A Three-Arm Randomized Phase II Study of Oral Vinorelbine Plus Capecitabine Versus Oral Vinorelbine and Capecitabine in Sequence Versus Docetaxel Plus Capecitabine in Patients with Metastatic Breast Cancer Previously Treated with Anthracyclines

卡培他滨 医学 长春瑞滨 多西紫杉醇 内科学 转移性乳腺癌 养生 蒽环类 胃肠病学 乳腺癌 氟尿嘧啶 癌症 人口 化疗 肿瘤科 外科 结直肠癌 顺铂 环境卫生
作者
Mario Campone,Natalya Dobrovolskaya,Serjei Tjulandin,Shin-Chen Chen,Sameul Fourie,F. Mefti,Maria Konstantinova,Florence Lefresne,N Meheust,Jacek Jassem
出处
期刊:Breast Journal [Wiley]
卷期号:19 (3): 240-249 被引量:18
标识
DOI:10.1111/tbj.12098
摘要

Owing to the increased number of patients treated with anthracycline-based adjuvant chemotherapy, there is a need for new effective and tolerable nonanthracycline regimens in metastatic breast cancer. Patients with HER2-negative metastatic breast cancer previously treated with anthracyclines in (neo)adjuvant setting were randomized to fully oral 3 weekly cycles of the combination of oral vinorelbine with capecitabine (V + C), to the same drugs alternating every three cycles (V↔C), or to the combination of docetaxel and capecitabine (D + C). V was given at 80 mg/m2 (after the first cycle at 60 mg/m2) on days 1 and 8 in the V + C arm and weekly in the V↔C arm, C at 1,000 mg/m2 bid from days 1 to 14, and D on day 1 at 75 mg/m2. The primary end point was disease control rate (CR + PR + NC ≥ 3 months). A total of 139 patients were randomly assigned to V + C (44 patients), V↔C (47 patients), and D + C (48 patients). After an independent review, the disease control rate in the intent-to-treat population in the V + C, V↔C, and D + C arms [95% CI] was 70.5% [54.8–83.2], 37.0% [23.2–52.5], and 70.8% [55.9–83.1], and the median overall survival 22.2, 19.4, and 24.2 months, respectively. When taken into account the disease control rate, the alternating V↔C regimen seems to be less effective compared with V + C or D + C combinations. Combinations of V + C or D + C showed similar efficacy and a different toxicity profile; V + C induced less neutropenia, infection, hand-foot syndrome, fatigue/asthenia, and alopecia, whereas D + C – less gastrointestinal toxicity. V + C combination constitutes a valuable fully oral alternative option to D + C in patients with metastatic breast cancer previously treated with anthracyclines in (neo)adjuvant setting, while offering the advantages of an all-oral treatment.
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