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NCT01398085Fut, nem toboroz2/3. fázis

IoN- Is Ablative Radio-iodine Necessary for Low Risk Differentiated Thyroid Cancer Patients

Is Ablative Radio-iodine Necessary for Low Risk Differentiated Thyroid Cancer Patients

Forrás: ClinicalTrials.gov · Utoljára frissítve: 2026. máj. 7.

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Rövid összefoglaló (regiszter, angolul)

IoN is a phase II/III trial that will look to ascertain whether or not radio-iodine ablation is necessary for low risk differentiated thyroid cancer patients.

Állapot (regiszter)
Fut, nem toboroz
Fázis (regiszter)
2/3. fázis
Vizsgálattípus
Beavatkozással járó
Résztvevők száma
504 (tényleges)
Első benyújtás
2011. júl. 6.
Kezdés
2012. jún. 26.
Elsődleges befejezés
2031. márc.
Fő szponzor
University College, London
NCT-szám
NCT01398085
EudraCT-szám
2011-000144-21

Mit vállalsz

  • Vizsgálat típusa: Beavatkozással járó · 2/3. fázis
  • Bevont résztvevők: 504
  • 2012. jún. 26. és az elsődleges befejezés (2031. márc.) között
  • 36 helyszín, 1 országban
  • Vizitek és vizsgálatok: kérdezd a vizsgálat csapatát, a regiszter nem sorolja fel őket

A(z) ClinicalTrials.gov regisztermezőiből összeállítva. A vizsgálat felépítését írja le.

Ki nem vehet részt

Szó szerint a(z) ClinicalTrials.gov forrásból, témák szerint csoportosítva. Hogy ki vehet részt, azt csak a vizsgálat csapata dönti el.

Korábbi kezelés

  • Incomplete resection or lobectomy
  • 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)
  • Incomplete resection or lobectomy
  • 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)

Más betegség

  • 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)
  • 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
  • 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:
  • 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)
  • 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
  • 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

Egyéb

  • pT1a - Papillary and Follicular carcinoma which is unifocal and ≤1cm in size, without any positive nodes or unfavourable clinical features, treated by lobectomy.
  • non-invasive follicular tumour with papillary-like nuclei (NIFTP)
  • Anaplastic, poorly differentiated or medullary carcinoma
  • R1 or R2 thyroidectomy
  • Patients with:
    • pN1b
    • M1
  • pT4a and pT4b or macroscopic and microscopic tumour invasion of loco-regional tissues or structures
  • Pregnant women or women who are breast feeding
  • pT1a - Papillary and Follicular carcinoma which is unifocal and ≤1cm in size, without any positive nodes or unfavourable clinical features, treated by lobectomy.
  • 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
  • pT3b, pT4a and pT4b or macroscopic and microscopic tumour invasion of loco-regional tissues or structures
  • Pregnant women or women who are breast feeding

Kiket keres a vizsgálat

  • 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).
  • 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.

A regiszterben nem jelölt feltételek

  • 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:

Életkor a regiszterben: 16 év – - · Nem: nők és férfiak · Egészséges önkénteseket nem fogad

A teljes feltétellista: ClinicalTrials.gov

Helyszínek (36)

Helyszínek a regiszter sorrendjében. Ha a profilodba mented a városodat, távolság szerint rendeződnek.

HelyszínVárosOrszágHelyszín állapota
Belfast Health and Social Care TrustBelfastEgyesült KirályságIsmeretlen állapot
University Hospitals Birmingham NHS Foundation TrustBirminghamEgyesült KirályságIsmeretlen állapot
University Hospitals Sussex NHS Foundation TrustBrightonEgyesült KirályságIsmeretlen állapot
University Hospital Bristol NHS Foundation TrustBristolEgyesült KirályságIsmeretlen állapot
Cambridge University Hospitals NHS Foundation TrustCambridgeEgyesült KirályságIsmeretlen állapot
East Kent Hospitals University NHS Foundation TrustCanterburyEgyesült KirályságIsmeretlen állapot
Velindre NHS TrustCardiffEgyesült KirályságIsmeretlen állapot
Mid and South Essex NHS Foundation TrustChelmsfordEgyesült KirályságIsmeretlen állapot
Gloucestershire Hospitals NHS TrustCheltenhamEgyesült KirályságIsmeretlen állapot
Royal Derby Hospital NHS Foundation TrustDerbyEgyesült KirályságIsmeretlen állapot
NHS LothianEdinburghEgyesült KirályságIsmeretlen állapot
Royal Devon and Exeter Hospital NHS Foundation TrustExeterEgyesült KirályságIsmeretlen állapot
Glasgow and Clyde NHS TrustGlasgowEgyesült KirályságIsmeretlen állapot
The Royal Surrey County Hospital NHS Foundation TrustGuildfordEgyesült KirályságIsmeretlen állapot
Hull University Teaching Hospitals NHS TrustHullEgyesült KirályságIsmeretlen állapot
Ipswich Hospital NHS TrustIpswichEgyesült KirályságIsmeretlen állapot
Leeds Teaching Hospitals NHS TrustLeedsEgyesült KirályságIsmeretlen állapot
University Hospitals of Leicester NHS TrustLeicesterEgyesült KirályságIsmeretlen állapot
Barts Health NHS TrustLondonEgyesült KirályságIsmeretlen állapot
Royal Marsden NHS Foundation TrustLondonEgyesült KirályságIsmeretlen állapot
Guy's and St Thomas' NHS Foundation TrustLondonEgyesült KirályságIsmeretlen állapot
University College London Hospitals NHS Foundation TrustLondonEgyesült KirályságIsmeretlen állapot
Imperial College Healthcare NHS TrustLondonEgyesült KirályságIsmeretlen állapot
Maidstone and Tunbridge Wells NHS TrustMaidstoneEgyesült KirályságIsmeretlen állapot
The Christie NHS Foundation TrustManchesterEgyesült KirályságIsmeretlen állapot
South Tees Hospitals NHS TrustMiddlesbroughEgyesült KirályságIsmeretlen állapot
Newcastle Upon Tyne Hospitals NHS Foundation TrustNewcastleEgyesült KirályságIsmeretlen állapot
Norfolk and Norwich University Hospitals NHS Foundation TrustNorwichEgyesült KirályságIsmeretlen állapot
Nottingham University Hospitals NHS TrustNottinghamEgyesült KirályságIsmeretlen állapot
University Hospitals Dorset NHS Foundation TrustPooleEgyesült KirályságIsmeretlen állapot
Portsmouth Hospitals University NHS TrustPortsmouthEgyesült KirályságIsmeretlen állapot
Sheffield Teaching Hospitals NHS Foundation TrustSheffieldEgyesült KirályságIsmeretlen állapot
Southend University Hospitals NHS TrustSouthendEgyesült KirályságIsmeretlen állapot
East and North Hertfordshire NHS TrustStevenageEgyesült KirályságIsmeretlen állapot
University Hospitals of North Midlands NHS TrustStoke-on-TrentEgyesült KirályságIsmeretlen állapot
Royal Wolverhampton Nhs TrustWolverhamptonEgyesült KirályságIsmeretlen állapot

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