首页> 外文期刊>Anti-cancer drugs >Is macrocytosis a potential biomarker of the efficacy of dose-dense paclitaxel-carboplatin combination therapy in patients with epithelial ovarian cancer?
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Is macrocytosis a potential biomarker of the efficacy of dose-dense paclitaxel-carboplatin combination therapy in patients with epithelial ovarian cancer?

机译:宏细胞症是一种潜在的生物标志物的潜在生物标志物,其剂量 - 密集紫杉醇 - 卡铂联合治疗在上皮性卵巢癌患者中的疗效?

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摘要

The aims of this study were to investigate a clinical observation that patients with epithelial ovarian cancer treated with first-line platinum-paclitaxel chemotherapy combination (TP) develop macrocytosis and to explore the possible predictive role of macrocytosis in response rate, progression-free survival (PFS), and overall survival. A retrospective analysis of laboratory and clinical data on 184 consecutive ovarian cancer patients treated with first-line TP chemotherapy in a single oncology center from 2004 to 2015 was carried out. Macrocytosis was defined as an increase in mean corpuscular volume of peripheral red blood cells above 97.2 fl during the treatment and/or 30 days after the last chemotherapy cycle. One hundred and forty-one patients were treated with a conventional 3-weekly TP schedule, whereas 43 patients were treated with a dose-dense schedule. Macrocytosis was induced in 35% of patients overall. It was induced significantly more often in patients treated with the dose-dense schedule than in those treated with the 3-weekly schedule (67 vs. 26%, P=1.29x10(-6)). Macrocytosis did not correlate with PFS and overall survival in the overall patient population, nor in patients treated with the 3-weekly schedule. It correlated with PFS (hazard ratio=0.42, 95% confidence interval=0.18-0.94, P=0.036) and objective response on therapy in patients treated with the dose-dense schedule (P=0.0285). Dose-dense TP chemotherapy induces macrocytosis significantly more often than does a 3-weekly schedule in ovarian cancer patients. In patients treated with a dose-dense schedule, macrocytosis can potentially be predictive for longer PFS and better response rate. This finding needs further confirmation, preferentially in a prospective study. Copyright c 2017 Wolters Kluwer Health, Inc. All rights reserved.
机译:本研究的目的是探讨临床观察,即用一线铂 - 紫杉醇化疗组合(TP)治疗上皮性卵巢癌的患者发育宏细胞症,并探讨宏细胞症在响应率,无进展存活中的可能预测作用( PFS)和整体生存。在2004年至2015年从2004年至2015年,在单一肿瘤学中心治疗的184名连续卵巢癌患者的实验室和临床数据的回顾性分析。宏细胞症定义为在治疗期间97.2F的周围红细胞的平均碎屑体积的增加和/或在最后化疗循环后30天。用常规的3-每周TP时间表治疗一百四十一名患者,而43名患者被用剂量密集的时间表进行治疗。宏细胞症在总体患者的35%诱导。在用剂量致密的时间表治疗的患者中诱导比用3-每周时间表(67 vs.26%,P = 1.29x10(-6))的患者显着诱导。宏细胞增多症与整体患者人口的PFS和整体生存率没有相关,也没有在3-每周时间表治疗的患者中存在。它与PFS(危险比= 0.42,95%置信区间= 0.18-0.94,p = 0.036)和对治疗剂量 - 致密时间表治疗的患者的客观反应(P = 0.0285)。剂量 - 致密TP化疗诱导宏髓变性更常见于卵巢癌患者的3-每周时间表。在用剂量致密的时间表治疗的患者中,宏细胞症可能会用于更长的PFS和更好的响应率的预测性。这一发现需要进一步确认,优先在预期的研究中。版权所有C 2017 Wolters Kluwer Health,Inc。保留所有权利。

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