<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yan Z</submitter><funding>Natural Science Foundation of Hebei Province</funding><pagination>163</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8978436</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>22(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Estimates of cervical lymph node (LN) metastasis in patients with middle and lower thoracic esophageal squamous cell carcinoma (ESCC) are important. A nomogram is a useful tool for individualized prediction.&lt;h4>Methods&lt;/h4>A total of 235 patients were enrolled in this study. Univariate and multivariate analyses were performed to screen for independent risk factors and construct a nomogram to predict the risk of cervical LN metastasis. The nomogram performance was assessed by discrimination, calibration, and clinical use.&lt;h4>Results&lt;/h4>Totally, four independent predictors, including the maximum diameter of tumor, paraesophageal lymph node status, recurrent laryngeal nerve lymph node status, and the CT-reported cervical LN status, were enrolled in the nomogram. The AUC of the nomogram model in the training and validation dataset were 0.833 (95% CI 0.762-0.905), 0.808 (95% CI 0.696-0.920), respectively. The calibration curve demonstrated a strong consistency between nomogram and clinical findings in predicting cervical LN metastasis. Decision curve analysis demonstrated that the nomogram was clinically useful.&lt;h4>Conclusion&lt;/h4>We developed a nomogram that could be conveniently used to predict the individualized risk of cervical LN metastasis in patients with middle and lower thoracic ESCC.</pubmed_abstract><journal>BMC gastroenterology</journal><pubmed_title>Development and validation of a nomogram for prediction of cervical lymph node metastasis in middle and lower thoracic esophageal squamous cell carcinoma.</pubmed_title><pmcid>PMC8978436</pmcid><funding_grant_id>No.H2021206259</funding_grant_id><pubmed_authors>You Y</pubmed_authors><pubmed_authors>Yan Z</pubmed_authors><pubmed_authors>Lu J</pubmed_authors><pubmed_authors>Xu T</pubmed_authors><pubmed_authors>Xu X</pubmed_authors><pubmed_authors>Xu J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Development and validation of a nomogram for prediction of cervical lymph node metastasis in middle and lower thoracic esophageal squamous cell carcinoma.</name><description>&lt;h4>Background&lt;/h4>Estimates of cervical lymph node (LN) metastasis in patients with middle and lower thoracic esophageal squamous cell carcinoma (ESCC) are important. A nomogram is a useful tool for individualized prediction.&lt;h4>Methods&lt;/h4>A total of 235 patients were enrolled in this study. Univariate and multivariate analyses were performed to screen for independent risk factors and construct a nomogram to predict the risk of cervical LN metastasis. The nomogram performance was assessed by discrimination, calibration, and clinical use.&lt;h4>Results&lt;/h4>Totally, four independent predictors, including the maximum diameter of tumor, paraesophageal lymph node status, recurrent laryngeal nerve lymph node status, and the CT-reported cervical LN status, were enrolled in the nomogram. The AUC of the nomogram model in the training and validation dataset were 0.833 (95% CI 0.762-0.905), 0.808 (95% CI 0.696-0.920), respectively. The calibration curve demonstrated a strong consistency between nomogram and clinical findings in predicting cervical LN metastasis. Decision curve analysis demonstrated that the nomogram was clinically useful.&lt;h4>Conclusion&lt;/h4>We developed a nomogram that could be conveniently used to predict the individualized risk of cervical LN metastasis in patients with middle and lower thoracic ESCC.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Apr</publication><modification>2025-04-04T08:24:23.959Z</modification><creation>2025-04-04T08:24:23.959Z</creation></dates><accession>S-EPMC8978436</accession><cross_references><pubmed>35369868</pubmed><doi>10.1186/s12876-022-02243-8</doi></cross_references></HashMap>