Risk factors for cervical lymph node metastasis in papillary thyroid microcarcinoma: a study of 1,587 patients.

OBJECTIVE: The purposes of this study were to identify risk factors for cervical lymph node metastasis and to examine the association between BRAF V600E status and clinical features in papillary thyroid microcarcinoma (PTMC).
METHODS: A total of 1,587 patients with PTMC, treated in Tianjin Medical University Cancer Institute and Hospital from January 2011 to March 2013, underwent retrospective analysis. We reviewed and analyzed factors including clinical results, pathology records, ultrasound results, and BRAF V600E status.
RESULTS: Multivariate logistic regression analyses demonstrated that gender (male) [odds ratio (OR) = 1.845, P = 0.000], age (< 45 years)(OR = 1.606,P = 0.000), tumor size (> 6 mm) (OR = 2.137,P = 0.000), bilateralism (OR = 2.011, P = 0.000) and extrathyroidal extension (OR = 1.555, P = 0.001) served as independent predictors of central lymph node metastasis (CLNM). Moreover, CLNM (OR = 29.354, P = 0.000) served as an independent predictor of lateral lymph node metastasis (LLNM). Among patients with a solitary primary tumor, those with tumor location in the lower third of the thyroid lobe or the isthmus were more likely to experience CLNM (P < 0.05). Univariate analyses indicated that CLNM, LLNM, extrathyroidal extension, and multifocality were not significantly associated with BRAF V600E mutation.
CONCLUSIONS: The present study suggested that prophylactic neck dissection of the central compartment should be considered in patients with PTMC, particularly in men with tumor size greater than 6 mm, age less than 45 years, extrathyroidal extension, and tumor bilaterality. Among patients with PTMC, BRAF V600E mutation is not significantly associated with prognostic factors. For a better understanding of surgical management of PTMC and the risk factors, we recommend multicenter research and long-term follow-up.

Introduction

Papillary thyroid microcarcinoma (PTMC) is defined by the World Health Organization (WHO) as a papillary thyroid carcinoma (PTC) ≤ 1 cm[1]. Clinically, fine needle aspiration biopsy (FNAB) and ultrasonography (US) are utilized to detect PTMC in patients without palpable thyroid nodes. Although PTMC has an indolent course, many cases have demonstrated highly aggressive clinical features, such as extrathyroidal extension and cervical lymph node metastasis. The incidences of central lymph node metastasis (CLNM) (24.1%–64.1%)[2-5] and lateral lymph node metastasis (LLNM) (3.7%–44.5%)[2] for PTMC are comparable with those of PTC.

BRAF mutation is a common genetic alternation in thyroid carcinoma. The most common and typical mutation in the BRAF gene is T1779A in exon 15, which results in a V600E amino acid substitution[6]. However, controversial results have been observed in studies of PTMC, as some research has shown that BRAFV600E mutation in PTMC led to more aggressive behavior[7,8], whereas other studies found that the BRAFV600E mutation was not significantly related to high-risk clinicopathologic characteristics[9].

As the clinical features of PTMC and the risk factors for CLNM have been previously investigated[10-13], the aim of the present study was to examine the risk factors for lymph node metastasis, including both CLNM and LLNM, based on US results and postoperative pathological records in the setting of a large cohort of Chinese patients with PTMC.

Materials and methods

Patients

A total of 3,789 patients with PTC were initially treated at Tianjin Medical University Cancer Institute and Hospital from January 2011 to March 2013. Among these patients, 1,587 were diagnosed with PTMC based on postoperative pathology.

All patients underwent indirect laryngoscopy before and after surgery. Preoperative US, performed in all cases, provided information regarding disease and possible cervical LNM. When preoperative findings were suspicious for LNM, computed tomography (CT) was performed. Preoperative FNAB was not performed routinely in patients with PTMC. Primary thyroid tumor location was divided into four regions: upper third, middle third, lower third, or isthmus, according to US imaging results.

