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Risk factors of lateral lymph node metastasis in cN0 papillary thyroid carcinoma

Abstract

Background

Cervical lymph node metastasis of papillary thyroid carcinoma (PTC) is common. However, whether undergoing prophylactic central lymph node (CLN) dissection or lateral lymph node (LLN) dissections to prevent metastasis is still controversial. This study aimed to retrospectively investigate the risk factors of LLN metastasis in clinical lymph node-negative (cN0) PTC patients.

Methods

We retrospectively studied 783 lymph node-negative (cN0) PTC patients who underwent total thyroidectomy plus CLN dissection and LLN dissection.

Results

The rates of CLN and LLN metastases were 68.2 and 47.4%, respectively. Large tumor size (> 20 mm) had a fourfold higher risk of LLN metastasis compared with small tumor size (≤ 20 mm; OR = 4.082, 95% CI 2.646–6.289; P = 0.001). Patients with tumor in the upper lobe had ~ 3-fold higher risk of LLN metastasis compared with patients with tumor in other locations (OR = 2.874, 95% CI 1.916–4.310; P = 0.001). Multifocality and extrathyroidal extension indicated a twofold higher risk of LLN metastasis. Having ≥ 2 CLN metastases dramatically increased the risk of LLN metastasis, compared with those with < 2 CLN metastases (OR = 6.536, 95% CI 4.630–9.259; P = 0.001).

Conclusions

Large tumor size (> 20 mm), tumor located in the upper lobe, multifocality, extrathyroidal extension, and ≥ 2 CLN metastases may increase the risk of LLN metastasis in cN0 PTC patients.

Background

Papillary thyroid carcinoma (PTC) is a common endocrine malignancy [1] and the most common type of thyroid cancer. In the USA, the annual incidence of PTC has increased during the last few decades, from 3.4/100,000 persons in 1975 to 12.5/100,000 persons in 2009 [2]. The etiology of PTC may associate with factors such as iodine deficiency, history of radiation on neck, Hashimoto’s thyroiditis, hereditary factors, and BRAF mutation [3, 4]. However, the increasing incidence cannot be fully explained by these risk factors. The majority of PTC patients have an excellent prognosis with low mortality rate, but early-stage metastasis may occur in the cervical lymph nodes.

Approximately 20–90% of PTC patients developed lymph node metastasis according to previous studies [5, 6]. These studies also indicate that lymph node metastasis predicts a higher recurrence rate. However, lymph node metastasis may not be associated with overall survival in PTC patients [7]. Therefore, the surgical treatment for metastasis of PTC remains controversial, especially the application of total thyroidectomy or lobectomy [8], and the prophylactic dissections of central and lateral lymph nodes (CLN and LLN, respectively) are also debatable [9].

In this retrospective cross-sectional study, we investigated the risk factors of LLN metastasis in clinical lymph node-negative (cN0) PTC patients.

Methods

A total of 1443 patients underwent surgery for thyroid cancer at the Department of Endocrine and Breast Surgery, First Affiliated Hospital of Chongqing Medical University, between January 2013 and December 2016. Patients with any of the following were excluded: non-PTC histology (n = 47), reoperation (n = 195), distant metastasis (n = 6), and clinical lymph node-positive (cN1) patients (n = 226). The inclusion criteria were as follows: no history of head or neck irradiation, and clinical lymph node-negative (cN0) confirmed by palpation and neck ultrasound. A total of 969 cN0 PTC patients underwent total thyroidectomy with CLN dissection and with or without LLN dissection. Routine ipsilateral central lymph node frozen biopsy is performed. Prophylactic LLN dissection was performed if CLN metastasis was confirmed by frozen biopsy. Because of the long-term clinical observation, some CLN-negative PTC patients diagnosed by intraoperative frozen biopsy, who still underwent prophylactic lateral lymph node dissection, meet the following conditions: extra thyroidal extension, diameter > 1 cm, tumor in the upper lobe, and multifocality (Fig. 1).

Fig. 1
figure 1

Flowchart of this retrospective study. CLND, central lymph node dissection; CLNM, central lymph node metastasis; LLND, lateral lymph node dissection

We sent all of the central compartment tissue for frozen biopsy after CLN dissection, and then, experienced pathologists dissected CLN from the fat tissue and examined the lymph nodes specimens. The frozen biopsy diagnosis takes about 30 min. All harvested lymph nodes were sent to postoperative pathological examination according to different regions and were diagnosed by three pathologists.

