OBJECTIVE: Evaluate the efficacy of cumulative doses (CDs) of 131I-iodide therapy (RIT) in differentiated thyroid cancer (DTC). SUBJECTS AND METHODS: The probability of progressive disease according to CDs was evaluated in patients < 45 years old and > 45 years old and correlated to tumor-node-metastasis (TNM), thyroglobulin values, histological types and variants, age, and zduration of the disease. RESULTS: At the end of a follow-up period of 69 ± 56 months, 85 out of 150 DTC patients submitted to fixed doses RIT had no evidence of disease, 47 had stable disease and 18 had progressive disease. Higher CDs were used in the more aggressive variants (p < 0.0001), higher TNM stages (p < 0.0001), and follicular carcinomas (p = 0.0034). Probability of disease progression was higher with CDs > 600 mCi in patients > 45 years old and with CDs > 800 mCi in patients < 45 years. CONCLUSION: Although some patients may still respond to high CDs, the impact of further RIT should be carefully evaluated and other treatment strategies may be warranted.
Cumulative dose; radioiodine therapy; 131I-iodide; differentiated thyroid cancer
OBJETIVO: Avaliar a eficácia de doses cumulativas (DCs) da terapia com iodeto-131I (RIT) no câncer diferenciado de tiroide (CDT). SUJEITOS E MÉTODOS: A probabilidade de doença em progressão conforme a DC foi calculada em pacientes com idade < 45 e > 45 anos e correlacionada com o TNM, valores de tiroglobulina sérica, tipos histológicos e variantes, idade e tempo de doença. RESULTADOS: Ao final de um seguimento de 69 ± 56 meses, 85 dos 150 pacientes CDT submetidos a doses fixas de RIT não tinham evidência de doença, 47 tinham doença estável e 18, doença progressiva. DCs mais elevadas foram usadas nas variantes agressivas (p < 0,0001), maior estágio TNM (p < 0,0001) e nos carcinomas foliculares (p = 0,0034). A probabilidade de doença em progressão foi maior com DCs > 600 mCi em pacientes > 45 anos e com DCs > 800 mCi em pacientes < 45 anos. CONCLUSÃO: Apesar de alguns pacientes ainda responderem a altas DCs, o impacto de RITs deve ser cuidadosamente avaliado e outras estratégias terapêuticas devem ser consideradas.
Dose cumulativa; radioiodoterapia; iodeto-131I; carcinoma diferenciado de tiroide
Cumulative doses of radioiodine in the treatment of differentiated thyroid carcinoma: knowing when to stop
Doses cumulativas de iodo radioativo no tratamento do carcinoma diferenciado de tireoide: sabendo a hora de parar
Raul Martins-FilhoI; Laura S. WardII; Barbara J. AmorimI; Allan O. SantosI; Mariana C. L. de LimaI; Celso D. RamosI; Patricia S. MatosIII; Lígia V. M. AssumpçãoIV; Edwaldo E. CamargoI; Elba C. S. C. EtchebehereI
IDivision of Nuclear Medicine, Faculdade de Ciências Médicas, Universidade Estadual de Campinas (FCM/Unicamp), São Paulo, SP, Brazil
IILaboratory of Cancer Molecular Genetics, FCM/Unicamp, São Paulo, SP, Brazil
IIIDepartment of Pathology, FCM/ Unicamp, São Paulo, SP, Brazil
IVDivision of Endocrinology, FCM/ Unicamp, São Paulo, SP, Brazil
OBJECTIVE: Evaluate the efficacy of cumulative doses (CDs) of 131I-iodide therapy (RIT) in differentiated thyroid cancer (DTC).
SUBJECTS AND METHODS: The probability of progressive disease according to CDs was evaluated in patients < 45 years old and > 45 years old and correlated to tumor-node-metastasis (TNM), thyroglobulin values, histological types and variants, age, and zduration of the disease.
