首页> 外文期刊>Journal of Clinical Oncology >Phase II proof-of-concept study of pazopanib monotherapy in treatment-naive patients with stage I/II resectable non-small-cell lung cancer.
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Phase II proof-of-concept study of pazopanib monotherapy in treatment-naive patients with stage I/II resectable non-small-cell lung cancer.

机译:在未经治疗的I / II期可切除非小细胞肺癌初治患者中,帕唑帕尼单药治疗的II期概念验证研究。

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PURPOSE: Patients with early-stage, resectable, non-small-cell lung cancer (NSCLC) are at risk for recurrent disease, and 5-year survival rates do not exceed 75%. Angiogenesis inhibitors have shown clinical activity in patients with late-stage NSCLC, raising the possibility that targeting the vascular endothelial growth factor pathway in earlier-stage disease may be beneficial. This proof-of-concept study examined safety and efficacy of short-term, preoperative pazopanib monotherapy in patients with operable stage I/II NSCLC. PATIENTS AND METHODS: Patients scheduled for resection received oral pazopanib 800 mg/d for 2 to 6 weeks preoperatively. Tumor response was measured by high-resolution computed tomography, permitting estimation of change in tumor volume and diameter. Gene-expression profiling was performed on 77 pre- and post-treatment lung samples from 34 patients. RESULTS: Of 35 patients enrolled, 33 (94%) had clinical stage I NSCLC and two (6%) had clinical stage II NSCLC. Median treatment duration was 16 days (range, 3 to 29 days). Thirty patients (86%) achieved tumor-volume reduction after pazopanib treatment. Two patients achieved tumor-volume reduction > or = 50%, and three patients had partial response according to Response Evaluation Criteria in Solid Tumors. Pazopanib was generally well tolerated. The most common adverse events included grade 2 hypertension, diarrhea, and fatigue. One patient developed pulmonary embolism 11 days after surgery. Several pazopanib target genes and other angiogenic factors were dysregulated post-treatment. CONCLUSION: Short-duration pazopanib was generally well tolerated and demonstrated single-agent activity in patients with early-stage NSCLC. Several target genes were dysregulated after pazopanib treatment, validating target-specific response and indicating a persistent pazopanib effect on lung cancer tissue. Further clinical evaluation of pazopanib in NSCLC is planned.
机译:目的:患有早期可切除的非小细胞肺癌(NSCLC)的患者有复发疾病的风险,并且5年生存率不超过75%。血管生成抑制剂已在晚期NSCLC患者中显示出临床活性,从而增加了在早期疾病中靶向血管内皮生长因子途径可能有益的可能性。这项概念验证研究检查了术前I / II期NSCLC患者短期术前帕唑帕尼单药治疗的安全性和有效性。患者与方法:计划切除的患者术前接受口服帕唑帕尼800 mg / d,持续2至6周。通过高分辨率计算机断层摄影术测量肿瘤反应,从而可以估计肿瘤体积和直径的变化。对来自34例患者的77例治疗前后的肺样品进行了基因表达谱分析。结果:在35名患者中,有33名(94%)患有临床I期非小细胞肺癌,有2名(6%)具有临床II期非小细胞肺癌。中位治疗时间为16天(范围3到29天)。帕唑帕尼治疗后有30例患者(86%)肿瘤缩小。根据实体瘤反应评估标准,两名患者的肿瘤体积减少≥50%,三名患者部分缓解。帕唑帕尼一般耐受良好。最常见的不良事件包括2级高血压,腹泻和疲劳。一名患者在手术后11天出现肺栓塞。治疗后一些帕唑帕尼靶基因和其他血管生成因子失调。结论:短期的帕唑帕尼一般耐受良好,并在早期NSCLC患者中表现出单药活性。帕唑帕尼治疗后几个靶基因失调,从而证实了靶标特异性反应并表明帕唑帕尼对肺癌组织具有持续的作用。计划对帕唑帕尼在NSCLC中进行进一步的临床评估。

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