In our institution, total thyroidectomy plus ipsilateral CLN dissection or ipsilateral LLN dissection is performed for unilateral PTC with a diameter > 1cm. For patients who have bilateral thyroid cancer with diameter > 1 cm, total thyroidectomy plus bilateral CLN dissection and bilateral LLN dissection is performed. For PTC with diameter <1 cm, lobectomy with ipsilateral CLN dissection is the basic operative treatment. If the ipsilateral central lymph node frozen biopsy suggests lymph node metastasis, we further perform contralateral lobectomy plus ipsilateral LLN dissection. The grading of each LLN level is based on the guidelines of the American Head and Neck Society [10]. Level I and level V lymph node metastases are rare in clinic, as previously reported [11, 12]. We performed selective LLN dissections, and the main regions of the LLN were graded as II, III, or IV.

Demographic and clinical pathology data were collected, including gender, age, extrathyroidal extension (ETE), multifocality, Hashimoto’s thyroiditis, tumor size, tumor location, bilaterality, and number of central lymph node metastases. If the patient had multiple lesions in one side of the thyroid gland, the diameter of the largest was recorded as the tumor size.

Postoperative complications were also evaluated and mainly concerned hemorrhage, hypoparathyroidism, recurrent laryngeal nerve injury, or chyle leakage. Serum calcium < 8 mg/dL within 6 months after surgery was defined as temporary hypoparathyroidism, while after 6 months was regarded as permanent hypoparathyroidism. Vocal cord paralysis, found by laryngoscopy within 6 months after the operation, was defined as temporary recurrent laryngeal nerve injury; vocal cord paralysis that lasted longer than 6 months was defined as permanent laryngeal nerve injury.

Recurrence can be seen as local or regional disease requiring reoperation or other treatment 6 months after the initial standard operation. It is diagnosed by ultrasound or ultrasound-guided fine needle aspiration cytology.

Statistical analysis

T test, chi-square, or Fisher’s exact test were used to compare differences in gender (male, female), age (≤ 45, > 45), tumor size (≤ 10, 10–20, > 20 mm), tumor location (upper lobe, middle lobe, lower lobe, isthmus, hole), ETE (yes, no), multifocality (yes, no), bilaterality (yes, no), Hashimoto’s thyroiditis (yes, no), and number of central lymph node metastases (≤ 1, ≥ 2) between the patients with or without LLN metastases. Univariate and multivariate analyses were used in this study. Two-sided P < 0.05 was regarded as statistically significant. SPSS version 21 software was used for all analyses. The study was approved by the local institutional ethics committee board.

Results

There were 783 PTC patients who underwent total thyroidectomy, plus prophylactic CLN dissection and LLN dissection from January 2013 to December 2016. All patients underwent ultrasonography, fibrolaryngoscope, and thyroid function before surgery. The mean follow-up time was 20.2 ± 12.7 months.

The total study population consisted of 576 (73.6%) women and 207 (26.4%) men (Table 1). The patient group with LLN metastasis comprised 256 women and 115 men; the group without LLN metastasis consisted of 320 women and 92 men (P = 0.06). The average age at diagnosis of the metastasis group was 41.0 ± 13.3, lower than that of the group without metastasis (P = 0.005). The tumor size in the metastasis group (20.8 ± 12.2 mm) was significantly larger than that of the patients without metastasis (14.0 ± 9.0 mm; P = 0.001). In the metastasis group, 105 (28.3%) patients had tumor in the upper lobe, while in the group without metastasis, this was true in only 68 (16.5%). The incidence of ETE, bilateral lesions, were also different between the two groups (all P < 0.05).

Table 1 Baseline characteristics of the study patients

LLN metastasis was significantly associated with gender, age at diagnosis, age group (≤ 45, > 45 years), tumor size, tumor size group, tumor location, ETE, multifocality, bilateral, and number of CLN metastasis in the univariate analysis (Table 1). In the multivariate analysis, compared to the women, the men tended to have a higher risk of LLN metastasis (OR = 1.435, 95% CI 0.982–2.092), although no statistical significance was found (P = 0.062; Table 2). No risk differences in LLN metastasis were found between the age groups (P = 0.373) and bilateral groups (P = 0.866). Large tumor size (> 20 mm) was observed with a fourfold higher risk of LLN metastasis compared with small tumor size (≤ 20 mm; OR = 4.082, 95% CI 2.646–6.289; P = 0.001). Patients with tumor found in the upper lobe had ~ 3-fold higher risk of LLN metastasis compared with patients with tumor in other locations (OR = 2.874, 95% CI 1.916–4.310; P = 0.001). Multifocality and ETE indicated a twofold higher risk of LLN metastasis. Having > 2 CLN metastases dramatically increased the risk of LLN metastasis, compared with those with < 2 CLN metastasis (OR = 6.536, 95% CI 4.630–9.259; P = 0.001).