Different therapeutic strategies were used for different types of PTMC, such as lobectomy with isthmectomy plus ipsilateral central lymph node dissection (CLND) for unilateral PTMC, isthmectomy plus prophylactic bilateral CLND for isthmus PTMC, and near-total thyroidectomy plus bilateral CLND for multiple tumors limited to a single thyroid lobe. Moreover, patients with multiple bilateral tumors were treated with total thyroidectomy with bilateral CLND, and patients with US and CT findings suspicious for LLNM were treated with ipsilateral lateral lymph node dissection, including levels II-V. Surgical treatments for the 1,587 patients are shown in .

Extrathyroidal extension, tumor size, tumor number, and presence of LLNM and CLNM were confirmed by two pathologists independently in a blinded fashion. Cases in which findings were inconsistent were discussed with a third pathologist. Extrathyroidal extension was defined according to gross infiltration evident at the time of surgery or by microscopic evidence on pathologic examination. Multifocality was defined as the presence of more than one tumor lesion in the thyroid. The maximum diameter of the primary tumor was defined as tumor size in multifocal cases.

Postoperative complications were also evaluated. Temporary hypoparathyroidism was defined as serum calcium < 8 mg/dL within 6 months after surgery. Permanent hypoparathyroidism was defined as low calcium levels in a patient with low/absent parathyroid hormone levels 6 months after surgery. Vocal cord paralysis was defined as temporary recurrent laryngeal nerve injury within 6 months after the operation; vocal cord paralysis continuing longer than 6 months was defined as permanent laryngeal nerve injury.

Follow-up data were available for all 1,587 patients, and the follow-up period ranged from 40 to 72 months. All patients underwent US every 3–6 months in our hospital during follow-up. This retrospective study was approved by the Institutional Review Board of Tianjin Medical University Cancer Institute and Hospital.

DNA extraction and analysis of BRAFV600E mutation

DNA was extracted from paraffin-embedded tissues using a kit (Tiangen, Beijing, China) according to the manufacturer’s instructions. Specifically, we selected unstained tumor tissue areas on 2 mm thick sections for comparison to hematoxylin and eosin-stained sections. For small tumors, we adopted laser-capture microdissection to collect tissues. Tumor samples were incubated in TE9 for 2 days at 37°C, with fresh proteinase K added daily. Samples were then centrifuged, and the supernatants were digested for an additional 2 days at 55°C. Chelex 100 resin (Bio-Rad Laboratories, Inc., Hercules, CA, USA) was added to each sample and incubated for 1 h, after which the supernatant was removed. DNA was extracted using phenol-chloroform, concentrated using ethanol precipitation, and resuspended in Tris-EDTA (1 mM EDTA and 10 mM Tris hydrochloride; pH 8.0).

The DNA samples extracted from tissues were then subjected to PCR analysis to explore the BRAFV600E mutation. The appropriate primers have been described in previous research[33]. PCR cycles were performed using the BigDye Terminator sequencing kit (Applied Biosystems, Foster City, CA, USA) and the sequencing products were analyzed with an ABI PRISM 310 Genetic Analyzer (Applied Biosystems).

Statistical analysis

SPSS 22.0 software (IBM Corp., Version 22.0, Armonk, NY, USA) was used to analyze the data. Data were presented as mean ± standard deviation. The χ2 test or Fisher’s exact test was used to compare cervical LNM and BRAFV600E mutation status with clinicopathologic features. We performed multivariate logistic regression analysis to assess independent risk factors for cervical LNM, using the factors screened by univariate analysis, with P < 0.05. We employed receiver operating characteristic curve (ROC) analysis to determine the optimal cutoff point of primary tumor size for determining the risk of CLNM. Values of P < 0.05 were considered statistically significant.

