Fax: (608) 263-8613
Phase II study of daily oral perifosine in patients with advanced soft tissue sarcoma†
Article first published online: 20 OCT 2006
Copyright © 2006 American Cancer Society
Volume 107, Issue 10, pages 2462–2467, 15 November 2006
How to Cite
Bailey, H. H., Mahoney, M. R., Ettinger, D. S., Maples, W. J., Fracasso, P. M., Traynor, A. M., Erlichman, C. and Okuno, S. H. (2006), Phase II study of daily oral perifosine in patients with advanced soft tissue sarcoma. Cancer, 107: 2462–2467. doi: 10.1002/cncr.22308
Informed consent for participation in this study was obtained from the subject(s) and/or guardian(s).
- Issue published online: 8 NOV 2006
- Article first published online: 20 OCT 2006
- Manuscript Accepted: 13 SEP 2006
- Manuscript Revised: 9 SEP 2006
- Manuscript Received: 12 JUN 2006
- NIH/NCI Phase 2 Consortium. Grant Number: CM17104
- Phase II trial
A multicenter Phase II study was performed to evaluate the clinical activity of an initial loading (150 mg every 6 hours × 4 doses) dose followed by continuous daily oral dosing (100 mg/day) of perifosine in patients with advanced soft tissue sarcomas (STSs).
Patients with measurable metastatic STS received perifosine as first-, second-, or third-line treatment and underwent disease assessment every 8 weeks until disease progression, excessive toxicity, or patient refusal.
Twenty-three patients received 66 cycles (1 cycle = 4 weeks) of perifosine. One partial response of 9 months duration was observed. The overall 3 and 6 month progression-free survival was 22% and 9%. NCI CTC (v2.0) Grade 1 to 2 gastrointestinal toxicity or fatigue were the most common (>50% of subjects) toxicities observed. The steady-state plasma perifosine levels (Css) were similar to prior experience (mean 6 μg/mL). Patients with Css levels >6 μg/mL appeared more likely to remain on study past 2 months than those with levels <6 μg/mL.
Despite not achieving the primary objective of ≥40% 6-month progression-free survival rate, optimism remains for this agent in STS patients. Prolonged responses in heavily pretreated STS patients continue to be observed with perifosine treatment. Continued assessment of perifosine in STS appears warranted, with special attention to specific histologies or tumor characteristics that might identify a more sensitive population and achieving perifosine Css levels >6 μg/mL. Cancer 2006 © 2006 American Cancer Society.