The role of prophylactic central compartment neck dissection in patients with T1–T2 cN0 papillary thyroid carcinoma
Highlight box
Key findings
• The effects of pCCND on recurrence pattern in PTC.
What is known and what is new?
• It remains controversial whether pCCND is necessary in cases of stage T1–T2 cN0 PTC.
• The omission of pCCND was found to be an independent risk factor for recurrence in the central compartment in patients with T1–T2 cN0 PTC.
What is the implication, and what should change now?
• pCCND did not reduce the overall RFS, but appeared to prevent recurrence in the central compartment area. A careful follow-up strategy to look for recurrence in the central compartment may be necessary for patients who do not undergo pCCND.
Introduction
Complete surgical resection of both the primary tumor and clinically significant lymph node metastases is the basic goal of cancer therapy and an important determinant of outcomes in patients with differentiated thyroid cancer (1). Central compartment neck dissection (CCND) is the surgical excision of all lymph nodes from the hyoid bone to the sternal notch between each side of carotid arteries (1). In cases of papillary thyroid carcinoma (PTC), it is known that central lymph node metastases are very common, and these malignant foci are discovered in 24–82% of patients with PTC without clinical evidence of central lymph node involvement during the preoperative evaluation (2-8). Lymph node metastases contribute to more frequent locoregional recurrence (LRR), and many studies suggest that the lymph node ratio (LNR) or the number of metastatic lymph nodes in the central compartment is a prognostic factor for PTC (6,9-11).
Although CCND is recommended in patients with clinically node-positive or invasive PTC, it is still debatable whether prophylactic CCND (pCCND) should be performed alongside thyroidectomy in patients with noninvasive and cN0 PTC (1,12). In studies favoring lymph node dissection, pCCND was thought to reduce LRR and improve disease-free survival (2,5,13-17). Some studies have demonstrated that the complications after the procedure were comparable in experienced surgeons (5,16,18). However, in studies skeptical of pCCND, the advantages of pCCND were vague (8,19-22) and significantly more complications occurred, such as permanent hypoparathyroidism or recurrent laryngeal nerve injury (8,21,22).
The purpose of this study was to investigate the effects of pCCND on cancer recurrence and its pattern in patients with T1–T2 cN0 PTC in a large patient cohort with an extensive follow-up period. We present the following article in accordance with the STROBE reporting checklist (available at https://gs.amegroups.com/article/view/10.21037/gs-22-550/rc).
Methods
Patients
We retrospectively reviewed the records of patients with PTC who underwent total thyroidectomy or unilateral thyroid lobectomy between 2006 and 2012 at Seoul St. Mary’s Hospital, College of Medicine, the Catholic University of Korea. A total of 3,872 surgeries related to thyroid cancer were found in the database. The demographic information, surgical records, clinicopathological data, and recurrence status were collected for analysis. To minimize bias, we analyzed data from all cohorts who met the eligibility criteria and included all surgeries performed by multiple surgeons within our institution. The pathology report was revised according to the American Joint Committee on Cancer Staging Manual, 8th edition (23).
Patients with cN0 PTC on preoperative ultrasonography and stage T1 or T2 PTC on the pathology report were enrolled. Patients with a cancer stage greater than T3 or with lateral neck node metastases at the time of the initial diagnosis were excluded. We excluded tall cell, columnar cell, hobnail, and diffuse sclerosing PTC variants, which are known to have a poorer prognosis than classic PTC. Thirty-five patients with a follow-up period within 6 months after surgery were excluded. Finally, data from 2,902 patients were reviewed. The cohort was divided into two groups for comparison: 2,099 patients who had undergone pCCND with thyroidectomy (pCCND group) and 803 patients who did not undergo pCCND (non-pCCND group).
