The optimal radioiodine treatment strategy for Graves’ disease is controversial as reflected in the differing guidance offered by international guidelines. The American Thyroid Association aims to render patients hypothyroid by administering 370–555 MBq (10–15 mCi) or 5.5 MBq (150 mCi) per gram of thyroid tissue 1. The Royal College of Physicians (UK) recommends a fixed activity of 400–600 MBq for rapid elimination of hyperthyroidism accepting that a significant proportion of patients will require life-long L-thyroxine with this approach 2. In contrast, the European Association of Nuclear Medicine recommends administration of an activity of radioiodine calculated to give an absorbed dose of 150 Gy to the thyroid where the aim is to restore euthyroidism 3.
A fixed activity approach has the advantages of cost-effectiveness, efficiency and early eradication of hyperthyroidism thus avoiding its adverse consequences 4–6. In contrast, an individualized approach on the basis of dosimetry aims to administer the minimum activity of radioiodine necessary to render a patient euthyroid for the maximum length of time in accordance with the ionizing radiation regulations, which are guided by the ALARA (as low as reasonably achievable) principle in radiation protection, that is to keep radiation doses ‘as low as reasonably achievable’ and stipulate that exposures of target volumes must be individually planned 7. The disadvantage of remaining on antithyroid medication for longer with this approach is offset by the delayed need for L-thyroxine replacement since ∼40% of patients on long-term L-thyroxine are either over-treated or under-treated, and hence at risk of associated morbidities 8.
Following an initial study that demonstrated that an absorbed dose of more than 40 Gy iodine-131 (131I) was needed to achieve short-term control of hyperthyroidism in Graves’ disease 9, the long-term prospective study presented here was performed to assess the feasibility and effectiveness of an activity administration calculated to deliver 60 Gy to the thyroid. Treatment outcomes, in terms of hyperthyroidism, hypothyroidism and euthyroidism were investigated with up to 10 years follow-up. In addition, clinical and 131I kinetic parameters that might predict treatment outcome were examined.
Patients and methods
Over a 10-year period (1999–2009), 284 patients [216 female, 67 male: mean age of 46.2 years (range: 18.1–81.6 years)] referred to the Thyroid Unit at the Royal Marsden Hospital for 131I treatment of Graves’ disease participated in this study, which was approved by the Royal Marsden Hospital Research Ethics Committee. Inclusion criteria stipulated clinical and biochemically proven Graves’ disease and no previous radioiodine treatment. All patients provided written informed consent after receiving detailed information about radioiodine treatment including printed radiation protection instructions. Patients with multinodular goitre, autonomous thyroid nodules or cardiac complications (heart failure or atrial fibrillation) were excluded from the study. Patients who were unable or unwilling to come up for the additional six visits required for dosimetry underwent standard treatment with a fixed radioactive iodine dose of 75 MBq.
The diagnosis of Graves’ disease was made according to standard criteria: typical clinical findings and the presence of thyroid-stimulating hormone (TSH) receptor autoantibodies. Those with a diffuse and homogenous pattern on technetium-99m-scintigraphy were classified as typical Graves’ disease (227 patients). The remaining 57 patients with nonuniform uptake on scintigraphy or nodular appearance on thyroid ultrasound scanning were classified as Graves’ disease in a nodular thyroid. Thyroid volume was determined immediately before a tracer administration of radioiodine. Radioiodine kinetics was determined following tracer and therapy administrations of Na131I.
The study schedule is shown in Table 1. Patients were advised to follow a low-iodine diet and to stop antithyroid medication commencing 3 days before radioiodine administration and continuing for 9 and 6 days for tracer and therapy, respectively. Tracer and therapy administrations were 14 days apart. This schedule ensured that patients were euthyroid at the time of 131I treatment, thus minimizing the risk of thyroid storm. In addition, it allowed tracer and therapy administrations to be given under the same physiological conditions. Those patients with clinical evidence of thyroid eye disease received 0.5 mg/kg oral prednisolone with the radioiodine at therapy and with the tracer administration to prevent ophthalmopathy worsening.