Results

Patient characteristics

There were 1,587 patients with PTMC, consisting of 1,251 (78.8%) women and 336 (21.2%) men. The mean age was 45.7 (11 to 73) years, and 333 (21.0%) patients were diagnosed with Hashimoto’s thyroiditis.

The mean size of primary tumors in the largest diameter was 5.9 ± 2.5 mm, with 586 (36.9%) tumors larger than 6 mm and 1,001 (63.1%) tumors smaller than or equal to 6 mm in diameter. Among all patients, 1,039 (65.5%) and 573 (36.1%) demonstrated extrathyroidal extension and multifocal lesions, respectively. Considering solitary lesions, 312 (30.8%) were in the upper third of the lobe, 268 (26.4%) were in the middle third, 407 (40.1%) were in the lower third, and 27 (2.7%) were in the isthmus.

CLNM occurred in 491 (30.9%) of the 1,587 patients, while LLNM was found in 73 (4.6%). Skip metastases, meaning LLNM without CLNM, were observed in 19 patients (1.2%). shows the clinical and pathologic characteristics of these patients.

Risk factors for CLNM

ROC curve analysis showed that primary tumor size of 6 mm was the optimal cutoff point to distinguish between patients with and without CLNM (area = 0.649, standard error = 0.015, asymptotic significance = 0.000, 95% confidence interval = 0.620–0.678).

Risk factors for CLNM were evaluated by univariate and multivariate analyses according to final pathological results. In univariate analysis, male gender, age < 45 years, primary tumor size greater than 6 mm, multifocality, bilateralism, and extrathyroidal extension ( P < 0.01) were significantly related to CLNM. Moreover, univariate analysis performed for the solitary primary tumor group showed that CLNM was significantly associated with tumor location ( P < 0.05); tumors located in the lower third and isthmus conferred a higher risk of CLNM than did those in the upper third. On multivariate analysis, male gender [odds ratio (OR) = 1.845, P = 0.000], age < 45 (OR = 1.606, P = 0.000), tumor size greater than 6 mm (OR = 2.137, P = 0.000), bilateralism (OR = 2.011, P = 0.000), and extrathyroidal extension (OR = 1.555, P = 0.001) were independent risk factors for CLNM, and number of primary tumors was not significantly correlated with CLNM (P > 0.05) ( ).

Risk factors for LLNM

According to univariate analysis, tumor size greater than 6 mm, CLNM, extrathyroidal extension, multifocality, bilateralism, and tumor location (P < 0.05) were characterized as risk factors for LLNM, whereas sex, age, and Hashimoto’s thyroiditis status were not significantly associated with LLNM ( P > 0.05). Tumor location in the middle third of the thyroid gland conferred a high risk for LLNM. However, multivariate analysis identified only CLNM and recurrence as independent predictors for LLNM in patients who underwent follow-up for 40 to 72 months ( ).

Correlation of clinicopathologic characteristics and BRAFV600E mutation

Among the 1,587 patients, BRAFV600E mutation was detected in 299 patients with a frequency of 83.3% (249/299). Univariate analysis showed that CLNM, LLNM, multifocality, and extrathyroidal extension were not significantly associated with BRAFV600E mutation. Among patients who underwent follow-up for 40 to 72 months, recurrence was not significantly associated with BRAFV600E ().

Complications, follow-up, and recurrence

Recurrent laryngeal nerve injury occurred in 14 patients (0.9%); among these, owing to direct tumor invasion, 8 patients underwent shaving procedures or intentional resection of the recurrent laryngeal nerve resulting in permanent vocal fold paralysis, while the injury in the other 6 patients was temporary. Of the 1,587 patients, 386 (24.3%) suffered postoperative hypocalcemia requiring calcium supplementation, and 4 (0.3%) experienced permanent hypocalcemia. Four patients developed a postoperative chylous fistula, and 1 patient required reoperation on the same day owing to postoperative bleeding.

