首页> 外文期刊>Breast cancer research and treatment. >Ixabepilone plus capecitabine in metastatic breast cancer patients with reduced performance status previously treated with anthracyclines and taxanes: a pooled analysis by performance status of efficacy and safety data from 2 phase III studies.
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Ixabepilone plus capecitabine in metastatic breast cancer patients with reduced performance status previously treated with anthracyclines and taxanes: a pooled analysis by performance status of efficacy and safety data from 2 phase III studies.

机译:伊沙贝比隆加卡培他滨治疗转移状态降低的乳腺癌患者,以前接受蒽环类和紫杉烷类药物治疗:通过两项3期临床研究的有效性和安全性数据进行合并分析。

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Patients with metastatic breast cancer (MBC) previously treated with anthracyclines and taxanes often have decreased performance status secondary to extensive tumor involvement. Here, we report the pooled analysis of efficacy and safety data from two similarly designed phase III studies to provide a more precise estimate of benefit of ixabepilone plus capecitabine in MBC patients with Karnofsky's performance status (KPS) 70-80. Across the studies, anthracycline/taxane-pretreated MBC patients were randomized to receive ixabepilone plus capecitabine or capecitabine alone. Individual patient data for KPS 70-80 subset (n = 606) or KPS 90-100 subset (n = 1349) from the two studies were pooled by treatment. Analysis included overall survival (OS), progression-free survival (PFS), objective response rate (ORR), and safety. In patients with reduced performance status (KPS 70-80), ixabepilone plus capecitabine was associated with improvements in OS (median: 12.3 vs. 9.5 months; HR, 0.75; P = 0.0015), PFS (median: 4.6 vs. 3.1 months; HR, 0.76; P = 0.0021) and ORR (35 vs. 19%) over capecitabine alone. Corresponding results in patients with high performance status (KPS 90-100) were median OS of 16.7 versus 16.2 months (HR, 0.98; P = 0.8111), median PFS of 6.0 versus 4.4 months (HR, 0.58; P = 0.0009), and ORR of 45 versus 28%. The safety profile of combination therapy was similar between the subgroups. Ixabepilone plus capecitabine appeared to show superior efficacy compared to capecitabine alone in MBC patients previously treated with anthracyclines and taxanes, regardless of performance status, with a possible OS benefit favoring KPS 70-80 patients (ClinicalTrials.gov identifiers: NCT00080301 and NCT00082433).
机译:先前接受蒽环类药物和紫杉烷类药物治疗的转移性乳腺癌(MBC)患者通常由于广泛的肿瘤受累而导致性能下降。在这里,我们报告了来自两项类似设计的三期研究的疗效和安全性数据的汇总分析,以更准确地评估依卡培比隆加卡培他滨对具有卡诺夫斯基功能状态(KPS)70-80的MBC患者的益处。在整个研究中,蒽环类/紫杉烷预处理的MBC患者被随机分配接受ixabepilone加卡培他滨或卡培他滨单独治疗。通过治疗合并来自两项研究的KPS 70-80子集(n = 606)或KPS 90-100子集(n = 1349)的个体患者数据。分析包括总生存期(OS),无进展生存期(PFS),客观缓解率(ORR)和安全性。在表现状态降低的患者(KPS 70-80)中,依沙贝比隆加卡培他滨与OS改善有关(中位数:12.3 vs. 9.5个月; HR,0.75; P = 0.0015),PFS(中位数:4.6 vs. 3.1个月;相对于单用卡培他滨而言,HR为0.76; P = 0.0021)和ORR(35比19%)。处于高性能状态(KPS 90-100)的患者的相应结果是OS的中位值分别为16.7和16.2个月(HR,0.98; P = 0.8111),PFS的中位值是6.0与4.4个月(HR,0.58; P = 0.0009), ORR分别为45和28%。在亚组之间,联合治疗的安全性相似。与以前的卡培他滨相比,在既往使用蒽环类和紫杉烷类药物治疗的MBC患者中,无论表现情况如何,伊沙贝比隆加卡培他滨似乎均显示出优于单独的卡培他滨的疗效,并且可能有利于KPS 70-80的患者受益于OS(ClinicalTrials.gov标识符:NCT00080301和NCT00082433)。

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