A new ultrasound technique called real-time elastography (RTE) is being tested in a large UK trial to see if it can reduce the number of inconclusive needle biopsies for thyroid nodules. Thyroid nodules are common, but current ultrasound-guided fine needle aspiration (FNAC) often fails to get a clear diagnosis—up to a fifth of samples come back "non-diagnostic," forcing patients to undergo repeat biopsies or even unnecessary surgery. RTE measures tissue stiffness, because malignant nodules are firmer than benign ones, potentially guiding radiologists to the most suspicious part of a nodule and improving the first biopsy's success rate. If RTE proves effective, it could cut the number of repeat procedures, reduce patient anxiety and surgical complications, and save the NHS money by streamlining the diagnostic pathway. The trial also includes a training module for UK radiologists, since the technique is not yet widely used here. Success would mean faster, more accurate diagnosis for thousands of patients each year, and fewer people undergoing thyroidectomy for what turns out to be benign disease.
View original technical description
DEFINITIONS: Please see Abstract below and diagram for definitions of different categories of the FNAC classification. DESIGN Pragmatic multicentre randomised trial with 1:1 randomisation, using the following minimisation variables: 1. Radiologist - as ultrasound is operator dependent. 2. Solitary nodule versus multi-nodular goitre - as multiple nodules can affect the utility and accuracy of RTE. 3. Size of nodule ( 4cm) - as size can affect accuracy of FNAC. 4. Completely cystic vs. solid or mixed solid and cystic nodules - as RTE cannot be used in a completely cystic lesion. INTERVENTION Real-time ultrasound elastography (RTE)–guided Fine Needle Aspiration cytology (FNAC). RTE is a technology that can be used at the same time as the routine ultrasound examination. RTE may help differentiate benign from malignant nodules based on the compression characteristics of the two (as benign nodules are less firm than malignant ones). This may then help reduce sampling errors and decrease the false negative rate of the first FNA, by guiding the radiologist to the nodule that is most likely to be malignant. RTE may also help guide the radiologist to the parts of large heterogeneous nodules that are most likely to contain malignant cells. This may also improve the nodule diagnostic rate (i.e. reduce the non-diagnostic rate). CONTROL Conventional grey scale and colour Doppler ultrasound-guided FNAC for all the FNACs required to obtain a definitive diagnosis for patients in the control arm. SETTING Secondary care radiology departments with radiologists who have undergone training and accreditation for RTE. Training and Accreditation: RTE is not yet commonly used in the UK, and so radiologists do not have experience in the technique. We have developed a training and accreditation module to address this. This will run concurrently in the first year with the set-up phase of the trial so that it does not delay the start of recruitment. It will include a workshop, a clinical observership, online tests and then a 'hot case' practical test, as well as second reading of the first 10 cases per radiologist. TARGET POPULATION Patients 18 years old or over with a thyroid nodule or nodules, detected on palpation by the clinician (clinically palpable) or identified incidentally by imaging performed for non-thyroid pathology e.g. cervical spondylosis. OUTCOME MEASURES Primary 1. The proportion of patients who have a non-diagnostic (Thy1) cytology result following the first FNAC. Secondary 1. Number of FNACs required to obtain a definitive diagnosis; 2. Time from first FNAC to obtaining a definitive diagnosis; 3. The proportion of patients with benign histology results following thyroidectomy; 4. Proportion of patients who have thyroidectomy; 5. Accuracy of a cytology result for first FNAC and repeated FNAC in relation to overall definitive diagnosis; 6. Accuracy of an imaging assessment on ultrasound (with or without RTE) alone diagnostic protocol in relation to overall definitive diagnosis; 7. Patient reported outcome measures of depression and anxiety, pain, and quality of life: the Hospital Anxiety and Depression rating Scale (HADS), Visual Analogue Pain Score (VAPS) and EQ-5D quality of life score; 8. Radiologist report of whether RTE had contributed to the radiologist's decisions, how easy they found using RTE, and whether they found it helpful above using US-alone in predicting malignancy; 9. Complication rate from any thyroidectomy at 30-days and 6-months post-surgery - to include haematoma rate and temporary hypocalcaemia rate rate at 30 days and vocal cord palsy and permanent hypocalcaemia at 6 months post-operative; 10. Resource usage for consultation time and diagnopstic testing procedures and subsequent management including consultations and surgical treatments. ASSESSMENT & FOLLOW-UP For both intervention and control arms, diagnosis and management will proceed as per the British Thyroid Association Guidelines for management of thyroid nodules. FNACs will be repeated until a diagnosis is obtained – either two benign (Thy2) FNAC results (patient can then be discharged), or one Thy2 FNAC with a benign ultrasound, or a Thy3/4/5 result necessitating surgery, or a decision is made to operate on a patient with at least 3 repeated Thy1 results (see diagram). QUALITY ASSURANCE Radiology The first 5 US elastography scans by each radiologist will be reviewed by the Trial Radiology Panel. Thereafter, a random sample of all scans will be reviewed by the Trial Radiology Panel. Cytology and histology All Thy 3,4 & 5 FNACs and a random sample of 5% of all Thy 1 & Thy 2 FNACs and all thyroidectomy histological samples will be reviewed by one of the experienced thyroid cyto/histopathologists of the Trial’s Reference Pathology laboratory. Any cases showing discordance between local and reference results will be reviewed by the full panel. Discordances will be fed back to the relevant pathologists. SAMPLE SIZE We will recruit a sample of 968 patients which will give over 90% power to detect a difference in the rate of non-diagnostic (Thy1) FNAC results at a 5% significance legel, allowing for 15% loss to follow-up. RECRUITMENT: 15 centres will recruit on average for 53 months, at a rate of 2.5 per month, or 30 patients per year, representing 25-30% of throughput of the interested centres. STATISTICAL ANALYSIS Analysis will be according to intention to test and treat principles at the patient level. TIMELINES 0- 18: set up of sites, and training and accreditation of radiologists. 6- 54: recruitment. 54-60: completion of follow-up. 60-72: trial closure, analysis and write-up. SUPPORTED BY: the British Thyroid Foundation (largest UK patient support group) and the European Society of Head and Neck Imaging.
Plain English summaries and category classifications on this site are generated by AI and may not perfectly reflect the original research.
Is something wrong? Let us know