Five surgeons at our institution were involved with the patients in this study. Four are certified general surgeons (S.N. Kim, MD; B.J. Song, MD; S.S. Jung, MD; and B.J. Choi, MD) who performed the thyroid surgeries between 2006 and 2012 but did not dissect central lymph nodes routinely. The patients who perithyroidal lymph nodes were removed incidentally during the procedure were classified as non-pCCND group. The other surgeon, J.S. Bae, MD, is an endocrine surgeon who performed pCCND for all study patients with a thyroid malignancy.
Preoperative evaluations consisted of ultrasonography, neck computed tomography (CT), and other laboratory tests including thyroid function tests. After surgery, the patients were administered levothyroxine to suppress thyroid-stimulating hormone levels (TSH suppression), according to the guidelines issued by the American Thyroid Association (ATA) (24-26). All patients who underwent total thyroidectomy also underwent radioactive iodine (RAI) ablation 4–6 weeks after surgery.
Serum thyroglobulin level measurements and neck ultrasonography were regularly performed every 6 or 12 months. The patients whose recurrence was confirmed pathologically were considered as positive for recurrence. Recurrence in this cohort was classified by location: central compartment, lateral lymph node, remnant thyroid, and distant from the site of origin. Recurrence in the post-thyroidectomy bed or level VI area was considered central compartment recurrence. The recurrence in the remnant thyroid was evaluated only among patients who underwent unilateral thyroid lobectomy.
Statistical analysis
Variables were compared between the groups using the chi-square test, the Mann-Whitney U test, the Student’s t test, or Fisher’s exact test, considering the characteristics of each variable. The Cox proportional hazard model was used to identify factors associated with recurrence-free survival (RFS). Survival analysis and comparisons between groups were performed using the life table method. All P values less than 0.05 were considered statistically significant. All statistical analyses were performed using SPSS software (SPSS Statistics for Windows, Version 24.0.; IBM, Armonk, NY, USA).
Ethical statement
The study was conducted in accordance with the Declaration of Helsinki (as revised in 2013). The study was approved by the institutional review board of Seoul St. Mary’s Hospital, the Catholic University of Korea (No. KC22WISI0219) and individual consent for this retrospective analysis was waived.
Results
Clinicopathologic characteristics
Of 2,937 T1–T2 cN0 PTC patients, a total of 2,902 patients who met the inclusion criteria were analyzed (Table 1). The entire cohort was divided into two groups, according to whether CCND was performed, for comparison. The mean follow-up period for all patients was 112±36.9 months (7–192 months). The mean age of the total cohort was 46.8±11.6 years (12–79 years), and the mean tumor size was 0.83±0.52 cm. The mean age of patients in the non-pCCND group was greater than that of patients in the pCCND group (47.9 vs. 46.4 years, P=0.002). There were no statistical differences in the distribution of patients with regard to sex, thyroidectomy extension, or tumor size.
Table 1
Variables | Non-pCCND (n=803) | pCCND (n=2,099) | P value |
---|---|---|---|
Age (years) | 47.9±11.6 [17–78] | 46.4±11.7 [12–79] | 0.002 |
<55 | 568 (70.7%) | 1,589 (75.7%) | |
≥55 | 235 (29.3%) | 510 (24.3%) | |
Sex | 0.092 | ||
Male | 154 (19.2%) | 347 (16.5%) | |
Female | 649 (80.8%) | 1,752 (83.5%) | |
Tumor size (cm) | 0.80±0.5 [0.1–3.7] | 0.84±0.5 [0.1–4.0] | 0.084 |
≤1 | 634 (79.0%) | 1,620 (77.2%) | |
>1 to 2 | 146 (18.2%) | 402 (19.2%) | |
>2 to 4 | 23 (2.9%) | 77 (3.7%) | |
Nodal status | n/a | ||
N0 | n/a | 1,216 (57.9%) | |
N1a | n/a | 883 (42.1%) | |
No. of MLN | n/a | 1.26±2.2 [0–20] | n/a |
No. of MLN in N1a cases | n/a | 3.0±2.6 [1–20] | n/a |
≤5 | n/a | 1,973 (94.0%) | |
>5 | n/a | 126 (6.0%) | |
No. of lymph node retrieved | 0.67±0.9 [0–3] | 9.0±5.6 [3–41] | <0.001 |
Thyroidectomy | 0.268 | ||
Unilateral lobectomy | 169 (21.0%) | 482 (23.0%) | |
Total thyroidectomy | 634 (79.0%) | 1,617 (77.0%) | |
Follow up period (months) | 117.4±44.7 [9–191] | 110.0±33.2 [7–192] | <0.001 |
Data were presented as Mean ± SD [Min–Max] or n (%). pCCND, prophylactic central compartment neck dissection; MLN, metastatic lymph node.
