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Population‐based study evaluating and predicting the probability of death resulting from thyroid cancer among patients with papillary thyroid microcarcinoma

BACKGROUND: Papillary thyroid microcarcinoma (PTMC) is an indolent carcinoma. The cumulative incidence of death from patients with PTMC and the nomogram built based on the competing risks model have not been described. METHODS: Patients diagnosed with PTMC were selected from the Surveillance, Epidem...

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Autores principales: Wang, Kun, Xu, Jing, Li, Shuyu, Liu, Shiyang, Zhang, Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6853812/
https://www.ncbi.nlm.nih.gov/pubmed/31588675
http://dx.doi.org/10.1002/cam4.2597
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author Wang, Kun
Xu, Jing
Li, Shuyu
Liu, Shiyang
Zhang, Lin
author_facet Wang, Kun
Xu, Jing
Li, Shuyu
Liu, Shiyang
Zhang, Lin
author_sort Wang, Kun
collection PubMed
description BACKGROUND: Papillary thyroid microcarcinoma (PTMC) is an indolent carcinoma. The cumulative incidence of death from patients with PTMC and the nomogram built based on the competing risks model have not been described. METHODS: Patients diagnosed with PTMC were selected from the Surveillance, Epidemiology, and End Results (SEER) program (1983‐2015). Cumulative incidence function was utilized to calculate the likelihood of death resulting from thyroid cancer. Gray's test was conducted to examine the difference in the cumulative incidence of death between groups. A proportional subdistribution hazard model was constructed and we further built a nomogram to quantify the likelihood of death using the model. A 10‐fold cross‐validation procedure was adopted to validate the model. RESULTS: A total of 46 662 patients diagnosed with PTMC were included. The median follow‐up time was 81 months (range, 1 to 407 months). The 5‐year, 10‐year, and 20‐year probabilities of death from thyroid carcinoma were 0.3%, 0.6%, and 1.4%, respectively. The age at diagnosis, sex, tumor extension, and lymph node involvement were related to the cumulative incidence of death. A proportional subdistribution hazard model was developed. The performance of the model was good. A nomogram was built based on the model to predict the likelihood of death in patients with PTMC. CONCLUSION: The survival rate of patients with PTMC is excellent. The nomogram constructed based on the well‐performed competing risks model is helpful for both patients and clinicians.
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spelling pubmed-68538122019-12-16 Population‐based study evaluating and predicting the probability of death resulting from thyroid cancer among patients with papillary thyroid microcarcinoma Wang, Kun Xu, Jing Li, Shuyu Liu, Shiyang Zhang, Lin Cancer Med Clinical Cancer Research BACKGROUND: Papillary thyroid microcarcinoma (PTMC) is an indolent carcinoma. The cumulative incidence of death from patients with PTMC and the nomogram built based on the competing risks model have not been described. METHODS: Patients diagnosed with PTMC were selected from the Surveillance, Epidemiology, and End Results (SEER) program (1983‐2015). Cumulative incidence function was utilized to calculate the likelihood of death resulting from thyroid cancer. Gray's test was conducted to examine the difference in the cumulative incidence of death between groups. A proportional subdistribution hazard model was constructed and we further built a nomogram to quantify the likelihood of death using the model. A 10‐fold cross‐validation procedure was adopted to validate the model. RESULTS: A total of 46 662 patients diagnosed with PTMC were included. The median follow‐up time was 81 months (range, 1 to 407 months). The 5‐year, 10‐year, and 20‐year probabilities of death from thyroid carcinoma were 0.3%, 0.6%, and 1.4%, respectively. The age at diagnosis, sex, tumor extension, and lymph node involvement were related to the cumulative incidence of death. A proportional subdistribution hazard model was developed. The performance of the model was good. A nomogram was built based on the model to predict the likelihood of death in patients with PTMC. CONCLUSION: The survival rate of patients with PTMC is excellent. The nomogram constructed based on the well‐performed competing risks model is helpful for both patients and clinicians. John Wiley and Sons Inc. 2019-10-06 /pmc/articles/PMC6853812/ /pubmed/31588675 http://dx.doi.org/10.1002/cam4.2597 Text en © 2019 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Cancer Research
Wang, Kun
Xu, Jing
Li, Shuyu
Liu, Shiyang
Zhang, Lin
Population‐based study evaluating and predicting the probability of death resulting from thyroid cancer among patients with papillary thyroid microcarcinoma
title Population‐based study evaluating and predicting the probability of death resulting from thyroid cancer among patients with papillary thyroid microcarcinoma
title_full Population‐based study evaluating and predicting the probability of death resulting from thyroid cancer among patients with papillary thyroid microcarcinoma
title_fullStr Population‐based study evaluating and predicting the probability of death resulting from thyroid cancer among patients with papillary thyroid microcarcinoma
title_full_unstemmed Population‐based study evaluating and predicting the probability of death resulting from thyroid cancer among patients with papillary thyroid microcarcinoma
title_short Population‐based study evaluating and predicting the probability of death resulting from thyroid cancer among patients with papillary thyroid microcarcinoma
title_sort population‐based study evaluating and predicting the probability of death resulting from thyroid cancer among patients with papillary thyroid microcarcinoma
topic Clinical Cancer Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6853812/
https://www.ncbi.nlm.nih.gov/pubmed/31588675
http://dx.doi.org/10.1002/cam4.2597
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