Skip to main content

Minimal extrathyroidal extension is associated with lymph node metastasis in single papillary thyroid microcarcinoma: a retrospective analysis of 814 patients

Abstract

Background

Extrathyroidal extension (ETE) is considered a major prognostic factor in papillary thyroid carcinoma (PTC). Patients with gross ETE are at increased risk of recurrence and mortality. The importance of minimal ETE still remains controversial, especially in patients with papillary thyroid microcarcinoma (PTMC). The purpose of this study was to evaluate the association between ETE and lymph node (LN) metastasis in single PTMC.

Methods

A retrospective analysis was performed of 1994 patients underwent thyroidectomy for PTC between 2012 and 2016 in a single institution. Patients with combined thyroid carcinoma of other types and those who underwent completion thyroidectomy were excluded. After further exclusion of PTC larger than 1 cm and multifocal tumors, 814 patients with single PTMC were included in the study.

Results

72.9% patients had no ETE, 25.1% minimal ETE, and 2.1% gross ETE. ETE was associated with lymphatic invasion, perineural invasion, and vascular invasion. Patients with minimal and gross ETE were also more likely to have LN metastasis, including lateral neck metastasis, compared to those without ETE. In univariate analysis, LN metastasis was associated with male gender, conventional PTC, lymphatic invasion, perineural invasion, and ETE. In multivariate analysis, male gender (OR = 1.987; 95% CI 1.369–2.884), lymphatic invasion (OR = 4.389; 95% CI 1.522–12.658), perineural invasion (OR = 6.545; 95% CI 1.262–33.948), and minimal ETE (OR = 1.852; 95% CI 1.298–2.643) were found to be independent risk factors of LN metastasis.

Conclusions

Minimal ETE is associated with LN metastasis in single PTMC, compared to no ETE. Minimal ETE should be considered in the management of patients with single PTMC, whether surgical or during active surveillance.

Background

Extrathyroidal extension (ETE) is considered an important prognostic factor in patients with papillary thyroid carcinoma (PTC) [1, 2]. ETE can be classified as minimal or gross, based on the extent of invasion of the tumor to adjacent structures. Both minimal and gross ETE were accepted as important variables during staging of differentiated thyroid carcinoma, regardless of tumor size [3, 4]. However, several studies have reported that minimal ETE has minimal influence on outcomes of the patient [5, 6]. These results were reflected in the eighth edition of TNM staging from the American Joint Committee on Cancer (AJCC), and minimal ETE has been removed from the T stage of differentiated thyroid carcinoma [7].

It is well accepted that patients with gross ETE have a worse outcome compared to those with minimal ETE. However, the oncological significance of minimal ETE still remains controversial. The association of ETE with tumor size and multifocality has been described in previous studies [8,9,10,11]. Tumor size is one of the most important prognostic factors in PTC, along with patient age, gender, and metastasis. Although not included in any of the prognostic classification systems, multifocality is generally regarded as a high-risk factor. Accordingly, tumor size and multifocality could be considered confounding variables, when investigating the clinical implications of ETE.

The relationship between ETE and lymph node (LN) metastasis has also been discussed in earlier studies [8, 12, 13], along with BRAF mutation, location of tumor, and iodine intake [14,15,16,17,18]. Controversy still exists on whether LN metastasis affects overall survival [19,20,21]. However, the association between LN metastasis and locoregional recurrence has been consistently confirmed through previous reports. Patients with recurred disease often require additional operations or radioactive iodine ablation, which can subsequently result in secondary complications.

The aim of this study was to investigate the clinicopathologic characteristics of minimal ETE in patients with single papillary thyroid microcarcinoma (PTMC) and its effects on LN metastasis.

Methods

Patients

Medical records of 1994 patients who underwent thyroidectomy for PTC at Chung-Ang University Hospital between 2012 and 2016 were retrospectively reviewed. After exclusion of patients with multifocal tumors and those with tumors larger than 1 cm, 814 patients with single PTMC were included in the study. Patients were according to the presence and extent of ETE into three groups (no ETE vs. minimal ETE vs. gross ETE), as appearing in the permanent pathology reports. Minimal ETE was defined as tumor invasion beyond the thyroid capsule detected on microscopy, and gross ETE was defined as obvious extension of the primary tumor to adjacent structures detected during operation. Gender, age, histologic variation, lymphovascular invasion, lymph node metastasis, BRAF mutation, and extent of surgery were reviewed. The study protocol was approved by the Institutional Review Board of Chung-Ang University Hospital (2203–019-19,411).