Comparison of overall recurrence between groups
Recurrence was then analyzed (Table 2). In terms of total recurrence, 20 (2.5%) cases of recurrence occurred in the non-pCCND group, and 47 (2.2%) cases occurred in the pCCND group. The 15-year cumulative RFS rates of patients in the non-pCCND and pCCND groups were 95% and 97%, respectively, but these values were not statistically different (P=0.687 and P=0.813, respectively).
Table 2
Variables | Non-pCCND (n=803) | pCCND (n=2,099) | P value |
---|---|---|---|
Recurrence (total), n (%) | 20 (2.5%) | 47 (2.2%) | 0.687 |
Site, n (%) | |||
Central compartment | 10 (1.2%) | 2 (0.1%) | <0.001 |
Lateral lymph node | 12 (1.5%) | 38 (1.8%) | 0.558 |
Remnant thyroid† | 2/167 (1.2%) | 6/482 (1.2%) | 0.950 |
Distant organ (lung) | 1 (0.1%) | 0 (0.0%) | 0.106 |
Nodal recurrent pattern in recurrence cases, n (%) | |||
Central compartment | 10/20 (50.0%) | 2/47 (4.3%) | <0.001 |
Central compartment only | 5/20 (25.0%) | 2/47 (4.3%) | <0.001 |
Lateral lymph node | 12/20 (60.0%) | 38/47 (80.9%) | 0.073 |
Lateral lymph node only | 7/20 (35.0%) | 38/47 (80.9%) | <0.001 |
Both central and lateral lymph node | 5/20 (25.0%) | 0/47 (0.0%) | <0.001 |
RFS | |||
Cumulative RFS (10/15 years) | 97%/95% | 98%/97% | 0.813 |
Cumulative central compartment RFS (10/15 years) | 99%/99% | 100%/100% | <0.001 |
†, remnant thyroid recurrence was analyzed in lobectomy cases. One case of recurrence from remnant thyroid tissue occurred 27 months after initial surgery in patients with total thyroidectomy and pCCND. This case was included total recurrence, but not considered as ‘remnant thyroid recurrence’. Central compartment: thyroidectomy bed or level IV. Remnant-contra lateral thyroid lobe was not included. pCCND, prophylactic central compartment neck dissection; RFS, recurrence free survival.
Comparison of nodal recurrence pattern between groups
The two groups showed significant differences in nodal recurrence pattern, especially related to the central compartment (Table 2). Ten cases of central compartment recurrence (1.2%) occurred in the non-pCCND group, which is significantly higher than those in the pCCND group (0.1%, P<0.001). In the non-pCCND group, half of the cases of recurrence consisted of central compartment lesions, which was significantly greater than cases in the pCCND group (50% vs. 4.3%, P<0.001). In the non-pCCND group, the recurrence involving the central compartment, such as “central compartment only” (25% vs. 4.3%, P<0.001) or “both central and lateral lymph node” (25% vs. 0%, P<0.001) were significantly more frequent than pCCND group. In contrast, the most frequent site of recurrence in the pCCND group was the “lateral lymph node only” (80.9%), which was significantly different from that in the non-pCCND group (35%, P<0.001). There were no cases in “both central and lateral lymph node” recurrence in the pCCND group.
