Preoperative serum thyroglobulin concentration as a predictive factor of malignancy in small follicular and Hürthle cell neoplasms of the thyroid gland

Thyroid nodules are a common clinical problem [1], and harbor thyroid cancer in 5% to 15% of cases [2]. A thyroid nodule is most accurately evaluated by an ultrasound-guided fine-needle aspiration biopsy (FNAB) [1]. However, in the preoperative diagnosis of follicular and Hürthle cell tumors, FNAB has limited usefulness [3‐5]. In follicular and Hürthle cell tumors, malignancy is confirmed by demonstration of transcapsular or vascular invasion, which cannot be seen on cytologic slides [3, 6‐9]. In follicular or Hürthle cell neoplasms, cytology cannot distinguish a malignant tumor from a benign one [8, 9]. Confirmation of malignancy is possible only with histological examination of the tumor. Therefore, patients with an FNAB-proven follicular or Hürthle cell neoplasm should be treated surgically. Unfortunately, intraoperative frozen-section analysis is not reliable and does not affect intraoperative decision-making [10, 11].

In the case of a follicular or Hürthle cell neoplasm, the American Thyroid Association guidelines recommend a lobectomy or total thyroidectomy [1]. Total thyroidectomy is preferable in patients who have bilateral nodular disease, who have large tumors (>4 cm), when marked atypia is seen on the biopsy, or who prefer to undergo bilateral thyroidectomy to avoid the possibility of requiring future surgery on the contralateral lobe [1]. A completion of thyroidectomy may be necessary if malignancy is confirmed by histologic examination after a lobectomy [1]. Reliable predictive factors for malignancy are needed, to decrease the number of thyroid reoperations [12‐14].

The levels of thyroglobulin (Tg) can be elevated in many thyroid diseases [1, 15]. So, according to the European and American Thyroid Associations, preoperative Tg measurement is an insensitive and non-specific diagnostic test for thyroid cancer [1, 15]. In subjects with mild-to-moderate iodine deficiency, the serum Tg concentration correlates with the size of the goiter, the presence of multinodularity and intake of iodine [16]. Furthermore, the thyroid volume, as well as the Tg concentration, is inversely related to iodine intake [16]. However, our previous studies in patients with large follicular or Hürthle cell neoplasms (median size 3 cm) showed that measurement of the preoperative serum Tg concentration may represent a useful preoperative diagnostic test. Namely, the concentration of serum Tg was higher in follicular and Hürthle cell cancers than in benign neoplasms [12‐14]. However, the majority of thyroid neoplasms are smaller than 2 cm [17]. The aim of our retrospective study was to find out if serum Tg is a predictive factor for malignancy in follicular or Hürthle cell neoplasms with a diameter of 2 cm or less.

The median age of the patients, tumor size, volume of the thyroid gland, median and mean concentration of preoperative Tg were 52 years (range, 9 to 82), 1.5 cm (range, 0.4 to 2), 20 ml (range, 5 to 162), 50 ng/ml (range, 1 to 3,424), and 125 (range 1 to 3,424) ng/ml, respectively. The histopathologic diagnoses were carcinoma, adenoma, and benign goiter in 62 (25.5%), 115 (47%), and 67 (27.5%) patients, respectively.

The median age of patients with carcinoma was 52.5 years, while the median age of those with a benign disease was 52 years. The median size of the tumor was 1.55 cm in patients with carcinoma and 1.5 cm in those with a benign disease. Tumor diameter did not correlate with malignancy rate (P = 0.225). These data are presented in Table 2 and Figures 1 and 2.

The median preoperative Tg concentrations in patients with and without carcinoma were 86 and 41 ng/ml, respectively. The mean preoperative Tg concentrations in patients with and without carcinoma were 215 and 95 ng/ml, respectively. The median preoperative Tg concentrations in benign tumors, papillary carcinomas, follicular carcinomas, and Hürthle cell carcinomas were 41, 87, 72, and 106 ng/ml (P < 0.05), respectively. The mean preoperative Tg concentrations in benign tumors, papillary carcinomas, follicular carcinomas, and Hürthle cell carcinomas were 95, 147, 433, and 269 ng/ml (P < 0.001), respectively. Tg concentrations in different types of carcinoma in the dominant nodule are listed in Table 3. As shown by logistic regression analysis, concentration of Tg (cut-off point of 80 ng/ml) was an independent predictive factor. The ROC analysis showed that the area under the curve was 0.613 (P = 0.008). The sensitivity and specificity of the test, positive predictive value, and negative predictive value (cut-off = Tg concentration of 80 ng/ml) for the presence of carcinomas in small follicular and Hürthle cell neoplasms of the thyroid gland were 54.8%, 31.1%, 35.4%, and 81%, respectively.

Predictive factors for malignancy in follicular or Hürthle cell neoplasms as shown by the chi-square test were: sex, volume of the thyroid gland, and Tg concentration (Table 1). The independent predictors of malignancy as shown by multivariate logistic regression were: sex and preoperative Tg concentration (Table 4). Male patients had a higher risk of carcinoma than female patients (odds ratio, 2.57). In male patients, the malignancy rate was 43%, while in female patients, it was 23%. Patients with a preoperative Tg concentration of 80 ng/ml or higher had a higher risk of malignancy than those with a lower concentration (odds ratio, 2.35). In patients with a Tg concentration of 80 ng/ml or more, the malignancy rate was 35%, while in those with a smaller Tg concentration, it was 19%.

