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Efficacy and safety of everolimus in combination with trastuzumab and paclitaxel in Asian patients with HER2+ advanced breast cancer in BOLERO-1.

Authors :
Toi, Masakazu
Toi, Masakazu
Shao, Zhimin
Hurvitz, Sara
Tseng, Ling-Ming
Zhang, Qingyuan
Shen, Kunwei
Liu, Donggeng
Feng, Jifeng
Xu, Binghe
Wang, Xiaojia
Lee, Keun Seok
Ng, Ting Ying
Ridolfi, Antonia
Noel-Baron, Florence
Ringeisen, Francois
Jiang, Zefei
Toi, Masakazu
Toi, Masakazu
Shao, Zhimin
Hurvitz, Sara
Tseng, Ling-Ming
Zhang, Qingyuan
Shen, Kunwei
Liu, Donggeng
Feng, Jifeng
Xu, Binghe
Wang, Xiaojia
Lee, Keun Seok
Ng, Ting Ying
Ridolfi, Antonia
Noel-Baron, Florence
Ringeisen, Francois
Jiang, Zefei
Source :
Breast cancer research : BCR; vol 19, iss 1, 47; 1465-5411
Publication Year :
2017

Abstract

BackgroundThe current exploratory analysis was performed to evaluate the efficacy and safety of everolimus for treatment of human epidermal growth factor receptor 2-positive (HER2+) advanced breast cancer in the Asian subset of patients in the BOLERO-1 trial.MethodsPostmenopausal women with HER2+ advanced breast cancer, who had not received systemic therapy for advanced disease, were randomized 2:1 to receive everolimus or placebo, plus trastuzumab and paclitaxel. The two primary end points were investigator-assessed progression-free survival (PFS) in the full population and in the hormone receptor-negative (HR-) subpopulation. Secondary end points included assessment of the objective response rate, the clinical benefit rate, and safety.ResultsIn the Asian subset, median PFS was similar in the everolimus (n = 198) and placebo (n = 105) arms in the full analysis set (hazard ratio = 0.82 (95% CI 0.61-1.11)). In the HR- subpopulation, everolimus prolonged median PFS by 10.97 months vs placebo (25.46 vs 14.49 months; hazard ratio = 0.48 (95% CI 0.29-0.79)). In the everolimus arm of the Asian subset, the most common adverse events of any grade were stomatitis (62.2%), diarrhea (48.0%), rash (43.4%) and neutropenia (42.3%). Neutropenia (grade 3: 27.6%; grade 4: 4.6%) and decreased neutrophil count (grade 3: 11.2%; grade 4: 3.6%) were the most frequent grade 3/4 adverse events. Serious adverse events included pneumonia (5.1%), pneumonitis (3.1%), and interstitial lung disease (3.1%). There were three deaths (1.5%) during treatment in the everolimus arm vs none in the placebo arm.ConclusionsThe efficacy and safety of everolimus plus trastuzumab and paclitaxel as first-line treatment for HER2+ advanced breast cancer in the Asian subset was consistent with that reported previously in the overall population.Trial registrationClinicalTrials.gov, NCT00876395 . Registered on 2 April 2009.

Details

Database :
OAIster
Journal :
Breast cancer research : BCR; vol 19, iss 1, 47; 1465-5411
Notes :
application/pdf, Breast cancer research : BCR vol 19, iss 1, 47 1465-5411
Publication Type :
Electronic Resource
Accession number :
edsoai.on1367474157
Document Type :
Electronic Resource