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Trial registered on ANZCTR
Registration number
ACTRN12616000715471
Ethics application status
Approved
Date submitted
24/05/2016
Date registered
30/05/2016
Date last updated
13/04/2018
Type of registration
Retrospectively registered
Titles & IDs
Public title
Molecular markers to delineate excision margins in head and neck squamous cell cancer - a bilateral prospective study in Australia and India
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Scientific title
Analysis of surgical margins with molecular markers, p53 and eIF4E to investigate the recurrence and prognosis in patients with head and neck squamous cell carcinoma at Royal Darwin Hospital, Northern Territory and Christian Medical College and Hospital Vellore, India - a prospective study
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Secondary ID [1]
289247
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None
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Head and neck squamous cell carcinoma
298823
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Condition category
Condition code
Cancer
298882
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0
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Head and neck
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Intervention/exposure
Study type
Observational
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Patient registry
False
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
As part of the routine management patients diagnosed with mucosal head and neck squamous cell carcinoma undergo wide local excision. The surgical margins are identified and labeled by the surgeon before the biopsy specimens are sent for routine histopathological analysis. The specimens that are reported to have all the margins free of tumour are enrolled in the study for Immunohistochemical analysis. The tumour free mucosal margins undergo further immunostaining with p53 and eIF4E. This study only involves the immunohistochemistry analysis using p53 and eIF4E.
The follow up period for each participant is minimum of 12 months for disease recurrence /progression
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Intervention code [1]
294788
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Diagnosis / Prognosis
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Comparator / control treatment
No control group
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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To assess
how many of the surgical margins free of tumour with routine Haematoxylin and Eosin show positivity with p53 and/or eIF4E ( by Immunohistochemistry)
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Assessment method [1]
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Timepoint [1]
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Tests to be done after the surgical margins are reported free of tumour on routine Haematoxylin and Eosin staining
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Primary outcome [2]
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how many of the patients with positive p53 and /or e IF4E surgical margins have recurrence of tumour or metastasis during their follow up visits.
This will be assessed by review of medical records for clinical outcomes
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Assessment method [2]
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Timepoint [2]
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The follow up review visits are scheduled until minimum of 12 months post surgery
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Secondary outcome [1]
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Can the recurrence of disease be correlated to positivity with p53 and e IF4E
This will be assessed by local examination, biopsy of a suspicious lesion, MRI scans and doing statistical analysis on the data collected
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Assessment method [1]
323910
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Timepoint [1]
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how soon post excision of tumour has the tumour recurred - 2, 3, 6 months
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Secondary outcome [2]
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Can the progression of disease be correlated to positivity with p53 and e IF4E
This will be assessed by local examination, biopsy of a suspicious lesions, MRI scans and doing statistical analysis on the data collected
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Assessment method [2]
324239
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Timepoint [2]
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how soon post excision of tumour has the tumour spread and metastasized - 2, 3, 6 months
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Eligibility
Key inclusion criteria
All patients diagnosed with mucosal head and neck squamous cell carcinoma with negative surgical margins on histopathology at the Royal Darwin Hospital and Christian Medical College Vellore
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Patients diagnosed with any other histological type of mucosal head and neck cancers, and whose primary modality of therapy was surgery.
*Patients whose surgical margins showed dysplasia, carcinoma – in – situ, tumour and was less than 5mm distant from invasive tumour on histopathological examination
*Patients with metastatic disease except a single regional lymph node with no extracapsular spread
*Patients with multiple foci of peri-neural invasion
Patients with lymphovascular invasion
*Patients with previous radiotherapy and chemotherapy
*Patients in whom the margins cannot be defined or with an unknown primary
*Patients under 18 years of age
*Patients who are pregnant
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Study design
Purpose
Screening
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Duration
Longitudinal
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Selection
Defined population
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Timing
Prospective
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Statistical methods / analysis
Sample size- The average number of patients at Darwin and Vellore are 20 and 70 per year respectively. Most patients present late and obtaining a tumour free margin is a challenge. We anticipate performing IHC on 30 to 40 patients.
The data on the surgical margins will be analysed statistically with SPSS software. Contingency table and the X2 test will be used to evaluate the association of e IF4E and p53 in the surgical margins with race, sex, stage, lymph node status, histological grade, post-operative radiation and e IF4E and p53 expression in the tumour and margins. A univariate analysis of clinical factors will be performed using Cox model to identify those variables significantly associated with prognosis. Multivariate analysis will be performed to test for simultaneous effect of two or more factors. Event –time distributions for recurrence will be estimated by Kaplan- Meier method and compared by the log rank test to determine the individual and combined effect of e IF4E and p53 expression in the margins. Similar curves will be performed to determine the effect of nodal status with e IF4E and p53 levels in the margins as nodal status is a significant prognostic factor in HNSCCs.
The consistency of protocol at both the sites will be assessed and the study will be periodically reviewed.