Thyroid volume was assessed by ultrasound performed immediately before tracer administration. Thyroid volume was calculated from the formula: Vlobe=length (cm)×width (cm)×depth (cm)×m (where m=0.479) taking the maximal linear dimensions of each lobe on a frozen B-scan image 10. Texture was graded as homogeneous, heterogeneous or nodular.
Following oral administration of a 0.37 MBq Na131I tracer administration, radioiodine uptake in the thyroid was measured using a sodium iodide detector with diverging collimator. Thyroid uptake was determined by comparison of the count rates from the patient’s thyroid and a known activity of 131I in a standard neck phantom. Background counts were measured with a lead shield positioned between the front of the collimator and the patient’s neck or phantom. Percentage thyroid uptake was determined at 1, 2 and 6 days following the tracer administration:
where U (%) is the percentage thyroid uptake, CRP is the patient count rate (cpm), AS is the activity of the standard (MBq), CRS is the count rate of the standard (cpm) and AP is the activity in the patient (MBq).
For each patient, the maximum recorded thyroid uptake (U) and the uptake at 6 days were used to determine the effective half-life (days). The effective half-life was set to 8 days in cases where it was calculated to be greater than this value.
The activity (A) of 131I needed to deliver 60 Gy to the thyroid was calculated from the following equation on the basis of the Medical Internal Radiation Dose schema:
where 60 is the target thyroid absorbed dose (Gy), M is the mass of the thyroid (g), U is the maximum uptake in the thyroid (%) and T is the effective half-life in the thyroid (days).
Radioiodine therapy was administered 1–2 weeks after the tracer study. At 24 h after therapy administration the thyroid uptake was measured using the same system and setup as for the tracer study. Owing to the high 131I activity present it was necessary to attach a secondary collimator to the diverging collimator to reduce the sensitivity of the system and thus avoid problems resulting from dead-time. The absorbed dose to the thyroid was then calculated using the thyroid volume and effective half-life calculated in the tracer study.
A gamma camera image was also taken at this time to assess heterogeneity of uptake.
Following radioiodine therapy, antithyroid medications were restarted and continued until patients were clinically and biochemically euthyroid. All patients received radiation protection advice regarding contact with children and time off work in line with standard guidelines. Patients were advised to avoid close contact with young children (<3 years) for 7 days and there was no restriction on work with adults unless contact with pregnant women was possible. Patients attended follow-up at regular visits for a minimum of 12 months up to 10 years with a median follow-up of 37.5 months. At each visit thyroid status was evaluated clinically and biochemically and patients were classified as hypothyroid requiring L-thyroxine (elevated TSH with or without low FT4), hyperthyroid requiring antithyroid treatment (elevated FT4 or FT3 and low TSH) or euthyroid on no specific thyroid medication (normal FT4, FT3 and measurable TSH). The requirement for a further administration of 131I was based on clinical assessment. A second administration of 131I was considered an outcome endpoint and any such patients left the study to be followed in the standard endocrine clinic.
Statistical analysis was performed using GraphPad Prism and Bell Laboratories statistical computing package (Graphpad software; San Diego, California, USA), ‘R’. Descriptive statistics are provided as mean±SD for normally distributed data or as median with 95% confidence intervals (CIs) and range for non-normally distributed data. Thyroid status was analysed at 6 months, 1, 3, 5 and 10 years. For the purpose of analysis it was assumed that patients who were hypothyroid on L-thyroxine replacement at discharge remained in the same state. For multivariate analysis to compare baseline variables (thyroid volume, age, 131I uptake, effective half-life) and thyroid status, we used logistic regression analysis. The coefficients of the independent variables in the regression were transformed to give the odds of a particular treatment outcome. The odds ratios (ORs) are expressed with 95% CIs. The regression was repeated at 3, 5 and 10 years with P value less than 0.05 taken as indicating statistical significance in all tests. All P values presented are two tailed.