Incidental carcinoma in a non-dominant tumor was detected in 13 patients. It was detected in patients with a benign disease and carcinoma of the dominant nodule in 9 (5%) and 4 (6%) of cases, respectively. In patients with carcinoma in the dominant nodule, final pathology additionally revealed a benign goiter, benign adenoma, and thyroiditis in 21, 10, and 27 cases, respectively.

The following predictive factors of malignancy have been reported in the literature [5, 13, 14, 17‐41]: the patient’s age [18, 19, 24, 25, 30‐33] and sex [5, 26], the tumor size [5, 18, 20‐22, 24‐26, 31‐36, 42], a solitary nodule [24, 26, 27], tumor fixation [25], a lesion that feels hard on palpation [27], Tg concentration [13, 14, 18], ultrasound characteristics [17, 27‐29, 41], cytologic characteristic [21], and gene expression diagnostic markers [37‐40]. Ultrasound characteristics predictive of malignancy are: the presence of internal blood flow (as detected by Doppler ultrasonography), the presence of hypervascularity, a solid echo structure, a hypoechoic lesion, or microcalcifications [17, 27‐29, 41]. New cytologic characteristics were also reported as factors predictive of malignancy: transgressing vessel [21] and nuclear grooves [21]. New gene expression diagnostic markers of malignancy are: miR-100, miR-125b, miR-138, miR-768-3p, miRNA-885-5p, and a combination of genes PVALB and C1orf24 [37‐40]. However, a vast majority of reports on predictive factors in follicular or Hürthle cell neoplasms included only a small number of patients; thus, the authors of these studies could perform only a univariate statistical analysis. To our knowledge, so far only eight publications [13, 14, 17, 18, 21, 25, 26, 41] have reported the results of multivariate logistic regression analysis of predictive factors in patients with follicular or Hürthle cell neoplasms.

Carcangiu et al. [30], Lopez-Penabad et al. [31], Taneri et al. [32], and Zhang et al. [33] stated that patients with carcinoma were older than those with a benign disease. However, the median age of our patients with carcinoma was not statistically different from the median age of those with a benign disease (52.5 years versus 52 years). Our findings are in agreement with the majority of reports from the literature.

Mihai et al. [5] and Tuttle et al. [26] found that the risk of carcinoma was higher in men than in women. This is in agreement with the findings of our study. In our study, men had a higher risk of carcinoma than women (an odds ratio of 2.57). The malignancy rate in men in our study was 43%, while in women it was 23%.

Many authors reported that the size of follicular neoplasms increases the risk of malignancy [5, 18, 20‐22, 24‐26, 28, 31‐36, 42]. Tuttle et al. [26] reported that the risk of carcinoma in a tumor larger than 4 cm was 40%, while in smaller tumors it was only 13%. In our patients with a tumor diameter of 2 cm or less, the risk of carcinoma was 25.5%. In Hürthle cell neoplasms, Taneri et al. [32] found that there was no malignancy among the tumors less than 1 cm in diameter. But our findings are quite the opposite. In our patients, the malignancy rate did not differ in patients with a tumor diameter of 1 cm or less versus bigger tumors (Table 1).

Hocevar and Auersperg [12] found that preoperative Tg concentration was higher in patients with follicular and Hürthle cell carcinoma than in patients with benign tumors. In Hürthle cell neoplasms, Sugino et al. [42] reported that in patients with carcinoma and benign disease the median Tg concentration was 1,782 ng/ml and 573 ng/ml, respectively. Strazisar et al. [14] and Petric et al. [13] reported that there was a statistical difference in preoperative Tg concentrations of benign tumors, papillary carcinomas, follicular carcinomas, and Hürthle cell carcinomas. Moreover, the results of the present study show that the mean preoperative Tg concentration was significantly different (P < 0.05) in benign tumors, papillary carcinomas, follicular carcinomas, and Hürthle cell carcinomas. The median preoperative Tg concentrations in benign tumors, papillary carcinomas, follicular carcinomas, and Hürthle cell carcinomas were 41, 87, 72, and 106 ng/ml, respectively. However, in contrast to our findings, Suh et al. [23] found, in only 39 patients with follicular or Hürthle cell neoplasms, that Tg was not an independent risk factor [23]. The median preoperative levels of the Tg serum were, in patients with malignant and in patients with benign tumors, 135 ng/ml and 116 ng/ml, respectively [23]. Their patients had bigger tumors than did the patients from our present study. Their patients’ Tg concentrations were larger than ours, probably because the median tumor size of their patients was bigger than in our study. The median diameter of their malignant and benign tumors was 2.8 cm and 2.4 cm, respectively.

The aim of this study was to find out whether Tg is a predictive factor of malignancy in 244 small (2 cm or less) follicular or Hürthle cell neoplasms. In our study, the concentration of Tg was an independent predictive factor of malignancy. Patients with a preoperative Tg concentration of at least 80 ng/ml had a higher risk of malignancy than those with a lower concentration (an odds ratio of 2.35). In patients with a Tg concentration of 80 ng/ml or more, the malignancy rate was 35%, while in those with a smaller Tg concentration, it was only 19%. We believe that determination of Tg concentration may be one of the factors that are useful in follicular or Hürthle cell neoplasms before determining the extent of the thyroid surgical procedure.

The malignancy rate in this study of 244 patients with follicular or Hürthle cell neoplasms with a tumor diameter of 2 cm or less was 25.5%. The independent predictors of malignancy in follicular or Hürthle cell neoplasms are: sex and preoperative Tg concentration.