Project Details
Abstract
Nasopharyngeal carcinoma (NPC) is a common cancer in Southeast Asia. It typically affects
middle-aged people and is commonly diagnosed in the late stage because of its deep location and
vague symptoms, and this late diagnosis leads to decreased survival.
Unfortunately, most of the NPC patients we encountered had Stage III or IV disease.
Although NPC is radiosensitive, 25% of NPC patients still suffer from local relapse in Taiwan, and
tumor recurrence also leads to a poor prognosis. Therefore, early diagnosis of newly diagnosed or
recurrent NPC is important to define appropriate therapeutic strategies.
Narrow-band imaging (NBI) is a novel optical technique that enhances the diagnostic sensitivity of
endoscopy for characterizing tissues by using narrow-bandwidth filters in a sequential
red-green-blue illumination system. The narrowband blue light, which has a short wavelength (415
nm), penetrates the mucosa and highlights the superficial vasculature. Thus, superficial mucosal
lesions that cannot usually be detected by regular white-light (WL) endoscopy can be identified on
the basis of their neoangiogenetic vasculature pattern by using blue light in NBI. In our pilot
study, we successfully detect newly diagnosed early NPC by irregular microvascular pattern or
side-difference, and early recurrent NPC by irregularities signs in NBI closer view.
Many studies showed that the detection of plasma Epstein-Barr virus (EBV) DNA might be helpful to
screen newly diagnosed NPC and monitor recurrence/treatment outcome of NPC post-irradiation. On the
other hand, NPC might be early detected during dysplastic stage by NBI in our previous study.
However, the diagnostic yield of NBI in the early detection of superficial NPC and diagnostic
accuracy between NBI and plasma EBV DNA has not been investigated. Therefore, we conducted a
prospective randomized controlled study to directly compare WL and NBI in the early diagnosis of
NPC among high-risk patients (post-treatment NPC in a state of remission, family history of NPC or
higher plasma EBV titer, unknown origin of neck mass and epistaxis). 320 patients with high-risk
were randomly assigned to primary WL followed by NBI (n = 160) or primary NBI followed by WL (n =
160) in a
back-to-back fashion. Regular endoscopy examination and plasma EBV DNA assay were scheduled every 3
to 6 months for these high risk populations. The primary aim was to compare the real-time detection
rates of superficial NPC between WL and NBI. The secondary aim was to evaluate the diagnostic
accuracy of these techniques. The third aim was to compare the diagnostic accuracy of early NPC
between NBI and plasma EBV DNA. Upon completion of this study, we will understand the definite
clinical value of NBI for early NPC and the difference between NBI and plasma EBV DNA for high risk
patients in Taiwan.
Project IDs
Project ID:PC10108-0685
External Project ID:NSC101-2314-B281-008
External Project ID:NSC101-2314-B281-008
Status | Finished |
---|---|
Effective start/end date | 01/08/12 → 31/07/13 |
Fingerprint
Explore the research topics touched on by this project. These labels are generated based on the underlying awards/grants. Together they form a unique fingerprint.