Baseline characteristics are shown in Tables 2 and 3. In comparison with patients with typical Graves’ disease, those with Graves’ in a nodular goitre were more likely to be male, older and to require more activity to achieve the target 60 Gy absorbed dose. The maximum uptake of 131I after tracer and therapy administrations was reduced in nodular glands although the 131I effective half-life was slightly but not significantly longer. Only five patients required 400 MBq or more to deliver a target absorbed dose of 60 Gy. The maximum thyroidal 131I uptake was very similar for the tracer and therapy (Table 3). The median thyroid volume was greater in the group with nodules. Five patients requiring over 400 MBq had significantly larger thyroid volumes (mean: 56.4 ml; range: 37.9–96.8 ml; P<0.05). Median effective half-life in Graves’ and Graves’ with nodules was not found to be statistically significant. Analysis of the whole patient cohort gave a median absorbed thyroid dose of 55.8 Gy (55.03–58.03).
Clinical outcomes for patients with typical Graves’ disease (n=227) and Graves’ in a nodular thyroid (n=57) are shown in Fig. 1. At 18 months, 44.2% of all study patients were euthyroid on no specific therapy, 9.0% were on replacement L-thyroxine, 11.6% were still taking antithyroid medication and 35.2% had required a second administration of 131I (fixed dose of 75 MBq) because of persistent hyperthyroidism requiring antithyroid medication.
The proportion of patients requiring further radioiodine increased to 43.8% by 3 years but thereafter changed little (47.0% at 5 years, 48.6% at 10 years). No serious adverse effects of radioiodine (post-therapy flare of hyperthyroidism or significant exacerbation of thyroid eye disease) were observed. At 3, 5 and 10 years after administration, 41.4, 37.7 and 30.0%, respectively of patients were euthyroid on no thyroid medication. The proportion of patients becoming hypothyroid increased from 12.9% at 3 years to 17.0% at 5 years and 21.4% at 10 years. After 3 years, a small percentage of patients were still on antithyroid medication usually because further 131I therapy was contraindicated. By 5 years no patients remained on antithyroid drugs.
In comparison with patients with typical Graves’ disease, those with Graves’ in a nodular thyroid became nonhyperthyroid sooner and none required antithyroid medication by 3 years (Fig. 1). At 10 years, a slightly greater proportion were euthyroid (33.3 vs. 29.2%) or hypothyroid (22.9 vs. 21.0%) and fewer had required a second administration of 131I (43.8 vs. 49.7%).
Factors affecting treatment outcomes
From multivariate analysis, increasing thyroid volume was found to be highly significant in the likelihood of a patient responding to a single administration of 131I. The ORs (95% CIs) for achieving a nonhyperthyroid state (euthyroidism or hypothyroidism on L-thyroxine) are shown in Table 4. At 3 years, OR was 1.044 (1.014–1.077, P=0.005), at 5 years the OR had decreased to 1.04 (1.011–1.074, P=0.008) and at 10 years to 1.032 (1.004–1.063, P=0.029). Thyroid volume did not correlate with effective 131I half-life or maximum percentage 131I uptake.
Age at treatment
Increasing age at the point of treatment was significantly associated with the likelihood of a patient successfully responding to a single administration (Fig. 2). The corresponding ORs at 3, 5 and 10 years were very similar at 0.976 (0.955–0.997), 0.97 and 0.969.
Effective iodine-131 half-life and maximum iodine-131 uptake
Neither effective half-life nor maximum 131I uptake were significantly associated with the need for further 131I treatment.
Duration of antithyroid treatment
We found no significant association between length of antithyroid treatment before 131I treatment and treatment outcomes.
The results of this study indicated that a targeted 60 Gy absorbed dose to the thyroid can delay the onset of hypothyroidism in about a quarter of patients with Graves’ disease. Using the protocol adopted in this study, 62% of patients were treated once with a mean 131I activity of 106 MBq. The remainder required a second 131I administration usually within 2 years. In patients receiving a single administration, euthyroidism persisted for 10 years and might be expected to continue for an average of 15 years 11. This approach was associated with continued requirement for oral antithyroid therapy in about a quarter of patients for 18 months. It should be noted that none became overtly hyperthyroid. Importantly, we excluded patients with cardiac complications in whom hyperthyroidism needed to be corrected more rapidly.
