Magnifying NBI for Occult NPC
Primary Purpose
Nasopharyngeal Carcinoma
Status
Recruiting
Phase
Not Applicable
Locations
Hong Kong
Study Type
Interventional
Intervention
Trans-oral magnifying endoscopy with NBI
Sponsored by
About this trial
This is an interventional screening trial for Nasopharyngeal Carcinoma focused on measuring nasopharyngeal carcinoma, Narrow band Imaging, Magnifying endoscopy
Eligibility Criteria
Inclusion Criteria:
- Male, age ≥ 18 years old
- Positive result on plasma EBV-DNA analysis
- No cancer identified on conventional investigations including nasoendoscopy and MRI
Exclusion Criteria:
- History of nasopharyngeal, oropharyngeal cancer
- Patients on anticoagulation (Including warfarin and other direct oral anti-coagulants)
- Bleeding tendency (International Normalized Ratio (INR) > 1.5 or Platelet < 50 x109/L)
- Trismus, unable to pass oral endoscope
- Allergic to local anaesthetic agents (Lignocaine)
- Failure of vital organ (heart, lungs, liver, or kidneys) function
- Other conditions deemed unsuitable for endoscopy
- Refusal to participate, or inability to sign consent for study
Sites / Locations
- Prince of Wales HospitalRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Trans-oral magnifying endoscopy with NBI
Arm Description
Transoral magnifying endoscopy with High Definition Upper Endoscope with Narrow Band Imaging enhancement (Olympus GIF-H290Z)
Outcomes
Primary Outcome Measures
Rate of Newly diagnosed Nasopharyngeal cancer
Newly diagnosed nasopharyngeal cancer with the novel endoscopic approach
Secondary Outcome Measures
Rate of Adverse event - overall
Rate of Adverse event related to the endoscopic procedure
Rate of adverse event - haemorrhage
Rate of haemorrhage related to the endoscopic procedure
Rate of adverse event - perforation
Rate of perforation related to the endoscopic procedure
Rate of adverse event - infection
Rate of infection related to the endoscopic procedure
Rate of adverse event - aspiration pneumonia
Rate of aspiration pneumonia related to the endoscopic procedure
Stage of the newly diagnosed nasopharyngeal cancer
TNM stage distribution of the newly diagnosed NPC
Duration of the endoscopic procedure
Duration from scope insertion to scope withdrawal
Full Information
NCT ID
NCT04593186
First Posted
October 13, 2020
Last Updated
September 6, 2023
Sponsor
Chinese University of Hong Kong
1. Study Identification
Unique Protocol Identification Number
NCT04593186
Brief Title
Magnifying NBI for Occult NPC
Official Title
Trans-oral Magnifying Endoscopy With Narrow Band Imaging for Screening of Nasopharyngeal Carcinoma
Study Type
Interventional
2. Study Status
Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
April 15, 2021 (Actual)
Primary Completion Date
October 31, 2023 (Anticipated)
Study Completion Date
November 30, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chinese University of Hong Kong
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Diagnosis of nasopharyngeal carcinoma (NPC) is currently made by trans-nasal endoscopy and biopsy. The small caliber endoscope provides only a limited view of the nasopharynx and may not be able to provide a thorough assessment of the nasopharynx. The investigators have developed a novel endoscopic approach to access the nasopharynx by using a trans-oral high definition endoscope with magnification and image enhancement function. In this cohort study, we aim to investigate the efficacy of diagnosing NPC by applying the novel technique in a high risk patient group with elevated plasma EBV DNA but with negative screening with conventional trans-nasal endoscopy.
Detailed Description
Nasopharyngeal carcinoma (NPC) is endemic in our region and is the 9th most common cancer in Hong Kong. Traditionally diagnosis has been through a nasoendoscopic examination of the nasopharynx with white light followed by a biopsy of suspicious lesions for a confirmatory diagnosis. However, given the geometry of the anatomy of the nasopharynx, with its inherent crevices and varying amounts of lymphoid tissues, lesions are not always easily identified leading to potential missed lesions. The non-specific aspect of white light also leads to excessive biopsies that are not without risk and of some discomfort to patients. Recent advances in liquid biopsies have also allowed for the detection of earlier and smaller lesions that are not always easily identified on nasoendoscopy but rather are seen on Magnetic Resonance Imaging (MRI).
