Radioactive iodine: unnecessary for some thyroid cancer patients?
NCT ID NCT01398085
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looks at whether low-risk thyroid cancer patients need radioactive iodine treatment after having their thyroid removed. About 504 participants are randomly assigned to receive either a standard dose of radio-iodine or no radio-iodine at all. The goal is to see if skipping this treatment affects cancer recurrence or survival, potentially sparing patients from unnecessary side effects.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Radioactive iodine (I131)
- What this could lead to
- If successful, this could show that many low-risk thyroid cancer patients can safely skip radioactive iodine treatment, avoiding its side effects.
- What could go wrong
- This is an early-to-mid stage trial with 504 participants, so results may not apply to all patients. There is a risk that skipping radio-iodine could lead to higher recurrence rates.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2/3
Runs two stages together: whether the treatment works, then large-scale confirmation.
- Participants
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504 people
The number who actually took part.
- Started
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Jun 2012
- Expected to finish
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Mar 2031
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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16 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
TNM eligibility is assessed against TNM7 (7th edition 2009) or TNM8 (8th edition 2017, in use in the UK from 01/01/2018). Eligibility Criteria using TNM7: Inclusion criteria: * Histological confirmation of well differentiated thyroid carcinoma: MDT decision for inclusion based on overall clinico-pathological assessment is critical. * R0 total thyroidectomy (in one or two stages, no residual disease present; Rx at the discretion of the MDT) within the last 6 months * Negative pregnancy test in women of child bearing potential * Aged 16 or over * WHO performance status 0 - 2, self-caring * Histological confirmation of differentiated thyroid carcinoma:MDT decision for inclusion based on overall clinico-pathological assessment * Papillary thyroid cancer (PTC): * Non aggressive histological features (small foci of aggressive histology allowed at the discretion of the MDT) * pT1a (≤1cm) unifocal with positive level VI lymph nodes (pN1a) * pT1a(m): all individual foci ≤1cm * pT1b and pT1b(m): \>1-2cm * pT2 and pT2(m): \>2-4cm * pT3 and pT3(m): \>4cm confined to the thyroid * pT3 R0 +/- (m): any size with minimal ETE if recommended by the MDT * pN0 * pN1a * pNX * Follicular thyroid cancer (FTC) (including oncocytic or Hürthle cell cancer): o minimally invasive FTC -which are considered low risk and are recommended by the specialist MDT based on overall clinico-pathological assessment * pT1b and pT2: \>1-4cm intrathyroidal * pT3 R0:any size up to 4 cm with minimal ETE if recommended by the MDT * Histological material available for Central Review (see section 9.7) * Willing to use contraception for the duration of the trial until 6 months post radioiodine treatment (for females) or 4 months post treatment (for males) (see section 6.4.2), if allocated to the ablation group. NB: Multifocal tumours (≥2 foci) of all histological types should be designated with "(m)", and the size of the largest focus determines the classification (as described in the TNM 7th edition). For example, if there are two foci, one 0.8cm and the other 3cm, the classification is based on the 3cm focus; i.e. pT2(m). Exclusion criteria: * pT1a - Papillary and Follicular carcinoma which is unifocal and ≤1cm in size, without any positive nodes or unfavourable clinical features, treated by lobectomy. * Up to 4cm non-invasive Encapsulated Follicular Variant of Papillary Thyroid Cancer (eFVPTC) with no capsular or vascular invasion (\>4 cm can be included at the discretion of the MDT) * non-invasive follicular tumour with papillary-like nuclei (NIFTP) * Anaplastic, poorly differentiated or medullary carcinoma * R1 or R2 thyroidectomy * Patients with: * pN1b * M1 * Aggressive Papillary thyroid cancer with any of the following features: * Widely invasive * Poorly differentiated * Anaplastic * Tall cell * Columnar cell * Diffuse sclerosing variants * Follicular thyroid cancer/Hürthle cell cancer with any of the following features: * Tumours greater than 4cm * Widely invasive * Poorly differentiated * Anaplastic * Incomplete resection or lobectomy * pT4a and pT4b or macroscopic and microscopic tumour invasion of loco-regional tissues or structures * Pregnant women or women who are breast feeding * Patients who have had CT