An absorbed thyroid dose of 60 Gy was chosen for this study after a previous study at this centre demonstrated a high rate of treatment failure at 12 months with lower absorbed doses 9. Howarth et al. 12 in a study of patients with Graves’ disease comparing 60 and 90 Gy absorbed doses to the thyroid reported 46% of patients were euthyroid on no specific medication with a median follow-up of 37.5 months. The authors concluded that 60 Gy was a better option than 90 Gy where the aim of treatment was to achieve euthyroidism and to delay the onset of hypothyroidism for as long as possible.
The difference between intended and therapeutically achieved target absorbed doses in Graves’ disease varies widely in previous publications. The coefficient of variation of 22.8% in this study compares well with previous reports of 18–28% 13,14 and is considerably lower than others 15. We noted a significant correlation between pretherapy thyroid volume (and hence thyroid mass) and treatment outcome and this may be relevant when comparing our results with other studies; Thyroid mass (>26 g) has previously been shown to be an important predictor of inadequate response to 131I therapy for patients treated with 60–90 Gy 12,13. The relatively small mean thyroid volume (18 ml) in this study is likely to be an important factor in determining the successful outcome of our patients.
Reliance on single measurements of 131I uptake at 24 h to determine activity is potentially inaccurate because of the variability of the biological half-life of 131I 16,17. Maximum 131I uptake occurs after 24 h in 54% of patients with Graves’ disease 18. This may be important in interpretation of the results of previous studies comparing individualized and fixed activity approaches 5,19,20. In our study, 131I uptake was measured over 6 days and there was good correlation between diagnostic and therapeutic maximum uptake values. A wide variation in 131I effective half-life was noted in this study although the mean of 5.3 days compares well with previous reports 12,13.
A shorter 131I effective half-life was found to be associated with an increased risk of hypothyroidism at 3 years in keeping with previous reports 21 although we did not find an association with maximum fractional 131I uptake. There may be a need to increase the target absorbed dose in cases where the effective half-life as determined from the tracer administration is found to be short.
Older patients in our study were more likely to become euthyroid after a single administration of 131I possibly indicating less severe hyperthyroidism at the outset. Pretreatment with propylthiouracil but not carbimazole may influence treatment outcomes after 131I therapy 22. However the use of this drug in our patients was limited to a small number of all ages who developed skin reactions to carbimazole.
The presence of nodules on ultrasonography in Graves’ patients may be an additional confounding factor in the comparison of outcomes from different studies. Patients with autonomous thyroid nodules or toxic adenomas were excluded from our study as with a number of other previously reported studies 12,20. Patients with nodular disease have conventionally been considered to be more radioresistant in comparison to those with typical Graves’ disease 23 although at least one study has noted that these patients may have better long-term results after a single administration of 131I therapy 24. Our data suggest that patients with Graves’ in a nodular thyroid have a good response to 131I therapy.
There have been few prospective randomized-controlled trials comparing individualized dosimetry versus fixed activity approaches 5,20,25. In an open randomized 12-month trial comparing three fixed 131I activities with an individualized absorbed dose equivalent to 70 Gy 20, 50% of patients treated by the individualized dose were euthyroid, 41% still required antithyroid treatment and 9% were hypothyroid. Results for the fixed activity approach were similar. No long-term data was presented. In another randomized trial, 98 patients with Graves’ disease received a fixed activity of 555 MBq and were compared by outcome at 6 months to 107 patients who were administered a planned absorbed dose of 100 Gy 25. A successful outcome, defined as elimination of hyperthyroidism, occurred in 71% of those receiving fixed activity versus 58% in the calculated absorbed dose group. This difference did not quite achieve significance. Long-term outcomes were not reported. Leslie et al.5 randomized 88 patients with Graves’ disease to either (i) 235 MBq; (ii) 350 MBq; (iii) 2.96 MBq/g thyroid (∼60 Gy) or (iv) 4.44 MBq/g thyroid (∼100 Gy). With a mean follow-up of 63 months, the investigators reported no significant differences in clinical outcomes. This study was considerably underpowered and clinically important differences between groups may have been missed.
