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Defining Markers of Susceptibility to Nasopharyngeal Carcinoma (NPC) Within High-Risk, Multiplex NPC Families

21 Years
Not Enrolling
Nasopharyngeal Carcinoma

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Trial Information

Defining Markers of Susceptibility to Nasopharyngeal Carcinoma (NPC) Within High-Risk, Multiplex NPC Families

The purpose of this proposed study is to evaluate the clinical utility of serum EBV antibody
testing for the identification of individuals at increased risk of nasopharyngeal carcinoma
(NPC) within high-risk, NPC multiplex families.

2,394 unaffected individuals from Taiwanese families, in which two or more relatives have
been diagnosed with NPC, have been identified and sampled as part of an ongoing
collaboration to identify genetic factors linked to NPC development. Serum from these
individuals has been tested for three anti-EBV antibodies (VCA IgA, EBNA1 IgA, and
anti-DNase) known to be associated with elevated risk of prevalent and incident NPC in
general population studies. Results from testing of our study population indicate that
apparently healthy individuals from high-risk multiplex families have a near 3-fold
elevation in their EBV antibody prevalence when compared to the EBV antibody prevalence
observed in the general community for these same EBV markers. However, the clinical
implications of this apparent elevation in EBV antibody reactivity are not yet understood.

Therefore, we propose to evaluate whether individuals within our previously conducted
high-risk family study with elevations in EBV antibody levels are at increased risk of
incident NPC. Individual markers (VCA IgA, EBNIA1 IgA and anti-DNase antibodies) and
combinations of markers will be evaluated to determine their performance as screening tests
for NPC risk in high-risk multiplex families.

To achieve this goal, we propose to invite the 2,394 unaffected individuals from our
multiplex family study, defined as those families with greater than or equal to 2 NPC. As a
result of our recruitment efforts, we expect approximately 1,600 subjects to participate in
an ear, nose, and throat (ENT) examination by an expert otolaryngologist to determine
whether any of these individuals has occult or symptomatic NPC. We will correlate the three
EBV antibody screening tests performed at the time of initial recruitment into our family
study with NPC detection in the period between initial recruitment into the family study and
the present study (median time between original EBV antibody testing and clinical evaluation
= 5.5 years; range = less than 1 year - 10 years).

In addition to histopathological specimens collected for NPC diagnosis, participants in this
study will be asked to agree to a brief risk factor questionnaire and to donate blood,
saliva, a nasopharyngeal swab, nasopharyngeal tissue, and urine for future studies.

No accepted clinical management protocol exists for screening unaffected members from
families at high-risk of NPC development. Results from this study have the potential to
significantly impact the clinical management and follow-up of individuals with a family
history of NPC.

Inclusion Criteria


The 2,394 unaffected family members who previously participated in the family study of
nasopharyngeal carcinoma (NPC) in Taiwan between 1996 and 2004.

Type of Study:


Study Design:


Principal Investigator

Allan Hildesheim, Ph.D.

Investigator Role:

Principal Investigator

Investigator Affiliation:

National Cancer Institute (NCI)


United States: Federal Government

Study ID:




Start Date:

June 2005

Completion Date:

Related Keywords:

  • Nasopharyngeal Carcinoma
  • Epidemiology
  • NPC
  • Genetic
  • Viruses
  • Cancer
  • Nasopharyngeal Carcinoma
  • Carcinoma
  • Nasopharyngeal Neoplasms