Open Access

Breast cancer in association with thyroid disorders

  • Orhan Turken1Email author,
  • Yavuz NarIn2,
  • Sezai DemIrbas3,
  • M Emin Onde4,
  • Ozkan Sayan5,
  • E Gokhan KandemIr1,
  • Mustafa YaylacI1 and
  • Ahmet Ozturk5
Breast Cancer Research20035:R110

https://doi.org/10.1186/bcr609

Received: 21 February 2003

Accepted: 24 April 2003

Published: 1 October 2003

Abstract

Background

The relationship between breast cancer and thyroid diseases is controversial. Discrepant results have been reported in the literature. The incidences of autoimmune and nonautoimmune thyroid diseases were investigated in patients with breast cancer and age-matched control individuals without breast or thyroid disease.

Methods

Clinical and ultrasound evaluation of thyroid gland, determination of serum thyroid hormone and antibody levels, and fine-needle aspiration of thyroid gland were performed in 150 breast cancer patients and 100 control individuals.

Results

The mean values for anti-thyroid peroxidase antibodies were significantly higher in breast cancer patients than in control individuals (P = 0.030). The incidences of autoimmune and nonautoimmune thyroid diseases were higher in breast cancer patients than in control individuals (38% versus 17%, P = 0.001; 26% versus 9%, P = 0.001, respectively).

Conclusion

Our results indicate an increased prevalence of autoimmune and nonautoimmune thyroid diseases in breast cancer patients.

Keywords

breast cancer thyroid

Introduction

Breast cancer is a hormone-dependent neoplasm. Conflicting results regarding the clinical correlation between breast cancer and thyroid diseases have been reported in the literature. Many studies showed that thyroid diseases are common among women with breast cancer [16], whereas other reports did not confirm such an association of breast cancer with thyroid diseases [711]. Almost every form of thyroid disease, including nodular hyperplasia [12], hyperthyroidism [13] and thyroid cancer [14, 15], has been identified in association with breast cancer. These findings have led to the investigation of the relationship between breast cancer and autoimmune thyroid diseases (AITDs). Such a relationship is not a new observation, and some authors have reported a higher prevalance of AITDs among breast cancer patients than in age-matched control individuals [1618]. The precise significance of this association remains elusive, and some reports have shown that the presence of thyroid peroxidase (TPO) antibodies is associated with a significant improvement in outcome among breast cancer patients [19] and is of similar importance to other prognostic indices such as axillary nodal status and tumour size [20]. The aim of the present prospective study was to determine the prevalence of thyroid diseases in patients with breast cancer as compared with that in the general female population.

Materials and methods

Patient selection

A total of 150 consecutive women with breast cancer and 100 age-matched control women were included in the present study, during the period from May 1998 to December 2002. Breast cancer patients were 38–80 years old (median age 63 years) and were without any known thyroid disease. Three or four weeks after surgical procedure, the patients were evaluated before starting chemotherapy, hormone therapy or radiotherapy.

Examinations

All patients underwent the following five examinations.

First, each patient underwent palpation of the thyroid gland.

Second, ultrasonographic evaluation of the thyroid gland was conducted by the same radiologist using an ultrasound scan fitted with a hand-held 6.6–11 MHz linear transducer. The volume of each lobe was calculated using the following formula: volume = length × width × height × 0.479 [19]. Upper and lower normal lobe volume limits were 18 ml and 10 ml, respectively.

Third, serum free triiodothyronine (T3) and free thyroxine (T4) levels were determined, based on a solid-phase I125 radioimmunoassay designed for the quantitative measurement of free T3 and free T4 levels in serum using Coat-A-Count kit containing radioactive I125-T3 or -T4 analogue (DPC, Los Angeles, CA, USA). Also, serum thyroid-stimulating hormone (TSH) levels were measured using a immunoradiometric assay designed for quantitative measurement of TSH in serum using Coat-A-Count kit containing radioactive I125-polyclonal anti-TSH (Diagnostics Products Coorporation, Los Angeles, CA, USA). The normal ranges were 2.2–6.8 pmol/l (1.4–4.4 pg/ml) for free T3, 0.8–2.0 ng/dl for free T4 and 0.3–5.0 μIU/ml for TSH.

