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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

Authors :
Lone Ottesen
Anthony P. Reeves
John D. Mitchell
David F. Yankelevitz
Thomas L. Bauer
Frederic W. Grannis
Anne Huff
Michael J. Guarino
Sabrina Tachdjian
R. Suzanne Swann
Enriqueta Felip
Maureen E. Lane
Paul C. Lee
Nasser K. Altorki
Harvey I. Pass
Nili Peylan-Ramu
Alfonso Gurpide
Debasish Roychowdhury
Source :
Journal of clinical oncology : official journal of the American Society of Clinical Oncology. 28(19)
Publication Year :
2010

Abstract

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.

Details

ISSN :
15277755
Volume :
28
Issue :
19
Database :
OpenAIRE
Journal :
Journal of clinical oncology : official journal of the American Society of Clinical Oncology
Accession number :
edsair.doi.dedup.....80d880a1b11f73a475d85c9d4b8f044e