Clinical and ultrasonic risk factors for high‐volume central lymph node metastasis in cN0 papillary thyroid microcarcinoma: A retrospective study and meta‐analysis
Objective Papillary thyroid microcarcinoma (PTMC) comprises more than 50% of all newly detected cases of papillary thyroid carcinoma (PTC). High‐volume lymph node metastasis (involving >5 lymph nodes) (hv‐LNM) is associated with PTMC recurrence. In half of the clinically node‐negative (cN0) PTMC...
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Published in | Clinical endocrinology (Oxford) Vol. 98; no. 4; pp. 609 - 621 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Wiley Subscription Services, Inc
01.04.2023
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Abstract | Objective
Papillary thyroid microcarcinoma (PTMC) comprises more than 50% of all newly detected cases of papillary thyroid carcinoma (PTC). High‐volume lymph node metastasis (involving >5 lymph nodes) (hv‐LNM) is associated with PTMC recurrence. In half of the clinically node‐negative (cN0) PTMC patients, central lymph node metastasis (CLNM) is pathologically present. However, clinical risk factors for high‐volume CLNM (hv‐CLNM) in cN0 PTMC have not been defined well. Therefore, we aimed to obtain evidence for hv‐CLNM risk factors in cN0 PTMC.
Design
Data on patients who visited our hospital between January 2020 and December 2021 were collected; a preoperative diagnosis of cN0 and a postoperative pathological confirmation of PTMC were obtained. After filtering by inclusion versus exclusion criteria, the obtained data (N = 2268) were included in the meta‐analysis. Relevant studies published as of 10 April 2022, were identified from the Web of Science, PubMed, WANFANG, and CNKI databases. These eligible studies were included in the meta‐analysis and the association between clinicopathological factors and hv‐CLNM in cN0 PTMC was assessed. SPSS and MetaXL were used for statistical analyses.
Results
The meta‐analysis included 10 previous studies (11,734 patients) and 2268 patients enroled in our hospital for a total of 14,002 subjects. The results of which suggested that younger age (<40, odds ratio [OR] = 3.28, 95% confidence interval [CI] = 2.75–3.92, p < .001 or <45 odds ratio [OR] = 2.93, 95% CI = 2.31–3.72, p < .001), male sex (OR = 2.81, 95% CI = 2.25–3.52, p < .001), tumour size >5 mm (OR = 1.85, 95% CI = 1.39–2.47, p < .001), multifocality (OR = 1.88, 95% CI = 1.56–2.26, p < .001), extrathyroidal extension (OR = 2.58, 95% CI = 2.02–3.30, p < .001), capsule invasion (OR = 2.02, 95% CI = 1.46–2.78, p < .001), microcalcification (OR = 3.25, 95% CI = 2.42–4.36, p < .001) and rich blood flow (OR = 1.65, 95% CI = 1.21–2.25, p = .002) were the significant factors related to an elevated hv‐CLNM risk in cN0 PTMC patients. Hashimoto thyroiditis (OR = 0.76, 95% CI = 0.55–1.07, p = .114), irregular margin (versus regular margin, OR = 0.96, 95% CI = 0.68–1.33, p = .787) and hypoechoic (versus nonhypoechoic, OR = 1.27, 95% CI = 0.84–1.92, p = .261) showed no significant association with hv‐CLNM.
