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