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AB073. Clinicopathologic characteristics, therapy and outcomes of primary ureteral small cell carcinoma: a case series and systematic review of the literature

BACKGROUND: To review the experience of diagnosis and treatment of primary small cell carcinoma (SCC) in our institution and discuss the clinicopathologic characteristics, treatments and outcomes of patients with primary ureteral SCC. METHODS: Patients diagnosed with ureteral SCC in our institution...

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Detalles Bibliográficos
Autores principales: Zhong, Wenlong, Li, Xuesong, Zhou, Liqun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5565533/
http://dx.doi.org/10.21037/tau.2017.s073
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author Zhong, Wenlong
Li, Xuesong
Zhou, Liqun
author_facet Zhong, Wenlong
Li, Xuesong
Zhou, Liqun
author_sort Zhong, Wenlong
collection PubMed
description BACKGROUND: To review the experience of diagnosis and treatment of primary small cell carcinoma (SCC) in our institution and discuss the clinicopathologic characteristics, treatments and outcomes of patients with primary ureteral SCC. METHODS: Patients diagnosed with ureteral SCC in our institution from January, 2007 to December, 2016 were reviewed. In addition, we performed a systematic literature review in October 2016 on case reports and case series of ureteral SCC. The clinicopathologic characteristics, treatments and outcomes of this rare disease were analyzed. RESULTS: A total of 32 patients were included in our analysis (4 cases from our institution and 28 cases from the literature). Most patients (71.0%) were male with an average age of 66.6 years (range, 48–80 years). The most common symptoms were hematuria (n=14, 48.3%) and flank pain (n=14, 48.3%). All patients received surgery, with 12 (37.5%) patients underwent multimodality therapy. Regional or distant recurrence occurred in 11 patients, among which only 1 patient presented bladder recurrence. The overall median survival for the patients was 17 months, with a 1- and 3-year survival rates 51.9% and 30.3%, respectively. In a univariate analysis, female (P=0.009), pure SCC (P=0.03), advanced T stage (P=0.04) were associated with worse overall survival. CONCLUSIONS: Ureteral SCCs are extremely rare neoplasms with aggressive natural history and poor prognosis. T stage, tumor components and gender may be important factors influencing prognosis. A multimodality treatment is recommended for the management. However, further studies are needed to improve the treatment strategy.
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spelling pubmed-55655332017-09-01 AB073. Clinicopathologic characteristics, therapy and outcomes of primary ureteral small cell carcinoma: a case series and systematic review of the literature Zhong, Wenlong Li, Xuesong Zhou, Liqun Transl Androl Urol Printed Abstracts BACKGROUND: To review the experience of diagnosis and treatment of primary small cell carcinoma (SCC) in our institution and discuss the clinicopathologic characteristics, treatments and outcomes of patients with primary ureteral SCC. METHODS: Patients diagnosed with ureteral SCC in our institution from January, 2007 to December, 2016 were reviewed. In addition, we performed a systematic literature review in October 2016 on case reports and case series of ureteral SCC. The clinicopathologic characteristics, treatments and outcomes of this rare disease were analyzed. RESULTS: A total of 32 patients were included in our analysis (4 cases from our institution and 28 cases from the literature). Most patients (71.0%) were male with an average age of 66.6 years (range, 48–80 years). The most common symptoms were hematuria (n=14, 48.3%) and flank pain (n=14, 48.3%). All patients received surgery, with 12 (37.5%) patients underwent multimodality therapy. Regional or distant recurrence occurred in 11 patients, among which only 1 patient presented bladder recurrence. The overall median survival for the patients was 17 months, with a 1- and 3-year survival rates 51.9% and 30.3%, respectively. In a univariate analysis, female (P=0.009), pure SCC (P=0.03), advanced T stage (P=0.04) were associated with worse overall survival. CONCLUSIONS: Ureteral SCCs are extremely rare neoplasms with aggressive natural history and poor prognosis. T stage, tumor components and gender may be important factors influencing prognosis. A multimodality treatment is recommended for the management. However, further studies are needed to improve the treatment strategy. AME Publishing Company 2017-08 /pmc/articles/PMC5565533/ http://dx.doi.org/10.21037/tau.2017.s073 Text en 2017 Translational Andrology and Urology. All rights reserved.
spellingShingle Printed Abstracts
Zhong, Wenlong
Li, Xuesong
Zhou, Liqun
AB073. Clinicopathologic characteristics, therapy and outcomes of primary ureteral small cell carcinoma: a case series and systematic review of the literature
title AB073. Clinicopathologic characteristics, therapy and outcomes of primary ureteral small cell carcinoma: a case series and systematic review of the literature
title_full AB073. Clinicopathologic characteristics, therapy and outcomes of primary ureteral small cell carcinoma: a case series and systematic review of the literature
title_fullStr AB073. Clinicopathologic characteristics, therapy and outcomes of primary ureteral small cell carcinoma: a case series and systematic review of the literature
title_full_unstemmed AB073. Clinicopathologic characteristics, therapy and outcomes of primary ureteral small cell carcinoma: a case series and systematic review of the literature
title_short AB073. Clinicopathologic characteristics, therapy and outcomes of primary ureteral small cell carcinoma: a case series and systematic review of the literature
title_sort ab073. clinicopathologic characteristics, therapy and outcomes of primary ureteral small cell carcinoma: a case series and systematic review of the literature
topic Printed Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5565533/
http://dx.doi.org/10.21037/tau.2017.s073
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