Conclusions
Younger age, tumour size >5 mm, males, extrathyroidal extension, multifocality, microcalcification, capsular invasion, and rich blood flow were the significant clinicopathological risk factors for hv‐CLNM risk in cN0 PTMC patients. These predictors may compensate for the sensitivity of imaging diagnosis in the preoperative period, thus helping in the effective identification of PTMCs with an invasive phenotype. |
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AbstractList | Papillary thyroid microcarcinoma (PTMC) comprises more than 50% of all newly detected cases of papillary thyroid carcinoma (PTC). High-volume lymph node metastasis (involving >5 lymph nodes) (hv-LNM) is associated with PTMC recurrence. In half of the clinically node-negative (cN0) PTMC patients, central lymph node metastasis (CLNM) is pathologically present. However, clinical risk factors for high-volume CLNM (hv-CLNM) in cN0 PTMC have not been defined well. Therefore, we aimed to obtain evidence for hv-CLNM risk factors in cN0 PTMC.OBJECTIVEPapillary thyroid microcarcinoma (PTMC) comprises more than 50% of all newly detected cases of papillary thyroid carcinoma (PTC). High-volume lymph node metastasis (involving >5 lymph nodes) (hv-LNM) is associated with PTMC recurrence. In half of the clinically node-negative (cN0) PTMC patients, central lymph node metastasis (CLNM) is pathologically present. However, clinical risk factors for high-volume CLNM (hv-CLNM) in cN0 PTMC have not been defined well. Therefore, we aimed to obtain evidence for hv-CLNM risk factors in cN0 PTMC.Data on patients who visited our hospital between January 2020 and December 2021 were collected; a preoperative diagnosis of cN0 and a postoperative pathological confirmation of PTMC were obtained. After filtering by inclusion versus exclusion criteria, the obtained data (N = 2268) were included in the meta-analysis. Relevant studies published as of 10 April 2022, were identified from the Web of Science, PubMed, WANFANG, and CNKI databases. These eligible studies were included in the meta-analysis and the association between clinicopathological factors and hv-CLNM in cN0 PTMC was assessed. SPSS and MetaXL were used for statistical analyses.DESIGNData on patients who visited our hospital between January 2020 and December 2021 were collected; a preoperative diagnosis of cN0 and a postoperative pathological confirmation of PTMC were obtained. After filtering by inclusion versus exclusion criteria, the obtained data (N = 2268) were included in the meta-analysis. Relevant studies published as of 10 April 2022, were identified from the Web of Science, PubMed, WANFANG, and CNKI databases. These eligible studies were included in the meta-analysis and the association between clinicopathological factors and hv-CLNM in cN0 PTMC was assessed. SPSS and MetaXL were used for statistical analyses.The meta-analysis included 10 previous studies (11,734 patients) and 2268 patients enroled in our hospital for a total of 14,002 subjects. The results of which suggested that younger age (<40, odds ratio [OR] = 3.28, 95% confidence interval [CI] = 2.75-3.92, p < .001 or <45 odds ratio [OR] = 2.93, 95% CI = 2.31-3.72, p < .001), male sex (OR = 2.81, 95% CI = 2.25-3.52, p < .001), tumour size >5 mm (OR = 1.85, 95% CI = 1.39-2.47, p < .001), multifocality (OR = 1.88, 95% CI = 1.56-2.26, p < .001), extrathyroidal extension (OR = 2.58, 95% CI = 2.02-3.30, p < .001), capsule invasion (OR = 2.02, 95% CI = 1.46-2.78, p < .001), microcalcification (OR = 3.25, 95% CI = 2.42-4.36, p < .001) and rich blood flow (OR = 1.65, 95% CI = 1.21-2.25, p = .002) were the significant factors related to an elevated hv-CLNM risk in cN0 PTMC patients. Hashimoto thyroiditis (OR = 0.76, 95% CI = 0.55-1.07, p = .114), irregular margin (versus regular margin, OR = 0.96, 95% CI = 0.68-1.33, p = .787) and hypoechoic (versus nonhypoechoic, OR = 1.27, 95% CI = 0.84-1.92, p = .261) showed no significant association with hv-CLNM.RESULTSThe meta-analysis included 10 previous studies (11,734 patients) and 2268 patients enroled in our hospital for a total of 14,002 subjects. The results of which suggested that younger age (<40, odds ratio [OR] = 3.28, 95% confidence interval [CI] = 2.75-3.92, p < .001 or <45 odds ratio [OR] = 2.93, 95% CI = 2.31-3.72, p < .001), male sex (OR = 2.81, 95% CI = 2.25-3.52, p < .001), tumour size >5 mm (OR = 1.85, 95% CI = 1.39-2.47, p < .001), multifocality (OR = 1.88, 95% CI = 1.56-2.26, p < .001), extrathyroidal extension (OR = 2.58, 95% CI = 2.02-3.30, p < .001), capsule invasion (OR = 2.02, 95% CI = 1.46-2.78, p < .001), microcalcification (OR = 3.25, 95% CI = 2.42-4.36, p < .001) and rich blood flow (OR = 1.65, 95% CI = 1.21-2.25, p = .002) were the significant factors related to an elevated hv-CLNM risk in cN0 PTMC patients. Hashimoto thyroiditis (OR = 0.76, 95% CI = 0.55-1.07, p = .114), irregular margin (versus regular margin, OR = 0.96, 95% CI = 0.68-1.33, p = .787) and hypoechoic (versus nonhypoechoic, OR = 1.27, 95% CI = 0.84-1.92, p = .261) showed no significant association with hv-CLNM.Younger age, tumour size >5 mm, males, extrathyroidal extension, multifocality, microcalcification, capsular invasion, and rich blood flow were the significant clinicopathological risk factors for hv-CLNM risk in cN0 PTMC patients. These predictors may compensate for the sensitivity of imaging diagnosis in the preoperative period, thus helping in the effective identification of PTMCs with an invasive phenotype.CONCLUSIONSYounger age, tumour size >5 mm, males, extrathyroidal extension, multifocality, microcalcification, capsular invasion, and rich blood flow were the significant clinicopathological risk factors for hv-CLNM risk in cN0 PTMC patients. These predictors may compensate for the sensitivity of imaging diagnosis in the preoperative period, thus helping in the effective identification of PTMCs with an invasive phenotype. Objective Papillary thyroid microcarcinoma (PTMC) comprises more than 50% of all newly detected cases of papillary thyroid carcinoma (PTC). High‐volume lymph node metastasis (involving >5 lymph nodes) (hv‐LNM) is associated with PTMC recurrence. In half of the clinically node‐negative (cN0) PTMC patients, central lymph node metastasis (CLNM) is pathologically present. However, clinical risk factors for high‐volume CLNM (hv‐CLNM) in cN0 PTMC have not been defined well. Therefore, we aimed to obtain evidence for hv‐CLNM risk factors in cN0 PTMC. Design Data on patients who visited our hospital between January 2020 and December 2021 were collected; a preoperative diagnosis of cN0 and a postoperative pathological confirmation of PTMC were obtained. After filtering by inclusion versus exclusion criteria, the obtained data (N = 2268) were included in the meta‐analysis. Relevant studies published as of 10 April 2022, were identified from the Web of Science, PubMed, WANFANG, and CNKI databases. These eligible studies were included in the meta‐analysis and the association between clinicopathological factors and hv‐CLNM in cN0 PTMC was assessed. SPSS and MetaXL were used for statistical analyses. Results The meta‐analysis included 10 previous studies (11,734 patients) and 2268 patients enroled in our hospital for a total of 14,002 subjects. The results of which suggested that younger age (<40, odds ratio [OR] = 3.28, 95% confidence interval [CI] = 2.75–3.92, p < .001 or <45 odds ratio [OR] = 2.93, 95% CI = 2.31–3.72, p < .001), male sex (OR = 2.81, 95% CI = 2.25–3.52, p < .001), tumour size >5 mm (OR = 1.85, 95% CI = 1.39–2.47, p < .001), multifocality (OR = 1.88, 95% CI = 1.56–2.26, p < .001), extrathyroidal extension (OR = 2.58, 95% CI = 2.02–3.30, p < .001), capsule invasion (OR = 2.02, 95% CI = 1.46–2.78, p < .001), microcalcification (OR = 3.25, 95% CI = 2.42–4.36, p < .001) and rich blood flow (OR = 1.65, 95% CI = 1.21–2.25, p = .002) were the significant factors related to an elevated hv‐CLNM risk in cN0 PTMC patients. Hashimoto thyroiditis (OR = 0.76, 95% CI = 0.55–1.07, p = .114), irregular margin (versus regular margin, OR = 0.96, 95% CI = 0.68–1.33, p = .787) and hypoechoic (versus nonhypoechoic, OR = 1.27, 95% CI = 0.84–1.92, p = .261) showed no significant association with hv‐CLNM. Conclusions Younger age, tumour size >5 mm, males, extrathyroidal extension, multifocality, microcalcification, capsular invasion, and rich blood flow were the significant clinicopathological risk factors for hv‐CLNM risk in cN0 PTMC patients. These predictors may compensate for the sensitivity of imaging diagnosis in the preoperative period, thus helping in the effective identification of PTMCs with an invasive phenotype. ObjectivePapillary thyroid microcarcinoma (PTMC) comprises more than 50% of all newly detected cases of papillary thyroid carcinoma (PTC). High‐volume lymph node metastasis (involving >5 lymph nodes) (hv‐LNM) is associated with PTMC recurrence. In