Table 2 Multivariate analysis of risk factors of LLN metastasis

Among the 783 PTC patients, only two cases of hemorrhage were found (Table 3). Temporary hypoparathyroidism was the most frequent comorbidity observed in both the metastasis and non-metastasis groups, with slightly more cases in the former (P = 0.019). Chyle leakage occurred more frequently in the patients with LLN metastasis (P = 0.031). No other differences were found regarding the occurrence of comorbidity. Five patients experienced recurrence, 4 of which were in the metastasis-positive group.

Table 3 Comorbidity and recurrence of LLN metastasis

Discussion

Our study indicates that large tumor size, tumor in the upper lobe, multifocality, ETE, and having ≥ 2 CLN metastases were all associated positively with risk of LLN metastasis. Gender, age, and bilateral lesions were not associated with risk of LLN metastasis.

The univariate analysis showed that the risk of LLN metastasis was significantly higher in men than in women, but this association did not hold true in the multivariate analysis. Previous studies found that male gender was associated with CLN metastasis, but was not associated with LLN metastasis [13, 14]. In the present study, age was not associated with risk of LLN metastasis, which is in agreement with two previous studies [13, 15].

Hunt et al. [16] suggested that the location of the tumor is closely related to LLN metastasis. More specifically, Zhang et al. [17] found that a tumor in the upper third of the thyroid was at greater risk of LLN metastasis, but at lower risk of CLN metastasis. Kwak et al. [18] also demonstrated that an upper pole location was an independent factor in predicting LLN metastasis.

Many studies have shown that lymph node metastasis is associated with tumor size. Nie et al. [15] suggested that a tumor diameter > 1.5 cm is an independent risk factor for LLN metastasis. However, another study suggested a cut-off point of 2 cm [13], which is in accord with the results of the current study.

In our study, multifocality was found to increase the risk of LLN metastasis. However, bilateral lesions were not a potential risk factor. Nie et al. [15] suggested that multifocality and bilateral were not risk factors for lymph node metastasis.

Much evidence has indicated that ETE is an important predictor of lymph node metastasis in PTC patients [19, 20]. Previous research has shown that CLN metastasis is an important risk factor for LLN metastasis [21, 22]. More specifically, our present study found that patients with ≥ 2 CLN metastases had higher risk of LLN metastasis, which could potentially provide support for performing LLN dissection.

Five cases of recurrence were found in the present study. Every patient had central lymph node and four patients had LLN metastasis during the initial treatment. Mercante et al. [23] found that lymph node metastasis was a risk factor of local recurrence. Chereau et al. [24] reported the LLN metastasis is an important prognostic factor for recurrence. Five patients were treated with iodine 131 after the initial operation. The average time of recurrence was 22.4 months (range from 12 to 35 months). In the current study, recurrence was in the LLN of each patient, which draws our particular attention to the question of LLN dissection.

Surgical complications are so important that they cannot be ignored. Common complications include parathyroid injury, recurrent laryngeal nerve, chyle leakage, and Horner’s syndrome. Moo et al. [25] reported that rates of temporary and permanent hypocalcemia were 47 and 0%, respectively, and the rates for temporary and permanent recurrent laryngeal nerve injury were 5 and 0%. Our data showed that the incidence of temporary parathyroid injury was high (417/783; 53.2%), but most patients had parathyroid function recovery after symptomatic treatment. There were very few patients with permanent parathyroid injury or permanent recurrent laryngeal nerve injury. Thirteen patients had chyle leakage, and each patient underwent level IV lymph node dissection; 11 of these underwent left level IV lymph node dissection. Twelve patients were treated successfully by strong negative pressure drainage, low-fat diet, or intracavitary injection of inactivated Pseudomonas aeruginosa. Only one patient underwent reoperation for thoracic duct ligation. We should pay special attention to left level IV lymph node dissection, as it may damage the branch or trunk of the thoracic duct because of its anatomical position.

We have gone through the process from roughly zoning and wide dissection to precise zoning and selective dissection. In our study, the recommended procedure for PTC patients is lobectomy with paratracheal, prelaryngeal, and ipsilateral tracheal lymph node dissections (we recommend posterior lymph nodes of recurrent laryngeal nerve dissection, if the lesions are located on the right side of the lobe). Then, the abovementioned central lymph node will undergo an intraoperative frozen biopsy, because the number of ipsilateral CLN metastases is very important.

If the total number of ipsilateral central metastases is ≥ 2, then prophylactic LLN dissection mainly in the ipsilateral level III and IV should be performed. Preoperative ultrasound showing enlarged lymph nodes in level II, intraoperative frozen biopsy prelaryngeal lymph node metastasis, and a primary tumor located in the upper pole of the thyroid gland is the basis of level II lymph node dissection.