Postsurgical clinical examinations were performed every 6 months; these included cervical US and serum thyroid stimulating hormone and thyroglobulin levels. The mean follow-up duration was 56 months (range, 40–72 months), and 121 patients were lost to follow-up. During the follow-up period, 16 patients experienced recurrence in the central cervical compartment. Among 88 patients who had undergone lateral neck dissection, 3 patients (0.19%) suffered from LLNM: 2 and 1 experienced ipsilateral and contralateral neck recurrence, respectively. Among patients without LLNM at the time of initial treatment, 7 patients (0.44%) suffered regional recurrence: ipsilateral neck recurrence was found in 4 patients, contralateral neck recurrence in 1, and bilateral neck recurrence in 2. Regional recurrence was frequent at levels III, IV, and II. Among 1,209 patients who did not undergo total thyroidectomy, 12 (0.99%) experienced malignant recurrence in the contralateral lobe. At the data cutoff point, no patient demonstrated distant metastasis. During the follow-up period, 2 patients died from adrenal insufficiency and pneumonia, and another died of heart failure. None of the patients died of PTMC.

Discussion

In this retrospective study, we evaluated the risk factors for CLNM and LLNM in 1,587 patients with PTMC. In previous reports, the prevalence of CLNM ranged from 24.1% to 64.1%[2-5], and that for LLNM ranged from 3.7% to 44.5%[2]. In the present study, the prevalence of CLNM and LLNM was 30.9% (491 of 1,587) and 4.6% (73 of 1,587), respectively. There were 19 patients (19 of 73) with skip metastases, meaning LLNM without CLNM.

In the present study, we used univariate and multivariate logistic regression analyses to evaluate risk factors for cervical LNM. Consistent with the results of previous reports, we found that male gender, age less than 45 years, extrathyroidal extension, and bilateralism were independent risk factors for CLNM[14-18]. Multifocality was not an independent predictor of CLNM, although significance was demonstrated on univariate analysis.

Tumor size is considered to be an essential prognostic factor in patients with PTMC[19]. Although the majority of previous studies used a tumor size of 5 mm as the size threshold[20-23], we assessed thresholds greater than 4 mm, 5 mm, 6 mm, 7 mm, and 8 mm by ROC curve analysis, and found that primary tumor size (> 6 mm) was significantly correlated with CLNM. Extrathyroidal extension was an evaluated risk factor for CLNM[22,24]. However, the diagnosis of extrathyroidal extension is subjective and controversial as there is not a well-defined true capsule in the thyroid gland. The thyroid capsule is usually made up of inconspicuous thin fibrous tissues and contains a variable amount of skeletal muscle, blood vessels, and adipose tissue. In the present study, most cases of PTMC with extrathyroidal extension exhibited extension to the perithyroid soft tissue, such as adipose tissue, rather than to the sternothyroid muscle. In this study, 1,039 (65.5%) patients showed extrathyroidal extension, as we selected intrathyroidal areas with low-risk thyroid carcinoma for observation rather than surgery.

Furthermore, the present study showed that tumor size greater than 6 mm, extrathyroidal extension, multifocality, bilateralism, and CLNM were statistically significant factors for LLNM, and CLNM was an independent risk factor. Although CLNM is not significantly associated with disease-free survival in PTMC[25-27], this outcome can be strongly associated with LLNM.

The connection between tumor location and LNM in patients with PTMC remains controversial. Wada et al.[28] first reported that the location of PTMC may be related to CLNM and LLNM, although the differences were not statistically significant. Xiang et al.[29] found a correlation between PTMC located in the middle third of the thyroid gland with both CLNM and LLNM. In contrast, Zhang et al.[14] showed that location of PTMC in the upper third of the thyroid conferred a lower risk for CLNM and a higher risk for LLNM. In the present study, we found that tumor location in the lower third of the thyroid gland and the isthmus was strongly associated with CLNM, whereas tumor location in the middle third was correlated with LLNM.

