Association of Hyperparathyroidism and Papillary Thyroid Cancer: A Multicenter Retrospective Study.

BACKGROUND: Concomitant papillary thyroid cancer (PTC) and hyperparathyroidism (HPT) have been reported in several studies. Our study aimed to investigate the incidence of concomitant PTC in HPT patients upon preoperative diagnosis and present a clinical opinion on detecting thyroid malignancy in case of parathyroidectomy.
METHODS: Patients who underwent parathyroidectomy between January 2009 and December 2019 in two medical centers were included. Of the 279 participants 154 were diagnosed as primary hyperparathyroidism (pHPT) and 125 as secondary hyperparathyroidism (sHPT). The incidence of concomitant PTC and its clinical characteristics were compared with 98 patients who underwent thyroidectomy and were diagnosed with classical PTC during the same period.
RESULTS: Concurrent PTC was detected in 14 patients (9.1%) with pHPT and in nine patients (7.2%) with sHPT. Ten (71.4%) and seven (77.8%) PTCs were microcarcinomas in the pHPT and sHPT cases respectively. In the pHPT patients, vitamin D was lower in the pHPT+PTC group (13.0±3.7 ng/mL) than in the pHPT-only group (18.5±10.4 ng/mL; P=0.01). Vitamin D levels were also lower in the sHPT+PTC group (12.3±5.6 ng/mL) than in the sHPT-only group (18.0±10.2 ng/mL; P=0.12). In the concomitant PTC group, lymph node ratio was higher than in the classical PTC group (P=0.00).
CONCLUSION: A high prevalence of concomitant PTC was seen in patients with pHPT and sHPT. Those concomitant PTCs were mostly microcarcinomas and had more aggressive features, suggesting that efforts should be made to detect concomitant malignancies in the preoperative parathyroidectomy evaluation.

INTRODUCTION

The prevalence of primary hyperparathyroidism (pHPT) is 0.1% to 0.4% in the general population [1] and its incidence is increasing, leading to an increased need for surgical management [2,3]. Usually, it is caused by a solitary parathyroid adenoma and surgical resection is the choice of treatment [4]. Secondary hyperparathyroidism (sHPT) results from compensatory parathyroid hyperfunction in response to chronic hypocalcemia caused by renal failure. Some patients with sHPT need parathyroidectomy in an attempt to reduce severe complications, such as renal osteodystrophy, caused by high levels of parathyroid hormone (PTH) [5]. The burden of sHPT is unknown, but despite the use of multiple medical therapies, the rate of parathyroidectomy in sHPT patients refractory to medical therapy has not declined in recent years [6].

Concomitant pHPT and thyroid malignancy have been reported in several studies since the first cases were reported by Ogburn and Black [7] in 1956. In pHPT patients, several studies reported the prevalence of papillary thyroid cancer (PTC) to range from 2% to 15% [8,9]. Data on the association between sHPT and PTC is more limited. sHPT and coexisting PTC have been reported in sporadic cases and studies are scarce [10]. Today, the number of experts proposing routine bilateral neck exploration has decreased and the paradigm has recently shifted to minimally invasive parathyroidectomy [11], offering a more limited exposure of the thyroid gland, making the detection of concomitant thyroid malignancy difficult during surgery. The presence of concomitant PTC can change the evaluation and surgical management of patients with hyperparathyroidism (HPT). In the coexistence of these two diseases, thyroid PTC must be identified prior to surgical management to minimize complications from additional surgical procedures, patient discomfort, and costs [12].

Thus, our study aimed to further investigate the incidence in our centers and the clinical characteristics of concomitant PTC in HPT patients with a special emphasis on preoperative diagnosis. We also aimed to provide a clinical opinion on the need for detecting PTC when preparing for parathyroidectomy.

METHODS

Data sources

We retrospectively evaluated 279 patients (patients from Seoul St. Mary’s Hospital and patients from Yeouido St. Mary’s Hospital) who underwent parathyroidectomy between January 2009 and December 2019. Patient clinical data and pathological results were obtained from the hospital’s electronic registry. Initially, 319 patients were screened, of whom 40 cases were excluded: due to multiple endocrine neoplasia syndrome (MEN) (n=15); parathyroid carcinoma (n=8); missing data or insufficient medical records (n=12); or because they underwent parathyroidectomy for diseases other than HPT (n=5). Of the 279 participants, 154 were diagnosed with pHPT and 125 with sHPT (Fig. 1). The clinical findings were compared between 98 age and sex-matched patients who underwent thyroidectomy and were diagnosed with classical PTC in our clinic during the same period. The study adhered to the tenets of the Declaration of Helsinki and was approved by the Institutional Review Board of Catholic Medical Center (No. KC19TESI0523). Informed consent was exempted by the review board since the study was a retrospective analysis.