performed with iv contrast less than 2-3 months before ablation * Previous treatment for thyroid cancer (except surgery in last 6 months) * Previous malignancies with limited life expectancy or likely to interfere with the patient's ability to be able to comply with treatment and/or follow-up for at least 5 years * The following GI conditions: dysphagia, oesophageal stricture, active gastritis, gastric erosions, peptic ulcer, suspected reduced gastrointestinal motility * MDT decision against ablation or suitability for trial in light of severe co-morbid condition/s including: * Unstable angina * Recent myocardial infarction or cerebrovascular accident (CVA) * Severe labile hypertension * Any patient who cannot comply with radiation protection including: * patients with learning difficulties * patients with dementia * patients with a tracheostomy that require nursing care * patients requiring frequent nursing/ medical supervision Eligibility Criteria using TNM8: Inclusion criteria: * Histological confirmation of well differentiated thyroid carcinoma: MDT decision for inclusion based on overall clinico-pathological assessment is critical. * R0 total thyroidectomy (in one or two stages, no residual disease present; Rx at the discretion of the MDT) within the last 6 months * Negative pregnancy test in women of child bearing potential * Aged 16 or over * WHO performance status 0 - 2, self-caring * Histological confirmation of differentiated thyroid carcinoma:MDT decision for inclusion based on overall clinico-pathological assessment * Papillary thyroid cancer (PTC): * Non aggressive histological features (small foci of aggressive histology allowed at the discretion of the MDT) * pT1a (≤1cm) unifocal with positive level VI lymph nodes (pN1a) * pT1a(m): all individual foci ≤1cm * pT1b and pT1b(m): \>1-2cm * pT2 and pT2(m): \>2-4cm * pT3a and pT3a(m): \>4cm confined to thyroid * pT1a/1b/2/3 (where minimal microscopic extra thyroidal extension (ETE) does not change the T score) +/- (m): any size with minimal ETE if recommended by the MDT * pN0 * pN1a * pNX * Follicular thyroid cancer (FTC) (including oncocytic or Hürthle cell cancer): o minimally invasive FTC -which are considered low risk and are recommended by the specialist MDT based on overall clinico-pathological assessment * pT1b and pT2: \>1-4cm intrathyroidal * pT1a/1b/2/3a (where minimal microscopic ETE does not change the T score): any size up to 4 cm with minimal ETE if recommended by the MDT * Histological material available for Central Review (see section 9.7) * Willing to use contraception for the duration of the trial until 6 months post radioiodine treatment (for females) or 4 months post treatment (for males) (see section 6.4.2), if allocated to the ablation group. Exclusion criteria: * pT1a - Papillary and Follicular carcinoma which is unifocal and ≤1cm in size, without any positive nodes or unfavourable clinical features, treated by lobectomy. * Up to 4cm non-invasive Encapsulated Follicular Variant of Papillary Thyroid Cancer (eFVPTC) with no capsular or vascular invasion (\>4 cm can be included at the discretion of the MDT) * non-invasive follicular tumour with papillary-like nuclei (NIFTP) * Anaplastic, poorly differentiated or medullary carcinoma * R1 or R2 thyroidectomy * Patients with: * pN1a with level VII involvement * pN1b * M1 * Aggressive Papillary thyroid cancer with any of the following features: * Widely invasive * Poorly differentiated * Anaplastic * Tall cell * Columnar cell * Diffuse sclerosing variants * Follicular thyroid cancer/Hürthle cell cancer with any of the following features: * Tumours greater than 4cm * Widely invasive * Poorly differentiated * Anaplastic * Incomplete resection or lobectomy * pT3b, pT4a and pT4b or macroscopic and microscopic tumour invasion of loco-regional tissues or structures * Pregnant women or women who are breast feeding * Patients who have had CT performed with iv contrast less than 2-3 months before ablation * Previous treatment for thyroid cancer (except surgery in last 6 months) * Previous malignancies with limited life expectancy or likely to interfere with the patient's ability to be able to comply with treatment and/or follow-up for at least 5 years * The following GI conditions: dysphagia, oesophageal stricture, active gastritis, gastric erosions, peptic ulcer, suspected reduced gastrointestinal motility * MDT decision against ablation or suitability for trial in light of severe co-morbid condition/s including: * Unstable angina * Recent myocardial infarction or cerebrovascular accident (CVA) * Severe labile hypertension * Any patient who cannot comply with radiation protection including: * patients with learning difficulties * patients with dementia * patients with a tracheostomy that require nursing care * patients requiring frequent nursing/ medical supervision
