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ISSN: 2155-9619
Journal of Nuclear Medicine & Radiation Therapy

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Radio-Active Iodine Ablation in Well-differentiated Thyroid Cancers

Russell N Moule*

Mount Vernon Cancer Centre, Northwood, Middlesex, HA6 2RN, UK

*Corresponding Author:
Russell N Moule
Mount Vernon Cancer Centre
Northwood, Middlesex, HA6 2RN, UK
E-mail: [email protected]

Received date: July 19, 2012; Accepted date: July 20, 2012; Published date: July 23, 2012

Citation: Moule RN (2012) Radio-Active Iodine Ablation in Well-differentiated Thyroid Cancers. J Nucl Med Radiat Ther 3:e103. doi:10.4172/2155-9619.1000e103

Copyright: © 2012 Moule RN. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Well differentiated thyroid cancers are relatively rare and are 1% of all cancer diagnoses. The main stay of treatment is thyroidectomy (hemi- and completion), followed by radioactive-iodine abalation. Radio-active iodine (131I) ablation after thyroidectomy in patients with well-differentiated thyroid cancers (Papillary, Follicular, and Mixed) is common practice although the optimal administered dose has been debated.

The management of thyroid cancer has been formalised like other cancers. The Royal College of Physicians (UK) and the American Thyroid Association have both produced guidance.

Recurrence and survival has been quoted at both 10 and 20 years depending on risk factors and the prognostic system used. The most commonly used are the AJCC TNM (Tumour, Node Metastasis) staging, and MACIS (Metastasis, Age at presentation, Completeness of surgical resection, Invasion – extra-thyroidal, and Size). Others scoring systems include AMES (Age at presentation, Metastases, Extent, Size of primary tumour), AGES (Age or presentation, Grade of Histology, Extent, Size of primary) and those from the EORTC.

Poor prognostic factors include: male, age greater than 40, tumour size greater than 5cm, widely invasive cancers or those with vascular invasion or poor differentiation, the presence of lymph node involvement or metastatic disease at presentation.

The use of 131I ablation (3.7 GBq) aims to kill any remaining thyroid cells, as well as any potentially residual microscopic disease. The serum thyroglobulin (Tg) measurements post-treatment will be more sensitive as Tg may be produced by normal thyroid cells and thyroid cancer cells. The rationale therefore is that any rise in the Tg after 131I ablation (providing the patient is adequately TSH suppressed on thyroxine) is due to the presence of thyroid cancer cells rather than normal thyroid cells and suggestive of persistent or recurrent disease. Also ablation reduces the risk of recurrence and prolongs survival.

The absolute indications of 131I ablation include T3 disease (>4cm), extra-thyroidal extension or capsular extension, lymph node involvement (with or without extra-capsular spread) or the presence of metastatic disease. Others include age greater than 45 years, tumour size 1 to 1.5cm. Very low risk patients for example completely excised tumours less than 1cm in size will not require ablative treatment.

However in patients with lower risk disease the decision to proceed with 131I ablation is not as clear cut and the use of a lower dose of 131I ablation may suffice. Hackshaw, et al. in 2007 [1] undertook a systematic review into the success of low-dose 131I ablation (1.1 GBq equivalent to 30 mCi) compared to a standard 3.7 Gbq (100 mCi) ablative dose. Unfortunately the data did not provide any robust conclusions.

The HiLO study [2] has specifically tried to address this issue. This study compared 1.1 GBq and 3.7 GBq ablative doses as well as the use of recombinantTSH (rTSH). Patients with T1 to T3 N0/1 M0 well differentiated thyroid cancer as well as Hurthle cell cancer we randomised to 1.1 GBq and 3.7 GBq radio-active iodine ablation and either rTSH (0.9mg day 1 and 2 pre-radioactive iodine) or standard withdrawal of thyroxine or liothyronine.

Out of the 438 patients that were recruited to the study 421 patients were evaluated. There was no significant difference in the ablation success between the two doses of radioactive iodine (85.0% vs. 88.9%). This was also the case for the use of rTSH. Nine and a half percent of patients who received 1.1 GBq required a further re-treatment compared to 4.1% in the 3.7 GBq group (p=0.02) However there was a significant reduction in the number of days admission. Patients who received 1.1 GBq were more likely to spend less time in hospital with 39.6% compared to 7.1% requiring only one day admission (p<0.001). Less side effects were also experienced in the 1.1 GBq group (21% vs. 33% p<0.007).

This study has provided important information as there was no difference in the ablation success rate between the low dose and high dose groups and similarly the use of rTSH did not have a significant impact on this rate.

As far as quality of life is concerned the use of 1.1 GBq radio-active iodine abaltion has significant advantages as the radiation protection issues surrounding administration are less and patients spend less time isolated and away from family life. For units that have pressure on treatment room usage 1.1 GBq in this group of patients allows a greater throughput and less treatment delays.

Following this study the same group attempting to answer the next question of whether radio-active iodine ablation is actually required in low-risk patients. This is being addressed through the IoN (Iodine or Not in low risk differentiated thyroid cancer) study.

There is no disadvantage with the use of low dose 1.1 GBq radioactive iodine ablation compared to 3.7 GBq in patients with low risk well differentiated thyroid cancers. The HiLo [3] study is a great step forward in the management of the patients and IoN will provide further valuable information over the coming years.


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