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A Phase 2 Study Of Perifosine As Second Line Therapy For Advanced Pancreatic Carcinoma
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. PURPOSE: Phase II trial to study the effectiveness of perifosine in treating patients who have locally advanced or metastatic pancreatic cancer.
OBJECTIVES: * Determine the efficacy of perifosine, in terms of 6-month survival, in patients with advanced adenocarcinoma of the pancreas. * Determine the safety and tolerability of this drug in these patients. * Determine median survival time and the 1-year survival rate of patients treated with this drug. * Determine the objective response rate (partial and complete), response duration, and time to progression in patients treated with this drug. * Determine the toxicity of this drug in these patients. OUTLINE: Patients receive oral perifosine daily for 3 weeks. Courses repeat every 4 weeks in the absence of disease progression or unacceptable toxicity. Patients are followed every 3 months. PROJECTED ACCRUAL: A total of 17-37 patients will be accrued for this study within 15 months.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Margaret and Charles Juravinski Cancer Centre
Hamilton, Ontario, Canada
Cancer Care Ontario-London Regional Cancer Centre
London, Ontario, Canada
Princess Margaret Hospital
Toronto, Ontario, Canada
Start Date
May 1, 2003
Primary Completion Date
May 1, 2006
Last Updated
July 23, 2015
perifosine
DRUG
Lead Sponsor
University Health Network, Toronto
Collaborators
NCT04550494
NCT05053971
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