Surgery

Five hundred sixty-one patients received a total thyroidectomy, 244 underwent unilateral lobectomy, and 9 patients had a wide isthmusectomy. Prophylactic central node dissection (CND) was routinely performed on the ipsilateral side of thyroid tumor. Bilateral therapeutic CND was performed on patients who underwent total thyroidectomy when there were suspicious lymph nodes on preoperative imaging studies. Lateral neck dissection was performed in 38 patients, who were preoperatively diagnosed with metastatic lymph nodes.

Statistical analysis

SPSS version 22 (SPSS, Inc., Chicago, IL, USA) was used for all statistical analyses. Continuous data were compared using analysis of variance (ANOVA). Nominal data were analyzed with chi-square test or Fisher’s exact test. Data are expressed as mean ± standard deviation or number (%). Multivariate analysis was performed using logistic regression to assess the impact of clinicopathological features in association to lymph node metastasis. Results are presented as the odds ratio (OR) with a 95% confidence interval (CI). A p-value < 0.05 defined statistical significance.

Results

Patients and tumor characteristics according to extent of ETE

Five hundred ninety-three (72.9%) patients had no ETE, 204 (25.1%) had minimal ETE, and 17 (2.1%) had gross ETE (Table 1). There was no significant difference in gender, age, and histologic variation between the groups. Both minimal and gross ETE were significantly associated with lymphatic invasion, perineural invasion, vascular invasion, and LN metastasis compared to the no ETE group. Furthermore, gross ETE showed a higher rate of lymphatic invasion, perineural invasion, vascular invasion, and LN metastasis in contrast to minimal ETE. The proportion of BRAF mutant tumors were significantly higher in the gross ETE group, when compared to the no ETE group (p = 0.005) but not the minimal ETE group (p = 0.095).

Table 1 Clinicopathological features of patients according to the presence and extent of ETE

Clinicopathological features according to LN metastasis

Table 2 shows the clinicopathological differences of patients in relation to lymph node metastasis. LN metastasis was significantly more common in male patients and younger patients. The proportion of patients with ETE was significantly higher in patients with LN metastasis (p < 0.001). BRAF mutation was similar between both groups.

Table 2 Clinicopathological features of patients according to lymph node metastasis

Risk factors for LN metastasis

Clinical and pathological variables that were significant in univariate analysis were included in the multivariate analysis regression for assessment as risk factors of lymph node metastasis (Table 3). Male gender, younger age, lymphatic invasion, perineural invasion, and minimal ETE were independently associated with LN metastasis. Patients with gross ETE were 2.1 times more likely to be accompanied by LN metastasis (95% CI 0.656–6.997) but with no statistical significance (p = 0.207).

Table 3 Multivariate logistic regression of lymph node metastasis in single PTMC

Recurrence

The mean follow-up period was 30.0 ± 15.7 months (range, 1 ~ 61 months). Recurrence was identified in 3 (0.4%) patients during follow-up. All three patients recurred in the lateral neck LN, and there were no distant metastases.

Discussion

Minimal ETE was first implemented in the TNM criteria by the AJCC in 2002. Differentiated thyroid carcinoma with minimal ETE was classified as T3, which upstaged tumors smaller than 4 cm [3]. Recent changes in the eight edition of the AJCC TNM staging system reflect the results from various studies that have invalidated the effects of minimal ETE on overall survival and mortality. Nonetheless, the oncological significance of minimal ETE still remains controversial. Minimal ETE is regarded in association with tumor size, multifocality, LN metastasis, and recurrence [8, 10,11,12, 19, 22, 23].

Papillary thyroid microcarcinoma is defined as a papillary thyroid carcinoma ≤ 1 cm in maximum diameter. PTMC is commonly viewed as non-progressive, due to its relatively indolent course. Disease-free survival and overall survival rate are commonly discussed when estimating the prognosis of a particular disease. Hay et al. reported cause-specific mortality rates of 0.1, 0.1, and 0.7% at 10, 20, and 40 years, respectively, in a study of 900 cases of PTMC during a 60-year period [24]. Many studies have shown that LN metastasis in PTMC is closely related to recurrence and disease-free survival [25, 26]. A retrospective study by Karatzas et al. concluded that LN metastasis was the strongest prognostic factor of tumor recurrence in patients with nonincidental PTMC [27].

