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Print version ISSN 0004-2730
Arq Bras Endocrinol Metab vol.53 no.6 São Paulo Aug. 2009
Área sob a curva de TSH após suspensão da levotiroxina versus administração do TSH recombinante humano: possíveis implicações no crescimento tumoral
Pedro Weslley Rosario; Daniela Santos Salles; Saulo Purisch
Departamento de Tireoide, Serviço de Endocrinologia, Santa Casa de Belo Horizonte, Belo Horizonte, MG, Brasil
OBJECTIVE: The levothyroxine withdrawal (L-T4) for some weeks results in prolonged exposure to elevated TSH. In contrast, administration of recombinant human TSH (rhTSH) promotes a short period of hyperthyrotropinemia. The objective of this study was to compare the area under the curve (AUC) of TSH obtained after L-T4 withdrawal versus administration of rhTSH.
METHODS: Thirty patients received 0.9 mg rhTSH for two consecutive days, and 64 were prepared by L-T4 withdrawal for four weeks, with the latter being reintroduced 48 hour after 131I. Measurement of TSH were performed before the first rhTSH ampoule; immediately before and seven and 14 days after 131I; before L-T4 withdrawal; and, weekly, up to two months after 131I.
RESULTS: The AUC obtained after rhTSH was 4.6 times smaller than that obtained after L-T4 withdrawal (532 versus 2,423 mIU/L per day). It should be emphasized that, on average, in the latter group, 58.5% of the AUC corresponded to the period after reintroduction of hormone therapy.
CONCLUSIONS: Surprising difference in the TSH AUC was demonstrated between rhTSH administration versus L-T4 withdrawal.
Keywords: Thyroid neoplasms; tumor growth; recombinant human TSH
OBJETIVO: A suspensão de levotiroxina (L-T4) por algumas semanas resulta em exposição prolongada ao TSH elevado. Em contraste, a administração do TSH recombinante (rhTSH) promove um curto período de hipertirotropinemia. O objetivo deste estudo foi comparar a área sob a curva (do inglês "area under the curve", AUC) do TSH obtida após suspensão da L-T4 versus a administração do rhTSH.
MÉTODOS: Trinta pacientes receberam 0,9 mg de rhTSH por dois dias consecutivos, e 64 foram preparados com suspensão da L-T4 por quatro semanas, com reintrodução dessa terapia 48 horas após o radioiodo. As medidas de TSH foram realizadas antes da primeira ampola de rhTSH; imediatamente antes e sete e 14 dias após o 131I; antes da suspensão da L-T4; e, semanalmente, até dois meses após o 131I.
RESULTADOS: A AUC do TSH obtida após rhTSH foi 4,6 vezes menor do que a alcançada após suspensão da L-T4 (532 versus 2.423 mUI/L ao dia). Enfatiza-se que, em média, no último grupo, 58,5% da AUC correspondeu ao período após a reintrodução da terapia hormonal.
CONCLUSÕES: Surpreendente diferença na AUC do TSH foi demonstrada entre a administração do rhTSH versus suspensão da L-T4.
Descritores: Neoplasias da glândula tireoide; crescimento tumoral; TSH recombinante humano
Stimulation of growth is one of the responses mediated by TSH in the normal thyroid. Well-differentiated tumors (papillary and follicular carcinomas) preserve, at least in part, this property of normal tissue. Therefore, although TSH is not the only stimulus and its effect is influenced by other factors, the role of this hormone in the recurrence of these tumors after surgery seems to be well-defined (1).
The classical preparation for ablation or therapy with 131I, which consists in levothyroxine withdrawal (L-T4) for some weeks, results in prolonged exposure to elevated levels of TSH, even after reintroduction of hormone therapy (2). In contrast, administration of recombinant human TSH (rhTSH) promotes a short period of hyperthyrotropinemia, with the perspective of distinct effects on tumor growth. In the present study, we compared the area under the curve (AUC) of TSH obtained after L-T4 withdrawal versus administration of rhTSH, considering that this is the best approach to evaluate the intensity of the TSH stimulus (3,4).
The characteristics of the patients have been published previously (5). In summary, 94 patients with well-differentiated thyroid carcinoma aged 18-65 years, who had been submitted to total thyroidectomy and presented no apparent disease after surgery, were studied. L-T4 therapy was initiated immediately after thyroidectomy and ablation with radioiodine (3.7 GBq (100 mCi) was performed between eight to ten weeks later. Thirty patients received 0.9 mg rhTSH for two consecutive days, followed by 131I administration on the third day; 64 patients were prepared by L-T4 withdrawal during four weeks (acquisition of rhTSH was not feasible), with the latter being reintroduced 48 hour after 131I administration (5). The groups were similar in terms of gender, age and tumor characteristics; all patients presented uptake in the thyroid bed < 2%, and none of them had distant metastases on RxWBS (5). The study was approved by the Ethics Committee on Research of our Institution (Santa Casa de Belo Horizonte), and the subjects gave written informed consent.
Samples for the measurement of TSH were collected before the first rhTSH ampoule; immediately before and seven and 14 days after 131I administration or before L-T4 withdrawal; and weekly, up to two months after ablation. The AUC values were calculated based on mean TSH levels using a standard trapezoidal model.
