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A multicenter NCI-sponsored phase II study was conducted to analyze the safety and efficacy of the combination of ixabepilone with trastuzumab in patients with metastatic HER2-positive breast cancer.Two cohorts were enrolled: cohort 1 had received no prior chemotherapy or trastuzumab for metastatic disease and cohort 2 had received 1-2 prior trastuzumab-containing regimens for metastatic disease. Patients in both cohorts received ixabepilone 40 mg/m(2) as a 3-h infusion and trastuzumab on day 1 of a 21-day cycle. Tumor biomarkers that may predict response to trastuzumab were explored.Thirty-nine women entered the study with 15 patients in cohort 1 and 24 patients in cohort 2. Across both cohorts, the overall RR was 44

作者:S M, Tolaney;J, Najita;J, Sperinde;W, Huang;W Y, Chen;J, Savoie;M, Fornier;E P, Winer;C, Bunnell;I E, Krop

来源:Annals of oncology : official journal of the European Society for Medical Oncology 2013 年 24卷 7期

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作者:
S M, Tolaney;J, Najita;J, Sperinde;W, Huang;W Y, Chen;J, Savoie;M, Fornier;E P, Winer;C, Bunnell;I E, Krop
来源:
Annals of oncology : official journal of the European Society for Medical Oncology 2013 年 24卷 7期
标签:
HER2 breast cancer ixabepilone trastuzumab
A multicenter NCI-sponsored phase II study was conducted to analyze the safety and efficacy of the combination of ixabepilone with trastuzumab in patients with metastatic HER2-positive breast cancer.Two cohorts were enrolled: cohort 1 had received no prior chemotherapy or trastuzumab for metastatic disease and cohort 2 had received 1-2 prior trastuzumab-containing regimens for metastatic disease. Patients in both cohorts received ixabepilone 40 mg/m(2) as a 3-h infusion and trastuzumab on day 1 of a 21-day cycle. Tumor biomarkers that may predict response to trastuzumab were explored.Thirty-nine women entered the study with 15 patients in cohort 1 and 24 patients in cohort 2. Across both cohorts, the overall RR was 44