In this study, we investigated the clinical and pathologic characteristics of ETE in 814 patients with single PTMC by excluding the effects of tumor size and multifocality. No ETE and gross ETE were also included for analysis in order to see the differences in this specific subset of patients with single PTMC, according to the extent of ETE, with emphasis on minimal ETE. Furthermore, the risk factors for LN metastasis in single PTMC were also assessed. Few studies have assessed the value of minimal ETE in PTMC. Moon et al. included 288 patients with conventional PTMC and found that minimal ETE was associated with tumor size and central LN metastasis but not recurrence [28]. Woo et al. evaluated the significance of minimal ETE in 144 patients with solitary PTMC and concluded that it had no significant influence on recurrence-free survival. This study included patients with 814 patients with single PTMC, which is a relatively larger population, compared with the former studies.

Minimal ETE was significantly associated with lymphatic invasion, perineural invasion, vascular invasion, and LN metastasis compared to the no ETE group but less than the gross ETE group. Minimal ETE was independently associated with LN metastasis, along with male gender, and younger age. These results are consistent with previous studies [8, 10, 12]. Since there were no mortality and only three cases of recurrence during 30 months (range, 1 ~ 61 months) of follow-up, we could not assess survival outcomes.

Two recent systematic reviews and meta-analyses that studied the impact of minimal ETE in differentiated thyroid cancer concluded that minimal ETE increases the risk of recurrence in PTC [29, 30]. In patients with PTMC, the impact of minimal ETE was non-significant [30]. We agree with previous reports that minimal ETE has no impact on survival, and the increase in risk of recurrence is small. However, LN metastasis in PTMC has been associated with recurrence. Thus, when there is suspicion of ETE at the time of operation, examination of the cervical lymph nodes is suggested. Similarly, in situations where ETE is suspected during active surveillance of small PTCs, careful inspection of metastatic LNs may be required.

A recent study of PTMC patients in Cyprus concluded that the prevalence of LN metastasis and ETE was especially higher in patients with multifocal tumors [31]. The main purpose of our study was to evaluate the effects of minimal ETE, and the associated LN metastasis in PTMC patients, which is why we chose to only include those with single tumors. However, multifocality is also associated LN metastasis and should be carefully looked for while assessing patients with PTMC.

There are some limitations to this study. The relatively short follow-up period and low recurrence rate made it difficult to assess the long term effects of minimal ETE in single PTMC patients. Most of the patients in the study were operated before the updates in thyroid cancer management guidelines were published in 2015 [32], and all patients received prophylactic central neck dissection, which may have impacted the number of LN metastasis detected. One may argue that information gained from prophylactic node dissection may upstage patients, leading to overtreatment. However, this information cannot be devalued, especially while managing PTMC patients before and after surgery.

Conclusions

Minimal ETE was significantly associated with lymphatic invasion, perineural invasion, vascular invasion, and LN metastasis in patients with single PTMC. Minimal ETE was independently associated with LN metastasis. Minimal ETE should be considered during the decision making in managing of patients with single PTMC, whether it be surgical or for active surveillance.

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Abbreviations

ETE:

Extrathyroidal extension

PTC:

Papillary thyroid carcinoma

PTMC:

Papillary thyroid microcarcinoma

LN:

Lymph node

CND:

Central node dissection

OR:

Odds ratio

CI:

Confidence interval

References

  1. Andersen PE, Kinsella J, Loree TR, Shaha AR, Shah JP. Differentiated carcinoma of the thyroid with extrathyroidal extension. Am J Surg. 1995;170(5):467–70.

    Article  CAS  Google Scholar 

  2. Wen X, Jin Q, Cen X, Qiu M, Wu Z. Clinicopathologic predictors of central lymph node metastases in clinical node-negative papillary thyroid microcarcinoma: a systematic review and meta-analysis. World J Surg Oncol. 2022;20(1):106.

    Article  Google Scholar 

  3. Edge SBBD, Compton CC, Fritz AG, Greene FL, Trotti A. AJCC Cancer Staging Handbook. 7th ed. New York: Springer-Verlag; 2010.

    Google Scholar 

  4. Hay ID, Grant CS, Taylor WF, McConahey WM. Ipsilateral lobectomy versus bilateral lobar resection in papillary thyroid carcinoma: a retrospective analysis of surgical outcome using a novel prognostic scoring system. Surgery. 1987;102(6):1088–95.

