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Spots Global Cancer Trial Database for Determination of Cetuximab Versus Cisplatin Early and Late Toxicity Events in HPV+ OPSCC

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Trial Identification

Brief Title: Determination of Cetuximab Versus Cisplatin Early and Late Toxicity Events in HPV+ OPSCC

Official Title: Determination of Epidermal Growth Factor Receptor-inhibitor (Cetuximab) Versus Standard Chemotherapy (Cisplatin) Early And Late Toxicity Events in Human Papillomavirus-positive Oropharyngeal Squamous Cell Carcinoma

Study ID: NCT01874171

Interventions

Cisplatin
Cetuximab

Study Description

Brief Summary: Oropharyngeal squamous cell carcinoma (OPSCC) incidence is increasing rapidly in the developed world. This has been attributed to a rise in Human Papillomavirus (HPV) infection. HPV+OPSCC is considered a distinct disease entity, affecting younger patients and has a good prognosis following treatment. Subsequently, patients can live with the considerable side effects for several decades. Radiotherapy and cetuximab (Epidermal Growth Factor Receptor-inhibitor) have demonstrated similar efficacy to 'platin' chemoradiotherapy (current standard treatment containing platinum-based compounds) in head and neck cancer, but is potentially less toxic. Results of this trial will be used to determine the optimum treatment of this debilitating cancer, with the primary aim of decreasing toxicity and improving quality of life for HPV+OPSCC patients.

Detailed Description:

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

St Luke's Hospital, Dublin, , Ireland

Beaumont Hospital, Dublin, , Ireland

VU University Medical Center, Amsterdam, , Netherlands

Aberdeen Royal Infirmary, Aberdeen, , United Kingdom

Royal United Hospital, Bath, , United Kingdom

Clatterbridge Cancer Centre, Bebington, , United Kingdom

Bradford Royal Infirmary, Bradford, , United Kingdom

Bristol Haematology & Oncology Centre, Bristol, , United Kingdom

Velindre Hospital, Cardiff, , United Kingdom

Cheltenham General Hospital, Cheltenham, , United Kingdom

Colchester General Hospital, Colchester, , United Kingdom

Castle Hill Hospital, Cottingham, , United Kingdom

University Hospitals Coventry & Warwickshire, Coventry, , United Kingdom

Royal Derby Hospital, Derby, , United Kingdom

Queen Elizabeth Hospital Birmingham, Edgbaston, , United Kingdom

Western General Hospital, Edinburgh, , United Kingdom

Royal Devon & Exeter Hospital, Exeter, , United Kingdom

Royal Surrey County Hospital, Guildford, , United Kingdom

St James's Institute of Oncology, Leeds, , United Kingdom

Leicester Royal Infirmary, Leicester, , United Kingdom

University College Hospital, London, , United Kingdom

Royal Marsden Hospital, London, , United Kingdom

James Cook University Hospital, Middlesbrough, , United Kingdom

New Cross Hospital, New Cross, , United Kingdom

Northampton General Hospital, Northampton, , United Kingdom

Norfolk & Norwich University Hospital, Norwich, , United Kingdom

Nottingham University Hopsital, Nottingham, , United Kingdom

Glan Clwyd Hospital, Rhyl, , United Kingdom

Weston Park Hospital, Sheffield, , United Kingdom

Royal Shrewsbury Hospital, Shrewsbury, , United Kingdom

Royal Marsden Hospital, Sutton, , United Kingdom

Singleton Hospital, Swansea, , United Kingdom

Musgrove Park Hospital, Taunton, , United Kingdom

Contact Details

Name: Hisham Mehanna, PhD, BMedSc (hons), FRCS

Affiliation: University of Birmingham

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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