RESULTS: At the end of a follow-up period of 69 ± 56 months, 85 out of 150 DTC patients submitted to fixed doses RIT had no evidence of disease, 47 had stable disease and 18 had progressive disease. Higher CDs were used in the more aggressive variants (p < 0.0001), higher TNM stages (p < 0.0001), and follicular carcinomas (p = 0.0034). Probability of disease progression was higher with CDs > 600 mCi in patients > 45 years old and with CDs > 800 mCi in patients < 45 years.
CONCLUSION: Although some patients may still respond to high CDs, the impact of further RIT should be carefully evaluated and other treatment strategies may be warranted.
Keywords: Cumulative dose; radioiodine therapy; 131I-iodide; differentiated thyroid cancer.
OBJETIVO: Avaliar a eficácia de doses cumulativas (DCs) da terapia com iodeto-131I (RIT) no câncer diferenciado de tiroide (CDT).
SUJEITOS E MÉTODOS: A probabilidade de doença em progressão conforme a DC foi calculada em pacientes com idade < 45 e > 45 anos e correlacionada com o TNM, valores de tiroglobulina sérica, tipos histológicos e variantes, idade e tempo de doença.
RESULTADOS: Ao final de um seguimento de 69 ± 56 meses, 85 dos 150 pacientes CDT submetidos a doses fixas de RIT não tinham evidência de doença, 47 tinham doença estável e 18, doença progressiva. DCs mais elevadas foram usadas nas variantes agressivas (p < 0,0001), maior estágio TNM (p < 0,0001) e nos carcinomas foliculares (p = 0,0034). A probabilidade de doença em progressão foi maior com DCs > 600 mCi em pacientes > 45 anos e com DCs > 800 mCi em pacientes < 45 anos.
CONCLUSÃO: Apesar de alguns pacientes ainda responderem a altas DCs, o impacto de RITs deve ser cuidadosamente avaliado e outras estratégias terapêuticas devem ser consideradas.
Descritores: Dose cumulativa; radioiodoterapia; iodeto-131I; carcinoma diferenciado de tiroide.
Differentiated thyroid cancer incidence has been rising all over the world and recent data demonstrate that rates have also increased for large and aggressive tumors diagnosed with distant metastasis (SEER stage) (1-3). Standard treatment for DTC patients includes total or near-total thyroidectomy followed by adjuvant radioiodine therapy (RIT) to destroy remnant, benign or malignant thyroid tissue (4-6). Two methods are widely available: the so-called fixed empirical method currently used by most medical services, and the dosimetric method. There is still no evidence of a clear advantage of one method over the other for the calculation of the administered dose (7).
The majority of patients with DTC have a good prognosis and high cure rates (8.9). However, the disease persists or recurs with a considerable impact on quality of life in up to 60% of the patients (8,9). Depending on the course of the disease additional treatments using radioiodine may become necessary. As long as metastases and recurrences are radioiodine-avid, it is the most effective treatment option and high response rates are achievable (10). Unfortunately, approximately 15% of these patients do not respond to RIT (8-11). Improved survival is associated with responsiveness to RIT (12).
There is no pre-established timing in the literature of when to stop RIT. Limits to 1,000 mCi have been suggested; however, they are empirical and do not consider all variables such as stage, tumor histology, age, tumor marker levels, clinical course, side effects and quality of life during RIT (5-7,12,13). Thus, many patients are submitted to cumulative doses of up to 2 Ci, however, the actual benefit of this is questionable.
The aim of this study was to evaluate the efficacy of RIT in DTC regarding cumulative doses and its relationship with the clinical course, primary tumor histology, stage, age and serum thyroglobulin (Tg) levels.
MATERIAL AND METHODS
This retrospective case-control study was approved by the Research Ethics Committee of the Faculty of Medical Sciences Universidade Estadual de Campinas (FCM-Unicamp). We analyzed the records of 232 DTC patients who were submitted to RIT with 131I-iodide. After excluding patients with incomplete data, 150 patients were selected for the study (125 women; mean age of 44.3 ± 14.6 years).
