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Paclitaxel vinorelbine and 5-fluorouracil in breast cancer patients pretreated with adjuvant anthracyclines

机译:辅助蒽环类药物预处理的乳腺癌患者中的紫杉醇长春瑞滨和5-氟尿嘧啶

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摘要

We investigated the activity and toxicity of a combination of vinorelbine (VNB), paclitaxel (PTX) and 5-fluorouracil (5-FU) continuous infusion administered as first-line chemotherapy in metastatic breast cancer patients pretreated with adjuvant anthracyclines. A total of 61 patients received a regimen consisting of VNB 25 mg m−2 on days 1 and 15, PTX 60 mg m−2 on days 1, 8 and 15 and continuous infusion of 5-FU at 200 mg m−2 every day. Cycles were repeated every 28 days. Disease response was evaluated by both RECIST and World Health Organization (WHO) criteria. Objective responses were recorded in 39 of 61 patients (64.0%) assessed by WHO and in 36 of 50 patients (72.0%) assessable by RECIST criteria. Complete remission occurred in 15 (24.6%) and 14 patients (28.0%), respectively. The median time to progression and overall survival of entire population was 10.6 and 27.3 months, respectively, and median duration of complete response was 14.8 months. The dose-limiting toxicity was myelosuppression (leucopenia grade 3/4 in 52.5% of patients). Grade 3/4 nonhaematologic toxicities included mucositis/diarrhoea in 13.1%, skin in 3.3% and cardiac in 1.6% of patients. Grade 2/3 neurotoxicity was observed in five patients (7.2%). The VNB, PTX and 5-FU continuous infusion combination regimen was active and manageable. Complete responses were frequent and durable.
机译:我们调查了长春瑞滨(VNB),紫杉醇(PTX)和5-氟尿嘧啶(5-FU)连续输注联合作为一线化疗在转移性乳腺癌患者中用辅助蒽环类药物预处理的活性和毒性。共有61例患者在第1和15天接受了由VNB 25NBmg m −2 组成的方案,在第1、8和15天以及每天以200 mg m −2 连续输注5-FU。每28天重复一次循环。 RECIST和世界卫生组织(WHO)均评估了疾病反应。世卫组织评估的61例患者中有39例(64.0%)记录了客观反应,RECIST标准评估的50例患者中有36例(72.0%)记录了客观反应。完全缓解分别发生在15(24.6%)和14例(28.0%)的患者中。整个人群的中位进展时间和总生存时间分别为10.6和27.3个月,完全缓解的中位持续时间为14.8个月。剂量限制性毒性是骨髓抑制(52.5%患者的白细胞减少症等级3/4)。 3/4级非血液学毒性包括粘膜炎/腹泻占13.1%,皮肤占3.3%,心脏占1.6%。五名患者(7.2%)观察到2/3级神经毒性。 VNB,PTX和5-FU连续输注联合方案十分活跃且易于管理。完整的回应是频繁且持久的。

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