Fig. 1

Enrollment of the study subjects. MEN, multiple endocrine neoplasia; pHPT, primary hyperparathyroidism; PTC, papillary thyroid cancer; sHPT, secondary hyperparathyroidism.

Indications for parathyroidectomy

The indications for parathyroidectomy were as follows. For the pHPT subjects, parathyroidectomy was recommended according to the following guidelines from the Fourth International Workshop [13]: (1) serum calcium >1 mg/dL above the upper limit of normal; (2) peri- or postmenopausal women and men age 50 and older with a T-score of −2.5 or less; (3) the presence of vertebral fracture; (4) a creatinine clearance of <60 mL/min; (5) the presence of renal stones or nephrocalcinosis in renal imaging; (6) the presence of marked hypercalciuria (>400 mg/day); and (7) age under 50 years. Parathyroidectomy for sHPT was indicated for patients refractory to medical therapy: (1) persistent hypercalcemia or hyperphosphatemia; (2) an elevated risk or presence of calciphylaxis; and (3) erythropoietin-resistant anemia [14].

Measurements

All patients underwent preoperative ultrasonography (US) and their thyroid nodules were screened. PTC was diagnosed by fine needle aspiration (FNA) of the suspected thyroid nodule seen in preoperative US or confirmed by pathology after resection. The baseline laboratory findings were measured before surgery. The biochemical and hormonal findings, including serum immuno-reactive intact PTH levels (reference range, 8 to 76 pg/mL; Cobra 5010, A Packard Bioscience Company, Meriden, CT, USA), total serum calcium (8 to 10 mg/dL), phosphorous (2.6 to 4.5 mg/dL), albumin, blood urea nitrogen, creatinine (Hitachi 7600, Hitachi, Tokyo, Japan), serum 25-hydroxyvitamin D (25(OH)D, 0 to 20 ng/mL; ADVIA Centaur XPT, Siemens Healthcare Diagnostics Inc., Tarrytown, NY, USA), and 24-hour urine calcium were evaluated. Serum calcium was corrected for changes in the serum albumin concentration according to the following formula: corrected calcium (mg/dL)=actual calcium+(4−serum albumin)×0.8. Body mass index was calculated as body weight in kilograms divided by height in meters squared. Bone mineral density was evaluated using dual-energy X-ray absorptiometry (Lunar Prodigy, GE Healthcare, Madison, WI, USA) before parathyroidectomy.

The PTC tumor size and pathology of the parathyroid specimens were described in the pathology analysis report. Tumor size was defined as the largest dimension. Microcarcinoma was defined as cancer where the greatest dimension was ≤1 cm. The calcification pattern was classified into the following three groups according to the consensus statement and recommendations proposed by the Korean Society of Thyroid Radiology and the Korean Society of Radiology [15]: (1) no calcification; (2) microcalcification defined as the presence of punctate echogenic foci of <1 mm with or without posterior shadowing; (3) macrocalcification defined as the presence of echogenic foci >1 mm with posterior shadowing [16]. The Korean Thyroid Imaging Reporting and Data System (K-TIRADS) was used to classify preoperative thyroid nodules for biopsy recommendation [17]. Lymph node metastases were considered positive if they were proven by pathology finding. Prophylactic central neck lymph node dissection was the standard surgical procedure for lymph node dissection in both institutions. The lymph node ratio (LNR) was defined as the number of metastatic lymph nodes divided by the number of lymph nodes removed. B-type Raf kinase (BRAF) mutations were analyzed by immunohistochemistry in the PTC specimens.

Statistical analysis

The continuous variables are expressed as mean±standard deviation or median (interquartile range) as appropriate. The categorical variables are presented as number and frequency (proportions, %). Comparisons of the means and proportions were performed with independent sample t tests or the Mann-Whitney test. The comparison of categorical variables was performed with Fisher’s exact test or chi-square analysis. A two-tailed P value of less than 0.05 was considered statistically significant. All statistical analyses were performed using IBM SPSS Statistics for Windows version 24.0 (IBM Corp., Armonk, NY, USA).