The BRAFV600E mutation, which occurs in about 29%–60% of PTC, has been identified as the most common genetic change in PTC[30,31]. These mutations activate the RAS/RAF/mitogen-activated protein kinase pathway and cause the malignant proliferation of cells[32]. Previous observations have indicated that the BRAFV600E mutation is correlated with highly aggressive factors, such as advanced stage of disease, extrathyroidal extension, and nodal metastasis in PTC[33-35]. The BRAFV600E mutational status of highly aggressive PTMC was analyzed by Lee et al.[32] who discovered that the rate of BRAFV600E mutation in patients with penetration of the capsule was higher than the rate in those without. The authors also found that mutations occurred in 50% of T3 or T4 stage tumors, meaning that the presence of BRAFV600E mutation can predict the existence of extrathyroidal metastasis. Moreover, the BRAFV600E mutation was discovered more commonly in highly aggressive subtypes, such as tall cell PTMC, indicating that BRAFV600E mutational status is significantly associated with poor tumor behavior. BRAFV600E is also observed in PTMC, and the mutation may thus be an early event in tumor development, perhaps facilitating the acquisition of secondary genetic events through induction of genomic instability. However, unlike the findings of previous studies, Sun et al.[8] observed that BRAFV600E mutation displayed a weakly negative association with PTMC neck and distant metastasis in a group of 101 patients. In the present study, we were unable to identify a significant correlation between BRAFV600E mutation and clinicopathologic characteristics such as multifocality, neck metastasis, and extrathyroidal extension. Accordingly, it seems that BRAFV600E mutation is not a prognostic factor for PTMC. In fact, most patients with PTMC have an extremely good prognosis following surgery. Large numbers of patients undergo very long-term follow-up, and it will be necessary to identify the clinical relevance of the BRAFV600E mutation in PTMC. Despite the restrictions of the current study, our data also suggest that larger studies are warranted to determine the relationships between the BRAFV600E mutation and clinical characteristics in patients with PTMC.

Although we analyzed a cohort of 1,587 patients with PTMC, there are nonetheless still several limitations in the present study. First, the incidence of LLNM was relatively low in our research sample, and patients who did not undergo LLND were regarded as negative. However, prophylactic LLND could only be performed in cases of LLNM proven by FNAB or with clinical suspicion on US. In fact, prophylactic LLDN is not recommended in the American Thyroid Association guidelines. Nevertheless, data based on prophylactic LLND are more accurate and meaningful. In PTMC, however, the complications of LLND cannot be weighed against its questionable effect on recurrence and survival. Second, long-term follow-up was not performed in the current study. Third, the BRAFV600E mutation analyses were performed in a relatively small number of patients (299); therefore, the rate of BRAFV600E mutation may be underestimated, leading to the absence of a significant correlation between BRAFV600E mutation and aggressive factors.

Conclusions

In conclusion, the present study showed that male sex, age less than 45 years, tumor size larger than 6 mm, presence of bilateralism, and extrathyroidal extension were all independent risk factors for CLNM. Moreover, larger primary tumor, extrathyroidal extension, multifocality, bilateralism, and CLNM were factors that conferred an increased risk of LLNM. Notably, the location of the tumor had an important association with cervical lymph node metastasis status in patients with a solitary primary tumor. Specifically, PTMC location in the lower third of the thyroid gland and the isthmus was associated with a higher risk of CLNM, and PTMC location in the middle third correlated with LLNM. In our studies including 299 patients, BRAFV600E mutation was not significantly associated with prognostic factors in patients with PTMC.

Acknowledgements

This work was supported by grants from the National Natural Science Foundation of China (Grant No. 81402392, 81472580, 81502322) and Tianjin Municipal Science and technology project (Grant No. 15JCQNJC12800 and 17YFZCSY00690).

Conflict of interest statement

No potential conflicts of interest are disclosed.

