Radioiodine Therapy for Multinodular Toxic Goiter FREE

MULTINODULAR goiter is a common cause of hyperthyroidism, especially in areas of mild to moderate iodine deficiency.¹ In these patients, hyperthyroidism cannot be expected to be permanently cured by antithyroid drug treatment. Radiolabeled iodine 131 therapy is in principle an attractive treatment modality, since the suppressed extranodular thyroid tissue is partly protected, and in recent years, the popularity of this treatment has increased. Therefore, it is of great importance to evaluate the long-term effects and possible side effects of this treatment. A 1-year follow-up of 70 patients was published from our department in 1986, demonstrating a 35% reduction of thyroid volume, and hypothyroidism developed in only 1 patient.² Studies evaluating the long-term effects of ¹³¹I treatment in patients with Graves disease,^3- 7 autonomously functioning solitary hot or toxic thyroid nodules,^8- 12 and multinodular nontoxic goiter have been performed.^13- 16 However, few studies^6- 7,17 have described the long-term effects of ¹³¹I treatment in patients with multinodular toxic goiter, and a precise evaluation of the long-term changes in thyroid volume is not available.

We therefore wanted to evaluate the long-term changes in thyroid function and volume using a precise and accurate ultrasonic technique¹⁸ in a large, prospective group of consecutive patients with multinodular toxic goiter treated with ¹³¹I. We used an algorithm for ¹³¹I dose calculation, taking volume and 24-hour ¹³¹I uptake into consideration.

The study population consisted of 130 consecutive patients treated with ¹³¹I for a multinodular toxic goiter and observed for a minimum of 1 year. Sixty-six patients were pretreated with antithyroid drugs, whereas 64 were not. Another 15 patients were treated in this period but were unavailable for follow-up within 12 months (7 were given antithyroid pretreatment). The patients were seen from November 1, 1979, through April 31, 1994. Type of thyroid gland was determined using technetium Tc 99m–pertechnetate scintigraphy and ultrasound, whereas the diagnosis of hyperthyroidism was based on the clinical picture, elevated free triiodothyronine (T₃) index (FT₃I) and/or free thyroxine (T₄) index (FT₄I), and suppressed serum thyrotropin level.

Sixty-six patients received antithyroid drugs before ¹³¹I treatment (propylthiouracil [n=54], methimazole [n=8], and carbimazole [n=4]). In these patients, antithyroid drug treatment was discontinued 5 days before ¹³¹I therapy and not resumed after ¹³¹I treatment. Sixty-four patients did not receive antithyroid pretreatment. Pretreatment was based on the degree of hyperthyroidism and the clinical status of the patients.

Permanent hypothyroidism was defined as decreased FT₄I accompanied by an elevated serum thyrotropin concentration. Euthyroidism was defined as FT₄I and FT₃I within the reference range. The ¹³¹I dose was calculated as 3.7 MBq/g total thyroid mass (evaluated using ultrasound), corrected to 100% uptake of ¹³¹I after 24 hours. The maximum single dose given was 740 MBq.

Serum concentrations of T₄ (reference range, 56-129 nmol/L [4-10 µg/dL]) and T₃ (reference range, 1.0-2.5 nmol/L) and T₃ resin uptake (reference range, 0.80-1.25 arbitrary units) were determined using in-house methods (assay variation was 6%, 10%, and 5%, respectively). The FT₄I (reference range, 62-158 arbitrary units) and FT₃I (reference range, 0.8-2.8 arbitrary units) were calculated as the total hormone concentration times the T₃ resin uptake. Serum concentrations of thyrotropin were determined using different commercial assays as described previously.³ Ultrasonic scanning and calculation of total thyroid volume (reference range, 9.6-27.6 mL) was performed as previously described¹⁸ using a compound scanner (type 3401 and type 1846; Brüel and Kjær, Nærum, Denmark).

Thyroid function variables and the size of the thyroid on ultrasonography were determined before and 34, 112, 3, 6, and 12 months after treatment, and thereafter, once every year. In patients becoming hypothyroid, no further volume or thyroid function data were included in the data evaluation after hypothyroidism was diagnosed.

Results are given as median and range or 25th and 75th percentiles. When percentage of change in thyroid volume is used, the median values of the individual changes are given. For statistical evaluation, Wilcoxon test for paired design, Mann-Whitney test for unpaired design, χ² test, and life-table analysis were used. The level of significance was chosen as P<.05.

