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Prognostic significance of maximum primary tumor diameter in nasopharyngeal carcinoma

BACKGROUND: To evaluate the prognostic value of maximum primary tumor diameter (MPTD) in nasopharyngeal carcinoma (NPC). METHODS: Three hundred and thirty-three consecutive, newly-diagnosed NPC patients were retrospectively reviewed. Kaplan-Meier analysis and the log-rank test were used to estimate...

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Autores principales: Liang, Shao-Bo, Deng, Yan-Ming, Zhang, Ning, Lu, Rui-Liang, Zhao, Hai, Chen, Hai-Yang, Li, Shao-En, Liu, Dong-Sheng, Chen, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3668272/
https://www.ncbi.nlm.nih.gov/pubmed/23710879
http://dx.doi.org/10.1186/1471-2407-13-260
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author Liang, Shao-Bo
Deng, Yan-Ming
Zhang, Ning
Lu, Rui-Liang
Zhao, Hai
Chen, Hai-Yang
Li, Shao-En
Liu, Dong-Sheng
Chen, Yong
author_facet Liang, Shao-Bo
Deng, Yan-Ming
Zhang, Ning
Lu, Rui-Liang
Zhao, Hai
Chen, Hai-Yang
Li, Shao-En
Liu, Dong-Sheng
Chen, Yong
author_sort Liang, Shao-Bo
collection PubMed
description BACKGROUND: To evaluate the prognostic value of maximum primary tumor diameter (MPTD) in nasopharyngeal carcinoma (NPC). METHODS: Three hundred and thirty-three consecutive, newly-diagnosed NPC patients were retrospectively reviewed. Kaplan-Meier analysis and the log-rank test were used to estimate overall survival (OS), failure-free survival (FFS), distant metastasis-free survival (DMFS) and local relapse-free survival (LRFS). Cox proportional hazards regression analysis was used to assess the prognostic value of MPTD. RESULTS: Median follow-up was 66 months (range, 2–82 months). Median MPTD in stage T1, T2, T3 and T4 was 27.9, 37.5, 45.0 and 61.3 mm, respectively. The proportion of T1 patients with a MPTD ≤ 30 mm was 62.3%; 72% and 62.9% of T2 and T3 patients had a MPTD > 30–50 mm, and 83.5% of T4 patients had a MPTD > 50 mm. For patients with a MPTD ≤ 30 mm, > 30–50 mm and > 50 mm, the 5-year OS, FFS, DMFS and LRFS rates were 85.2%, 74.2% and 56.3% (P < 0.001); 87%, 80.7% and 62.8% (P < 0.001); 88.7%, 86.4% and 72.5% (P = 0.003); and 98.2%, 93.2% and 86.3% (P = 0.012), respectively. In multivariate analysis, MPTD was a prognostic factor for OS, FFS and DMFS, and the only independent prognostic factor for LRFS. For T3-T4 patients with a MPTD ≤ 50 mm and > 50 mm, the 5-year OS, FFS and DMFS rates were 70.4% vs. 58.4% (P = 0.010), 77.5% vs. 65.2% (P = 0.013) and 83.6% vs. 73.6% (P = 0.047), respectively. In patients with a MPTD ≤ 30 mm, 5-year LRFS in T1, T2, T3 and T4 was 100%, 100%, 88.9% and 100% (P = 0.172). CONCLUSIONS: Our data suggest that MPTD is an independent prognostic factor in NPC, and incorporation of MPTD might lead to a further refinement of T staging.
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spelling pubmed-36682722013-06-01 Prognostic significance of maximum primary tumor diameter in nasopharyngeal carcinoma Liang, Shao-Bo Deng, Yan-Ming Zhang, Ning Lu, Rui-Liang Zhao, Hai Chen, Hai-Yang Li, Shao-En Liu, Dong-Sheng Chen, Yong BMC Cancer Research Article BACKGROUND: To evaluate the prognostic value of maximum primary tumor diameter (MPTD) in nasopharyngeal carcinoma (NPC). METHODS: Three hundred and thirty-three consecutive, newly-diagnosed NPC patients were retrospectively reviewed. Kaplan-Meier analysis and the log-rank test were used to estimate overall survival (OS), failure-free survival (FFS), distant metastasis-free survival (DMFS) and local relapse-free survival (LRFS). Cox proportional hazards regression analysis was used to assess the prognostic value of MPTD. RESULTS: Median follow-up was 66 months (range, 2–82 months). Median MPTD in stage T1, T2, T3 and T4 was 27.9, 37.5, 45.0 and 61.3 mm, respectively. The proportion of T1 patients with a MPTD ≤ 30 mm was 62.3%; 72% and 62.9% of T2 and T3 patients had a MPTD > 30–50 mm, and 83.5% of T4 patients had a MPTD > 50 mm. For patients with a MPTD ≤ 30 mm, > 30–50 mm and > 50 mm, the 5-year OS, FFS, DMFS and LRFS rates were 85.2%, 74.2% and 56.3% (P < 0.001); 87%, 80.7% and 62.8% (P < 0.001); 88.7%, 86.4% and 72.5% (P = 0.003); and 98.2%, 93.2% and 86.3% (P = 0.012), respectively. In multivariate analysis, MPTD was a prognostic factor for OS, FFS and DMFS, and the only independent prognostic factor for LRFS. For T3-T4 patients with a MPTD ≤ 50 mm and > 50 mm, the 5-year OS, FFS and DMFS rates were 70.4% vs. 58.4% (P = 0.010), 77.5% vs. 65.2% (P = 0.013) and 83.6% vs. 73.6% (P = 0.047), respectively. In patients with a MPTD ≤ 30 mm, 5-year LRFS in T1, T2, T3 and T4 was 100%, 100%, 88.9% and 100% (P = 0.172). CONCLUSIONS: Our data suggest that MPTD is an independent prognostic factor in NPC, and incorporation of MPTD might lead to a further refinement of T staging. BioMed Central 2013-05-27 /pmc/articles/PMC3668272/ /pubmed/23710879 http://dx.doi.org/10.1186/1471-2407-13-260 Text en Copyright © 2013 Liang et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Liang, Shao-Bo
Deng, Yan-Ming
Zhang, Ning
Lu, Rui-Liang
Zhao, Hai
Chen, Hai-Yang
Li, Shao-En
Liu, Dong-Sheng
Chen, Yong
Prognostic significance of maximum primary tumor diameter in nasopharyngeal carcinoma
title Prognostic significance of maximum primary tumor diameter in nasopharyngeal carcinoma
title_full Prognostic significance of maximum primary tumor diameter in nasopharyngeal carcinoma
title_fullStr Prognostic significance of maximum primary tumor diameter in nasopharyngeal carcinoma
title_full_unstemmed Prognostic significance of maximum primary tumor diameter in nasopharyngeal carcinoma
title_short Prognostic significance of maximum primary tumor diameter in nasopharyngeal carcinoma
title_sort prognostic significance of maximum primary tumor diameter in nasopharyngeal carcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3668272/
https://www.ncbi.nlm.nih.gov/pubmed/23710879
http://dx.doi.org/10.1186/1471-2407-13-260
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