All patients were managed according to a standard protocol which included total thyroidectomy. Patients with preoperatively or intraoperatively palpable neck node metastases underwent regional neck dissection. At the time of the initial treatment, surgical specimen was analyzed and classified according to the WHO classification, and patients were classified according to the sixth edition of the The American Joint Committee on Cancer (AJCC)/ International Union Against Cancer (UICC) TNM (14).
Radioiodine therapy (RIT)
RITs were performed with fixed doses, as follows: 3,700 MBq (100 mCi) for thyroid remnants, 5,550 MBq (150 mCi) for lymph node metastases, 7,400 MBq (200 mCi) for pulmonary metastases, 11,100 MBq (300 mCi) for bone metastases.
In patients who required second or third RIT the decision on the new dose was based on the location of the metastases, on the dose previously administered, on persistently elevated Tg levels (with or without positive WBI), and to some extent on tumor volume, normally adding 925 MBq to 1,850 MBq (25-50 mCi) to the new dose. For example, a patient with thyroid remnants after total thyroidectomy without lymph node metastases would initially receive 3,700 MBq (100 mCi) of 131I-iodide. If this patient presented with persistent thyroid remnants on follow-up scans, without lymph node metastases, another RIT would be performed with 4,625 5,550 MBq (125-150 mCi) of 131I-iodide. However, if this same patient required a new treatment due to the appearance of bone metastasis in follow-up, RIT would be performed with 11,100 MBq (300 mCi).
Lymph node metastases were diagnosed after total thyroidectomy with cervical neck dissection or during follow-up.
Patient follow-up ranged from 19 to 383 months (mean 69 ± 56 months, median 49.15 months). According to a routine protocol, follow-up included periodic total body scans, serum TSH and Tg measurements, as well as other eventual procedures to detect distant metastasis, including cervical ultrasound, chest CT, whole body iodide scan (WBI), whole body 99mTc- sestamibi scan (after the year 1992), 18F-FDG PET/CT (after the year 2007), and biopsy. Stimulated Tg levels were obtained when whole body scans (WBS) were performed. A first serum Tg result (Tg1) was obtained before patients underwent the first RIT, the second Tg (Tg2) was obtained after a second RIT (when indicated), and the same criterion was considered for the third (Tg3), fourth (Tg4) and ensuing Tg measurements. Using these parameters disease status was classified as: no evidence of disease (NED), stable disease (SD) and progressive disease (PD). This classification was established when the maximum tolerated dose for each patient was determined. There was no variation of this classification during the study.
NED was established as: undetectable Tg levels (with or without levothyroxine suppression), two consecutive WBI scans without local-regional uptake or distant metastases; other imaging studies (cervical ultrasounds, chest CTs, whole body 99mTc-sestamibi scans, 18F-FDG PET/CT scans) without evidence of disease; suppressed serum Tg level < 2.0 ng/mL and stimulated serum Tg level < 10.0 ng/mL.
SD was established as: unaltered Tg levels, persistent cervical uptake and/or metastases in annual WBI, suppressed serum Tg level > 2.0 ng/mL or serum Tg level > 10.0 ng/mL but without progressive elevation and no new metastatic foci.
PD was established as: increasing serum Tg levels despite RIT and/or new metastatic foci detected by imaging studies. Patients with PD were treated surgically whenever possible whether the metastases were loco-regional or distant. This approach was performed in order to improve the efficacy of RIT (15).
Table 1 summarizes median Tg levels and RIT doses administered to patients after the corresponding evaluation.
Seven patients with PD had non-avid radioiodine metastasis and one patient died after 8 years of DTC diagnosis, due to a second primary tumor. This patient had received a CD of 300 mCi.
