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Serum positive thyroglobulin antibodies: an old problem with new questions

INTRODUCTION

Serum thyroglobulin (Tg) is a cornerstone on the follow up of differentiated thyroid cancer (DTC) and is widely used for diagnostic and prognostic purposes (11. Haugen BR, Alexander EK, Bible KC, Doherty GM, Mandel SJ, Nikiforov YE, et al. 2015 American Thyroid Association Management Guidelines for Adult Patients with Thyroid Nodules and Differentiated Thyroid Cancer: The American Thyroid Association Guidelines Task Force on Thyroid Nodules and Differentiated Thyroid Cancer. Thyroid. 2016;26(1):1-133.). Some factors might interfere in the measurement, being the most common the presence of thyroglobulin antibodies (TgAB) (22. Spencer C, Petrovic I, Fatemi S, LoPresti J. Serum thyroglobulin (Tg) monitoring of patients with differentiated thyroid cancer using sensitive (second-generation) immunometric assays can be disrupted by false-negative and false-positive serum thyroglobulin autoantibody misclassifications. J Clin Endocrinol Metab. 2014;99(12):4589-99.). This is known to happen in nearly one third of patients. In this scenario, image modalities become even more important during follow up as serum Tg measurement in not reliable and TgAB absolute values and/or TgAB’s curve over time is not as accurate. Furthermore, it is also known that lymph node metastasis can be found in more than 50% of patients at diagnosis and it is the most common site of persistence/recurrence of disease (11. Haugen BR, Alexander EK, Bible KC, Doherty GM, Mandel SJ, Nikiforov YE, et al. 2015 American Thyroid Association Management Guidelines for Adult Patients with Thyroid Nodules and Differentiated Thyroid Cancer: The American Thyroid Association Guidelines Task Force on Thyroid Nodules and Differentiated Thyroid Cancer. Thyroid. 2016;26(1):1-133.). The appropriate initial surgical procedure can lower the frequency of persistence/recurrence of lymph node metastatic disease.

In addition to a well-performed neck ultrasound, the ultrasound guided fine needle aspiration biopsy (FNAB) should be performed in every suspicious lymph node in order to confirm malignancy. As these biopsies still carry up to 10% of false negative results (33. Ahuja AT, Chow L, Chick W, King W, Metreweli C. Metastatic cervical nodes in papillary carcinoma of the thyroid: ultrasound and histological correlation. Clin Radiol. 1995;50(4):229-31.) recommended to measure Tg levels in needle washouts (Tg-FNAB). Therefore, another issue came up during the last couple of years: does the presence of serum TgAB interfere with the measurement of Tg-FNAB as they are present also in the washouts?

METHODS

Martins-Costa and cols. (44. Martins-Costa MC, Maciel RMB, Kasamatsu TS, Nakabashi CCD, Camacho CP, Crispim F, et al. Clinical impact of thyroglobulin (Tg) and Tg autoantibody (TgAb) measurements in needle washouts of neck lymph node biopsies with papillary thyroid carcinoma. Arch Endocrinol Metab. 2017;61(2):108-14.), assessed 232 FNAB samples obtained from suspicious lymph neck nodes from 144 DTC patients. Regular cytology, Tg-FNAB, TgAB in the washouts and also serum Tg and TgAB were performed in all patients. They have used the literature-validated cutoffs. Tg-FNAB was performed using a commercially available assay with functional sensitivity of 1.0 ng/mL and if Tg-FNAB was lower than 10 ng/mL and patient had serum Tg AB positivity, another assay with lower sensitivity was used to exclude contamination by TgAB.

RESULTS

Patients were divided into two groups: group 1 (203 FNAB samples): serum negative TgAB and group 2 (29 FNAB samples): serum positive TgAB. In the first group, all patients with Tg-FNAB > 10 ng/mL had metastatic disease confirm by histology or I131 uptake, however, only 57% had positive cytology. When Tg-FNAB was < 10 ng/mL, only 10% had confirm metastatic disease and FNAB was able to identify only 2%. In group 2, when Tg-FNAB was above 10 ng/mL, also all patients had confirmed metastatic disease and positive cytology but when less than 10 ng/mL, around 45% had confirmed metastatic disease by histology or I131 uptake but only 25% had positive cytology. In both groups there were a high frequency of non-diagnostic cytology FNABs when Tg-FNAB was less than 10 ng/mL, showing that neither Tg-FNAB nor cytology were able to identify those cases of lymph node metastasis.