An alternative imaging technique is the use of Narrow Band Imaging (NBI) to view the vasculature of the mucosa to identify suspicious lesions for pre-malignancy and malignancy that has been popularized in the gastrointestinal tract. In NPC, NBI with the flexible nasoendoscopes has been used in the diagnosis of NPC with varying success. Researchers at Chinese University of Hong Kong has found that in NPC NBI has limitations arising from a lack of consensus on vascular findings on NBI that constitute malignancy, lack of magnification and long focal length of current nasoendoscopes1. Flexible endoscopy using conventional esophago-gastroscopy endoscope (OGD) with NBI and magnification power up to 80x overcome the limitations of current nasoendoscopes. The passage of the endoscope through the mouth and retroflexion at oropharynx could visualize the nasopharynx clearly and detailed assessment is feasible.
Here in this study the investigators will seek to use a trans-oral magnifying endoscopy with NBI and retroflexion into the nasopharynx to view the nasopharynx to evaluate the feasibility in the diagnosis of occult nasopharyngeal carcinoma.
The aim of this study is to investigate the clinical usefulness of trans-oral magnifying endoscopy with NBI as a screening tool for patients at increased risk of nasopharyngeal carcinoma (NPC).
The investigators hypothesize that with the use of magnifying NBI trans-oral endoscopy, the nasopharynx could improve the diagnostic yield of NPC in high risk patients with negative test on conventional investigations. As a result, such endoscopic screening tool could be used routinely to identify early NPC in patients deemed at risk.
Study Design
This study is a prospective single arm study designed to evaluate the diagnostic yield of trans-oral magnifying NBI endoscopic assessment of nasopharynx in patients who are deemed elevated risk of NPC but with negative traditional endoscopic and radiological screening.
In a previous study conducted by the Department of Chemical Pathology and Otorhinolaryngology, screening of 20000 asymptomatic individuals was performed using plasma Epstein Barr Virus DNA analysis. The presence of plasma EBV DNA consisting of short DNA fragments released by NPC cells helped identify NPC patients. In the published results, 34 NPC was identified in 300-screened positive individuals. In the rest of the cohort, NPC was not identified with initial nasoendoscopy and biopsy. A few more cancers was subsequently identified on Magnetic Resonance Imaging upon follow-up at 3 years and was confirmed with repeated endoscopic biopsies. In the current study the investigators would invite patients with persistently positive screening on plasma EBV-DNA analysis and no cancer found on usual diagnostic tests to undergo the novel screening endoscopy.
Individuals would be screened for eligibility at the clinic follow-up at the Department of Otorhinolaryngology. Study consent would be taken if they agree to participate in the current study.
Endoscopic procedures would be performed by endoscopists with expertise on performing magnifying NBI endoscopy at the Combined Endoscopy Center, Prince of Wales Hospital. It would be conducted at the Combined Endoscopy Center, Prince of Wales Hospital. Topical local anaesthetic will be applied to the oropharynx and nasopharynx. In addition, intravenous sedation by use of Midazolam and Fentanyl would be given. Endoscopes with magnification and NBI function would be used (GF-H290Z, Olympus Medical Corporations, Tokyo, Japan). A soft black hood would be attached to the tip of the endoscope for better focal length adjustment.
Upon insertion through a mouthpiece, the scope will then be retroflexed into the nasopharynx and the lateral walls into the Fossa of Rosenmuller and the posterior nasopharyngeal wall will be systematically examined with white light and NBI. Target suspicious areas would be examined by use of magnification with the power up to 80X. Biopsy would be taken if suspicious lesion is identified during the procedure.