The chi-squared test or the Fisher's exact test was performed in order to verify associations or compare proportions. The Mann-Whitney test was applied to compare continuous variables between two groups. For three or more variables among groups, the Kruskal - Wallis test followed by the Tukey's test was used to locate these differences. Spearman's linear coefficient was applied to verify the relationship among continuous variables. A multiple logistic regression analysis adjusting age and follow-up time was used to identify factors associated with the evidence of disease. In order to calculate the estimated probability of disease status (NED, SD or PD), we created a model that took into account the age (above or below 45 years) and the cumulative dose. The significance level applied was 5%.
Papillary carcinomas (PC) were found in 125 cases and follicular carcinomas (FC) in the remaining 25 cases. An experienced pathologist (PSM) classified the tumors as "classic DTC" (116 cases) or as having an "aggressive histology"; the latter included 34 patients (22.7%) presenting Hürthle cell, invasive FC, tall cell variant, diffuse sclerosis variant or columnar cell variant of PC. Eighty-five cases (56.7%) were considered a TNM stage I, 28 were stage II (18.7%); 14 stage III (9.3%), and 23 stage IV (15.3%). Table 2 summarizes the patient data.
Eighty-five out of the 150 patients (56.7%) were classified as NED; 47 patients had SD (31.3%), and the remaining 18 patients had PD (12.0%).
Tg1 levels ranged from 0 to 6,000 ng/mL; Tg2 levels were obtained in 71 patients and ranged from 0.2 ng/mL to 6,000 ng/mL; Tg3 levels were obtained in 31 patients and ranged from 0.2 ng/mL to 3,000 ng/ mL, and Tg4 levels were obtained in 11 patients and also ranged from 0.2 ng/mL to 3,000 ng/mL.
Among the 49 patients with Tg1 levels above 10 ng/ mL that evolved with NED, in 7 patients this occurred after the first RIT dose while 42 patients required more treatment sessions. Thus, RIT was completely effective in treating thyroid remnants in 14% of the cases and was effective treating the actual disease in 86% of the patients.
After the first RIT, 79 patients were deemed with SD or NED. Hence, the RIT was effective and no new treatment was necessary for these cases. Tg levels ranged from 0 to 86 ng/mL in this group. The remaining 71 patients required a second RIT. After the second RIT, 40 patients were considered with SD or NED and their Tg levels ranged from 0 to 516 ng/mL. The remaining 31 patients required a third RIT. After the third RIT, 20 patients were classified as presenting SD or NED and their Tg levels ranged from 0 to 170 ng/ mL. The remaining 11 patients required a fourth RIT.
A striking response was seen in a few patients with high serum Tg levels. Six out of the 150 patients had Tg1 levels above 500 ng/mL. All 6 patients presented with pulmonary metastases although in 2 of them the WBI scans were negative. The only patient with Tg1 above 6,000 ng/mL had bone and pulmonary metastases. Among the 6 patients that had serum Tg1 levels > 500 ng/mL after a second RIT, two patients responded to RIT treatment and 4 patients maintained Tg2 levels above 700 ng/mL and pulmonary metastases. Among these 4 patients with serum Tg2 levels > 700 ng/mL one patient responded to RIT and the remaining 3 maintained serum Tg levels above 500 ng/mL (two with pulmonary metastases and one with a mediastinal lymph node).
Table 3 summarizes the positive associations confirmed by a multiple logistic regression analysis that showed the disease status was associated with the TNM stage and age on the occasion of diagnosis, with the initial stimulated serum Tg levels and with the cumulative dose.
Higher cumulative doses were used in the more aggressive histologic variants (p < 0.0001), higher TNM stage tumors (p < 0.0001), and follicular carcinomas (p = 0.0034), while no association was observed with gender (p = 0.1469). Patients with aggressive histologic variants received almost twice the dose (464 ± 318 mCi) of the non-aggressive variants (240 ± 192 mCi;p < 0.0001). The highest cumulative dose given in this group was 1,100 mCi.
The statistic model was created in order to estimate the probability of disease status (RD, SD or PD) according to the cumulative dose in patients above and below 45 years of age and is displayed in figures 1 and 2.
