREL trial [A Study of Avastin (Bevacizumab) in Combination With Herceptin (Trastuzumab)/Docetaxel in Patients With HER2-Positive Metastatic Breast Cancer] evaluated first-line bevacizumab-containing therapy for human epidermal growth factor receptor 2 (HER2) –positive locally recurrent/metastatic breast cancer (LR/MBC). Patients and Methods Patients with measurable/evaluable HER2-positive LR/MBC who had not received trastuzumab or chemotherapy for LR/MBC were stratified by prior adjuvant trastuzumab, prior (neo)adjuvant taxane, hormone receptor status, and measurable disease and were randomly assigned to receive docetaxel 100 mg/m2 plus trastuzumab 8 mg/kg loading dose followed by 6 mg/kg either with bevacizumab 15 mg/kg or without bevacizumab, all administered every 3 weeks. The primary end point was progression-free survival (PFS). Additional end points included overall survival, response rate (RR), safety, quality of life, and translational research. Results Baseline characteristics of the 424 patients were balanced between treatment arms. Most patients had visceral metastases, 43% had a disease-free interval less than 12 months, and 85% had measurable disease. Median follow-up was 26 months. The hazard ratio for investigator-assessed PFS was 0.82 (95% CI, 0.65 to 1.02; P = .0775; median PFS, 13.7 v 16.5 months in the non-bevacizumab and bevacizumab arms, respectively; PFS events in 72%). The Independent Review Committee–assessed PFS hazard ratio was 0.72 (95% CI, 0.54 to 0.94; P = .0162; median PFS, 13.9 v 16.8 months, respectively; PFS events in 53%). The RR was 70% versus 74%, respectively (P = .3492). Grade ≥ 3 febrile neutropenia and hypertension were more common with bevacizumab-containing therapy. High baseline plasma vascular endothelial growth factor A (VEGF-A) concentrations were associated with greater bevacizumab benefit (not statistically significant). Conclusion Combining bevacizumab with docetaxel and trastuzumab did not significantly improve investigator-assessed PFS. The potential predictive value of plasma VEGF-A is consistent with findings in HER2-negative LR/MBC, warranting prospective evaluation.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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