RESULTS

Clinical and biochemical characteristics of pHPT patients

The demographic, clinical, biochemical, and histopathological characteristics of the pHPT patients are described in Table 1. Concurrent PTC was detected in 14 patients (9.1%) with pHPT. pHPT was more prevalent in females (75.7%). There was no difference in sex and age between the subjects with pHPT and those with pHPT+PTC. The PTH level was 206.8±164.3 pg/mL in the pHPT-only group and 207.4±138.7 pg/mL in the pHPT+ PTC group, with no significant difference between the two groups (P=0.53). The serum calcium and 24-hour urine calcium levels were not different between the two groups. 25(OH)D levels were significantly higher in the pHPT-only group (18.5±10.4 ng/mL) than in the pHPT+PTC group (13.0±3.7 ng/mL) (P=0.01) (Table 1).

Table 1

The Clinical and Biochemical Features in Primary Hyperparathyroidism

Variable	Primary HPT (n=140)	Primary HPT+PTC (n=14)	P value
Age, yr	54.8±11.8	54.1±15.4	0.10
Sex
Male	34 (24.3)	3 (21.4)	1.00
Female	106 (75.7)	11 (78.6)
Body mass index, kg/m2	24.0±3.8	24.4±4.9	0.12
PTH, pg/mL	206.8±164.3	207.4±138.7	0.53
BMD, g/cm2
Lumbar	0.975±0.167	0.931±0.275	0.42
Total hip	0.812±0.119	0.838±0.206	0.89
Parathyroid pathology
Adenoma	117 (83.6)	14 (100)	0.70
Hyperplasia	23 (16.4)	0
Calcium, mg/dL	10.8±1.0	11.3±1.1	0.87
Phosphorus, mg/dL	2.7±0.5	2.4±0.4	0.19
25(OH)D, ng/mL	18.5±10.4	13.0±3.7	0.01
Blood urea nitrogen, mg/dL	14.3±4.8	15.2±3.1	0.14
Creatinine, mg/dL	0.80±0.20	0.75±0.20	0.39
24-hr urine calcium, mg/day	345.7±141.9	402.1±110.1	0.14

Values are expressed as mean±standard deviation or number (%). Serum calcium level is adjusted calcium for albumin. A two-tailed P value of less than 0.05 was considered statistically significant.

HPT, hyperparathyroidism; PTC, papillary thyroid cancer; PTH, parathyroid hormone; BMD, bone mineral density; 25(OH)D, 25-hydroxyvitamin D.

Clinical and biochemical characteristics of sHPT patients

Table 2 shows the baseline characteristics of the sHPT patients. Concurrent PTC was detected in nine patients (7.2%) with sHPT. There was no difference in sex and age between the subjects with sHPT and those with sHPT+PTC. The PTH level was 1,368.5±1,076.8 pg/mL in the sHPT-only group and 962.2±788.2 pg/mL in the sHPT+PTC group, with no significant difference between the two groups (P=0.43). No specific biochemical variables were significantly different between the two groups. However, 25(OH)D levels were higher in the sHPT-only group (18.0±10.2 ng/mL) than in the sHPT+PTC group (12.3±5.6 ng/mL) (P=0.12) (Table 2).

Table 2

The Clinical and Biochemical Features in Secondary Hyperparathyroidism

Variable	Secondary HPT only (n=116)	Secondary HPT+PTC (n=9)	P value
Age, yr	49.4±11.4	58.0±9.8	0.43
Sex			0.30
Male	52 (44.8)	2 (22.2)
Female	64 (55.2)	7 (77.8)
Body mass index, kg/m2	22.7±4.1	21.1±2.2	0.13
PTH, pg/mL	1,368.5±1,076.8	962.2±788.2	0.43
BMD, g/cm2
Lumbar	1.022±0.164	0.957±0.093	0.27
Total hip	0.798±0.164	0.751±0.095	0.32
Parathyroid pathology
Adenoma	8 (6.9)	2 (22.2)	0.00
Hyperplasia	108 (93.1)	7 (77.8)
Calcium, mg/dL	10.3±1.3	10.1±1.2	0.66
Phosphorus, mg/dL	4.8±2.0	4.0±1.6	0.31
25(OH)D, ng/mL	18.0±10.2	12.3±5.6	0.12
Blood urea nitrogen, mg/dL	44.3±23.8	38.1±29.7	0.33
Creatinine, mg/dL	6.6±4.6	5.2±5.4	0.38

Values are expressed as mean±standard deviation or number (%). Serum calcium level is adjusted calcium for albumin. A two-tailed P value of less than 0.05 was considered statistically significant.