Irrespective of whether the objective of 131I therapy is the elimination of hyperthyroidism or the maintenance of euthyroidism for as long as possible, the principle of ensuring that radiation doses as low as reasonably achievable (ALARA) should be applied 7,26. This principle is not always respected in the treatment of thyroid disease 11. In our study, a very wide range of activity (mean: 106 MBq; range 17.4–1377 MBq) was associated with a targeted absorbed dose of 60 Gy reflecting the poor correlation between administered activity and the absorbed dose. Only five of our patients required the Royal College of Physicians recommended fixed activity of 400 MBq. Even a fixed activity of 370 MBq may result in some two-thirds of patients being unnecessarily over-irradiated 4,11.
It is acknowledged that a dosimetric approach entails more visits to hospital with associated costs and the increased risk of recurrent hyperthyroidism in comparison with a fixed ablative dose. In patients with cardiovascular disease this could have serious consequences, and hence significant cardiac disease is, in our view, a contraindication to this approach. Furthermore, if patients are lost to follow-up, there is the potential for untreated hypothyroidism but this is also the case for patients receiving fixed doses.
The strengths of this study include: (i) a well-characterized cohort of patients all treated in one centre using a standard protocol, in whom cardiac disease was excluded and in whom the presence of thyroid nodules was taken into account in the analysis; (ii) achievement of the targeted absorbed dose of 60 Gy with an acceptable coefficient of variation; (iii) prolonged follow-up with results at 10 years and (iv) outcome measurement of euthyroidism requiring no specific therapy as the preferred measure of successful treatment. A limitation of the study is that we did not directly compare outcomes with patients treated with fixed 131I activities in a randomized-controlled trial design.
On the basis of our results, a dosimetric approach would have resulted in nearly two-thirds of patients receiving an average of three to five times less radioiodine compared with standard fixed radiation activities of 370–550 MBq. Further research is needed to identify the optimal absorbed dose for different patient cohorts and investigate which patients would benefit most from this approach.
The authors acknowledge the invaluable help provided by our specialist nurses.
This work was supported by the NIHR Clinical Research Network.
Conflicts of interest
There are no conflicts of interest.
1. Ross DS, Birch HB, Cooper DS, Greenlee MC, Laurberg P, Maia AL, et al. 2016 American Thyroid Association GUIDELINES for diagnosis and management of hyperthyroidism
and other causes of thyrotoxicosis. Thyroid 2016; 26:1343–1421.
2. Royal College of Physicians. Radioiodine
in the management of benign thyroid disease
Clinical guidelines Report of a working party. London, UK: RCP; 2007.
3. Stokkel MP, Handkiewicz Junak D, Lassmann M, Dietlein M, Luster M. EANM procedure guidelines for therapy of benign thyroid disease
. Eur J Nucl Med Mol Imaging 2010; 37:2218–2228.
4. Allahabaida A, Daykin J, Sheppard M, Gough SC, Franklyn JA. Radioiodine
treatment of hyperthyroidism
-prognostic factors for outcome. J Clin Endocrinol Metab 2001; 86:3611–3617.
5. Leslie WD, Ward L, Salamon EA, Ludwig S, Rowe RC, Cowden EA. A randomised comparison of radioiodine
doses in Graves’ hyperthyroidism
. J Clin Endocrinol Metab 2003; 88:978–983.
6. Metso S, Jaatinen P, Huhtala H, Luukkaala T, Oksala H, Salmi J. Long term follow-up study of radioiodine
treatment of hyperthyroidism
. Clin Endocrinol (Oxf) 2004; 61:641–648.
7. European Union. European Council Directive 2013/59 Euratom on basic safety standards for the protection against the dangers arising from the exposure to ionising radiation and repealing directives 89/618/Euratom, 90/641/Euratom, 96/29/Euratom, 97/43/ Euratom and 2003/122/Euratom. OJEU 2014; 57:1–73.
8. Canaris GJ, Manowitz NR, Mayor G, Ridgway EC. The Colorado thyroid disease prevalence study. Arch Intern Med 2000; 160:526–534.
9. Flower MA, Al-Saadi A, Harmer CL, McCready R, Ott RJ. Dose–response study on thyrotoxic patients undergoing positron emission tomography and radioiodine
therapy. Eur J Nucl Med 1994; 21:531–536.