Clinical data for the 130 patients are given in Table 1. The median follow-up was 72 months (12-180 months). Patients pretreated with antithyroid drugs did not differ significantly from those not receiving antithyroid pretreatment with regard to age, sex, ¹³¹I dose, follow-up, or the proportion needing more than 1 ¹³¹I dose. The patients receiving antithyroid pretreatment had significantly lower FT₄I and FT₃I at the time of ¹³¹I treatment than patients not receiving antithyroid pretreatment ( Table 1). Thyroid function variables before antithyroid pretreatment were not available in all patients and are therefore not given. The pretreated group had a significantly higher 24-hour ¹³¹I uptake (Table 1). The median initial thyroid volume was higher in the pretreated group (59 mL [16-430 mL] vs 43 mL [18-125 mL]), but the difference was not significant (P=.09; Table 1). However, comparing the initial volume in patients needing more than 1 ¹³¹I dose, a highly significant difference was seen (74 mL [21-430 mL] in the pretreated group vs 47 mL [23-125 mL] in the group not pretreated) (P<.005).

The median initial ¹³¹I dose was 313 MBq (93-925 MBq), whereas the median total dose was 370 MBq (93-1850 MBq). More than 1 dose was given due to persistent hyperthyroidism in 41 patients and to reduce goiter size in 8.

The median time to become euthyroid after ¹³¹I therapy was 5 weeks (range, 3 weeks to 24 months) after the last ¹³¹I treatment (Table 2). There were no significant differences between patients given antithyroid pretreatment and those who were not. Sixty-eight patients (52%) were euthyroid within 3 months after the first ¹³¹I treatment. Eight patients did not become euthyroid after ¹³¹I treatment. Three of these 8 patients had 1 ¹³¹I treatment, 4 patients had 2 treatments, and 1 patient had 3 treatments. These patients did not want subsequent ¹³¹I treatment and were given long-term antithyroid drug treatment.

Median initial thyroid volume was 59 mL (16-430 mL). Twenty-five of the 66 patients were treated with more than 1 ¹³¹I dose. In these patients, ¹³¹I doses not leading to euthyroidism caused a 27% decrease in thyroid volume from a median of 74 mL (21-430 mL) to 50 mL (13-315 mL) (P<.005), and 24 months after the last ¹³¹I dose, a further decrease to 24 mL (8-108 mL) (P<.005). The median volume reduction after more than 1 ¹³¹I dose was 50%. Thyroid volume before and after ¹³¹I therapy in relation to the latest ¹³¹I dose is demonstrated in Figure 1. A gradual 45% reduction from a median of 45 mL (13-315 mL) to 23 mL (8-120 mL) 24 months after treatment was observed (P<.005). Hereafter, no further significant changes were observed. Within the observation period, 11 patients became hypothyroid. In these patients, the median thyroid volume was reduced from 24 mL (17-66 mL) to 16 mL (8-72 mL) at the time when hypothyroidism was diagnosed (P=.01). Within the first 3 months after ¹³¹I therapy, 68% of the total volume reduction was seen.

Median initial thyroid volume was 43 mL (18-125 mL). Twenty-four of the 64 patients were treated with more than 1 ¹³¹I dose. In these patients, ¹³¹I doses not leading to euthyroidism caused a 21% decrease in thyroid volume from a median of 47 mL (23-125 mL) to 44 mL (15-99 mL) (P=.03), and 24 months after the last ¹³¹I dose, a further decrease to 29 mL (8-76 mL) (P<.005). The median volume reduction after more than 1 ¹³¹I dose was 32%. Thyroid volume before and after ¹³¹I therapy in relation to the latest ¹³¹I dose is demonstrated in Figure 2. A gradual 40% reduction from a median of 43 mL (15-115 mL) to 27 mL (8-85 mL) 24 months after treatment was observed (P<.005). Hereafter, no further significant changes were observed. Within the observation period, 3 patients became hypothyroid. In these patients, the median thyroid volume was reduced from 19 mL (15-42 mL) to 10 mL (8-12 mL), measured at the time hypothyroidism was diagnosed. Within the first 3 months after ¹³¹I therapy, 72% of the total volume reduction was seen.