HPT, hyperparathyroidism; PTC, papillary thyroid cancer; PTH, parathyroid hormone; BMD, bone mineral density; 25(OH)D, 25-hydroxyvitamin D.

Clinical features of PTC in HPT and classical PTC patients

The mean size of the PTC nodules in the HPT patients (concomitant PTC group) was 0.86±0.70 cm. Among 23 cases, 17 (73.9%) were microcarcinomas. All PTC nodules were either K-TIRADS 4 or K-TIRADS 5 in preoperative US examination. Extrathyroidal extension was found in 10 (43.5%) cases. Lymph node metastasis was confirmed in 10 (43.5%) cases, and the LNR was 21.8%±33.2% in the concomitant PTC group.

The mean size of the PTC nodules in the classical PTC group was 0.90±0.60 cm; 71 nodules (72.4%) were microcarcinomas. Extrathyroidal invasion was found in 34 (34.7%) cases. Lymph node metastasis was confirmed in 32 (32.6%) cases, and the LNR was 10.3%±20.3% in patients with classical PTC. Extrathyroidal extension and lymph node metastasis were more common in the concomitant PTC group than in the classical PTC group, but the difference was not statistically significant (P= 0.47 and P=0.34, respectively). The LNR was significantly higher in the concomitant PTC group than in the classical PTC group (P=0.00) (Table 3).

Table 3

Clinical Differences between Concomitant Papillary Thyroid Cancer and Classical Papillary Thyroid Cancer

Variable	Concomitant PTC (n=23)	Classical PTC (n=98)	P value
Age, yr	55.0±13.5	52.0±11.6	0.54
Sex
Male	5 (21.8)	22 (22.4)	1.00
Female	18 (78.2)	76 (77.6)
Tumor size, cm	0.86±0.70	0.90±0.60	0.92
Microcarcinoma	17 (73.9)	71 (72.4)	1.00
Echogenicity
Hypoechoic	20 (87.0)	77 (78.6)	0.56
Isoechoic	3 (13.0)	21 (21.4)
Hyperechoic	0	0
Margin
Ill-defined	6 (26.1)	33 (33.7)	0.62
Well-defined	17 (73.9)	65 (66.3)
Shape
Parallel	13 (56.5)	55 (56.1)	1.00
Non-parallel	10 (43.5)	43 (43.2)
K-TIRADS
4	6 (26.1)	37 (37.8)	0.34
5	17 (73.9)	61 (62.2)
Extrathyroidal extension	10 (43.5)	34 (34.7)	0.47
Lymph node metastasis	10 (43.5)	32 (32.6)	0.34
LNR, %	21.8±33.2	10.3±20.3	0.00
BRAF mutation
Yes	13 (56.5)	86 (87.8)	0.00
No	2 (8.7)	11 (11.2)
Unknown	8 (34.8)	1 (1.0)

Values are expressed as mean±standard deviation or number (%). Concomitant PTC includes PTC in primary hyperparathyroidism and secondary hyperparathyroidism. A two-tailed P value of less than 0.05 was considered statistically significant.

PTC, papillary thyroid cancer; K-TIRADS, Korean Thyroid Imaging Reporting and Data System; LNR, lymph node ratio; BRAF, B-type Raf kinase.

DISCUSSION

In our research, 9.1% of the pPHT cases and 7.2% of the sPHT cases requiring parathyroidectomy had concomitant PTC. The serum 25(OH)D levels were lower in the group with concomitant PTC+HPT than in the group with HPT only. The coexisting cases of PTC were mostly microcarcinomas and had more aggressive features.

In previous literature, the prevalence of concomitant PTC in pPHT ranged from 2% to 15%, consistent with our results. Preda et al. [18] recently reported the incidence of thyroid cancer in patients with sHPT to be 11.7%, which was higher than our findings of 7.2%. Our study demonstrated that the incidence of PTC was high and similar in both patients with pHPT and sHPT.