The 15-year cumulative central compartment RFS in the non-pCCND group was significantly lower than that in the pCCND group (99% vs. 100%, respectively, P<0.001, Figure 1).
Central compartment recurrence status in 12 patients
The detailed status of central compartment recurrence is shown in Table 3. There were ten patients with recurrence in the non-pCCND group. Of these 10 patients, 4 patients underwent surgical treatment. During the re-operation of patient No. 1, only thyroid cartilage, and soft tissue with PTC on thyroidectomy bed were resected due to local adhesion. Two years later, second recurrence occurred at subcutaneous and trachea, and excision of tumor mass and reconstruction of trachea were performed. Single recurrent laryngeal nerve was sacrificed with this operation. For patients No. 2 to 4, CCND and lateral neck dissection were performed to the affected lesion. Ethanol ablation or radiofrequency ablation were attempted to 5 patients with recurrence (No. 5 to 9). One patient was lost to follow-up after the diagnosis of recurrence.
Table 3
Patients | CCND | LNY | MLN | Thyroidectomy | Age | Sex | Tumor size (cm) | ETE | Concurrent recurrence | Treatment (MLN/LNY) | Time to recurrence (months) |
---|---|---|---|---|---|---|---|---|---|---|---|
1* | No | 0 | n/a | Total thyroidectomy | 68 | F | 3.5 | Min | None | Excision (PTC was found in thyroid cartilage and soft tissue on level VI), RAI | 91 |
2 | No | 3 | 2 | Total thyroidectomy | 25 | F | 1 | None | LLN | CCND (2/4) with lateral neck dissection (1/13), RAI | 25 |
3 | No | 0 | n/a | Total thyroidectomy | 51 | F | 0.7 | Min | LLN | CCND (1/5) with lateral neck dissection (8/64), RAI | 44 |
4 | No | 0 | n/a | Total thyroidectomy | 33 | F | 1.5 | None | LLN | Transferred to CCND with lateral neck dissection | 24 |
5 | No | 2 | 2 | Total thyroidectomy | 47 | F | 1.8 | Min | None | RFA | 81 |
6 | No | 0 | n/a | Total thyroidectomy | 49 | M | 1.5 | None | None | RFA | 64 |
7 | No | 0 | n/a | Total thyroidectomy | 50 | F | 0.4 | Min | LLN | Ethanol ablation for level VIRFA for level IV | 5 |
8 | No | 0 | n/a | Total thyroidectomy | 45 | F | 0.8 | Min | None | RFA, RAI | 13 |
9 | No | 0 | n/a | Total thyroidectomy | 26 | F | 0.6 | None | None | RFA, RAI | 10 |
10 | No | 0 | n/a | Total thyroidectomy | 38 | F | 1 | None | LLN | Follow-up loss | 31 |
11 | Right CCND | 6 | 0 | Right thyroid lobectomy | 48 | F | 0.6 | None | None | Completion thyroidectomy with CCND (1/7), RAI | 53 |
12 | Bilateral CCND | 16 | 11 | Total thyroidectomy | 49 | M | 2.8 | Min | None | Active surveillance | 58 |
*, second recurrence occurred at subcutaneous and trachea (thyroidectomy bed), 2 years after treatment of first recurrence. Excision of tumor mass and reconstruction of trachea were performed. pCCND, prophylactic central compartment neck dissection; CCND, central compartment neck dissection; LNY, lymph node yield; the total number of lymph node harvest; MLN, metastatic lymph node; the total number of metastatic lymph node; ETE, extrathyroidal extension; LLN, lateral lymph node; PTC, papillary thyroid carcinoma; RAI, radioactive iodine; RFA, radiofrequency ablation.
