Valproic Acid in the Induction of EBV Lytic Cycle Antigen Expression in Nasopharyngeal Carcinoma

NCT ID: NCT00181220

Last Updated: 2020-05-18

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: PHASE1
• Study Classification: INTERVENTIONAL
• Study Start Date: 2004-04-30
• Study Completion Date: 2006-09-30

Brief Summary

The proposed study will test the safety and efficacy of sodium valproate in the induction of Epstein-Barr virus (EBV) lytic cycle antigen expression in tumor tissue of patients undergoing primary therapy for nasopharyngeal carcinoma. Up to 20 patients will be given valproic acid for 2 weeks. The primary surrogate endpoint for efficacy will be expression of EBV lytic antigens by immunohistochemistry in tumor tissue. Biopsies of primary tumor will be taken after 2 weeks with achievement of a therapeutic concentration of valproate. Expression of immunodominant EBV latency antigens in tumor tissue, EBV viral load by real time PCR, and valproate levels will be measured. Adverse events associated with valproate in NPC patients will be described.

Conditions

Nasopharyngeal Carcinoma

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Interventions

valproic acid

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

All subjects must fulfill the following criteria to be eligible for study admission:

• Subjects are of age 18 years and above
• Biopsy proven nasopharyngeal carcinoma - WHO type 3
• Must have tumor which is accessible to biopsy
• For patients with disease localized to the PNS, the lesion must be visualized by endoscopy
• Subjects with metastatic disease with disease accessible to biopsy in the PNS if they are deemed by their treating physicians not to require treatment for at least two weeks.
• An ECOG performance status of 0-2
• For sexually active women of child-bearing potential, negative pregnancy test within 14 days of enrolling on trial
• Must be able to give informed consent

Exclusion Criteria

• For patients with localized NPC, PNS lesions that cannot be visualized by endoscopy
• Patients with disease inaccessible to biopsy
• History of anaphylaxis after exposure to valproic acid
• Hepatic dysfunction as defined by total bilirubin 1.0x upper limit of normal. AST (SGOT) and ALT (SGPT) 3x upper limit of normal
• Hemoglobin 8g/dl, Absolute neutrophil count 1500 cells/mm, and Platelet count 100,000 /mm
• Creatinine 3x upper limit of normal
• PT/PTT blood test result not within normal range
• Patients who require treatment with an anticonvulsant besides valproic acid during the course of valproate prescribed by the protocol
• ECOG Performance status 3-4
• Patients who are pregnant or breast feeding (Sexually active women of childbearing potential must use contraception during course of therapy and within 4 weeks of completion of trial)
• Participation in another clinical trial involving therapeutic intervention within 4 weeks of enrollment.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

National University Hospital of Singapore

UNKNOWN

Sponsor Role: collaborator

Johns Hopkins University

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Wen-son Hsieh, M.D.

Role: PRINCIPAL_INVESTIGATOR

Johns Hopkins University

Locations

Johns Hopkin Singapore International Medical Center

Singapore, , Singapore

Countries

Singapore

Other Identifiers

Valproic Acid NPC

Identifier Type: -

Identifier Source: org_study_id