Phase II Proof-of-Concept Study of Pazopanib Monotherapy in Treatment-Naive Patients With Stage I/II Resectable Non-Small-Cell Lung Cancer

被引:112
作者
Altorki, Nasser [1 ]
Lane, Maureen E.
Bauer, Thomas
Lee, Paul C.
Guarino, Michael J.
Pass, Harvey
Felip, Enriqueta
Peylan-Ramu, Nili
Gurpide, Alfonso
Grannis, Frederic W.
Mitchell, John D.
Tachdjian, Sabrina
Swann, R. Suzanne
Huff, Anne
Roychowdhury, Debasish F.
Reeves, Anthony
Ottesen, Lone H.
Yankelevitz, David F.
机构
[1] Cornell Univ, Weill Med Coll, New York, NY 10021 USA
关键词
VINORELBINE PLUS CISPLATIN; PULMONARY NODULES; CT; TRIAL; VARIABILITY; GROWTH; SIZE; BEVACIZUMAB; SORAFENIB; SUNITINIB;
D O I
10.1200/JCO.2009.23.9749
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 >= 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.
引用
收藏
页码:3131 / 3137
页数:7
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