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

被引:13
作者
Jones, Benjamin S. [1 ,2 ,3 ]
Jerome, Mary S. [1 ,2 ,3 ]
Miley, Deborah [1 ,2 ,3 ]
Jackson, Bradford E. [1 ,2 ,3 ]
DeShazo, Mollie R. [1 ,2 ,3 ]
Reddy, Vishnu V. B. [1 ,2 ,3 ]
Singh, Karan P. [1 ,2 ,3 ]
Brown, Olivia C. [1 ,2 ,3 ]
Robert, Francisco [1 ,2 ,3 ]
机构
[1] Univ Alabama Birmingham, Comprehens Canc Ctr, Div Hematol Oncol, 1824 Sixth Ave South,WTI 210B, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Comprehens Canc Ctr, Div Prevent Med, Birmingham, AL USA
[3] Univ Alabama Birmingham, Comprehens Canc Ctr, Div Lab Med, Birmingham, AL USA
关键词
Metronomic chemotherapy; Non-small cell lung cancer; Bevacizumab; PACLITAXEL PLUS CARBOPLATIN; ANTIANGIOGENIC ACTIVITY; TRIAL; VINORELBINE; CISPLATIN; GEMCITABINE; EXPRESSION; REGIMENS;
D O I
10.1016/j.lungcan.2017.02.004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 80 mg/m(2) and gemcitabine 300 mg/m(2) weekly for three weeks, plus bevacizumab 10 mg/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. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:125 / 130
页数:6
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