The mechanism of the relationship between HPT and concomitant PTC is still unclear. Pickard et al. [19] reported that thyroid malignancy was the most prevalent cancer among patients whose primary disorder was pHPT. Several possible explanations have been proposed as the mechanism for the association. First, high PTH levels have been reported to affect phagocytosis, T-cell sensitivity, and B-cell function, thus contributing to the immune dysfunction of patients and increasing the incidence of cancer [20]. Some authors postulated that PTH could increase the hepatic synthesis of insulin-like growth factor 1 [21], leading to thyroid cell growth [22]. Likewise, a study suggested that high levels of PTH might predict the existence of PTC in pHPT patients [23]. Second, long-term exposure to elevated calcium has also been reported to be carcinogenic. The goitrogenic effect of calcium is due to the inhibition of thyroxine synthesis. Hypercalcemia and the excessive production of calcitonin in response to hypercalcemia have been proposed as a common pathogenic mechanism [24]. Third, low levels of vitamin D were associated with concomitant PTC in patients with HPT in our study. A previous study also reported low vitamin D concentrations in patients with severe pHPT [23]. It is well known that vitamin D is associated with anti-proliferative, pro-differentiative, pro-apoptotic, and anti-inflammatory actions within the tumor microenvironment [25]. Several clinical studies have suggested low vitamin D levels as a risk factor for thyroid cancer associated with incidence and worse outcome [26,27]. The level of vitamin D can vary according to outdoor activity, diet, and the time of measurement. However, considering that the mean vitamin D level in Korea was reported to be 18.5±8.1 ng/mL [28], our study showing significantly lower levels of vitamin D in HPT patients with concomitant PTC has some implications. Further research is needed to clarify the association of vitamin D with HPT in patients with concomitant PTC.

Lymph node metastasis and extrathyroidal invasion are associated with aggressive features in PTC [16,29-31]. Of the concomitant PTC cases, 43.5% had lymph node metastasis and presented with extrathyroidal invasion, suggesting high-risk features [16,29-31]. A previous study reported that the optimal LNR threshold value for predicting PTC recurrence was 17.86% [32]. Our study showing high LNRs in concomitant PTC (21.8%±33.2%) compared to the control group (10.3%±20.3%), might represent a high risk of recurrence in these groups. Therefore, our study suggests that PTC in HPT patients represents a higher risk feature than PTC incidentally found in the general population.

A high rate of microcarcinoma has been reported in patients with concomitant HPT [33], consistent with our research showing 16 cases (73.9%) of microcarcinoma (10 in pHPT and seven in sHPT) in 23 thyroid papillary cancers. Subcentimeter microcarcinoma is associated with a low disease-specific mortality, and certain authors and guidelines have recommended active surveillance instead of surgery as a reasonable option for papillary microcarcinoma [34]. However, considering the highly aggressive feature of concomitant PTC in our study, we suggest that active surveillance should be considered carefully, even in cases of microcarcinoma. Further study is needed to clarify the implication of concomitant PTC.

The routine FNA of K-TIRADS five nodules lesser than 1 cm in size is not recommended by the Korean Thyroid Association guidelines unless suspicious malignant features are present. Moreover, the guidelines do not recommend FNA of subcentimeter K-TIRADS four nodules since they have a low risk of malignancy [17]. However, in our study, several subcentimeter K-TIRADS four nodules were proven malignant and presented aggressive features. Thus, efforts should be made to detect the coexistent PTC in HPT patients for any subcentimeter nodule prior to parathyroidectomy. Considering the aggressiveness of concomitant PTC, overlooking subcentimeter concomitant thyroid nodules in HPT patients may mean missing PTC with high-risk features that can lead to multiple surgeries and several complications [35]. Vaiman et al. [36] reported that injury to the recurrent laryngeal nerve occurred in 1.4% of the primary thyroidectomy compared to 3% of the patients undergoing reoperation thyroidectomy. To avoid reoperation, preoperative US evaluation is necessary before parathyroidectomy. By searching for concomitant thyroid nodules with preoperative US, indeterminate lesions that require additional evaluation can be detected.

There are several limitations in our study. First, since this study is retrospective, we were unable to clarify the causal relationships and underlying mechanisms in the research. Second, we were unable to investigate several factors that could have affected serum calcium and vitamin D levels, such as taking health supplements or other medication, a lack of sun exposure, and exercising. Lastly, the small sample size without a control group is a limitation. A study with a larger population may allow more significant conclusions about PTC in HPT patients to be drawn.

In conclusion, to our knowledge, this is the first study evaluating the incidence of concomitant PTC in patients with HPT in Korea. A high prevalence of concomitant PTC in pHPT and sHPT patients was shown and concomitant PTC had more aggressive features than incidentally detected PTC. As a minimally invasive approach for parathyroidectomy has replaced bilateral neck exploration, thorough preoperative thyroid evaluation is necessary to identify concomitant PTC.