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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04151134
Other study ID # CCR5065
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date November 1, 2019
Est. completion date December 1, 2028

Study information

Verified date May 2024
Source Royal Marsden NHS Foundation Trust
Contact John C Hardman, MBChB
Phone +442073528171?
Email johncharles.hardman@nhs.net
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Squamous cell carcinoma (SCC) is a cancer that originates from the cells lining the body and can spread into the lymph glands and beyond. Some patients first present with an SCC which has moved to the lymph glands of the neck. Clinical examination and imaging investigations are performed to try and identify the site where the cancer has originated. However, if no original site can be identified, then the investigators call these 'cancers of an unknown primary' (CUP) of the head and neck. One region where these cancers could have originated from is the oropharynx. There are two areas in the oropharynx were cancers commonly arise. One area is the palatine tonsils, which can be removed for analysis with an operation called tonsillectomy. The other area is the tissue lining the back of the tongue, known as the tongue base. A relatively new surgical technique called 'tongue base mucosectomy' (TBM) allows removal of this tissue to see if the primary cancer is contained within it. This study will then use a histological method called 'step serial sectioning' (SSS) to look in more detail at the tonsils and tongue base, hoping to increase the detection rate of the primary cancer. Centres performing TBM will be asked to participate. Patients will be asked to consent to their tissue being used for SSS after it has undergone conventional histology. Anonymised samples will be sent to a central laboratory in Newcastle for processing. Other anonymised data regarding the patients' diagnosis and care will be collated. Patients will be asked to complete questionnaires regarding pain and swallowing recovery following surgery. A smaller cohort of patients will also be interviewed as part of a qualitative research process to establish their views on CUP and the acceptability of the above treatment.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date December 1, 2028
Est. primary completion date December 1, 2027
Accepts healthy volunteers No
Gender All
Age group 16 Years and older
Eligibility Inclusion Criteria: - Aged 16 or over - Both sexes - Cervical metastatic SCC, confirmed with cytology or biopsy, undergoing TBM for identification of primary site Exclusion Criteria: - Primary site identified by any means prior to being indicated for TBM - Patients undergoing targeted biopsies or resections - Patients known to have a history of previous H&N cancers - Patients known to have undergone previous radiation to the H&N region

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Step serial sectioning histological processing
Step serial sectioning histological processing

Locations

Country Name City State
United Kingdom University Hospitals Birmingham NHS Foundation Trust Birmingham

Sponsors (3)

Lead Sponsor Collaborator
Royal Marsden NHS Foundation Trust Institute of Cancer Research, United Kingdom, Oracle Cancer Trust

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of Primary Cancers Identified Cancer identified in tonsil and tongue base resections Within one year of surgery
Secondary Pain after tongue base mucosectomy Numeric Pain Scale. A person rates their pain on a scale of 0 to 10 week 0 , 3 weeks, 6 weeks, 12 weeks, 26 weeks and 52 weeks
Secondary Swallow function after tongue base mucosectomy Patients will be given the MDADI questionnaire in which they will be asked a series of questions with the following possible answers: completely agree, agree, uncertain, disagree, completely disagree week 0 , 3 weeks, 6 weeks, 12 weeks, 26 weeks and 52 weeks
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