Fourth, all patients underwent serological determination of thyroid autoantibodies based on a direct Anti-TPO radioimmunoassay kit for quantitative determination of anti-TPO autoantibodies (Immunotech, Prague, Czech Republic). Also, autoantibodies specific for thyroglobulin were measured using a quantitative indirect enzyme immunoassay based on the sandwich method (antithyroglobulin immunoradiometric assay kit; Immunotech, Prague, Czech Republic). The normal ranges were 0–60 IU/ml for antithyroglobulin antibodies and 0–20 IU/ml for anti-TPO antibodies.

Finally, after informed consent had been obtained from each patient, fine-needle aspiration (FNA) of the thyroid gland was performed in breast cancer patients who had a palpable thyroid nodule. The aspiration was performed using a 22 guage needle and the smears were air dried and dyed with May–Gruenwald–Giemsa dye. FNA smears were considered diagnostic for autoimmune thyroiditis if there was an abundance of lymphocytes and plasmacytes in a diffuse pattern and/or coexistence of many lymphocytes and oxyphilic epithelial cells.

Patients were separated into three groups according to clinical and ultrasound findings: normal gland, diffuse goitre and nodular goitre. Those women without any breast or thyroid disease were the control group. Patients were also classified into the following subgroups according to menopausal and oestrogen receptor (ER) status: premenopausal and postmenopausal; and ER negative and ER positive.

Statistics

Results are expressed as the mean ± standard deviation. Clinical and other data were analyzed using Mann–Whitney U and student t-test, as applied by the computerized statistical program SPSS (SPSS Inc., Chicago, IL, USA).

Results

The separation of patients into groups on the basis of histopathological diagnosis is shown in Table 1. A total of 118 (79%) patients had invasive ductal carcinoma, 15 (10%) had invasive lobular carcinoma and 17 (11%) had mixed (invasive ductal and lobular) carcinoma. In breast cancer patients, diffuse goitre was identified in 12 cases (8%) and nodular goitre in 75 cases (50%). In the remaining (42%) patients, thyroid glands were totally normal by ultrasound and physical examination. In the control group, diffuse goitre was identified in four (4%) and nodular goitre in 26 (26%). Thus, the prevalence of nodular goitre in the cancer group was higher, and this finding was statistically significant (50% versus 26%; P = 0.001; Table 1). With respect to thyroid volumes, measured ultrasonographically, the mean volumes of diffuse thyroid gIand were 23.1 ml (range 17–26 ml) in the breast cancer patients and 21.9 ml (range 16–27 ml) in the control group. The mean volumes of nodular goitre in breast cancer patients and in the control group were 19.2 ml (range 13–21 ml) and 18.7 ml (range 11–21 ml), respectively.
Table 1

Patient distribution according to clinical and ultrasound evaluation of thyroid gland

 

Patients (n [%])

Control (n [%])

P

Normal gland

63 (42)

70 (70)

0.001

Diffuse goitre

12 (8)

4 (4)

0.29

Nodular goitre

75 (50)

26 (26)

0.001

Evaluation of thyroid function was based on serum thyroid hormones. The mean values for serum thyroid hormones were 8.47 ± 0.75 pmol/l for free T3, 2.64 ± 0.91 ng/dl for free T4 and 3.12 ± 1.40 μIU/ml for TSH in breast cancer patients, and 4.48 ± 0.75 pmol/l, 1.42 ± 0.31 ng/dl and 1.46 ± 0.82 μIU/ml, respectively, in the control group. The differences between breast cancer patients and the control group in mean serum free T3, free T4 and TSH levels were not statistically significant (Table 2). Nontoxic goitre was found in 77 (51%) of the breast cancer patients and in 29 (29%) of the control individuals (P = 0.001; Table 3).
Table 2

Serum thyroid hormone and antibody levels

 

Patients

Control

P

Free T3 (pmol/l)

8.47 ± 0.75

4.48 ± 0.75

0.48

Free T4 (ng/dl)

2.64 ± 0.91

1.42 ± 0.31

0.51

TSH (μIU/ml)

3.12 ± 1.40

1.46 ± 0.82

0.27

TPO antibodies (IU/ml)

105.82 ± 21.46

23.08 ± 4.16

0.030

Tyroglobulin antibodies (IU/ml)

140.92 ± 21.52

27.75 ± 7.60

0.094

T3, triiodothyronine; T4, thyroxine; TPO, thyroid peroxidase; TSH, thyroid-stimulating hormone.