There are many studies discussing clinical, pathological and molecular factors related to the prognosis of DTC. However, only a few authors have focused on the impact of the cumulative dose of RIT. The relatively long follow-up period in the present study (up to 32 years) has made it possible to evaluate tumor behavior compared to RIT cumulative doses and their effect on survival. As expected, patients with higher serum Tg levels during the course of the disease had progressive disease and therefore required higher and more frequent therapeutic 131I-iodide doses. Also, in accordance to others, we observed that patients with Hürthle cell, invasive FC, tall cell, diffuse sclerosis variant, columnar cells had the worst prognosis (16). These variants have high vascularity and therefore have a higher risk of hematogenic spread. They also frequently present metastases at diagnosis (16), which explains why these patients had PD and therefore significant higher cumulative doses of RIT. The association between cumulative dose and TNM stage was also expected considering that the higher stages (III and IV) have a worse prognosis (17,18). However, there are conflicting reports in the literature regarding the influence of the histological type (PC vs. FC) on DTC prognosis (19). Mazzaferri and cols. reported similar progression rates when distant metastases were excluded at diagnosis, with FC and PC similar mortality rates (10% vs. 6%, p = N/S) (20).
Patients with higher staging (III and IV), above 45 years of age, and aggressive variants have a worse prognosis, greater chances of local recurrence and distant metastases, and require higher and more RIT doses. Consequently, higher cumulative doses are seen in this subgroup of patients as the endpoint is prolonging overall survival. In order to estimate the probability of the possible outcome of these patients, a probability model was created. The estimated probability model was designed to evaluate the relationship between cumulative dose and disease status and thus determine a specific cumulative dose for which the probability of disease progression would be high despite the RIT dose. With our patient population, based on this model, we may suppose that a patient below the age of 45 years has approximately 70% chance of complete remission of the disease with a cumulative dose of only 100 mCi while the same patient, if requiring cumulative doses in the 1 Ci range may still have a 27% chance of stabilizing the disease.
We observed that there is a high probability of disease progression with cumulative doses of 600 mCi in patients above 45 years of age, although a few individuals do respond to cumulative doses above 1,000 mCi. The disease will only continue to progress in younger patients (< 45 years) with higher cumulative doses (800 mCi or higher), despite the fact that some patients may still respond to cumulative doses above 1,000 mCi.
A recent study of 77 DTC patients with distant metastases followed-up for a median of 6.1 years reported similar data concluding that age had significantly greater influence on survival than iodine avidity (21,22).
The evaluation of Tg levels throughout this long period of time is challenging and some variability existed since new techniques with less false negative results have emerged throughout the years. Reference values were determined according to the period in which they were analyzed and in patients in whom these values were discrepant with history and imaging studies, new analyses were performed. Treatment strategies were always based on discussion with a multidisciplinary team to minimize possible discrepancies (23).
Unfortunately, we were not able to evaluate the impact on overall survival vs. cumulative dose since the mean follow-up time was below 10 years. A longer follow-up time with a larger number of patients is necessary in order to evaluate the impact of this information on patient management.
In conclusion, although there is no actual cutoff point indicating when RIT should not be considered for therapy, these data indicate caution in patients above 45 years old receiving cumulative doses higher than 600 mCi, as well as in younger patients who have already received cumulative doses above 800 mCi. Although some patients may still respond to cumulative doses above these levels, we should carefully evaluate the impact of further RIT on their quality of life considering the disease progression rate in between treatments and the availability of other measures, including surgical excision of metastasis, ethanol ablation, chemo-embolization or the emerging targeted molecular therapies.
Disclosure: no potential conflict of interest relevant to this article was reported.
Received on May/17/2010
Accepted on Nov/3/2010
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Correspondence to:Elba C. S. C.Etchebehere Serviço de Medicina NuclearHospital de Clínicas, UnicampAv. Zeferino Vaz, s/nCaixa postal 6142 13081-970 − Campinas, SP, Brazil
Publication in this collection
08 Feb 2011
Date of issue
17 May 2010
03 Nov 2010