half of the clinically node‐negative (cN0) PTMC patients, central lymph node metastasis (CLNM) is pathologically present. However, clinical risk factors for high‐volume CLNM (hv‐CLNM) in cN0 PTMC have not been defined well. Therefore, we aimed to obtain evidence for hv‐CLNM risk factors in cN0 PTMC.DesignData on patients who visited our hospital between January 2020 and December 2021 were collected; a preoperative diagnosis of cN0 and a postoperative pathological confirmation of PTMC were obtained. After filtering by inclusion versus exclusion criteria, the obtained data (N = 2268) were included in the meta‐analysis. Relevant studies published as of 10 April 2022, were identified from the Web of Science, PubMed, WANFANG, and CNKI databases. These eligible studies were included in the meta‐analysis and the association between clinicopathological factors and hv‐CLNM in cN0 PTMC was assessed. SPSS and MetaXL were used for statistical analyses.ResultsThe meta‐analysis included 10 previous studies (11,734 patients) and 2268 patients enroled in our hospital for a total of 14,002 subjects. The results of which suggested that younger age (<40, odds ratio [OR] = 3.28, 95% confidence interval [CI] = 2.75–3.92, p < .001 or <45 odds ratio [OR] = 2.93, 95% CI = 2.31–3.72, p < .001), male sex (OR = 2.81, 95% CI = 2.25–3.52, p < .001), tumour size >5 mm (OR = 1.85, 95% CI = 1.39–2.47, p < .001), multifocality (OR = 1.88, 95% CI = 1.56–2.26, p < .001), extrathyroidal extension (OR = 2.58, 95% CI = 2.02–3.30, p < .001), capsule invasion (OR = 2.02, 95% CI = 1.46–2.78, p < .001), microcalcification (OR = 3.25, 95% CI = 2.42–4.36, p < .001) and rich blood flow (OR = 1.65, 95% CI = 1.21–2.25, p = .002) were the significant factors related to an elevated hv‐CLNM risk in cN0 PTMC patients. Hashimoto thyroiditis (OR = 0.76, 95% CI = 0.55–1.07, p = .114), irregular margin (versus regular margin, OR = 0.96, 95% CI = 0.68–1.33, p = .787) and hypoechoic (versus nonhypoechoic, OR = 1.27, 95% CI = 0.84–1.92, p = .261) showed no significant association with hv‐CLNM.ConclusionsYounger age, tumour size >5 mm, males, extrathyroidal extension, multifocality, microcalcification, capsular invasion, and rich blood flow were the significant clinicopathological risk factors for hv‐CLNM risk in cN0 PTMC patients. These predictors may compensate for the sensitivity of imaging diagnosis in the preoperative period, thus helping in the effective identification of PTMCs with an invasive phenotype. Papillary thyroid microcarcinoma (PTMC) comprises more than 50% of all newly detected cases of papillary thyroid carcinoma (PTC). High-volume lymph node metastasis (involving >5 lymph nodes) (hv-LNM) is associated with PTMC recurrence. In half of the clinically node-negative (cN0) PTMC patients, central lymph node metastasis (CLNM) is pathologically present. However, clinical risk factors for high-volume CLNM (hv-CLNM) in cN0 PTMC have not been defined well. Therefore, we aimed to obtain evidence for hv-CLNM risk factors in cN0 PTMC. Data on patients who visited our hospital between January 2020 and December 2021 were collected; a preoperative diagnosis of cN0 and a postoperative pathological confirmation of PTMC were obtained. After filtering by inclusion versus exclusion criteria, the obtained data (N = 2268) were included in the meta-analysis. Relevant studies published as of 10 April 2022, were identified from the Web of Science, PubMed, WANFANG, and CNKI databases. These eligible studies were included in the meta-analysis and the association between clinicopathological factors and hv-CLNM in cN0 PTMC was assessed. SPSS and MetaXL were used for statistical analyses. The meta-analysis included 10 previous studies (11,734 patients) and 2268 patients enroled in our hospital for a total of 14,002 subjects. The results of which suggested that younger age (<40, odds ratio [OR] = 3.28, 95% confidence interval [CI] = 2.75-3.92, p < .001 or <45 odds ratio [OR] = 2.93, 95% CI = 2.31-3.72, p < .001), male sex (OR = 2.81, 95% CI = 2.25-3.52, p < .001), tumour size >5 mm (OR = 1.85, 95% CI = 1.39-2.47, p < .001), multifocality (OR = 1.88, 95% CI = 1.56-2.26, p < .001), extrathyroidal extension (OR = 2.58, 95% CI = 2.02-3.30, p < .001), capsule invasion (OR = 2.02, 95% CI = 1.46-2.78, p < .001), microcalcification (OR = 3.25, 95% CI = 2.42-4.36, p < .001) and rich blood flow (OR = 1.65, 95% CI = 1.21-2.25, p = .002) were the significant factors related