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
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Actual
18/09/2014
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Date of last participant enrolment
Anticipated
30/09/2016
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Actual
3/09/2016
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Date of last data collection
Anticipated
30/09/2017
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Actual
3/09/2017
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Sample size
Target
40
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Accrual to date
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Final
43
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Recruitment in Australia
Recruitment state(s)
NT
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Recruitment hospital [1]
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Royal Darwin Hospital - Tiwi
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Recruitment outside Australia
Country [1]
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India
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State/province [1]
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Tamil Nadu
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Funding & Sponsors
Funding source category [1]
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University
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Name [1]
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Charles Darwin University
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Address [1]
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Charles Darwin University
Ellengowan Drive,
PO Box 40146
Casuarina
Darwin
Northern Territory 0811
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Country [1]
293626
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Australia
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Primary sponsor type
Individual
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Name
Rama Jayaraj
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Address
Faculty of Engineering, Health, Science and the Environment
CHARLES DARWIN UNIVERSITY
Ellengowan Drive,
Casuarina
Darwin 0909
Northern Territory
AUSTRALIA
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Country
Australia
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Secondary sponsor category [1]
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Individual
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Name [1]
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Mahiban Thomas
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Address [1]
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Department of Maxillofacial surgery
Royal Darwin Hospital
105 Rocklands Drive,
Tiwi
Darwin
NT 0810
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Country [1]
292458
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Australia
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Other collaborator category [1]
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Hospital
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Name [1]
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Christian Medical College and Hospital
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Address [1]
278997
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Norman Pathology,
IDA Scudder Rd,
Vellore,
Tamil Nadu 632004,
India
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Country [1]
278997
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India
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Human Reseach Ethics Committee of the Northern Territory
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Ethics committee address [1]
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Menzies school of health Research John Mathews Building Building 58 Royal Darwin Hospital Campus Rocklands Drive, Tiwi Darwin NT 0810
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
295063
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10/05/2013
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Approval date [1]
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12/11/2013
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Ethics approval number [1]
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HREC 13- 2036
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Ethics committee name [2]
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Institustional Review Board Christian Medical College Vellore
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Ethics committee address [2]
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Bagayam Thorapadi, Vellore Tamil Nadu 632002
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Ethics committee country [2]
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India
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Date submitted for ethics approval [2]
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30/06/2014
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Approval date [2]
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04/09/2014
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Ethics approval number [2]
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IRB Min. No. 8967
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Summary
Brief summary
The primary purpose of this study is to evaluate whether the presence of two antibodies, eIF4E and p53, in samples of tissue from the edge of surgically removed tumours in the head and neck may correspond with cancer progression and recurrence. Who is it for? You may be eligible to participate in this study if you are aged 18 or over, and have been diagnosed with mucosal head and neck squamous cell carcinoma with negative surgical margins on histopathology at the Royal Darwin Hospital or the Christian Medical College, Vellore (India). Study details: All participants enrolled in this study will have tests carried out on tissue samples which were taken at the time of surgery, and which have already been shown to be tumour-free. These tests will assess for the presence of the two antibodies eIF4E and p53. Participants will then be followed-up for minimum of 12 months - end of study period by review of medical records, to see if any correlation exists between presence of the antibodies and cancer recurrence. It is hoped that the findings of this study may provide information on whether these antibodies may be used as a marker for prognosis in head and neck cancer patients at the time of surgery.
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Trial website
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Trial related presentations / publications
Joseph, S., et al. (2017). "Predictability of Recurrence using Immunohistochemistry to delineate Surgical Margins in mucosal Head and Neck Squamous Cell Carcinoma (PRISM-HNSCC): study protocol for a prospective, observational and bilateral study in Australia and India." BMJ Open 7(10): e014824.
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Public notes
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Contacts
Principal investigator
Name
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Dr Mahiban Thomas
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Address
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Department of Maxillo-facial surgery,
Royal Darwin Hospital
105 Rocklands Drive,
Tiwi
Darwin
NT 0810
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Country
65958
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Australia
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Phone
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+ 61 8 8922 8888
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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Sheela Joseph
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Address
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Centre for Remote Health
Corner of Simpson and Skinner street
Alice Springs
PO Box 4066
NT 0870
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Country
65959
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Australia
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Phone
65959
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+61 8 89514781
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Fax
65959
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Email
65959
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[email protected]
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Contact person for scientific queries
Name
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Sheela Joseph
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Address
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Centre for Remote Health
Corner of Simpson and Skinner street
Alice Springs
PO Box 4066
NT 0870
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Country
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Australia
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Phone
65960
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+61 8 89514781
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Fax
65960
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Email
65960
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
Source
Title
Year of Publication
DOI
Dimensions AI
Predictability of Recurrence using Immunohistochemistry to delineate Surgical Margins in mucosal Head and Neck Squamous Cell Carcinoma (PRISM-HNSCC): study protocol for a prospective, observational and bilateral study in Australia and India
2017
https://doi.org/10.1136/bmjopen-2016-014824
N.B. These documents automatically identified may not have been verified by the study sponsor.
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