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 (VC), or to the combination of docetaxel and capecitabine (D+C). V was given at 80mg/m2 (after the first cycle at 60mg/m2) on days 1 and 8 in the V+C arm and weekly in the VC arm, C at 1,000mg/m2 bid from days 1 to 14, and D on day 1 at 75mg/m2. The primary end point was disease control rate (CR+PR+NC3months). A total of 139 patients were randomly assigned to V+C (44 patients), VC (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, VC, and D+C arms [95% CI] was 70.5% [54.883.2], 37.0% [23.252.5], and 70.8% [55.983.1], and the median overall survival 22.2, 19.4, and 24.2months, respectively. When taken into account the disease control rate, the alternating VC 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.

  • 出版日期2013-6

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