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Establishment of an innovative staging system for extramedullary plasmacytoma

BACKGROUND: Extramedullary plasmacytoma (EMP) is a rare malignant disease that lacks a unique clinical staging system to predict the survival of EMP patients and to design individualized treatment. Instead, clinicians have chosen to use the multiple myeloma (MM) staging system. METHODS: Forty-eight...

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Autores principales: Zhu, Qian, Zou, Xiong, You, Rui, Jiang, Rou, Zhang, Meng-Xia, Liu, You-Ping, Qian, Chao-Nan, Mai, Hai-Qiang, Hong, Ming-Huang, Guo, Ling, Chen, Ming-Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5055682/
https://www.ncbi.nlm.nih.gov/pubmed/27717354
http://dx.doi.org/10.1186/s12885-016-2824-x
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author Zhu, Qian
Zou, Xiong
You, Rui
Jiang, Rou
Zhang, Meng-Xia
Liu, You-Ping
Qian, Chao-Nan
Mai, Hai-Qiang
Hong, Ming-Huang
Guo, Ling
Chen, Ming-Yuan
author_facet Zhu, Qian
Zou, Xiong
You, Rui
Jiang, Rou
Zhang, Meng-Xia
Liu, You-Ping
Qian, Chao-Nan
Mai, Hai-Qiang
Hong, Ming-Huang
Guo, Ling
Chen, Ming-Yuan
author_sort Zhu, Qian
collection PubMed
description BACKGROUND: Extramedullary plasmacytoma (EMP) is a rare malignant disease that lacks a unique clinical staging system to predict the survival of EMP patients and to design individualized treatment. Instead, clinicians have chosen to use the multiple myeloma (MM) staging system. METHODS: Forty-eight EMP patients treated between 1996 and 2014 were included in this study. The new clinical stages were established according to independent survival factors using Cox regression model. RESULTS: Lymph node metastasis and a larger primary tumor (≥5 cm) were the only two independent poor prognostic factors for overall survival (OS) and disease-free survival (P < 0.05). Stage I was defined as the disease without those two poor prognostic factors. Stage II was defined as the presence of either factor, and Stage III was defined as the presence of both factors. OS was significantly different in each stage of the new staging system (P < 0.001), with a median follow-up time for Stage I, Stage II and Stage III of 68, 23 and 14 months. The new staging system had enhanced prognostic value compared to the MM staging system (the area under ROC 0.763 versus 0.520, P = 0.044). Although no difference was observed between treatments in Stage I, the combination treatment was associated with a significantly beneficial OS in the late stages (5-year OS: 15.3 % versus 79.5 %; P = 0.032). CONCLUSIONS: The new staging system exhibited a promising prognostic value for survival and could aid clinicians in choosing the most suitable treatment for EMP patients.
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spelling pubmed-50556822016-10-19 Establishment of an innovative staging system for extramedullary plasmacytoma Zhu, Qian Zou, Xiong You, Rui Jiang, Rou Zhang, Meng-Xia Liu, You-Ping Qian, Chao-Nan Mai, Hai-Qiang Hong, Ming-Huang Guo, Ling Chen, Ming-Yuan BMC Cancer Research Article BACKGROUND: Extramedullary plasmacytoma (EMP) is a rare malignant disease that lacks a unique clinical staging system to predict the survival of EMP patients and to design individualized treatment. Instead, clinicians have chosen to use the multiple myeloma (MM) staging system. METHODS: Forty-eight EMP patients treated between 1996 and 2014 were included in this study. The new clinical stages were established according to independent survival factors using Cox regression model. RESULTS: Lymph node metastasis and a larger primary tumor (≥5 cm) were the only two independent poor prognostic factors for overall survival (OS) and disease-free survival (P < 0.05). Stage I was defined as the disease without those two poor prognostic factors. Stage II was defined as the presence of either factor, and Stage III was defined as the presence of both factors. OS was significantly different in each stage of the new staging system (P < 0.001), with a median follow-up time for Stage I, Stage II and Stage III of 68, 23 and 14 months. The new staging system had enhanced prognostic value compared to the MM staging system (the area under ROC 0.763 versus 0.520, P = 0.044). Although no difference was observed between treatments in Stage I, the combination treatment was associated with a significantly beneficial OS in the late stages (5-year OS: 15.3 % versus 79.5 %; P = 0.032). CONCLUSIONS: The new staging system exhibited a promising prognostic value for survival and could aid clinicians in choosing the most suitable treatment for EMP patients. BioMed Central 2016-10-08 /pmc/articles/PMC5055682/ /pubmed/27717354 http://dx.doi.org/10.1186/s12885-016-2824-x Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Zhu, Qian
Zou, Xiong
You, Rui
Jiang, Rou
Zhang, Meng-Xia
Liu, You-Ping
Qian, Chao-Nan
Mai, Hai-Qiang
Hong, Ming-Huang
Guo, Ling
Chen, Ming-Yuan
Establishment of an innovative staging system for extramedullary plasmacytoma
title Establishment of an innovative staging system for extramedullary plasmacytoma
title_full Establishment of an innovative staging system for extramedullary plasmacytoma
title_fullStr Establishment of an innovative staging system for extramedullary plasmacytoma
title_full_unstemmed Establishment of an innovative staging system for extramedullary plasmacytoma
title_short Establishment of an innovative staging system for extramedullary plasmacytoma
title_sort establishment of an innovative staging system for extramedullary plasmacytoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5055682/
https://www.ncbi.nlm.nih.gov/pubmed/27717354
http://dx.doi.org/10.1186/s12885-016-2824-x
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