Conclusions

In conclusion, our study found that large tumor size, tumor in the upper lobe, multifocality, ETE, or ≥ 2 CLN metastases may increase the risk of LLN metastasis. Recurrence was high among patients with LLN metastasis, and therefore, we support that PTC patients need routine central lymph node dissection, not only for more accurate clinical staging but also because of the high incidence of central lymph node metastasis.

We recommend that prophylactic LLN dissection should be considered for PTC patients with large tumor size (> 20 mm), primary tumor in the upper lobe, multifocality, ETE, or ≥ 2 CLN metastases.

Abbreviations

CLN:

Central lymph node

cN0:

Clinical lymph node negative

LLN:

Lateral lymph node

PTC:

Papillary thyroid carcinoma

References

  1. Shaha AR. Prognostic factors in papillary thyroid carcinoma and implications of large nodal metastasis. Surgery. 2004;135:237–9.

    Article  PubMed  Google Scholar 

  2. Davies L, Welch HG. Current thyroid cancer trends in the United States. JAMA Otolaryngol Head Neck Surg. 2014;140:317–22.

    Article  PubMed  Google Scholar 

  3. Pellegriti G, Frasca F, Regalbuto C, Squatrito S, Vigneri R. Worldwide increasing incidence of thyroid cancer: update on epidemiology and risk factors. J Cancer Epidemiol. 2013;2013:965212.

    Article  PubMed  PubMed Central  Google Scholar 

  4. Kimura ET, Nikiforova MN, Zhu Z, Knauf JA, Nikiforov YE, Fagin JA. High prevalence of BRAF mutations in thyroid cancer: genetic evidence for constitutive activation of the RET/PTC-RAS-BRAF signaling pathway in papillary thyroid carcinoma. Cancer Res. 2003;63:1454–7.

    CAS  PubMed  Google Scholar 

  5. Cooper DS, Doherty GM, Haugen BR, Kloos RT, Lee SL, Mandel SJ, Mazzaferri EL, McIver B, Pacini F, Schlumberger M, et al. Revised American Thyroid Association management guidelines for patients with thyroid nodules and differentiated thyroid cancer. Thyroid. 2009;19:1167–214.

    Article  PubMed  Google Scholar 

  6. Hay ID, Hutchinson ME, Gonzalez-Losada T, McIver B, Reinalda ME, Grant CS, Thompson GB, Sebo TJ, Goellner JR. Papillary thyroid microcarcinoma: a study of 900 cases observed in a 60-year period. Surgery. 2008;144:980–7. discussion 987-988

    Article  PubMed  Google Scholar 

  7. Podnos YD, Smith D, Wagman LD, Ellenhorn JD. The implication of lymph node metastasis on survival in patients with well-differentiated thyroid cancer. Am Surg. 2005;71:731–4.

    PubMed  Google Scholar 

  8. Adam MA, Pura J, Gu L, Dinan MA, Tyler DS, Reed SD, Scheri R, Roman SA, Sosa JA. Extent of surgery for papillary thyroid cancer is not associated with survival: an analysis of 61,775 patients. Ann Surg. 2014;260:601–5. discussion 605-607

    Article  PubMed  PubMed Central  Google Scholar 

  9. Evans DB. Papillary carcinoma of the thyroid: balancing principles of oncology with emerging technology. Surgery. 2011;150:1015–22.

    Article  PubMed  Google Scholar 

  10. Carty SE, Cooper DS, Doherty GM, Duh QY, Kloos RT, Mandel SJ, Randolph GW, Stack BC Jr, Steward DL, Terris DJ, et al. Consensus statement on the terminology and classification of central neck dissection for thyroid cancer. Thyroid. 2009;19:1153–8.

    Article  PubMed  Google Scholar 

  11. Kupferman ME, Patterson M, Mandel SJ, LiVolsi V, Weber RS. Patterns of lateral neck metastasis in papillary thyroid carcinoma. Arch Otolaryngol Head Neck Surg. 2004;130:857–60.

    Article  PubMed  Google Scholar 

  12. Kim SK, Park I, Hur N, Lee JH, Choe JH, Kim JH, Kim JS. Should level V be routinely dissected in N1b papillary thyroid carcinoma? Thyroid. 2017;27:253–60.

    Article  CAS  PubMed  Google Scholar 

  13. Lee DJ, Lee KH, Kim JH, Kwon KH, Yoon DY, Rho YS. Posterosuperior lesion has a high risk of lateral and central nodal metastasis in solitary papillary thyroid cancer. World J Surg. 2015;39:387–92.

