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Brief Title: Phase Ib Study of Alpelisib With Cisplatin in Patients With HPV+ Solid Tumor Malignancies
Official Title: A Phase Ib, Open-label Study of Alpelisib (BYL719) in Combination With Cisplatin in Patients With HPV+ Solid Tumor Malignancies
Study ID: NCT02620839
Brief Summary: This phase Ib trial studies the best dose and side effects of alpelisib and cisplatin in treating patients with human papillomavirus (HPV) positive solid tumor malignancies. Alpelisib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as cisplatin, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving alpelisib and cisplatin may work better in treating patients with solid tumor malignancies.
Detailed Description: PRIMARY OBJECTIVES: I. To determine the maximally tolerated dose and recommended phase 2 dose of alpelisib in combination with weekly cisplatin. SECONDARY OBJECTIVES: I. To determine the objective response rate and median progression-free survival with the treatment combination in HPV positive (+) solid tumor malignancies. II. To characterize the safety profile of the combination. OUTLINE: This is a dose escalation study. Patients receive alpelisib orally (PO) once daily (QD) on days 1-14 or 1-21, and cisplatin intravenously (IV) over 1-2 hours on days 1 and 8, or days 1, 8, and 15. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed up at 30 days.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
UCSF Helen Diller Family Comprehensive Cancer Center, San Francisco, California, United States
Name: Pamela Munster, MD
Affiliation: University of California, San Francisco
Role: PRINCIPAL_INVESTIGATOR