Although most thyroid cancers are treated and cured successfully there are still 30% who recur after many years. This will eventually progress and at this point may become incurable with treatment options including complex and high risk surgery. The overall efficacy of systemic treatment in advanced thyroid cancer has a good initial response in most patients but not all. The study will collect tissues and blood samples for various protein analysis, nucleic acid extraction and live cell analysis in order to try and detect the presence of plasma ctDNA at baseline of eligible patients.
The treatment decisions are based on relying on radiological parameters such as using the RECIST criteria and measuring the rise in certain serum tumour biomarkers. However, the disadvantage of this is that this method can take many months to detect a change in disease volume. An improved understanding of genetics and cancer and potential gene sequencing can help achieve personalised treatment for patients. However, there are many questions and issues that still need to be answered and require urgent attention before being able to achieve optimate patient stratification. We need to identify better tumour biomarkers to detect disease progression, show real time response to treatment and understand why tumours evolve to becoming more aggressive. This study hopes to address these issues by proposing a multicentre prospective study to investigate the presence and role of ctDNA in advanced thyroid cancer including differentiated thyroid cancer , medullary thyroid cancer and Anaplastic Thyroid Cancer.
Study Type
OBSERVATIONAL
Enrollment
120
Sample collection only
The Royal Marsden NHS Foundation Trust
London, United Kingdom
RECRUITINGThe primary objective of the proposed study is to determine the sensitivity of detecting the presence of plasma ctDNA in patients with advanced and recurrent thyroid cancer
The primary objective of the proposed study is to determine the sensitivity of detecting the presence of plasma ctDNA in patients with advanced and recurrent thyroid cancer
Time frame: 5 years
Specificity of the absence of plasma ctDNA in patients with advanced and recurrent thyroid cancer at baseline
Specificity of the absence of plasma ctDNA in patients with advanced and recurrent thyroid cancer at baseline
Time frame: 5 years
Association of ctDNA levels as biomarker of disease burden compared with standard biochemical markers and radiological response
Association of ctDNA levels as biomarker of disease burden compared with standard biochemical markers and radiological response
Time frame: 5 years
Changes in ctDNA levels as biomarker of disease burden compared with standard biochemical markers and radiological response
Changes in ctDNA levels as biomarker of disease burden compared with standard biochemical markers and radiological response
Time frame: 5 years
ctDNA as a biomarker of response to systemic therapy (levels and timing) compared with standard biochemical markers and radiological response in patients starting/during systemic therapy
ctDNA as a biomarker of response to systemic therapy (levels and timing) compared with standard biochemical markers and radiological response in patients starting/during systemic therapy
Time frame: 5 years
ctDNA as a biomarker of progression free and overall survival
ctDNA as a biomarker of progression free and overall survival
Time frame: 5 years
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