There was no significant difference between the patients receiving and those not receiving antithyroid drug pretreatment in relation to changes in thyroid volume seen after the ¹³¹I dose that cured the hyperthyroidism.

Hypothyroidism occurred significantly more often in patients pretreated with antithyroid drugs (11/66 [17%]) than in those not receiving such treatment (3/64 [5%]) (P=.03). After evaluation using life-table analysis, hypothyroidism was seen in 14% of the entire group within 5 years. Hereafter, no further cases of hypothyroidism occurred. Life-table analysis showed a hypothyroidism rate of 20% within 5 years in patients treated with antithyroid premedication, whereas patients in the group not given antithyroid drug pretreatment had a significantly lower hypothyroidism rate of 6% (P<.005) (Figure 3). Hypothyroidism was diagnosed after a median of 42 months (3-60 months). No significant differences in time to hypothyroidism, time to serum thyrotropin values greater than 4 µIU/mL, and time from these values to hypothyroidism were seen between patients who were given antithyroid drug pretreatment and those who were not (Table 2). In Table 2, 12 patients are described as having serum values of greater than 4 µIU/mL without progression to overt hypothyroidism. These patients had serum thyrotropin values in the range of 5 to 11 µIU/mL during follow-up (in 1 patient, a single measurement of 17 µIU/mL was found). In all patients, FT₄I and FT₃I were within the normal range, with no symptoms of hypothyroidism.

Recurrence of hyperthyroidism after a longer period of euthyroidism without antithyroid drugs was seen in 1 patient treated with 400 MBq of ¹³¹I. The patient was euthyroid with a slightly suppressed serum thyrotropin level for 10 years; then hyperthyroidism recurred and, after a further ¹³¹I dose, the patient again became euthyroid.

None of the patients had symptoms of a radioiodine-induced thyroiditis. An increase (more than 5%) in thyroid volume was seen in 9 patients the first months after ¹³¹I treatment. The median increase was 23% (11%-60%). In these 9 patients, the median thyroid volume was 33 mL (19-133 mL) before treatment. The largest increase was seen in a patient with an initial volume of 28 mL. None of these patients had increased pressure symptoms, and none needed surgical intervention. Three patients had a second ¹³¹I dose, not because of compression symptoms, but because of continued hyperthyroidism.

In 1 patient, a disseminated follicular thyroid carcinoma was diagnosed 3 years after ¹³¹I treatment of 488 MBq. The time from ¹³¹I treatment to the diagnosis of a disseminated thyroid follicular cancer is too short to relate the cancer to the ¹³¹I treatment.

The magnitude of thyroid volume reduction found in our study is of the same order as that seen after ¹³¹I therapy in toxic diffuse³ and autonomous solitary toxic thyroid adenomas^2,12 as well as in nontoxic diffuse^19- 20 and nontoxic multinodular goiter.¹³ As in these long-term follow-up studies,^3,12- 13 we found that the most pronounced reduction is seen within the first 3 months, with a continuous size-reducing effect of ¹³¹I on thyroid volume lasting 2 years. One could speculate that if the ¹³¹I is only taken up in the hyperfunctioning nodules, the reduction in the thyroid volume would be based on the changes in these nodules, leaving the paranodular tissue unaffected with a potential of growth. The result could be a primary reduction of the thyroid volume followed by a reincrease related to growth of the paranodular tissue. We did not see this secondary regrowth of the thyroid volume in a rather long follow-up, indicating that the ¹³¹I affects not only the hyperfunctioning nodules but also the paranodular tissue. To our knowledge, these are the first long-term data on thyroid volume and function in multinodular toxic goiter, using an accurate thyroid size evaluation, and on ¹³¹I therapy, taking thyroid size and ¹³¹I uptake into consideration.

