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A Study of Patients with Primary Mediastinal Germ Cell Tumors Treated Using Multimodal Therapy
OBJECTIVES: Primary mediastinal germ cell tumors (PMGCTs) are rare, which often makes them difficult to treat. Herein, we examined patients with PMGCTs who underwent multimodal treatment. METHODS: We examined 6 patients (median age: 25 years, range: 19–27 years) with PMGCTs who underwent multimodal...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5467274/ https://www.ncbi.nlm.nih.gov/pubmed/28634489 http://dx.doi.org/10.1155/2017/1404610 |
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author | Tanaka, Yutaro Okamura, Takehiko Nagai, Takashi Kobayashi, Daichi Kobayashi, Takahiro Akita, Hidetoshi Moritoki, Yoshinobu Yasui, Takahiro |
author_facet | Tanaka, Yutaro Okamura, Takehiko Nagai, Takashi Kobayashi, Daichi Kobayashi, Takahiro Akita, Hidetoshi Moritoki, Yoshinobu Yasui, Takahiro |
author_sort | Tanaka, Yutaro |
collection | PubMed |
description | OBJECTIVES: Primary mediastinal germ cell tumors (PMGCTs) are rare, which often makes them difficult to treat. Herein, we examined patients with PMGCTs who underwent multimodal treatment. METHODS: We examined 6 patients (median age: 25 years, range: 19–27 years) with PMGCTs who underwent multimodal treatment between April 2001 and March 2015. Three patients had seminomas, 2 patients had yolk sac tumors, and 1 patient had choriocarcinoma. The median observation period was 32.5 months (range: 8–84 months). RESULTS: Three of the 6 patients received initial operation followed by 3-4 courses of chemotherapy (bleomycin, etoposide, and cisplatin (BEP) or etoposide and cisplatin (EP)). One patient developed multiple lung metastases 17 months after surgery; received salvage chemotherapy with vinblastine, ifosfamide, and cisplatin; and achieved complete remission. The remaining 3 patients received initial BEP and EP chemotherapy. Multiple lung metastases and supraclavicular lymph node metastases were detected in 2 of these patients at the initial diagnosis. The patients underwent resections to remove residual tumor after treatment, and no viable tumor cells were found. CONCLUSIONS: Reliable diagnosis and immediate multimodal treatments are necessary for patients with PMGCTs. The 6 patients treated in our hospital have never experienced recurrence after the multimodal treatment. |
format | Online Article Text |
id | pubmed-5467274 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-54672742017-06-20 A Study of Patients with Primary Mediastinal Germ Cell Tumors Treated Using Multimodal Therapy Tanaka, Yutaro Okamura, Takehiko Nagai, Takashi Kobayashi, Daichi Kobayashi, Takahiro Akita, Hidetoshi Moritoki, Yoshinobu Yasui, Takahiro Adv Urol Clinical Study OBJECTIVES: Primary mediastinal germ cell tumors (PMGCTs) are rare, which often makes them difficult to treat. Herein, we examined patients with PMGCTs who underwent multimodal treatment. METHODS: We examined 6 patients (median age: 25 years, range: 19–27 years) with PMGCTs who underwent multimodal treatment between April 2001 and March 2015. Three patients had seminomas, 2 patients had yolk sac tumors, and 1 patient had choriocarcinoma. The median observation period was 32.5 months (range: 8–84 months). RESULTS: Three of the 6 patients received initial operation followed by 3-4 courses of chemotherapy (bleomycin, etoposide, and cisplatin (BEP) or etoposide and cisplatin (EP)). One patient developed multiple lung metastases 17 months after surgery; received salvage chemotherapy with vinblastine, ifosfamide, and cisplatin; and achieved complete remission. The remaining 3 patients received initial BEP and EP chemotherapy. Multiple lung metastases and supraclavicular lymph node metastases were detected in 2 of these patients at the initial diagnosis. The patients underwent resections to remove residual tumor after treatment, and no viable tumor cells were found. CONCLUSIONS: Reliable diagnosis and immediate multimodal treatments are necessary for patients with PMGCTs. The 6 patients treated in our hospital have never experienced recurrence after the multimodal treatment. Hindawi 2017 2017-05-28 /pmc/articles/PMC5467274/ /pubmed/28634489 http://dx.doi.org/10.1155/2017/1404610 Text en Copyright © 2017 Yutaro Tanaka et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Study Tanaka, Yutaro Okamura, Takehiko Nagai, Takashi Kobayashi, Daichi Kobayashi, Takahiro Akita, Hidetoshi Moritoki, Yoshinobu Yasui, Takahiro A Study of Patients with Primary Mediastinal Germ Cell Tumors Treated Using Multimodal Therapy |
title | A Study of Patients with Primary Mediastinal Germ Cell Tumors Treated Using Multimodal Therapy |
title_full | A Study of Patients with Primary Mediastinal Germ Cell Tumors Treated Using Multimodal Therapy |
title_fullStr | A Study of Patients with Primary Mediastinal Germ Cell Tumors Treated Using Multimodal Therapy |
title_full_unstemmed | A Study of Patients with Primary Mediastinal Germ Cell Tumors Treated Using Multimodal Therapy |
title_short | A Study of Patients with Primary Mediastinal Germ Cell Tumors Treated Using Multimodal Therapy |
title_sort | study of patients with primary mediastinal germ cell tumors treated using multimodal therapy |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5467274/ https://www.ncbi.nlm.nih.gov/pubmed/28634489 http://dx.doi.org/10.1155/2017/1404610 |
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