1

Surgical treatment in 1,587 patients

Treatment	n (%)
Thyroid surgery
Lobectomy with isthmectomy	987 (62.2)
Isthmectomy	27 (1.7)
Near-total thyroidectomy	195 (12.3)
Total thyroidectomy	378 (23.8)
Lymph node dissection
Ipsilateral central lymph node dissection	974 (61.4)
Bilateral central lymph node dissection	613 (38.6)
Ipsilateral lateral lymph node dissection	98 (6.2)
No resection	0

2

Characteristics of patients

Characteristics	Case n = 1,587 (%)	CLNM+/-	LLNM+/-
		Positive (%)	Positive (%)
PTMC: papillary thyroid microcarcinoma; HT: Hashimotos thyroiditis; CLNM: Central lymph node metastasis; LLNM: Lateral neck lymph node metastasis; +, Positive; -, Negative.
Gender
Female	1251 (78.8)	351/900 (28.1)	53/1198 (4.2)
Male	336 (21.2)	140/196 (41.7)	20/316 (6.0)
Age, mean±SD (years)	45.7±9.4
< 45	726 (45.7)	259/467 (35.7)	40/686 (5.5)
≥ 45	861 (54.3)	232/629 (26.9)	33/828 (3.8)
PTMC with HT
Yes	333 (21.0)	105/228 (31.5)	18/315 (5.4)
No	1254 (79.0)	386/868 (30.8)	55/1199 (4.4)
Tumor size, mean±SD (mm)	5.9±2.5
> 6	586 (36.9)	256/330 (43.7)	45/541 (7.7)
≤ 6	1001 (63.1)	235/766 (23.5)	28/973 (2.8)
Extrathyroidal extension
Yes	1039 (65.5)	372/667 (35.8)	63/976 (6.1)
No	548 (34.5)	119/429 (21.7)	10/538 (1.8)
Tumor location
Multifocal letion	573 (36.1)	237/336 (41.4)	44/529 (7.7)
Solitary letion	1014 (63.9)	266/748 (26.2)	29/985 (2.9)
Upper third	312 (30.8)	72/240 (23.1)	15/297 (4.8)
Middle third	268 (26.4)	62/206 (23.1)	3/265 (1.1)
Lower third	407 (40.1)	126/281 (31.0)	11/396 (2.7)
Isthmus	27 (2.7)	6/21 (22.2)	0/27 (0)
Bilateralism
Yes	378 (23.8)	177/201 (46.8)	29/349 (7.7)
No	1209 (76.2)	314/895 (26.0)	44/1165 (3.6)
Subtype
Classical	1474 (92.9)	450/1024 (30.5)	68/1406 (4.6)
Follicular variant	102 (6.4)	36/66 (35.3)	5/97 (5.0)
Hürthle cell variant	11 (0.7)	5/6 (45.5)	0/11 (0)

3

Univariate and multivariate logistic regression for CLNM

Independent variable	Univariate			Multivariate
	OR (95% CI)	P		OR (95% CI)	P
aThe P-value means the difference between the group multifocal lesion and solitary lesions. bThe P-value means the difference among the upper third, top third, lower third, and isthmus in group of solitary lesion.
Gender		0.000			0.000
Female	1 (reference)			1 (reference)
Male	1.832 (1.427–2.351)			1.845 (1.419–2.399)
Age, years		0.000			0.000
< 45	1 (reference)			1 (reference)
≥ 45	0.665 (0.537–0.824)			0.624 (0.498–0.782)
PTMC with HT		0.790
Yes	1 (reference)			-	-
No	0.966 (0.744–1.253)			-
Tumor size (> 6 mmvs. ≤ 6 mm)		0.000			0.000
≤ 6 mm	1 (reference)			1 (reference)
> 6 mm	2.529 (2.013–3.148)			2.137 (1.694–2.697)
Extrathyroidal extension		0.000			0.001
Yes	1 (reference)			1 (reference)
No	0.497 (0.391–0.632)			0.643 (0.498–0.782)
Multifocal		0.000a			0.782
Yes	1 (reference)			1 (reference)
No	0.504 (0.406–0.627)			0.953 (0.679–1338)
Bilateralism		0.000			0.000
Yes	1 (reference)			1 (reference)
No	0.397 (0.312–0.504)			0.495 (0.343–0.715)
Subtype		0.017
Classical	1 (reference)			1 (reference)
Follicular variant	2.732 (1.253–5.957)	0.009		2.101 (0.932–4.738)	0.074
Hürthle cell variant	3.512 (0.585–21.098)	0.143		1.926 (0.298–12.440)	0.491
Solitary letion		0.049b
Upper third	1 (reference)			-	-
Middle third	1.003 (0.681–1.478)	1.000		-
Lower third	1.495 (1.067–2.093)	0.023		-
Isthmus	5.675 (1.989–16.087)	0.003		-