    Article  PubMed  Google Scholar 

  14. Giordano D, Frasoldati A, Kasperbauer JL, Gabrielli E, Pernice C, Zini M, Pedroni C, Cavuto S, Barbieri V. Lateral neck recurrence from papillary thyroid carcinoma: predictive factors and prognostic significance. Laryngoscope. 2015;125:2226–31.

    Article  PubMed  Google Scholar 

  15. Nie X, Tan Z, Ge M, Jiang L, Wang J, Zheng C. Risk factors analyses for lateral lymph node metastases in papillary thyroid carcinomas: a retrospective study of 356 patients. Arch Endocrinol Metab. 2016;60:492–9.

    Article  PubMed  Google Scholar 

  16. Hunt JP, Buchmann LO, Wang L, Abraham D. An analysis of factors predicting lateral cervical nodal metastases in papillary carcinoma of the thyroid. Arch Otolaryngol Head Neck Surg. 2011;137:1141–5.

    Article  PubMed  Google Scholar 

  17. Zhang L, Wei WJ, Ji QH, Zhu YX, Wang ZY, Wang Y, Huang CP, Shen Q, Li DS, Wu Y. Risk factors for neck nodal metastasis in papillary thyroid microcarcinoma: a study of 1066 patients. J Clin Endocrinol Metab. 2012;97:1250–7.

    Article  CAS  PubMed  Google Scholar 

  18. Kwak JY, Kim EK, Kim MJ, Son EJ, Chung WY, Park CS, Nam KH. Papillary microcarcinoma of the thyroid: predicting factors of lateral neck node metastasis. Ann Surg Oncol. 2009;16:1348–55.

    Article  PubMed  Google Scholar 

  19. Ito Y, Kudo T, Takamura Y, Kobayashi K, Miya A, Miyauchi A. Prognostic significance of carcinoma extension from primary lesions and metastatic nodes in papillary thyroid carcinoma: appropriateness of three subdivisions of extension. Endocr J. 2011;58:961–7.

    Article  PubMed  Google Scholar 

  20. Chung YS, Kim JY, Bae JS, Song BJ, Kim JS, Jeon HM, Jeong SS, Kim EK, Park WC. Lateral lymph node metastasis in papillary thyroid carcinoma: results of therapeutic lymph node dissection. Thyroid. 2009;19:241–6.

    Article  PubMed  Google Scholar 

  21. Xiao GZ, Gao L. Central lymph node metastasis: is it a reliable indicator of lateral node involvement in papillary thyroid carcinoma? World J Surg. 2010;34:237–41.

    Article  PubMed  Google Scholar 

  22. Ducoudray R, Tresallet C, Godiris-Petit G, Tissier F, Leenhardt L, Menegaux F. Prophylactic lymph node dissection in papillary thyroid carcinoma: is there a place for lateral neck dissection? World J Surg. 2013;37:1584–91.

    Article  PubMed  Google Scholar 

  23. Mercante G, Frasoldati A, Pedroni C, Formisano D, Renna L, Piana S, Gardini G, Valcavi R, Barbieri V. Prognostic factors affecting neck lymph node recurrence and distant metastasis in papillary microcarcinoma of the thyroid: results of a study in 445 patients. Thyroid. 2009;19:707–16.

    Article  CAS  PubMed  Google Scholar 

  24. Chereau N, Buffet C, Tresallet C, Tissier F, Leenhardt L, Menegaux F. Recurrence of papillary thyroid carcinoma with lateral cervical node metastases: predictive factors and operative management. Surgery. 2016;159:755–62.

    Article  PubMed  Google Scholar 

  25. Moo TA, Umunna B, Kato M, Butriago D, Kundel A, Lee JA, Zarnegar R, Fahey TJ 3rd. Ipsilateral versus bilateral central neck lymph node dissection in papillary thyroid carcinoma. Ann Surg. 2009;250:403–8.

    PubMed  Google Scholar 

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Contributions

XS and DH designed the study. JZ, WH, JP, YC, YM, and WX collected the data. HR, YD, QX, and DH performed the statistical analyses. XS and DH reviewed the results, interpreted the data, and wrote the manuscript. All authors read and approved the final version of the paper.

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Correspondence to Xinliang Su.

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This work was supported by the ethics committee of The First Affiliated Hospital of Chongqing Medical University.

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Hu, D., Zhou, J., He, W. et al. Risk factors of lateral lymph node metastasis in cN0 papillary thyroid carcinoma. World J Surg Onc 16, 30 (2018). https://doi.org/10.1186/s12957-018-1336-3

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