Table 3

Classification of patients in relation to functional thyroid diseases

 

Patients (n [%])

Control (n [%])

P

Hyperthyroidism

6 (4)

1 (1)

0.24

Hypothyroidism

4 (3)

-

0.152

Nontoxic goitre

77 (51)

29 (29)

0.001

The mean values for serum thyroid autoantibodies were 105.82 ± 21.46 IU/ml for anti-TPO antibodies and 140.92 ± 21.52 IU/ml for antithyroglobulin antibodies in breast cancer patients, and 23.08 ± 4.16 IU/ml and 27.75 ± 7.60 IU/ml, respectively, in the control group. Thus, the mean value for serum anti-TPO antibodies was higher in breast cancer patients than in the control group (P = 0.030), whereas the difference between the groups in mean values for serum antithyroglobulin antibodies was not statistically significant (P = 0.094). Autoimmune thyroiditis was defined by increased serum levels of at least one thyroid autoantibody or diagnostic FNA findings, or both. Among the breast cancer patients, autoimmune thyroiditis was diagnosed by autoantibodies in 42 (28%), by FNA in four (2%) and by both in 11 (7%). The difference in the frequency of autoimmune thyroiditis between breast cancer patients and control group was statistically significant (P = 0.001; Table 4). On the other hand, non-AITD was identified, with neither thyroid autoantibody in plasma nor FNA findings specific to autoimmune thyroiditis, in the patients with nodular or diffuse goitre.
Table 4

Classification of patients based on autoimmune and non-autoimmune thyroid disorders

 

Patients (n [%])

Controls (n [%])

P

Normal

54 (36)

74(74)

0.0001

Non-AITD

39 (26)

9 (9)

0.001

Autoimmune thyroiditis

57 (38)

17 (17)

0.001

AITD, autoimmune thyroid disease.

The mean thyroid hormone and autoantibody values were compared between breast cancer patients and the control group, according to menopausal and ER status. The differences between two groups according to both menopausal status and ER status were not significant.

Discussion

The coincidence of thyroid disease and breast cancer has long been a subject of debate. Although associations with hyperthyroidism, hypothyroidism, thyroiditis and nontoxic goitre have been reported in the literature, no convincing evidence exists of a causal role for overt thyroid disease in breast cancer. Geographical variations in the incidence of breast cancer have been attributed to differences in dietary iodine intake, and an effect of iodine on the breast has been postulated [1]. The possible interactions between thyroid gland and breast tissue are based on the common property of the mammary and thyroid epithelial cell to concentrate iodine by a membrane active transport mechanism [18] as well as on the presence of TSH receptors in fatty tissue, which is abundant in mammary gland [21]. Additionally, some endocrine stimuli identified in thyroid products that exert a simultaneous action on the breast and the various thyroid antibodies, which could also interact with receptors on breast tumours, have been postulated to be responsible for the coincidence of mammary and thyroid gland disorders [15, 22].

The present study found a high prevalance of goitre as well as a high prevalence of autoimmune thyroiditis, confirmed mainly by antibody positivity, in breast cancer patients. An association of autoimmune thyroid disease with breast cancer has been reported in the literature [1, 16]. In those studies, increased serum levels of thyroid antibodies were identified. Although Mittra and coworkers [1] found the levels of thyroid antibodies in British women to be lower than those in Japanese women, they found no differences between incidences in breast cancer among women of either race. With the use of specific immunoassays for TPO and thyroglobulin antibodies, an increased level of TPO has been demonstrated in breast cancer.

