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首页> 外文期刊>Cancer investigation >Phase I study of vinorelbine and docetaxel with granulocyte colony-stimulating factor support in the treatment of metastatic breast cancer.
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Phase I study of vinorelbine and docetaxel with granulocyte colony-stimulating factor support in the treatment of metastatic breast cancer.

机译:长春瑞滨和多西紫杉醇联合粒细胞集落刺激因子支持的I期研究用于转移性乳腺癌的治疗。

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PURPOSE: Vinorelbine and docetaxel are two active agents in the treatment of metastatic breast cancer. When given together, these drugs exhibit synergistic antitumor activity without significant pharmacokinetic interaction. The dose-limiting toxicities of this combination are neutropenic fever and mucositis. Adding granulocyte colony-stimulating factor (G-CSF) might lessen the toxicity and increase the maximum tolerated dose (MTD) of this combination. The aim of this study was to determine the MTD of vinorelbine and docetaxel given in combination with G-CSF. PATIENTS AND METHODS: Between August 1997 and December 1998, 14 patients with metastatic breast cancer were enrolled in this study. All patients had received doxorubicin-based therapy, and 46% had received paclitaxel in the adjuvant or neoadjuvant setting. Patients were treated with vinorelbine at a starting dose of 20 mg/m2 intravenously over 10 min on days 1 and 5 and docetaxel at a starting dose of 85 mg/m2 intravenously over 1 hr on day 1, following the vinorelbine. Treatments were repeated every 21 days. Prophylactic G-CSF 5 mcg/kg was given subcutaneously on days 3-10. Toxicity was graded according to the National Cancer Institute's grading system. RESULTS: A total of 65 cycles was administered at dose levels 0, -1, -2, and -3. The median absolute granulocyte count nadir for all courses was 200 mm(-3) (range, 0.1-7700 mm(-3)), and the median time to this nadir was 9 days (range, 7-30). The median platelet nadir was 163 (range, 27-401 k), and the median time to this nadir was 8 days (range, 7-30). The most common grade 3 nonhematologic toxicities for all courses were fatigue and myalgia, which occurred in 32 and 10 cycles, respectively. Neutropenic fever was encountered in 11 cycles. Three patients developed colitis-like pictures, two of whom died as a result. Consequently, the protocol was closed to accrual before a MTD was reached. CONCLUSION: The combination of vinorelbine, docetaxel, and G-CSF in our hands has proven to be a toxic regimen, even when relatively low doses of vinorelbine and docetaxel are given. Meticulous observation of patients receiving this combination is warranted since the combination resulted in two deaths in this study.
机译:目的:长春瑞滨和多西他赛是治疗转移性乳腺癌的两种活性药物。当一起使用时,这些药物表现出协同的抗肿瘤活性,而没有明显的药代动力学相互作用。这种组合的剂量限制性毒性是中性粒细胞减少症和粘膜炎。添加粒细胞集落刺激因子(G-CSF)可能会降低毒性并增加该组合的最大耐受剂量(MTD)。这项研究的目的是确定长春瑞滨和多西他赛与G-CSF联合使用的MTD。患者与方法:1997年8月至1998年12月,本研究纳入了14例转移性乳腺癌患者。所有患者均接受了以阿霉素为基础的治疗,其中46%的患者在辅助或新辅助治疗中接受了紫杉醇治疗。在长春瑞滨后,患者在第1天和第5天以10分钟静脉注射长春瑞滨以20 mg / m2的起始剂量接受治疗,在第1天经1小时静脉内以85 mg / m2的起始剂量以多西他赛治疗。每21天重复治疗一次。在第3-10天皮下给予预防性G-CSF 5mcg / kg。毒性根据国家癌症研究所的分级系统进行分级。结果:以剂量水平0,-1,-2和-3总共进行了65个循环。所有疗程的中位数绝对粒细胞计数最低点为200 mm(-3)(范围为0.1-7700 mm(-3)),到该最低点的中值时间为9天(范围7-30)。血小板最低值的中位数为163(范围27-401 k),该最低点的中位时间为8天(范围7-30)。所有疗程中最常见的3级非血液学毒性是疲劳和肌痛,分别发生在32和10个周期中。在11个周期中发生了中性粒细胞减少。三名患者出现了类似结肠炎的照片,其中两人因此死亡。因此,在达到MTD之前,该协议已无法累计。结论:即使给予相对较低剂量的长春瑞滨和多西他赛,长春瑞滨,多西他赛和G-CSF联合使用已被证明是一种毒性疗法。必须认真观察接受该组合的患者,因为该组合在本研究中导致两人死亡。

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