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o RIGINAL ARTICLE Phase-I/II Study of Bortezomib in Combination with Carboplatin and Bevacizumab as First-Line Therapy in Patients With Advanced Non–Small-Cell Lung Cancer Bilal Piperdi, MD,* William V. Walsh, MD,† Kendra Bradley, RN,† Zheng Zhou, MD, PhD,† Venu Bathini, MD,† Meredith Hanrahan-Boshes, RN,† Lloyd Hutchinson, PhD,‡ and Roman Perez-Soler, MD* (44%). The response rate, PFS, and overall survival in all patients Background: This study aimed to establish the maximum tolerated were 37.5% (95%CI 13.8%–61.2%), 5.0 months (95%CI: 3.1–8.4), dose (MTD) of weekly bortezomib in combination with fixed stan - 9.9 months (95% CI: 8.2–14.1), and among the 9 patients in phase-II dard doses of carboplatin and bevacizumab, and to estimate the effi - portion are 44% (95%CI 15.3%–77.3%), 5.5 months (95%CI: 3.1– cacy (response rate and progression free survival [PFS]) and safety of 2.2) and 10.9 months (95%CI: 8.0–14.1). combination therapy with carboplatin, bortezomib, and bevacizumab Conclusion: The recommended phase-II dose for this combination as first-line therapy in patients with advanced non–small-cell lung is: carboplatin AUC 6, bevacizumab 15 mg/kg on day 1 and bort- cancer (NSCLC). ezomib 1.8 mg/m on day 1 and day 8 on every 21-day cycle. The Methods: Patients were assigned to three dose levels
Journal of Thoracic Oncology – Wolters Kluwer Health
Published: Jun 1, 2012
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