    CAS  PubMed  Google Scholar 

  5. Ito Y, Tomoda C, Uruno T, Takamura Y, Miya A, Kobayashi K, et al. Prognostic significance of extrathyroid extension of papillary thyroid carcinoma: massive but not minimal extension affects the relapse-free survival. World J Surg. 2006;30(5):780–6.

    Article  Google Scholar 

  6. Hay ID, Johnson TR, Thompson GB, Sebo TJ, Reinalda MS. Minimal extrathyroid extension in papillary thyroid carcinoma does not result in increased rates of either cause-specific mortality or postoperative tumor recurrence. Surgery. 2016;159(1):11–9.

    Article  Google Scholar 

  7. Amin MB, Edge S, Greene F, Byrd DR, Brookland RK, Washington MK, et al. (Eds.). AJCC Cancer Staging Manual 8th ed. American Joint Commission on Cancer. New York: Springer International Publishing; 2017.

  8. Park JS, Chang JW, Liu L, Jung SN, Koo BS. Clinical implications of microscopic extrathyroidal extension in patients with papillary thyroid carcinoma. Oral Oncol. 2017;72:183–7.

    Article  Google Scholar 

  9. Ahn D, Sohn JH, Jeon JH, Jeong JY. Clinical impact of microscopic extrathyroidal extension in patients with papillary thyroid microcarcinoma treated with hemithyroidectomy. J Endocrinol Invest. 2014;37(2):167–73.

    Article  CAS  Google Scholar 

  10. Jin BJ, Kim MK, Ji YB, Song CM, Park JH, Tae K. Characteristics and significance of minimal and maximal extrathyroidal extension in papillary thyroid carcinoma. Oral Oncol. 2015;51(8):759–63.

    Article  Google Scholar 

  11. Radowsky JS, Howard RS, Burch HB, Stojadinovic A. Impact of degree of extrathyroidal extension of disease on papillary thyroid cancer outcome. Thyroid. 2014;24(2):241–4.

    Article  Google Scholar 

  12. Youngwirth LM, Adam MA, Scheri RP, Roman SA, Sosa JA. Extrathyroidal extension is associated with compromised survival in patients with thyroid cancer. Thyroid. 2017;27(5):626–31.

    Article  CAS  Google Scholar 

  13. Clain JB, Scherl S, Dos Reis L, Turk A, Wenig BM, Mehra S, et al. Extrathyroidal extension predicts extranodal extension in patients with positive lymph nodes: an important association that may affect clinical management. Thyroid. 2014;24(6):951–7.

    Article  Google Scholar 

  14. Zhou SL, Guo YP, Zhang L, Deng T, Xu ZG, Ding C, et al. Predicting factors of central lymph node metastasis and BRAF(V600E) mutation in Chinese population with papillary thyroid carcinoma. World J Surg Oncol. 2021;19(1):211.

    Article  Google Scholar 

  15. Zeng Z, Li K, Wang X, Ouyang S, Zhang Z, Liu Z, et al. Low urinary iodine is a protective factor of central lymph node metastasis in papillary thyroid cancer: a cross-sectional study. World J Surg Oncol. 2021;19(1):208.

    Article  Google Scholar 

  16. Li X, Zhang H, Zhou Y, Cheng R. Risk factors for central lymph node metastasis in the cervical region in papillary thyroid carcinoma: a retrospective study. World J Surg Oncol. 2021;19(1):138.

    Article  CAS  Google Scholar 

  17. Dou Y, Hu D, Chen Y, Xiong W, Xiao Q, Su X. PTC located in the upper pole is more prone to lateral lymph node metastasis and skip metastasis. World J Surg Oncol. 2020;18(1):188.

    Article  Google Scholar 

  18. Ryu YJ, Cho JS, Yoon JH, Park MH. Identifying risk factors for recurrence of papillary thyroid cancer in patients who underwent modified radical neck dissection. World J Surg Oncol. 2018;16(1):205.

    Article  Google Scholar 

  19. Toniato A, Boschin I, Casara D, Mazzarotto R, Rubello D, Pelizzo M. Papillary thyroid carcinoma: factors influencing recurrence and survival. Ann Surg Oncol. 2008;15(5):1518–22.