4

Univariate and multivariate logistic regression for LLNM

Independent variable	Univariate			Multivariate
	OR (95%CI)	P		OR (95%CI)	P
Gender		0.242
Female	1 (reference)			-	-
Male	1.403 (0.828–2.378)			-
Age, years		0.119
< 45	1 (reference)			-	-
≥ 45	0.684 (0.426–1.096)			-
PTMC with HT		0.461
Yes	1 (reference)			-	-
No	0.803 (0.465–1.387)			-
Tumor size (mm)		0.000			0.219
≤ 6	1 (reference)			1 (reference)
> 6	2.890 (1.783–4.687)			1.392 (0.822–2.359)
Extrathyroidal extension		0.000			0.055
Yes	1 (reference)			1 (reference)
No	0.288 (0.147–0.566)			0.496 (0.242–1.015)
Multifocal		0.000			0.267
Yes	1 (reference)			1 (reference)
No	0.382 (0.235–0.622)			0.668 (0.328–1.362)
Bilateralism		0.002			0.582
Yes	1 (reference)			1 (reference)
No	0.455 (0.280–0.737)			1.224 (0.595–2.519）
Subtype		0.759
Classical	1 (reference)			-	-
Follicular	1.646 (0.381–7.115)	0.808		-	-
Hürthle cell variant	1.051 (1.038–1.063)	1.000		-
Solitary letion		0.046
Upper third	1 (reference)			-	-
Middle third	0.224 (0.064–0.783)	0.014		-
Lower third	0.550 (0.249–1.215)	0.159		-
Isthmus	1.051 (1.025–1.077)	0.619		-
CLNM		0.000			0.000
Negative	1 (reference)			1 (reference)
Positive	35.077 (14.048–87.587)			29.354 (11.631–74.084)
Recurrence		0.000			0.000
Yes	1 (reference)			1 (reference)
No	30.051 (12.458–80.551)			25.254 (10.352–66.217)

5

Correlation between clinicopathological characteristics and BRAFV600E mutation in PTMC

Parameter	Case (n=299)	BRAF V600E mutation (n=249)	BRAF V600E wild-type (n=50)	P
CLNM				0.265
Positive	140 (46.8)	113 (80.7)	27 (19.3)
Negative	159 (53.2)	136 (85.5)	23 (14.5)
Multifocal
Yes	143 (47.8)	122 (85.3)	21 (14.7)	0.366
No	156 (52.2)	127 (81.4)	29 (18.6)
Extrathyroidal extension
Yes	233 (77.9)	192 (82.4)	41 (17.6)	0.447
No	66 (22.1)	57 (86.4)	9 (13.6)
LLNM
Positive	23 (7.7)	22 (95.7)	1 (4.3)	0.075
Negative	276 (92.3)	227 (82.2)	49 (17.8)
Recurrence
No	283 (94.6)	234 (82.7)	49 (17.3)	0.088
Yes	16 (5.4)	15 (93.8)	1 (6.2)