In addition, non-contrast Magnetic Resonance Imaging (MRI) of the nasopharynx would be performed if the participants have not received a similar scan in recent 6 months and have no contra-indications to MRI. The MRI finding would be correlated with the endoscopic and histological findings.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nasopharyngeal Carcinoma
Keywords
nasopharyngeal carcinoma, Narrow band Imaging, Magnifying endoscopy
7. Study Design
Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Trans-oral magnifying endoscopy with Narrow Band Imaging assessment of nasopharynx
Masking
None (Open Label)
Allocation
N/A
Enrollment
246 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Trans-oral magnifying endoscopy with NBI
Arm Type
Experimental
Arm Description
Transoral magnifying endoscopy with High Definition Upper Endoscope with Narrow Band Imaging enhancement (Olympus GIF-H290Z)
Intervention Type
Procedure
Intervention Name(s)
Trans-oral magnifying endoscopy with NBI
Intervention Description
Endoscopic procedures would be performed by endoscopists with expertise on performing magnifying NBI endoscopy. Topical local anaesthetic will be applied to the oropharynx and nasopharynx. In addition, intravenous sedation by use of Midazolam and Fentanyl would be given. Endoscopes with magnification and NBI function would be used (GF-H290Z, Olympus Medical Corporations, Tokyo, Japan). A soft black hood would be attached to the tip of the endoscope for better focal length adjustment.
Upon insertion through a mouthpiece, the scope will then be retroflexed into the nasopharynx and the lateral walls into the Fossa of Rosenmuller and the posterior nasopharyngeal wall will be systematically examined with white light and NBI. Target suspicious areas would be examined by use of magnification with the power up to 80X. Biopsy would be taken if suspicious lesion is identified during the procedure.
Primary Outcome Measure Information:
Title
Rate of Newly diagnosed Nasopharyngeal cancer
Description
Newly diagnosed nasopharyngeal cancer with the novel endoscopic approach
Time Frame
1 month
Secondary Outcome Measure Information:
Title
Rate of Adverse event - overall
Description
Rate of Adverse event related to the endoscopic procedure
Time Frame
7 days
Title
Rate of adverse event - haemorrhage
Description
Rate of haemorrhage related to the endoscopic procedure
Time Frame
7 days
Title
Rate of adverse event - perforation
Description
Rate of perforation related to the endoscopic procedure
Time Frame
7 days
Title
Rate of adverse event - infection
Description
Rate of infection related to the endoscopic procedure
Time Frame
7 days
Title
Rate of adverse event - aspiration pneumonia
Description
Rate of aspiration pneumonia related to the endoscopic procedure
Time Frame
7 days
Title
Stage of the newly diagnosed nasopharyngeal cancer
Description
TNM stage distribution of the newly diagnosed NPC
Time Frame
1 month
Title
Duration of the endoscopic procedure
Description
Duration from scope insertion to scope withdrawal
Time Frame
1 day
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Male, age ≥ 18 years old
Positive result on plasma EBV-DNA analysis
No cancer identified on conventional investigations including nasoendoscopy and MRI
Exclusion Criteria:
History of nasopharyngeal, oropharyngeal cancer
Patients on anticoagulation (Including warfarin and other direct oral anti-coagulants)
Bleeding tendency (International Normalized Ratio (INR) > 1.5 or Platelet < 50 x109/L)
Trismus, unable to pass oral endoscope
Allergic to local anaesthetic agents (Lignocaine)
Failure of vital organ (heart, lungs, liver, or kidneys) function
Other conditions deemed unsuitable for endoscopy
Refusal to participate, or inability to sign consent for study
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Hon Chi Yip, MBChB, FRCSEd
Phone
35052956
Email
hcyip@surgery.cuhk.edu.hk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hon Chi Yip, MBChB, FRCSEd
Organizational Affiliation
Chinese University of Hong Kong
Official's Role
Principal Investigator
Facility Information:
Facility Name
Prince of Wales Hospital
City
Hong Kong
Country
Hong Kong
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hon Chi YIP, FRCSEd
Phone
35052627
Email
hcyip@surgery.cuhk.edu.hk
12. IPD Sharing Statement
Plan to Share IPD
No
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Magnifying NBI for Occult NPC
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