    Article  Google Scholar 

  20. Liu FH, Kuo SF, Hsueh C, Chao TC, Lin JD. Postoperative recurrence of papillary thyroid carcinoma with lymph node metastasis. J Surg Oncol. 2015;112(2):149–54.

    Article  Google Scholar 

  21. Jeon MJ, Kim WG, Kim TH, Kim HK, Kim BH, Yi HS, et al. Disease-specific mortality of differentiated thyroid cancer patients in Korea: a multicenter cohort study. Endocrinol Metab. 2017;32(4):434–41.

    Article  Google Scholar 

  22. Lee HS, Park C, Kim SW, Park T, Chun BK, Hong JC, et al. Correlation of minimal extrathyroidal extension with pathologic features of lymph node metastasis in patients with papillary thyroid carcinoma. J Surg Oncol. 2015;112(6):592–6.

    Article  CAS  Google Scholar 

  23. Seifert R, Schafers MA, Heitplatz B, Kerschke L, Riemann B, Noto B. Minimal extrathyroid extension in papillary micro carcinoma of the thyroid is an independent risk factor for relapse through lymph node and distant metastases. J Nucl Med. 2021;62(12):1702–9.

    Article  CAS  Google Scholar 

  24. Hay ID, Hutchinson ME, Gonzalez-Losada T, McIver B, Reinalda ME, Grant CS, et al. Papillary thyroid microcarcinoma: a study of 900 cases observed in a 60-year period. Surgery. 2008;144(6):980–7 discussion 7-8.

    Article  Google Scholar 

  25. Besic N, Pilko G, Petric R, Hocevar M, Zgajnar J. Papillary thyroid microcarcinoma: prognostic factors and treatment. J Surg Oncol. 2008;97(3):221–5.

    Article  Google Scholar 

  26. Siddiqui S, White MG, Antic T, Grogan RH, Angelos P, Kaplan EL, et al. Clinical and pathologic predictors of lymph node metastasis and recurrence in papillary thyroid microcarcinoma. Thyroid. 2016;26(6):807–15.

    Article  CAS  Google Scholar 

  27. Karatzas T, Vasileiadis I, Kapetanakis S, Karakostas E, Chrousos G, Kouraklis G. Risk factors contributing to the difference in prognosis for papillary versus micropapillary thyroid carcinoma. Am J Surg. 2013;206(4):586–93.

    Article  Google Scholar 

  28. Moon HJ, Kim EK, Chung WY, Yoon JH, Kwak JY. Minimal extrathyroidal extension in patients with papillary thyroid microcarcinoma: is it a real prognostic factor? Ann Surg Oncol. 2011;18(7):1916–23.

    Article  Google Scholar 

  29. Yin DT, Yu K, Lu RQ, Li X, Xu J, Lei M. Prognostic impact of minimal extrathyroidal extension in papillary thyroid carcinoma. Medicine. 2016;95(52): e5794.

    Article  Google Scholar 

  30. Diker-Cohen T, Hirsch D, Shimon I, Bachar G, Akirov A, Duskin-Bitan H, et al. Impact of minimal extra-thyroid extension in differentiated thyroid cancer: systematic review and meta-analysis. J Clin Endocrinol Metab. 2018. https://doi.org/10.1210/jc.2018-00081.

  31. Papaioannou C, Lamnisos D, Kyriacou K, Lyssiotis T, Constantinides V, Frangos S, et al. Lymph node metastasis and extrathyroidal extension in papillary thyroid microcarcinoma in cyprus: suspicious subcentimeter nodules should undergo FNA when multifocality is suspected. J Thyroid Res. 2020;2020:3567658.

    Article  Google Scholar 

  32. 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.

    Article  Google Scholar 

Download references

Acknowledgements

Not applicable

Funding

This research was supported by the Chung-Ang University Research Grants in 2020.

Author information

Authors and Affiliations

Authors

Contributions

RYS and KHK analyzed and interpreted the patient data. HSK performed the histological examination. RYS was the major contributor in writing the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Ra-Yeong Song.

Ethics declarations

Ethics approval and consent to participate

This study was approved by the Institutional Review Board of Chung-Ang University Hospital.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Song, RY., Kim, H.S. & Kang, K.H. Minimal extrathyroidal extension is associated with lymph node metastasis in single papillary thyroid microcarcinoma: a retrospective analysis of 814 patients. World J Surg Onc 20, 170 (2022). https://doi.org/10.1186/s12957-022-02629-8

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12957-022-02629-8

Keywords