Only two cases of central compartment recurrence occurred in the pCCND group. One patient (No. 11) underwent right thyroid lobectomy with ipsilateral pCCND for the initial procedure, no metastatic lymph node among the six lymph nodes removed at the initial surgery. The recurrence occurred in the operation bed in level VI, the patient underwent completion thyroidectomy with redo CCND and RAI ablation therapy. The other patient (No.12) initially underwent total thyroidectomy with bilateral CCND due to right thyroid cancer, the initial LNR was 11/16. The recurrence occurred at ipsilateral central compartment area, and he was followed without further treatment with active surveillance.
Factors associated with central compartment RFS
Results of a Cox regression analysis to determine factors affecting central compartment RFS are shown in Table 4. A univariate Cox regression analysis was performed for each variable, including age group, sex distribution, thyroidectomy extension, tumor size, and pCCND group. The variables of non-pCCND and tumor size larger than 2 cm were the only factors that predicted a worse central compartment RFS (Table 4). In the multivariate analysis using the forward conditional method, non-pCCND remained the only independent risk factor related to central compartment RFS; the hazard ratio was 13.362 (95% CI: 2.928–60.986; P<0.001).
Table 4
Variables | Hazard ratio [95% CI] | P value |
---|---|---|
Univariate analysis | ||
Age, years | ||
<55 vs. ≥55 | 0.262 [0.34–2.032] | 0.2 |
Sex | ||
Male vs. female | 1.045 [0.229–4.770] | 0.955 |
Thyroidectomy | ||
Lobectomy vs. total thyroidectomy | 3.094 [0.401–24.073] | 0.278 |
Size, cm | ||
≤1 | Ref. | |
>1 to 2 | 1.764 [ 0.456–6.823] | 0.411 |
>2 to 4 | 6.192 [1.286–29.804] | 0.023 |
pCCND vs. non-pCCND | 13.362 [2.928–60.986] | 0.001 |
Multivariate analysis | ||
pCCND vs. non-pCCND | 13.362 [2.928–60.986] | 0.001 |
pCCND, prophylactic central compartment neck dissection.
Discussion
The controversy associated with pCCND still remains. Weighing the risks and benefits of lymph node dissection is at the center of this controversy. However, results from different studies are conflicting.
The increase in complications, such as recurrent laryngeal nerve or parathyroid gland injury, associated with lymph node dissection is an important consideration when performing pCCND (8,21). Viola et al. reported that permanent hypoparathyroidism occurred more frequently in patients who underwent total thyroidectomy with pCCND compared to patients who underwent total thyroidectomy only, but the rate of recurrent laryngeal nerve injury did not differ between the two groups in this prospective randomized controlled study (22). Many studies that compared the complication rates between patients undergoing total thyroidectomy alone and those undergoing total thyroidectomy with pCCND reached similar conclusions (3,20,27). In another prospective randomized controlled study by Sippel et al., there was no difference in patient complications between those undergoing total thyroidectomy only and those undergoing total thyroidectomy with pCCND (28). Other studies reported that CCND did not increase the risk of complications (5,16). The experience of the surgeon may contribute to this discrepancy. Complications related to thyroid surgery may be affected by the volume of surgery, which is determined by the number of surgeries performed by the surgeon per year (29).
It is not simple to demonstrate positive oncologic outcomes associated with pCCND in patients with PTC, as it is difficult to demonstrate reduced recurrence. Carling et al. proposed that 5,840 patients in a prospective trial would be necessary to have sufficient statistical power to prove positive effects on recurrence rate (30). Nevertheless, some studies have suggested that pCCND protects against recurrence (2,5,13-17). Liu et al. demonstrated that the addition of pCCND to total thyroidectomy reduces the risk of local recurrence compared to total thyroidectomy alone in their meta-analysis (14).