COMMENTS

The authors nicely showed that Tg-FNAB is a useful tool to diagnose lymph node metastasis as they proved that, when above 10 ng/mL, all patients had confirmed metastatic disease, independently on the Tg-AB serum status. Thus, if Tg-FNAB is high in a suspicious lymph node, is likely that will be confirmed as metastatic disease. Interestingly, Tg-FNAB was even more accurate than cytology. That information reinforces the recommendation that Tg-FNAB should be measured when suspicious lymph nodes are biopsied in order to increase sensitivity.

Conversely, when Tg-FNAB was lower, the accuracy was not as good but neither was cytology.

Even more important, in the present study, the authors also showed that the same phenomenon occurs in serum TgAB positive and negative patients, suggesting that the presence of TgAB in the serum does not interfere significantly in Tg-FNAB measurement. This is an ongoing discussion in the literature. Shin and cols., studied 239 lymph nodes from 201 PTC patients and found that the presence of serum TgAB in fact interfered with Tg-FNAB measurement (55. Shin HJ, Lee HS, Kim EK, Moon HJ, Lee JH, Kwak JY. A Study on Serum Antithyroglobulin Antibodies Interference in Thyroglobulin Measurement in Fine-Needle Aspiration for Diagnosing Lymph Node Metastasis in Postoperative Patients. PLoS One. 2015;10(6):e0131096.) and similarly, Jo and cols. suggested that serum TgAB might lower Tg-FNAB. This last study proposed to lower the Tg-FNAB cutoff for serum TgAb positive patients (66. Jo K, Kim MH, Lim Y, Jung SL, Bae JS, Jung CK, et al. Lowered cutoff of lymph node fine-needle aspiration thyroglobulin in thyroid cancer patients with serum anti-thyroglobulin antibody. Eur J Endocrinol. 2015;173(4):489-97.). However, those studies performed FNAB of suspicious lymph nodes before thyroid surgery when serum TgAB levels were higher than in Martins-Costa’s and cols. study. Therefore, the interference of serum TgAB in Tg-FNAB measurement might be significant when serum TgAB are higher and differences in cutoffs for both measurements should be considered in those situations.

REFERENCES

  • 1
    Haugen BR, Alexander EK, Bible KC, Doherty GM, Mandel SJ, Nikiforov YE, et al. 2015 American Thyroid Association Management Guidelines for Adult Patients with Thyroid Nodules and Differentiated Thyroid Cancer: The American Thyroid Association Guidelines Task Force on Thyroid Nodules and Differentiated Thyroid Cancer. Thyroid. 2016;26(1):1-133.
  • 2
    Spencer C, Petrovic I, Fatemi S, LoPresti J. Serum thyroglobulin (Tg) monitoring of patients with differentiated thyroid cancer using sensitive (second-generation) immunometric assays can be disrupted by false-negative and false-positive serum thyroglobulin autoantibody misclassifications. J Clin Endocrinol Metab. 2014;99(12):4589-99.
  • 3
    Ahuja AT, Chow L, Chick W, King W, Metreweli C. Metastatic cervical nodes in papillary carcinoma of the thyroid: ultrasound and histological correlation. Clin Radiol. 1995;50(4):229-31.
  • 4
    Martins-Costa MC, Maciel RMB, Kasamatsu TS, Nakabashi CCD, Camacho CP, Crispim F, et al. Clinical impact of thyroglobulin (Tg) and Tg autoantibody (TgAb) measurements in needle washouts of neck lymph node biopsies with papillary thyroid carcinoma. Arch Endocrinol Metab. 2017;61(2):108-14.
  • 5
    Shin HJ, Lee HS, Kim EK, Moon HJ, Lee JH, Kwak JY. A Study on Serum Antithyroglobulin Antibodies Interference in Thyroglobulin Measurement in Fine-Needle Aspiration for Diagnosing Lymph Node Metastasis in Postoperative Patients. PLoS One. 2015;10(6):e0131096.
  • 6
    Jo K, Kim MH, Lim Y, Jung SL, Bae JS, Jung CK, et al. Lowered cutoff of lymph node fine-needle aspiration thyroglobulin in thyroid cancer patients with serum anti-thyroglobulin antibody. Eur J Endocrinol. 2015;173(4):489-97.

Publication Dates

  • Publication in this collection
    Apr 2017

History

  • Received
    23 Mar 2017
  • Accepted
    23 Mar 2017
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