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NCT Number: NCT01744587

Epstein-Barr Virus Reactivation and the Effect of EGCG on Virus Reactivation in Remission Patients

The purpose of this study is to investigate the EBV reactivation rate in post-radiation and remission NPC patients, evaluate the safety and tolerance of EGCG and analyze the observational correlation between EBV reactivation and clinical outcome.

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Key information

Conditions

NPC

Age range

20 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Taiwan Cooperative Oncology Group, National Health Research Institutes

Zhunan, Miaoli, 350, Taiwan

About this study

Patients with pathologically proven NPC, stage II-IVB and finishing curative RT ≧70 Gy within 6 months (± induction/concurrent/adjuvant chemotherapy) will be candidates for this study. Before entry, 8 CC venous blood will be obtained for EBV DNA and antibody screen tests after patient's consent. Those who have undetectable plasma EBV DNA (0 copy/ml) and fulfilled with all inclusion and exclusion criteria will be registered.

Routine re-staging work-ups after RT should show no active lesion in nasopharynx, neck and distant organs. Re-staging survey should include nasopharyngoscope, pEBV DNA assay, CBC, platelet count, renal and liver function tests, CXR, abdominal sonography or CT scan, whole body bone scan, MRI or CT scan of the head and neck region.

Within one week after finishing registration, EGCG or placebo should be started. A blood sample before taking EGCG/placebo will be collected for antibodies test and pEBV DNA assay.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Histologically proven NPC.
  • 2010 AJCC stage II-IVB.
  • Age ≧ 20 years old.
  • Performance status of ECOG ≦ 2.
  • Finished RT ≧66 Gy within 6 months (± induction/concurrent/adjuvant chemotherapy).
  • Clinical complete remission by re-staging work-ups within 3 months before entry.
  • Plasma EBV DNA = 0 copy/ml within 4 weeks before entry.
  • Adequate liver, renal, and bone marrow function:Serum total bilirubin level ≦ 2.5 mg/dl. Serum creatinine ≦ 1.6 mg/dl. WBC ≧ 3,000/ul. Platelet count ≧ 100,000/ul.
  • No intake of EGCG or similar dietary supplements.
  • Signed informed consent.
  • No further anti-cancer treatment.

Exclusion criteria

  • Occurrence of locoregional recurrence or distant metastasis.
  • Inadequate RT or finishing RT > 6 months.
  • Not complete remission by re-staging work-ups within 3 months before entry.
  • Plasma EBV DNA > 0 copy/ml within 4 weeks before entry.
  • Intake of EGCG or similar dietary supplements during recent 3 months.
  • Severe cardiopulmonary diseases (unstable angina and/or congestive heart failure or peripheral vascular disease requiring hospitalization within the last 12 months; chronic obstructive pulmonary disease exacerbation other respiratory illness requiring hospitalization) or clinically significant psychiatric disorders.

Treatment and study plan

Epigallocatechin Gallate (EGCG)

Other

EGCG 600 mg per day will be provided to the test group.Four capsules will be taken daily (2# bid) by the test individuals.

Other names: EGCHAC-purified EGCG 90% capsules

Placebo

Dietary Supplement

Placebo qd (2# bid) for 3 years

Primary outcomes

  1. EBV reactivation rates between EGCG and placebo group

    Time frame: every 3 months for the first 3 years and every 6 months thereafter for antibodies tests and pEBV DNA assay (total 5 years)

    Reactivation of EBV is defined as

    1.Antibody against EBV VCA: The IgA antibody titers will be detected by a commercial EBV VCA ELISA kit (RE 562 71, Immuno-Biological Laboratories, Germany) Patient's serum with anti-EBV VCA greater than 10U/ml will be considered as reactivation of EBV.

Secondary outcomes

  1. Correlation between EBV reactivation and OS/RFS

    Time frame: q 3 months for first 3 years and q 6 months for the

    Observational analysis of the correlation between EBV reactivation and clinical outcome

Sponsors and collaborators

Lead sponsor

National Health Research Institutes, Taiwan

Other

Collaborators

  • Chang Gung Memorial Hospital
  • China Medical University Hospital
  • Mackay Memorial Hospital
  • National Cheng-Kung University Hospital
  • National Taiwan University Hospital
  • Taichung Veterans General Hospital

Registry information

Official study title

Study of Epstein-Barr Virus Reactivation and the Effect of Dietary Supplement Epigallocatechin Gallate (EGCG) on Virus Reactivation in Remission Patients With Nasopharyngeal Carcinoma - A Randomized Trial

Acronym: NPC

Important dates

Study start
2013
Primary completion
2023
Study completion
2023
First posted
Dec 6, 2012
Registry last updated
Aug 15, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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