Because there are conflicting studies about the role of lymph nodes in cancer recurrence, there may also be disagreements about the need for lymph node resection. In several studies, lymph nodes may play a role as education centers of the immune system and anti-tumor immunity (31,32). According to these studies, it seems that the removal of lymph nodes has adverse effects on oncologic outcome. On the other hand, according to recent research, lymph node colonization can induce cancer metastasis (33). However, it is difficult to study the effect of occult lymph node metastasis on thyroid cancer recurrence because it is impossible to determine whether lymph node metastasis exists without pCCND in clinically N0 patients with thyroid cancer. Forty-two percent of patients in pCCND group had occult lymph node metastasis in this study and generally the rate of occult lymph node metastasis in PTC has been reported up to 82% (2-8). Considering this, we may estimate that undissected-occult lymph nodes induced local recurrence in central compartment in non-pCCND group.
Despite these controversies, pCCND is not recommended for noninvasive, T1–T2 cN0 PTC according to the ATA 2015 guidelines (1). In this study, we compared a large number of patients with PTC to investigate the benefits of pCCND during a relatively long follow-up period. The total recurrence rate and RFS of the non-pCCND group were not statistically different with pCCND group. Prophylactic CCND did not appear to have any effect on preventing the overall recurrence of T1–T2 cN0 disease. Considering these non-different results and the easier accessibility to the non-dissected central compartment lymph node during the re-operation rather than to the dissected area, it seems impossible to conclude that pCCND is necessary to patients with thyroid cancer to improve overall outcome.
However, it is clear that pCCND reduces recurrence in the central area and affects the distribution of the sites of recurrence. When pCCND was not performed, the risk of central compartment recurrence was about 13 times higher than that of the pCCND group [13.362 (95% CI: 2.928–60.986)] (P<0.001). The elimination of central neck lymph nodes appears to prevent local recurrence around the site of the previous malignant tumor even at early stages (T1–T2 cN0, without ETE) of thyroid cancer. Performing of pCCND would have reduced unnecessary additional procedures due to recurrence. Considering the psychological adverse effects of local-regional recurrence of thyroid cancer (34) or expected complications followed by re-operation, pCCND can be applied depending on the surgeon’s performance.
There are several limitations of our study. First, the study design was retrospective. Second, the incidence of complications due to pCCND was not investigated in this study due to a lack of data. In addition, a longer follow-up period could contribute to a more thorough investigation, considering that PTC is indolent, and cases in this study were all early stage.
Conclusions
In this study, pCCND did not reduce the overall recurrence rate or RFS in patients with T1–T2 cN0 PTC. However, the omission of pCCND was determined to be an independent risk factor for worse recurrence in the central compartment, which was the primary site of recurrence in this study. A careful follow-up strategy to look for recurrence in the central compartment may be necessary for patients who do not undergo pCCND.
Acknowledgments
Funding: None.
Footnote
Reporting Checklist: The authors have completed the STROBE reporting checklist. Available at https://gs.amegroups.com/article/view/10.21037/gs-22-550/rc
Data Sharing Statement: Available at https://gs.amegroups.com/article/view/10.21037/gs-22-550/dss
Peer Review File: Available at https://gs.amegroups.com/article/view/10.21037/gs-22-550/prf
Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at https://gs.amegroups.com/article/view/10.21037/gs-22-550/coif). The authors have no conflicts of interest to declare.
Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved. The study was conducted in accordance with the Declaration of Helsinki (as revised in 2013). The institutional review board of Seoul St. Mary’s Hospital, the Catholic University of Korea approved the study (No. KC22WISI0219) and individual consent for this retrospective analysis was waived.
Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
References
- Haugen BR, Alexander EK, Bible KC, 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;26:1-133. [Crossref] [PubMed]
- Lang BH, Ng SH, Lau LL, et al. A systematic review and meta-analysis of prophylactic central neck dissection on short-term locoregional recurrence in papillary thyroid carcinoma after total thyroidectomy. Thyroid 2013;23:1087-98. [Crossref] [PubMed]
- Som PM, Curtin HD, Mancuso AA. Imaging-based nodal classification for evaluation of neck metastatic adenopathy. AJR Am J Roentgenol 2000;174:837-44. [Crossref] [PubMed]
- Wada N, Duh QY, Sugino K, et al. Lymph node metastasis from 259 papillary thyroid microcarcinomas: frequency, pattern of occurrence and recurrence, and optimal strategy for neck dissection. Ann Surg 2003;237:399-407. [Crossref] [PubMed]
- Hall CM, Snyder SK, Maldonado YM, et al. Routine central lymph node dissection with total thyroidectomy for papillary thyroid cancer potentially minimizes level VI recurrence. Surgery 2016;160:1049-58. [Crossref] [PubMed]
- Kwon O, Lee S, Bae JS. The Prognostic Value of Central Lymph Node Yield and Ratio in Papillary Thyroid Carcinoma Patients Who Underwent Thyroidectomy with Prophylactic Central Compartment Neck Dissection. Int J Thyroidol 2019;12:19-27.
- American Thyroid Association Surgery Working Group. Consensus statement on the terminology and classification of central neck dissection for thyroid cancer. Thyroid 2009;19:1153-8. [Crossref] [PubMed]
- Ywata de Carvalho A, Chulam TC, Kowalski LP. Long-term Results of Observation vs Prophylactic Selective Level VI Neck Dissection for Papillary Thyroid Carcinoma at a Cancer Center. JAMA Otolaryngol Head Neck Surg 2015;141:599-606. [Crossref] [PubMed]
- Pereira JA, Jimeno J, Miquel J, et al. Nodal yield, morbidity, and recurrence after central neck dissection for papillary thyroid carcinoma. Surgery 2005;138:1095-100, discussion 1100-1. [Crossref] [PubMed]
- Mazzaferri EL, Jhiang SM. Long-term impact of initial surgical and medical therapy on papillary and follicular thyroid cancer. Am J Med 1994;97:418-28. [Crossref] [PubMed]
- Lee YC, Na SY, Park GC, et al. Occult lymph node metastasis and risk of regional recurrence in papillary thyroid cancer after bilateral prophylactic central neck dissection: A multi-institutional study. Surgery 2017;161:465-71. [Crossref] [PubMed]
- Zhu W, Zhong M, Ai Z. Systematic evaluation of prophylactic neck dissection for the treatment of papillary thyroid carcinoma. Jpn J Clin Oncol 2013;43:883-8. [Crossref] [PubMed]
- Caliskan M, Park JH, Jeong JS, et al. Role of prophylactic ipsilateral central compartment lymph node dissection in papillary thyroid microcarcinoma. Endocr J 2012;59:305-11. [Crossref] [PubMed]
- Liu H, Li Y, Mao Y. Local lymph node recurrence after central neck dissection in papillary thyroid cancers: A meta analysis. Eur Ann Otorhinolaryngol Head Neck Dis 2019;136:481-7. [Crossref] [PubMed]
- Su H, Li Y. Prophylactic central neck dissection and local recurrence in papillary thyroid microcarcinoma: a meta-analysis. Braz J Otorhinolaryngol 2019;85:237-43. [Crossref] [PubMed]
- Barczyński M, Konturek A, Stopa M, et al. Prophylactic central neck dissection for papillary thyroid cancer. Br J Surg 2013;100:410-8. [Crossref] [PubMed]
- Ji YB, Yoo HS, Song CM, et al. Predictive factors and pattern of central lymph node metastasis in unilateral papillary thyroid carcinoma. Auris Nasus Larynx 2016;43:79-83. [Crossref] [PubMed]