It has been proposed that the presence of thyroid abnormalities may influence breast cancer progression [19]. A recent report suggested a better prognosis for breast cancer among patients with increased levels of TPO [19]. It has been proposed that the immune response might be directed both by tumour and by thyroid tissue [20], or that the tumour and thyroid tissue share common properties, as they both express TPO and the sodium iodide symporter gene [23, 24]. Although high TPO level has been shown to be a very important factor in antibody-dependent cell cytotoxicity in the thyroid, and there may be a possible association between autoimmune thyroiditis and the immune system, there is no agreement on the significance of its association with breast cancer.

The relationship between thyroiditis and prognostic factors for breast cancer such as ER and stage has been investigated. In one study [1], a higher frequency of thyroiditis was described in more advanced stages of breast cancer. In another study reported by Giani and coworkers [18] no relationship was found between ER status and the presence of serum thyroid antibodies. We found no correlations among ER status, menopausal status and thyroid antibody levels.

In addition to the reported high prevalance of autoimmune thyroiditis among breast cancer patients, the incidence of breast cancer among patients with chronic thyroiditis has been investigated. In a study conducted by Ito and Maruchi [2], those investigators reported that there was an increase in risk for breast cancer among patients with Hashimoto's thyroiditis.

Conclusion

In this paper, we have studied thyroid autoantibody levels and thyroid function tests in breast cancer patients and controls. Abnormal thyroid gland characteristics were revealed in the breast cancer patients compared with the control group. The incidence of nodular goitre was significantly higher in the patients with breast cancer. Regarding functional thyroid disorders, nontoxic goitre was significantly associated with breast carcinoma. There was a significant difference between the groups in terms of TPO Ab levels; however, no difference was demonstrated for other variables, such as Tg Ab and TFT.

These results indicate a significant association between breast cancer and autoimmune and non-autoimmune thyroid disorders. However, more research on this subject is required to confirm this association.

Abbreviations

AITD: 

autoimmune thyroid disease

ER: 

oestrogen receptor

FNA: 

fine-needle aspiration

T3

triiodothyronine

T4

thyroxine

TSH: 

thyroid-stimulating hormone

TPO: 

thyroid peroxidase.

Declarations

Authors’ Affiliations

(1)
GATA Haydarpasa Training Hospital, Medical Oncology Department
(2)
GATA Haydarpasa Training Hospital, Nuclear Medicine Department
(3)
GATA Haydarpasa Training Hospital, General Surgery Department
(4)
GATA Haydarpasa Training Hospital, Endocrinology Department
(5)
GATA Haydarpasa Training Hospital, Hematology Department