TSH was measured with a chemiluminescent assay (Advia Centaur System, Bayer Corporation), with an inter-assay coefficient of variation < 6% for values ranging from 0.26 to 83 mIU/L, and reference values of 0.3 to 5 mIU/L (euthyroid).
Means were compared between groups by the Student's t-test or the nonparametric Mann-Whitney U test. The Fisher exact test or χ2 test was used to detect differences in the proportion of cases. A p-value of less than 0.05 was considered significant.
TSH levels were similar in the two groups before rhTSH administration and before L-T4 withdrawal (TSH < 0.1 mIU/L, 40 versus 37.5%; TSH < 2 mIU/L, 90 versus 92.2%, respectively), but were higher in the rhTSH Group immediately before 131I administration (118 ± 28 versus 85 ± 23 mIU/L, p < 0.05) (5). The average daily L-T4 dose was 178 μg or 2.2 μg/kg, with no difference between groups.
The AUC obtained after rhTSH administration was 4.6 times smaller than that obtained after L-T4 withdrawal (532 versus 2,423 mIU/L per day; p < 0.0001) (Figure 1). The AUC ranged from 305 to 906 mIU/L per day in the rhTSH Group and from 996 to 4,022 mIU/L per day after L-T4 withdrawal. It should be emphasized that, on average, in the latter group, 58.5% (range: 45% to 71%) of the AUC corresponded to the period after reintroduction of hormone therapy.
The intensity of the TSH stimulus on responsive tissues has better evaluation if based on the AUC than when the peak TSH is used (3,4). The AUC was approximately 4.5 times smaller after rhTSH administration than after L-T4 withdrawal for four weeks, even in the presence of higher peak TSH, demonstrating that, if adjusted for the same peak concentration, this difference is even greater. Considering only the period after reintroduction of L-T4, Maini, Sciuto and Tofani (6) reported an AUC (mean TSH) of 2,797 mIU/L per day, for a daily dose of 100 μg, and 1,634 mIU/L per day, for a daily dose of 150 μg. In the present study, this value was 1,415 mIU/L per day, since the patients reinitiated therapy using the same daily L-T4 dose that was previously able to normalize TSH (< 2 mIU/L in > 90% of cases), on average, 178 μg or 2.2 μg/kg. Thus, the administration of daily doses of 100 μg or < 2 μg/kg, unless they were able to normalize or suppress TSH previously, probably resulted in a greater AUC than that demonstrated here. Interestingly, this period (after reintroduction of L-T4) corresponds to the main portion of the TSH AUC but, on this occasion, elevated TSH has no longer any desired purpose since thyroglobulin had already been measured, and radioiodine was taken up by tissues.
The clinical consequences of the difference demonstrated here deserve some comments. With respect to thyroglobulin secretion, the serum levels of this protein are, in fact, lower after rhTSH administration when compared with hypothyroidism, but there is no difference in the sensitivity of detection of metastases (7-9). Even if 131I uptake is lower with rhTSH, other mechanisms, such as a longer effective half-life, guarantee a similar radiation in the target tissue (10,11). In this respect, the efficacy of rhTSH in remnant ablation has been widely demonstrated (5,10,12-15). Thus, the difference in the TSH stimulus does not compromise the efficiency of rhTSH in situations in which its use is suggested and recommended (3,8,9).
On the other hand, the lower TSH stimulus associated with the administration of rhTSH may have implications in tumor growth. The impact of this difference might be dramatic in patients with known metastases, but there is no comparative studies about the efficacy of rhTSH versus hypothyroidism in this group; rhTSH has still not been approved for this purpose. The advantage of rhTSH in providing a smaller AUC of TSH is only explored in cases of metastases at critical sites, in which tumor expansion is limited and L-T4 withdrawal would increase the chance of severe symptomatic growth (3,8,9). Although possible, the increase of metastases after administration of rhTSH results from edema and intralesional hemorrhage and is probably prevented by preparation with corticosteroids (8). In thyroid remnant ablation, although not presenting apparent disease, some patients are at high risk of persistent occult metastases (16,17). These patients may particularly benefit from preparation with rhTSH by preventing the progression of these metastases with a TSH stimulus, that is much lower than that obtained with L-T4 withdrawal.
Although the efficacy of rhTSH in stimulating serum thyroglobulin and in the ablation of thyroid remnants has been well-documented in the literature, the surprising difference in the TSH AUC demonstrated between rhTSH administration and L-T4 withdrawal suggests the perspective of distinct effects on tumor growth and indicates an interesting potential advantage of preparation with rhTSH.
Acknowledgements: this study was not supported by research funds.
Disclosure: no potential conflict of interest relevant to this article was reported.
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Pedro Weslley Rosario
Centro de Estudos e Pesquisa
Clínica de Endocrinologia e Metabologia (Cepcem)
Av. Francisco Sales, 1.111, 5ºD - Santa Efigênia
30150-221 - Belo Horizonte, MG, Brasil
Received in Feb/25/2009
Accepted in June/2/2009