We demonstrated a cumulated risk for hypothyroidism of 14% within 5 years of ¹³¹I therapy. No cases of hypothyroidism were seen beyond 5 years in this follow-up ranging from 1 to 15 years. This pattern of hypothyroidism is different from that seen in patients treated with ¹³¹I for Graves disease. In the latter group, hypothyroidism was seen in approximately 20% within 1 year and thereafter with a constant incidence of 2% to 3% per year, eventually reaching 100% if the patients lived long enough.^3- 5 In our study, the incidence of hypothyroidism is similar to that found in patients with other nonimmunological thyroid diseases such as autonomously functioning solitary thyroid nodules^11- 12 and nontoxic multinodular goiter.¹³ Few published studies have addressed this issue in groups of patients all treated with ¹³¹I for multinodular goiter. Franklyn et al²¹ demonstrated hypothyroidism in 11.4% of 44 patients with a 1-year follow-up. Danaci et al⁶ investigated 21 patients and found a cumulative 5-year hypothyroidism rate of 24%, giving a fixed dose of 444 MBq. Berg et al,⁷ giving a calculated dose of 100 Gy, found that 47% were given thyroxine treatment 48 months after treatment. On the other hand, Wiener,¹⁷ studying 88 patients only, found 1 patient with hypothyroidism in a follow-up ranging from 1 to 17 years (average, 5.3 years).

We found a significantly higher hypothyroidism rate in patients pretreated with antithyroid drugs (20%) compared with patients not given antithyroid premedication (6%). An explanation could be that in patients given antithyroid drugs before ¹³¹I treatment, serum thyrotropin was not suppressed at the time of treatment, and the ¹³¹I was taken up, not only in the hyperfunctioning nodules but in the whole thyroid gland. In a recent study, Hancock et al²² found a significantly higher failure rate in patients treated with propylthiouracil until 4 to 7 days before ¹³¹I therapy for Graves disease compared with patients not given antithyroid pretreatment, or patients whose therapy was discontinued for more than 1 week, suggesting that antithyroid drugs have a radioprotective effect. Corresponding results have been found by us and by others.^21,23 In our study, we could not demonstrate a similar radioprotective effect of antithyroid pretreatment, as evidenced by a similar volume reduction in both groups as well as similar time to achieve euthyroidism and similar fraction of patients needing more than 1 dose of ¹³¹I. However, the patients were not randomized to receive or not receive antithyroid pretreatment. The patients receiving antithyroid drug pretreatment were those with the most severe disease. To illuminate these questions, a randomized prospective study is warranted.

Using a relatively low dose of ¹³¹I calculated according to ¹³¹I uptake and thyroid volume, we found that 52% of our patients were cured within 3 months of therapy. This figure is lower than that found for Graves disease³ and solitary autonomous thyroid nodules,¹² where cure rates of 75% are seen using corresponding doses. However, only 8 patients (6%) were not cured following this regimen. An increase in ¹³¹I dose should theoretically reduce the number of initial failures and thus retreatment, reduce thyroid volume even more, and possibly lead to a higher incidence of hypothyroidism. Again, prospective studies are needed to substantiate this.

A potential major side effect of ¹³¹I treatment is cancer, and several studies have addressed this question.^24- 32 All of these studies conclude that there is no evidence of cancer induced by ¹³¹I, when given in doses to treat benign thyroid diseases in adults. When ¹³¹I treatment is given to patients with Graves disease, all thyroid cells receive a high amount of radiation, which reduces their ability to replicate. In nodular goiter, the paranodular tissue receives only small amounts of radiation, and it has recently been proposed that this tissue would be at risk for subsequent neoplastic transformation.³³ This hypothesis could be supported by the results of a 1998 study by Ron et al,³² in which they found a small but statistically significant increase in thyroid cancer risk in patients with toxic nodular goiter. However, the major increase in mortality was seen in the first 5 years after treatment, indicating that the thyroid cancer was present before ¹³¹I treatment. If this hypothesis was to be correct, one would also expect an increased number of thyroid cancers in patients examined with diagnostic doses of ¹³¹I. It has not been possible to demonstrate such a correlation.²⁷

We saw a cure rate of 52% within 3 months after 1 ¹³¹I treatment for multinodular toxic goiter. One hundred nineteen patients (92%) were cured with 1 or 2 treatments. The median thyroid volume was reduced by 43%, and hypothyroidism was only seen in 14% within 5 years of treatment. Radioiodine, therefore, should be the treatment of choice in these patients.

Accepted for publication October 8, 1998.

This study was supported by grants from Agnes and Knut Mørks Foundation, Copenhagen, Denmark.

Corresponding author: Birte Nygaard, MD, PhD, Department of Endocrinology F112, Herlev Hospital, University of Copenhagen, Herlev Ringvej, DK-2730 Herlev, Denmark (e-mail: birte.nygaard@dadlnet.dk).