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Barts Health NHS Trust
London, United Kingdom
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Belfast Health and Social Care Trust
Belfast, BT9 7AB, United Kingdom
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Cambridge University Hospitals NHS Foundation Trust
Cambridge, CB2 0QQ, United Kingdom
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East Kent Hospitals University NHS Foundation Trust
Canterbury, CT1 3NG, United Kingdom
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East and North Hertfordshire NHS Trust
Stevenage, SG1 4AB, United Kingdom
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Glasgow and Clyde NHS Trust
Glasgow, G12 0YN, United Kingdom
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Gloucestershire Hospitals NHS Trust
Cheltenham, United Kingdom
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Guy's and St Thomas' NHS Foundation Trust
London, United Kingdom
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Hull University Teaching Hospitals NHS Trust
Hull, HU16 5JU, United Kingdom
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Imperial College Healthcare NHS Trust
London, W6 8RF, United Kingdom
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Ipswich Hospital NHS Trust
Ipswich, IP4 5PD, United Kingdom
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Leeds Teaching Hospitals NHS Trust
Leeds, LS9 7TF, United Kingdom
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Maidstone and Tunbridge Wells NHS Trust
Maidstone, ME16 9QQ, United Kingdom
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Mid and South Essex NHS Foundation Trust
Chelmsford, United Kingdom
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NHS Lothian
Edinburgh, EH4 2XU, United Kingdom
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Newcastle upon Tyne Hospitals NHS Foundation Trust
Newcastle, NE7 7DN, United Kingdom
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Norfolk and Norwich University Hospitals NHS Foundation Trust
Norwich, United Kingdom
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Nottingham University Hospitals NHS Trust
Nottingham, NG5 1PB, United Kingdom
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Portsmouth Hospitals University NHS Trust
Portsmouth, PO6 3LY, United Kingdom
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Royal Derby Hospital NHS Foundation Trust
Derby, DE223NE, United Kingdom
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Royal Devon and Exeter Hospital NHS Foundation Trust
Exeter, EX2 5DW, United Kingdom
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Royal Marsden NHS Foundation Trust
London, SW3 6JJ, United Kingdom
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Royal Wolverhampton NHS Trust
Wolverhampton, United Kingdom
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Sheffield Teaching Hospitals NHS Foundation Trust
Sheffield, S10 2SJ, United Kingdom
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South Tees Hospitals NHS Trust
Middlesbrough, TS4 3BW, United Kingdom
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Southend University Hospitals NHS Trust
Southend, SS0 0RY, United Kingdom
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The Christie NHS Foundation Trust
Manchester, M20 4BX, United Kingdom
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The Royal Surrey County Hospital NHS Foundation Trust
Guildford, GU1 4JW, United Kingdom
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University College London Hospitals NHS Foundation Trust
London, United Kingdom
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University Hospital Bristol NHS Foundation Trust
Bristol, BS1 3NU, United Kingdom
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University Hospitals Birmingham NHS Foundation Trust
Birmingham, United Kingdom
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University Hospitals Dorset NHS Foundation Trust
Poole, DT1 2JY, United Kingdom
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University Hospitals Sussex NHS Foundation Trust
Brighton, BN2 5BE, United Kingdom
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University Hospitals of Leicester NHS Trust
Leicester, LE1 5WW, United Kingdom
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University Hospitals of North Midlands NHS Trust
Stoke-on-Trent, ST4 6QG, United Kingdom
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Velindre NHS Trust
Cardiff, CF15 7QZ, United Kingdom
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Other studies related to the condition(s) this trial covers.
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