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Pharmacokinetics of metronomic chemotherapy: a neglected but crucial aspect.节拍化疗的药代动力学:一个被忽视但至关重要的方面。
Nat Rev Clin Oncol. 2016 Nov;13(11):659-673. doi: 10.1038/nrclinonc.2016.64. Epub 2016 May 17.
2
Metronomic oral vinorelbine as first-line treatment in elderly patients with advanced non-small cell lung cancer: results of a phase II trial (MOVE trial).口服节拍性长春瑞滨作为老年晚期非小细胞肺癌患者的一线治疗:一项II期试验(MOVE试验)的结果
BMC Cancer. 2015 May 6;15:359. doi: 10.1186/s12885-015-1354-2.
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The pharmacological bases of the antiangiogenic activity of paclitaxel.紫杉醇抗血管生成活性的药理学基础。
Angiogenesis. 2013 Jul;16(3):481-92. doi: 10.1007/s10456-013-9334-0. Epub 2013 Feb 7.
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Prognostic or predictive plasma cytokines and angiogenic factors for patients treated with pazopanib for metastatic renal-cell cancer: a retrospective analysis of phase 2 and phase 3 trials.帕唑帕尼治疗转移性肾细胞癌患者的预后或预测性血浆细胞因子和血管生成因子: 2 期和 3 期试验的回顾性分析。
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Dose-ranging study of metronomic oral vinorelbine in patients with advanced refractory cancer.口服节拍式长春瑞滨治疗晚期难治性癌症的剂量范围研究。
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Paclitaxel-carboplatin alone or with bevacizumab for non-small-cell lung cancer.单独使用紫杉醇-卡铂或联合贝伐单抗治疗非小细胞肺癌。
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Antiangiogenic activity of paclitaxel is associated with its cytostatic effect, mediated by the initiation but not completion of a mitochondrial apoptotic signaling pathway.紫杉醇的抗血管生成活性与其细胞生长抑制作用相关,该作用由线粒体凋亡信号通路的启动而非完成介导。
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The anti-angiogenic basis of metronomic chemotherapy.节拍化疗的抗血管生成基础。
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Three-arm randomized study of two cisplatin-based regimens and paclitaxel plus gemcitabine in advanced non-small-cell lung cancer: a phase III trial of the European Organization for Research and Treatment of Cancer Lung Cancer Group--EORTC 08975.两种基于顺铂的方案与紫杉醇加吉西他滨治疗晚期非小细胞肺癌的三臂随机研究:欧洲癌症研究与治疗组织肺癌组的III期试验——EORTC 08975
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Thrombospondin 1, a mediator of the antiangiogenic effects of low-dose metronomic chemotherapy.血小板反应蛋白1,低剂量节拍化疗抗血管生成作用的介质。
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节拍化疗联合贝伐单抗治疗晚期非鳞状非小细胞肺癌的II期试验性研究

Pilot phase II study of metronomic chemotherapy in combination with bevacizumab in patients with advanced non-squamous non-small cell lung cancer.

作者信息

Jones Benjamin S, Jerome Mary S, Miley Deborah, Jackson Bradford E, DeShazo Mollie R, Reddy Vishnu V B, Singh Karan P, Brown Olivia C, Robert Francisco

机构信息

Division of Hematology/Oncology, Comprehensive Cancer Center, University of Alabama at Birmingham, United States; Division of Preventive Medicine, Comprehensive Cancer Center, University of Alabama at Birmingham, United States; Division of Laboratory Medicine, Comprehensive Cancer Center, University of Alabama at Birmingham, United States.

Division of Hematology/Oncology, Comprehensive Cancer Center, University of Alabama at Birmingham, United States; Division of Preventive Medicine, Comprehensive Cancer Center, University of Alabama at Birmingham, United States; Division of Laboratory Medicine, Comprehensive Cancer Center, University of Alabama at Birmingham, United States.

出版信息

Lung Cancer. 2017 Apr;106:125-130. doi: 10.1016/j.lungcan.2017.02.004. Epub 2017 Feb 9.

DOI:10.1016/j.lungcan.2017.02.004
PMID:28285686
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5667666/
Abstract

INTRODUCTION

The goal of this study was to explore the efficacy and tolerability of metronomic chemotherapy, a novel anti-angiogenic treatment strategy, in combination with bevacizumab in patients with advanced non-small cell lung cancer (NSCLC).

METHODS

Subjects with newly diagnosed stage IV NSCLC were treated with 4-week cycles of paclitaxel 80mg/m and gemcitabine 300mg/m weekly for three weeks, plus bevacizumab 10mg/kg every two weeks. Radiologic assessments were performed every 8 weeks. The primary endpoint was progression free survival (PFS). An exploratory objective was to correlate plasma levels of angiogenic biomarkers with treatment response.

RESULTS

Thirty-nine subjects were included in the intent to treat (ITT) analysis. The objective response rate (ORR) was 56%, the median PFS was 8.5 months, and median overall survival (OS) was 25.5 months. The PFS rate at 6, 12, and 24 months was 61%, 21%, and 11% respectively. The OS rate at 12 and 24 months was 74% and 53% respectively. Treatment was well tolerated, without significant myelosuppressive, gastrointestinal, or neurologic events. Subjects with less than median baseline values of angiopoietin-2 and IL-8 experienced significantly longer PFS. Longer OS was associated with subjects with less than the median baseline values for PLGF and angiopoietin-2. There were statistically significant differences in median values of several biomarkers between cycles 1 and 3 in subjects with objective responses.

CONCLUSIONS

The combination of paclitaxel and gemcitabine, delivered in a metronomic schedule, in combination with bevacizumab, appears to be an effective and tolerable treatment strategy in patients with advanced NSCLC.

摘要

引言

本研究的目的是探讨节拍化疗(一种新型抗血管生成治疗策略)联合贝伐单抗治疗晚期非小细胞肺癌(NSCLC)患者的疗效和耐受性。

方法

新诊断为IV期NSCLC的受试者接受为期4周的周期治疗,每周一次,连续三周给予紫杉醇80mg/m²和吉西他滨300mg/m²,每两周给予贝伐单抗10mg/kg。每8周进行一次影像学评估。主要终点是无进展生存期(PFS)。一个探索性目标是将血管生成生物标志物的血浆水平与治疗反应相关联。

结果

39名受试者纳入意向性分析(ITT)。客观缓解率(ORR)为56%,中位PFS为8.5个月,中位总生存期(OS)为25.5个月。6、12和24个月时的PFS率分别为61%、21%和11%。12和24个月时的OS率分别为74%和53%。治疗耐受性良好,无明显骨髓抑制、胃肠道或神经系统事件。血管生成素-2和IL-8基线值低于中位数的受试者PFS明显更长。OS更长与胎盘生长因子(PLGF)和血管生成素-2基线值低于中位数的受试者相关。客观缓解的受试者在第1周期和第3周期之间几种生物标志物的中位数存在统计学显著差异。

结论

节拍给药的紫杉醇和吉西他滨联合贝伐单抗,似乎是晚期NSCLC患者一种有效且耐受性良好的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/caf1/5667666/fdd08c432e5d/nihms903486f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/caf1/5667666/fdd08c432e5d/nihms903486f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/caf1/5667666/fdd08c432e5d/nihms903486f1.jpg