- Chen Y, Chen S, Lin X, et al. Clinical Analysis of Cervical Lymph Node Metastasis Risk Factors and the Feasibility of Prophylactic Central Lymph Node Dissection in Papillary Thyroid Carcinoma. Int J Endocrinol 2021;2021:6635686. [Crossref] [PubMed]
- Randolph GW, Duh QY, Heller KS, et al. The prognostic significance of nodal metastases from papillary thyroid carcinoma can be stratified based on the size and number of metastatic lymph nodes, as well as the presence of extranodal extension. Thyroid 2012;22:1144-52. [Crossref] [PubMed]
- Zetoune T, Keutgen X, Buitrago D, et al. Prophylactic central neck dissection and local recurrence in papillary thyroid cancer: a meta-analysis. Ann Surg Oncol 2010;17:3287-93. [Crossref] [PubMed]
- Dobrinja C, Troian M, Cipolat Mis T, et al. Rationality in prophylactic central neck dissection in clinically node-negative (cN0) papillary thyroid carcinoma: Is there anything more to say? A decade experience in a single-center. Int J Surg 2017;41:S40-7. [Crossref] [PubMed]
- Viola D, Materazzi G, Valerio L, et al. Prophylactic central compartment lymph node dissection in papillary thyroid carcinoma: clinical implications derived from the first prospective randomized controlled single institution study. J Clin Endocrinol Metab 2015;100:1316-24. [Crossref] [PubMed]
- Lamartina L, Grani G, Arvat E, et al. 8th edition of the AJCC/TNM staging system of thyroid cancer: what to expect (ITCO#2). Endocr Relat Cancer 2018;25:L7-L11.
- Singer PA, Cooper DS, Daniels GH, et al. Treatment guidelines for patients with thyroid nodules and well-differentiated thyroid cancer. American Thyroid Association. Arch Intern Med 1996;156:2165-72.
- American Thyroid Association (ATA) Guidelines Taskforce on Thyroid Nodules and Differentiated Thyroid Cancer. Revised American Thyroid Association management guidelines for patients with thyroid nodules and differentiated thyroid cancer. Thyroid 2009;19:1167-214. [Crossref] [PubMed]
- Cooper DS, Doherty GM, Haugen BR, et al. Management guidelines for patients with thyroid nodules and differentiated thyroid cancer. Thyroid 2006;16:109-42. [Crossref] [PubMed]
- Lang BH, Chan DT, Wong KP, et al. Predictive factors and pattern of locoregional recurrence after prophylactic central neck dissection in papillary thyroid carcinoma. Ann Surg Oncol 2014;21:4181-7. [Crossref] [PubMed]
- Sippel RS, Robbins SE, Poehls JL, et al. A Randomized Controlled Clinical Trial: No Clear Benefit to Prophylactic Central Neck Dissection in Patients With Clinically Node Negative Papillary Thyroid Cancer. Ann Surg 2020;272:496-503. [Crossref] [PubMed]
- Hauch A, Al-Qurayshi Z, Randolph G, et al. Total thyroidectomy is associated with increased risk of complications for low- and high-volume surgeons. Ann Surg Oncol 2014;21:3844-52. [Crossref] [PubMed]
- Carling T, Carty SE, Ciarleglio MM, et al. American Thyroid Association design and feasibility of a prospective randomized controlled trial of prophylactic central lymph node dissection for papillary thyroid carcinoma. Thyroid 2012;22:237-44. [Crossref] [PubMed]
- von Andrian UH, Mempel TR. Homing and cellular traffic in lymph nodes. Nat Rev Immunol 2003;3:867-78. [Crossref] [PubMed]
- Binnewies M, Mujal AM, Pollack JL, et al. Unleashing Type-2 Dendritic Cells to Drive Protective Antitumor CD4 T Cell Immunity. Cell 2019;177:556-71.e16. [Crossref] [PubMed]
- Reticker-Flynn NE, Zhang W, Belk JA, et al. Lymph node colonization induces tumor-immune tolerance to promote distant metastasis. Cell 2022;185:1924-42.e23. [Crossref] [PubMed]
- Misra S, Meiyappan S, Heus L, et al. Patients' experiences following local-regional recurrence of thyroid cancer: a qualitative study. J Surg Oncol 2013;108:47-51. [Crossref] [PubMed]