to an elevated hv-CLNM risk in cN0 PTMC patients. Hashimoto thyroiditis (OR = 0.76, 95% CI = 0.55-1.07, p = .114), irregular margin (versus regular margin, OR = 0.96, 95% CI = 0.68-1.33, p = .787) and hypoechoic (versus nonhypoechoic, OR = 1.27, 95% CI = 0.84-1.92, p = .261) showed no significant association with hv-CLNM. Younger age, tumour size >5 mm, males, extrathyroidal extension, multifocality, microcalcification, capsular invasion, and rich blood flow were the significant clinicopathological risk factors for hv-CLNM risk in cN0 PTMC patients. These predictors may compensate for the sensitivity of imaging diagnosis in the preoperative period, thus helping in the effective identification of PTMCs with an invasive phenotype. |
Author | Zhang, Ting Ji, Xiaoyu Zhang, Hao Wu, Pu He, Liang Sun, Wei Wang, Zhihong Wang, Zhiyuan Dong, Wenwu Shi, Jinyuan Gui, Zhiqiang Huang, Jiapeng Zhang, Dalin Shao, Liang |
Author_xml | – sequence: 1 givenname: Zhiyuan orcidid: 0000-0003-2237-7960 surname: Wang fullname: Wang, Zhiyuan organization: The First Hospital of China Medical University – sequence: 2 givenname: Zhiqiang surname: Gui fullname: Gui, Zhiqiang organization: The First Hospital of China Medical University – sequence: 3 givenname: Zhihong orcidid: 0000-0002-4465-1441 surname: Wang fullname: Wang, Zhihong organization: The First Hospital of China Medical University – sequence: 4 givenname: Jiapeng surname: Huang fullname: Huang, Jiapeng organization: The First Hospital of China Medical University – sequence: 5 givenname: Liang surname: He fullname: He, Liang organization: The First Hospital of China Medical University – sequence: 6 givenname: Wenwu surname: Dong fullname: Dong, Wenwu organization: The First Hospital of China Medical University – sequence: 7 givenname: Dalin surname: Zhang fullname: Zhang, Dalin organization: The First Hospital of China Medical University – sequence: 8 givenname: Ting surname: Zhang fullname: Zhang, Ting organization: The First Hospital of China Medical University – sequence: 9 givenname: Liang surname: Shao fullname: Shao, Liang organization: The First Hospital of China Medical University – sequence: 10 givenname: Jinyuan surname: Shi fullname: Shi, Jinyuan organization: The First Hospital of China Medical University – sequence: 11 givenname: Pu surname: Wu fullname: Wu, Pu organization: The First Hospital of China Medical University – sequence: 12 givenname: Xiaoyu surname: Ji fullname: Ji, Xiaoyu organization: The First Hospital of China Medical University – sequence: 13 givenname: Hao orcidid: 0000-0002-9938-8433 surname: Zhang fullname: Zhang, Hao organization: The First Hospital of China Medical University – sequence: 14 givenname: Wei surname: Sun fullname: Sun, Wei email: sun19890208@126.com organization: The First Hospital of China Medical University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/36263602$$D View this record in MEDLINE/PubMed |
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Keywords | meta-analysis thyroid cancer thyroid lymph node metastasis |
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Papillary thyroid microcarcinoma (PTMC) comprises more than 50% of all newly detected cases of papillary thyroid carcinoma (PTC). High‐volume lymph... Papillary thyroid microcarcinoma (PTMC) comprises more than 50% of all newly detected cases of papillary thyroid carcinoma (PTC). High-volume lymph node... ObjectivePapillary thyroid microcarcinoma (PTMC) comprises more than 50% of all newly detected cases of papillary thyroid carcinoma (PTC). High‐volume lymph... |
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SubjectTerms | Blood flow Diagnosis Humans lymph node metastasis Lymph nodes Lymph Nodes - pathology Lymphatic Metastasis - pathology Lymphatic system Male Meta-analysis Metastases Metastasis Papillary thyroid carcinoma Patients Phenotypes Retrospective Studies Risk Factors Statistical analysis thyroid Thyroid cancer Thyroid gland Thyroid Neoplasms - pathology Thyroiditis Tumors Ultrasonics |
Title | Clinical and ultrasonic risk factors for high‐volume central lymph node metastasis in cN0 papillary thyroid microcarcinoma: A retrospective study and meta‐analysis |
URI | https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fcen.14834 https://www.ncbi.nlm.nih.gov/pubmed/36263602 https://www.proquest.com/docview/2785192309 https://www.proquest.com/docview/2726923001 |
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