I-124 PET/CT Based Remnant Radioiodine Ablation Decision Concept in Differentiated Thyroid Cancer

NCT01704586 · tracked via the Priya Life Science Germany tracker

Sponsor

University of Wuerzburg

Phase

Not applicable

Started

2015-05

Last updated

2026-10-09

Condition(s) studied

Differentiated Thyroid Carcinoma

Investigational drug(s) / intervention(s)

Radioiodine I-131I-124

Radioiodine I-131: Radioiodine will be used for ablation therapy, dosimetry and posttherapeutic whole body scan, as well as low dose I-131 imaging.

I-124: I-124 will be used for imaging to assess uptake inside and outside of thyroid bed, using PET/CT whole body scanning, followed by I-131 therapy as necessary as per protocol.

Study summary

Thyroid nodules are a common clinical problem. Epidemiologic studies have shown the prevalence of palpable thyroid nodules to be approximately 5% in women and 1% in men living in iodine-sufficient parts of the world and up to 30% in iodine deficient regions, such as Germany. The clinical importance of thyroid nodules rests with the need to exclude thyroid cancer which occurs in 5-15%. Differentiated thyroid cancer (DTC), which includes papillary and follicular cancer, comprises the vast majority (90%) of all thyroid cancers. In Germany, approximately 7,000 new cases will be diagnosed in 2011. The yearly incidence has increased from 3.6 per 100,000 in 1973 to 8.7 per 100,000 in 2002, and this trend appears to be continuing. Recurrence-free survival is generally excellent and depends on the risk group.

The role of postoperative remnant radioiodine ablation (RRIA) as the most serious question regarding the initial management of DTC still needs to be resolved even after decades of radioiodine use. American Thyroid Association directions for future research addressing these questions include:

* Better understanding of the long-term risks of radioiodine use;
* Improved risk stratification;

Randomized controlled trials are still missing in which RRIA has proven its worth as a safe and very effective treatment that results in an improved life expectancy and a reduced recurrence rate. Many observational studies lack sufficiently high evidence. Evidence grade is rated mainly on "expert level", based on non-randomized retrospective observation studies. Although RRIA in Europe is established as adjuvant standard treatment for all patients with DTC, except those with stage T1a, it remains to be shown throughout if it is beneficial for low risk and medium risk patients without metastases (M0), also known as stage I patients according to UICC/AJCC classification, accounting for 40-90% of all patients.

Blood doses due to cumulative radioiodine therapy may well exceed 2 Gy, and RRIA induces an average blood dose of 0.28 Gy to the entire body. Risks as estimated from that dose are not insignificant. The question is whether or not the condition after remnant ablation justifies such an increased risk of a secondary malignancy. The probability of causation for a pharyngeal or breast tumour can well exceed the margin of a 50% after being exposed to RRIA or consecutive I-131 diagnostic imaging to explore measureable Tg levels. Even though radioiodine therapy can benefit some patients with advanced thyroid carcinoma, it is still unknown whether the risks of RRIA outweigh any discernable benefit. Undoubtedly, quality of life may be affected by adjuvant use of I-131.

Study Hypothesis:

The I-124 study arm may have considerable benefits for the patient included in the study. These include

* enhanced tumour and risk stratification,
* avoidance of unnecessary I-131 exposure in 30-89 percent of patients who were classified with "low risk" tumour (MACIS or AMES scoring) or "stage I disease" (UICC-AJCC TNM staging system), and,
* improved quality of life at the same or better morbidity and mortality rates in the I-124 arm.

Environmental and hospital staff related benefits include prevention or saving of I-131 exposure.

This study is designed to compare effectiveness of treatments following and evaluating guideline recommendations in two assignment arms.

Eligibility

Sex

ALL

Min age

18 Years

Max age

80 Years

Healthy volunteers

Inclusion criteria common for all study subjects prior to randomisation: * Histologically confirmed new diagnosis of DTC (including Hürthle-cell carcinoma) * Age 18-80 years * Performance Status of 0-2 * Tumor stage T1a(m) to T4 with the possibility of lymph node involvement and distant metastasis according to the \[TNM\] staging system * One- or two stage thyroidectomy, with or without central lymph node dissection * Patient´s written informed consent * Ability to comply with the protocol procedures Exclusion criteria for all study subjects prior to randomisation: * Anaplastic or medullary carcinoma * History of prior malignancy within the past 5 years with limited life-time expectancy, except for cured non-melanoma skin cancer, cured in situ cervical carcinoma, or other treated malignancies with no evidence of disease for at least three years. * Positive pregnancy test or breast feeding * Any other severe acute or chronic medical or psychiatric condition, or laboratory abnormality that would impart, in the judgment of the investigator, excess risk associated with study participation, or which, in the judgment of the investigator, would make the patient inappropriate for entry into this study. * Recent iodine contamination After Randomisation: I-124 arm (Arm 1): A: Inclusion criteria for no remnant ablation (low risk DTC): * Papillary or follicular carcinoma with the possibility of lymph node involvement but no distant metastasis and no macroscopical (R2) residual disease (Patient age \<45y: T1-T2, T3 limited to the thyroid, any N, M0; Patient age 45y or older: T1-T2, N0, M0) * I-124 uptake only in thyroid bed * Microscopical residual disease (R1) and/or aggressive malignant histologic subtypes, including tall-cell, insular, poorly differentiated and diffuse sclerosing thyroid cancer, columnar cell variant: according to the recommendation of the local tumour board B: Inclusion criteria (high risk DTC): * All other \[TNM\] stages (stage II to stage IV C) and T3 (any size with minimal extrathyroidal extension) * R2 (if no redo surgery) * Microscopical residual disease (R1) and/or aggressive malignant histologic subtypes, including tall-cell, insular, poorly differentiated and diffuse sclerosing thyroid cancer, columnar cell variant: according to the recommendation of the local tumour board * AND I-124 uptake in or outside thyroid bed * OR low risk showing 124 uptake outside of the thyroid bed Standard arm (Arm 2): · Standard I-131 ablation concept as defined for all T1a(m) to T4 subjects.

Primary outcome measure(s)

Mean blood dose after complete remission — 18 months after thyroid surgery
Both study arms result in different I-131 activity assigned to be administered, depending on remnant ablation and/or metastasis treatment decision. I-131 activity will be standard or less in the standard arm, none in the I-124 arm in patients identified as per protocol not to be administered an ablation activity.

Trial sites (2)

Facility	City	Region	Status
Clinic of Nuclear Medicine, University Clinic Essen	Essen	Germany
University Clinic Würzburg	Würzburg	Germany

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT01704586 on ClinicalTrials.gov ↗ ← All trials in Germany