References

  1. Mittra I, Perrin J, Kumaoka S: Thyroid and other autoantibodies in British and Japanese women: an epidemiological study of breast cancer. BMJ. 1976, 1: 257-259.View ArticlePubMedPubMed CentralGoogle Scholar
  2. Ito K, Maruchi N: Breast cancer in patients with Hashimoto's thyroiditis. Lancet. 1975, 2: 1119-1121. 10.1016/S0140-6736(75)91006-5.View ArticlePubMedGoogle Scholar
  3. Kapdi JJ, Wolfe JN: Breast cancer relationship to thyroid supplements for hypothyroidism. JAMA. 1976, 236: 1124-1127. 10.1001/jama.236.10.1124.View ArticlePubMedGoogle Scholar
  4. Rasmusson B, Rasmussen UF, Hegedus L, Perrild H, Bech K, Hoier-Madsen M: Thyroid function in patients with breast cancer. J Cancer Clin Oncol. 1987, 23: 553-556.View ArticleGoogle Scholar
  5. Mittra I, Haysward JL: Hypothalamic-pituitary-thyroid axis in breast cancer. Lancet. 1974, 1: 885-888. 10.1016/S0140-6736(74)90344-4.View ArticlePubMedGoogle Scholar
  6. Shering SG, Zbar AP, Moriatry M: Thyroid disorders and breast cancer. Eur J Cancer Prev. 1996, 5: 504-506.PubMedGoogle Scholar
  7. Maruchi N, Annegers JF, Kurland LT: Hashimoto's thyroiditis and breast cancer. Mayo Clin Proc. 1976, 51: 263-265.PubMedGoogle Scholar
  8. Lemmarie M, Baugnet-Mahieu L: Thyroid function in women with breast cancer. Eur J Cancer Clin Oncol. 1986, 22: 301-307.View ArticleGoogle Scholar
  9. Moossa AR, Price-Evans DA, Brewer AC: Thyroid status and breast cancer: reappraisal of an old relationship. Ann R Coll Surg. 1973, 53: 178-188.Google Scholar
  10. Kurland LT, Annegers JF: Breast cancer and Hashimoto's thyroiditis [letter]. Lancet. 1976, 1: 808-10.1016/S0140-6736(76)91650-0.View ArticlePubMedGoogle Scholar
  11. Anker GB, Lonning PE, Aakvaag : Thyroid function in post-menopausal breast cancer patients treated with tamoxifen. Scand J Clin Lab Invest. 1998, 58: 103-107. 10.1080/00365519850186670.View ArticlePubMedGoogle Scholar
  12. Smyth PPA, Smith DF, McDermott P, Murray J, Geraghty JG, O'Higgins NJ: A direct relationship between thyroid enlargement and breast cancer. J Clin Endocrinol Metabol. 1996, 81: 937-941.Google Scholar
  13. Goldman MB: Thyroid diseases and breast cancer. Epidemiology Rev. 1990, 12: 28-30.Google Scholar
  14. McThernan A, Weiss NS, Daling JR: Incidence of thyroid cancer in women in relation to known or suspected risk factors for breast cancer. Cancer Res. 1987, 47: 292-294.Google Scholar
  15. Ron E, Curtis R, Hooffman DA, Flannery JT: Multiple primary breast and thyroid cancer. Br J Cancer. 1984, 49: 87-90.View ArticlePubMedPubMed CentralGoogle Scholar
  16. Gogas J, Kouskos E, Tseleni-Balafouta S, Markopoulos C, Revenas K, Gogas G, Kostakis A: Autoimmune thyroid disease in women with breast carcinoma. Eur J Surg Oncol. 2001, 27: 626-630. 10.1053/ejso.2001.1204.View ArticlePubMedGoogle Scholar
  17. Myhil J, Reeve TS, Hales IB: Thyroid function in breast cancer. Acta Endocrinol. 1966, 51: 290-300.Google Scholar
  18. Giani C, Fierabracci P, Bonacci R, Gigliotti A, Campani D, DeNegri F, Cecchetti D, Martino E, Pinchera A: Relationship between breast cancer and thyroid disease: relevance of autoimmune thyroid disorders in breast malignancy. J Endocr Metab. 1986, 81: 990-994.Google Scholar
  19. Smyth PPA, Kilbane MT, Murray MJ, Mc Dermott EWM, Smith DF, O'Higgins NJ: Serum thyroid peroxidase autoantibodies, thyroid volume and outcome in breast cancer. Clin Endocr Metab. 1988, 83: 2711-2716.Google Scholar
  20. Smyth PPA: Autoimmune thyroid disease and breast cancer: a chance association. J Endocrinol Invest. 2000, 23: 42-43.View ArticlePubMedGoogle Scholar
  21. Davies TF: The thyrotrophin receptors spread themselves around. J Clin Endocrinol Metabol. 1994, 79: 1232-1238.Google Scholar
  22. Dumont JE, Maenhaut C: Growth factors controlling the thyroid gland. Baillieres Clin Endocrinol Metabol. 1991, 5: 727-753.View ArticleGoogle Scholar
  23. Spitzweg C, Joba W, Eisenmenger W, Heufelder A: Analysis of human sodium iodide symporter gene expression in extrathyroidal tissues and cloning of its complementary deoxyribonucleic acids from salivary gland, mammary gland and gastric mucosa. J Clin Endocrinol Metab. 1998, 83: 1746-1751.View ArticlePubMedGoogle Scholar
  24. Kilbane MTTA, Shering SG, Symith DF, McDermott EWM, O'Higgins NJ, Symith PPA: Thyroid peroxidase (TPO): an autoantigen common to the thyroid and breast. J Endocrinol. 1998, 156: 323-View ArticleGoogle Scholar

Copyright

© Turken et al., licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL. 2003