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Clinical analysis of 13 males with primary choriocarcinoma and review of the literature
OBJECTIVE: To analyze the management and prognosis of primary choriocarcinoma (PCC) in male patients. METHODS: The clinical records of males with PCC who were treated at Peking Union Medical College Hospital between 1990 and 2012 were analyzed retrospectively. The literature regarding this clinical...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4074184/ https://www.ncbi.nlm.nih.gov/pubmed/25018640 http://dx.doi.org/10.2147/OTT.S62561 |
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author | Jiang, Fang Xiang, Yang Feng, Feng-Zhi Ren, Tong Cui, Zhu-Mei Wan, Xi-Run |
author_facet | Jiang, Fang Xiang, Yang Feng, Feng-Zhi Ren, Tong Cui, Zhu-Mei Wan, Xi-Run |
author_sort | Jiang, Fang |
collection | PubMed |
description | OBJECTIVE: To analyze the management and prognosis of primary choriocarcinoma (PCC) in male patients. METHODS: The clinical records of males with PCC who were treated at Peking Union Medical College Hospital between 1990 and 2012 were analyzed retrospectively. The literature regarding this clinical condition was also reviewed. RESULTS: The median survival interval of the 13 patients treated at Peking Union Medical College Hospital was 54 months (range, 6–115 months), and the 1- and 3-year survival rates were 53.8% and 43.1%, respectively. All patients were treated with surgery; 12 were treated with combined chemotherapy. After including 100 cases found in the literature, for a total of 113 patients, the median survival interval was 10 months (range, 6.4–13.6 months). The testis was the most common primary site (36.2%). Most patients (70.9%) had metastatic lesions at diagnosis. Univariate and multivariate analyses revealed that longer median overall survival was significantly associated with patient age <34 years old (48 months vs 10 months, odds ratio [OR] =0.47, P=0.029), the presence of other histological components (54 months vs 11 months, OR =0.54, P=0.011), and combined chemotherapy and surgical treatments (14 months vs 2.5 months, OR =0.18, P=0.002). CONCLUSION: PCC is an extremely rare disease among men, and its prognosis is much worse than that of gestational choriocarcinoma. The complete resection of the primary site and metastases followed by chemotherapy seems to provide patients with the best chance at survival. Furthermore, additional chemotherapy cycles might facilitate better progress. |
format | Online Article Text |
id | pubmed-4074184 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-40741842014-07-11 Clinical analysis of 13 males with primary choriocarcinoma and review of the literature Jiang, Fang Xiang, Yang Feng, Feng-Zhi Ren, Tong Cui, Zhu-Mei Wan, Xi-Run Onco Targets Ther Case Series OBJECTIVE: To analyze the management and prognosis of primary choriocarcinoma (PCC) in male patients. METHODS: The clinical records of males with PCC who were treated at Peking Union Medical College Hospital between 1990 and 2012 were analyzed retrospectively. The literature regarding this clinical condition was also reviewed. RESULTS: The median survival interval of the 13 patients treated at Peking Union Medical College Hospital was 54 months (range, 6–115 months), and the 1- and 3-year survival rates were 53.8% and 43.1%, respectively. All patients were treated with surgery; 12 were treated with combined chemotherapy. After including 100 cases found in the literature, for a total of 113 patients, the median survival interval was 10 months (range, 6.4–13.6 months). The testis was the most common primary site (36.2%). Most patients (70.9%) had metastatic lesions at diagnosis. Univariate and multivariate analyses revealed that longer median overall survival was significantly associated with patient age <34 years old (48 months vs 10 months, odds ratio [OR] =0.47, P=0.029), the presence of other histological components (54 months vs 11 months, OR =0.54, P=0.011), and combined chemotherapy and surgical treatments (14 months vs 2.5 months, OR =0.18, P=0.002). CONCLUSION: PCC is an extremely rare disease among men, and its prognosis is much worse than that of gestational choriocarcinoma. The complete resection of the primary site and metastases followed by chemotherapy seems to provide patients with the best chance at survival. Furthermore, additional chemotherapy cycles might facilitate better progress. Dove Medical Press 2014-06-20 /pmc/articles/PMC4074184/ /pubmed/25018640 http://dx.doi.org/10.2147/OTT.S62561 Text en © Jiang et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Case Series Jiang, Fang Xiang, Yang Feng, Feng-Zhi Ren, Tong Cui, Zhu-Mei Wan, Xi-Run Clinical analysis of 13 males with primary choriocarcinoma and review of the literature |
title | Clinical analysis of 13 males with primary choriocarcinoma and review of the literature |
title_full | Clinical analysis of 13 males with primary choriocarcinoma and review of the literature |
title_fullStr | Clinical analysis of 13 males with primary choriocarcinoma and review of the literature |
title_full_unstemmed | Clinical analysis of 13 males with primary choriocarcinoma and review of the literature |
title_short | Clinical analysis of 13 males with primary choriocarcinoma and review of the literature |
title_sort | clinical analysis of 13 males with primary choriocarcinoma and review of the literature |
topic | Case Series |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4074184/ https://www.ncbi.nlm.nih.gov/pubmed/25018640 http://dx.doi.org/10.2147/OTT.S62561 |
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