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Small Cell Carcinoma of the Esophagus: Clinicopathological Features and Outcome of 22 Cases

BACKGROUND: Small cell esophageal carcinoma (SCEC) is a highly aggressive and rare neoplasm. OBJECTIVES: This study aimed to report the characteristics, prognostic factors, and treatment outcomes of 22 patients with SCEC. PATIENTS AND METHODS: This brief report was carried out by reviewing the medic...

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Autores principales: Hosseini, Sare, Salek, Roham, Nasrolahi, Hamid, Mohammadianpanah, Mohammad, Judi, Mona
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kowsar 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4698141/
https://www.ncbi.nlm.nih.gov/pubmed/26734479
http://dx.doi.org/10.5812/ircmj.20353
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author Hosseini, Sare
Salek, Roham
Nasrolahi, Hamid
Mohammadianpanah, Mohammad
Judi, Mona
author_facet Hosseini, Sare
Salek, Roham
Nasrolahi, Hamid
Mohammadianpanah, Mohammad
Judi, Mona
author_sort Hosseini, Sare
collection PubMed
description BACKGROUND: Small cell esophageal carcinoma (SCEC) is a highly aggressive and rare neoplasm. OBJECTIVES: This study aimed to report the characteristics, prognostic factors, and treatment outcomes of 22 patients with SCEC. PATIENTS AND METHODS: This brief report was carried out by reviewing the medical records of 22 patients with newly histologically proven SCEC that were treated between 2000 and 2010 at 2 tertiary academic hospitals. All the potential prognostic variables, including the patients’ characteristics, tumor features, and treatment modalities were analyzed to establish their influence on the patients’ survival rates. RESULTS: This study was conducted on 7 males and 15 females with a median age of 61 years. Dysphagia and weight loss were the most prevalent symptoms. According to the results, 14 patients (64%) had limited diseases and 8 cases (36%) had extensive diseases. In those with extensive diseases, liver, lung, and lymph nodes (LNs) were the most metastatic sites. Besides, most tumors were located in lower (50%) and middle (32%) part of the esophagus. Most patients (91%) were treated with sequential (55%) or concurrent (36%) chemoradiation (CRT). Surgical resection was also performed for 7 patients. Chemotherapy regimen consisted of cisplatin and etoposide in 14 patients (64%). The median follow up time was 12 months. The 1, 3, and 5-year overall survival rates were 27%, 14%, and 4%, respectively. Yet, no prognostic factors were found because of the small sample size of the study. CONCLUSIONS: Primary SCEC is a rare and highly aggressive tumor. However, prognosis is poor and long-term survival is exceptional. CRT could be an appropriate alternative to operation.
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spelling pubmed-46981412016-01-05 Small Cell Carcinoma of the Esophagus: Clinicopathological Features and Outcome of 22 Cases Hosseini, Sare Salek, Roham Nasrolahi, Hamid Mohammadianpanah, Mohammad Judi, Mona Iran Red Crescent Med J Brief Report BACKGROUND: Small cell esophageal carcinoma (SCEC) is a highly aggressive and rare neoplasm. OBJECTIVES: This study aimed to report the characteristics, prognostic factors, and treatment outcomes of 22 patients with SCEC. PATIENTS AND METHODS: This brief report was carried out by reviewing the medical records of 22 patients with newly histologically proven SCEC that were treated between 2000 and 2010 at 2 tertiary academic hospitals. All the potential prognostic variables, including the patients’ characteristics, tumor features, and treatment modalities were analyzed to establish their influence on the patients’ survival rates. RESULTS: This study was conducted on 7 males and 15 females with a median age of 61 years. Dysphagia and weight loss were the most prevalent symptoms. According to the results, 14 patients (64%) had limited diseases and 8 cases (36%) had extensive diseases. In those with extensive diseases, liver, lung, and lymph nodes (LNs) were the most metastatic sites. Besides, most tumors were located in lower (50%) and middle (32%) part of the esophagus. Most patients (91%) were treated with sequential (55%) or concurrent (36%) chemoradiation (CRT). Surgical resection was also performed for 7 patients. Chemotherapy regimen consisted of cisplatin and etoposide in 14 patients (64%). The median follow up time was 12 months. The 1, 3, and 5-year overall survival rates were 27%, 14%, and 4%, respectively. Yet, no prognostic factors were found because of the small sample size of the study. CONCLUSIONS: Primary SCEC is a rare and highly aggressive tumor. However, prognosis is poor and long-term survival is exceptional. CRT could be an appropriate alternative to operation. Kowsar 2015-11-01 /pmc/articles/PMC4698141/ /pubmed/26734479 http://dx.doi.org/10.5812/ircmj.20353 Text en Copyright © 2015, Iranian Red Crescent Medical Journal. http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.
spellingShingle Brief Report
Hosseini, Sare
Salek, Roham
Nasrolahi, Hamid
Mohammadianpanah, Mohammad
Judi, Mona
Small Cell Carcinoma of the Esophagus: Clinicopathological Features and Outcome of 22 Cases
title Small Cell Carcinoma of the Esophagus: Clinicopathological Features and Outcome of 22 Cases
title_full Small Cell Carcinoma of the Esophagus: Clinicopathological Features and Outcome of 22 Cases
title_fullStr Small Cell Carcinoma of the Esophagus: Clinicopathological Features and Outcome of 22 Cases
title_full_unstemmed Small Cell Carcinoma of the Esophagus: Clinicopathological Features and Outcome of 22 Cases
title_short Small Cell Carcinoma of the Esophagus: Clinicopathological Features and Outcome of 22 Cases
title_sort small cell carcinoma of the esophagus: clinicopathological features and outcome of 22 cases
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4698141/
https://www.ncbi.nlm.nih.gov/pubmed/26734479
http://dx.doi.org/10.5812/ircmj.20353
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