10. Crawford DC, Flower MA, Pratt BE, Hill C, Zweit J, McCready, R, Harmer CL. Thyroid volume measurement in thyrotoxic patients: comparison between ultrasonography and iodine-124 positron emission tomography. Eur J Nucl Med 1997; 24:1470–1478.
11. Van Isselt JW, de Klerk JMH, Lips CJM. Radioiodine
treatment of hyperthyroidism
: fixed or calculated doses; intelligent design or science. Eur J Nucl Med Mol Imaging 2007; 34:1883–1884.
12. Howarth D, Epstein M, Lan L, Tan P, Booker J. Determination of the optimal minimum radioiodine
dose in patients with Graves’ disease
: a clinical outcome study. Eur J Nucl Med 2001; 28:1489–1495.
13. Reinhardt MJ, Brink I, Joe AY, von Mallek D, Ezziddin S, Palmedo H, Krause TM. Radioiodine
therapy in Graves’ disease
based on tissue absorbed dose calculations: effect of pre-treatment thyroid volume on clinical outcome. Eur J Nucl Med 2002; 29:1118–1124.
14. Bockisch A, Jamitzky T, Derwanz R, Biersack HJ. Optimised dose planning of radioiodine
therapy of benign thyroidal diseases. J Nucl Med 1993; 34:1632–1638.
15. Catargi B, Leprat F, Guyot M, Valli N, Dominique Ducassou D, Tabarin A. Optimized radioiodine
therapy of Graves’ disease
: analysis of the delivered dose and of other possible factors affecting outcome. Eur J Endocrinol 1999; 141:117–121.
16. Kaplan MM, Meier DA, Dworkin JJ. Treatment of hyperthyroidism
with radioactive iodine. Endocrinol Metab Clin North Am 1998; 27:205–223.
17. Van Isselt JW, Broekhuizen-de Gast HS. The radioiodine
turnover rate as a determinant of radioiodine
treatment outcome in Graves’ disease
. Hell J Nucl Med 2010; 13:2–5.
18. Vemulakonda US, Atkins FB, Ziessman HA. Therapy dose calculation in Graves’ disease
using early I-123 uptake measurements. Clin Nucl Med 1996; 21:102–105.
19. De Rooij A, Vandenbroucke JP, Smit JWA, Stokkel MPM, Dekkers OM. Clinical outcomes after estimated versus calculated activity of radioiodine
for the treatment of hyperthyroidism
: systematic review and meta-analysis. Eu J Endocrinol 2009; 161:771–777.
20. Jarlov VAE, Hegedus L, Kristensen LO, Nygaard B, Hansen JM. Is calculation of the dose in radioiodine
therapy of hyperthyroidism
worthwhile? Clin Endocrinol (Oxf) 1995; 431:325–329.
21. Krohn T, Hanscheid H, Muller B, Behrendt FF, Heinzel A, Mottaghy FM, Verburg FA. Maximum dose rate is a determinant of hypothyroidism after 131
I therapy of Graves’ disease
but the total thyroid absorption dose is not. J Clin Endocrinol Metab 2014; 99:4109–4115.
22. Weetman AP. Radioiodine
treatment for benign thyroid diseases. Clin Endocrinol (Oxf) 2007; 66:757–764.
23. Farrar JJ, Toft AD. Iodine-131 treatment of hyperthyroidism
: current issues. Clin Endocrinol (Oxf) 1991; 35:207–212.
24. Delgrange E, Weber E, Michel L, deCoster P, Buysschaert M, Donckier J. Status of three years of hyperthyroidism
treatment with iodine 131. Acta Clin Belg 1994; 49:200–2007.
25. Peters H, Fischer C, Bogner U, Reiners C, Schleusener H. Radioiodine
therapy of Graves’ hyperthyroidism
: standard vs calculated 131 iodine activity. Results from a prospective, randomised, multicentre study. Eur J Clin Invest 1995; 25:186–193.
26. Buscombe J, Hirji H, Witney-Smith C. Nuclear medicine in the management of thyroid disease. Expert Rev Anticancer Ther 2008; 8:1425–1431.
Keywords:Copyright © 2018 Wolters Kluwer Health, Inc. All rights reserved.
benign thyroid disease; dosimetry; Graves’ disease; hyperthyroidism; radioiodine