Literature DB >> 28920241

Comparative analysis of PET findings and clinical outcome in patients with primary mediastinal seminoma.

Tomonobu Koizumi1, Akane Katou2, Kayoko Ikegawa2, Mitsuru Kosaka2, Kazunari Tateishi2, Toshiki Yokoyama2, Atsuto Ushiki2, Shintaro Kanda2, Kenji Tsushima2, Hiroshi Yamamoto2, Masayuki Hanaoka2, Keishi Kubo2, Kazuo Yoshida2, Kazuhiko Oguchi3.   

Abstract

BACKGROUND: Primary mediastinal seminoma is a rare neoplasm. Cisplatin-based chemotherapy is the standard treatment, but management of post-chemotherapy seminoma residuals is still controversial. We encountered four cases of primary mediastinal seminoma and reviewed the clinical characteristics and outcomes, focusing on tumor size and F-18 fluorodeoxyglucose positron emission tomography (FDG-PET) findings after chemotherapy.
METHODS: A retrospective review was performed of four consecutive patients with primary mediastinal seminoma treated in our institution between 2006 and 2010. All patients were young adult males with a median age of 31.3 years (range: 20-46 years). All patients were treated with three to four cycles of a combination of cisplatin, bleomycin, and etoposide, and FDG-PET was performed after chemotherapy.
RESULTS: The response to chemotherapy was good in all patients. After chemotherapy, the findings of the FDG-PET were negative in three subjects. Two of the patients, with tumors measuring over 30 mm, underwent surgical resection for the residual mass and revealed necrotic tissues and no viable cells. A third patient remained stable without salvage surgery. The size of the residual mass in the remaining patient was less than 30 mm, but the FDP-PET result was positive and the mass considered inoperable because of the involvement of large vessels. Subsequently, radiotherapy was added for the residual tumor, but disease progression was seen seven months after the initiation of chemotherapy.
CONCLUSIONS: FDG-PET findings after chemotherapy could be useful as a tool for the prediction of viable residual tumor in post chemotherapy residual mediastinal seminoma.
© 2012 Tianjin Lung Cancer Institute and Wiley Publishing Asia Pty Ltd.

Entities:  

Keywords:  BEP; MEN; PET; SUVmax; chemotherapy; germ cell tumor

Year:  2013        PMID: 28920241     DOI: 10.1111/1759-7714.12002

Source DB:  PubMed          Journal:  Thorac Cancer        ISSN: 1759-7706            Impact factor:   3.500


  2 in total

1.  Primary mediastinal adenocarcinoma originating from a calcified nodule.

Authors:  Gang Chen; Xiaoming Qiu; Yi Liu; Yanjie Qiao; Tao Shi; Jun Chen; Qinghua Zhou
Journal:  Int J Clin Exp Med       Date:  2014-07-15

2.  Chemoradiotherapy is an alternative choice for patients with primary mediastinal seminoma.

Authors:  Yirui Zhai; Bo Chen; Xiaoli Feng; Kan Liu; Shulian Wang; Zhouguang Hui; Qinfu Feng; Junling Li; Zefen Xiao; Jima Lv; Yushun Gao; Yueping Liu; Hui Fang; Jianyang Wang; Lei Deng; Wenyang Liu; Wenqing Wang; Zongmei Zhou; Ye-Xiong Li
Journal:  Radiat Oncol       Date:  2022-03-26       Impact factor: 3.481

  2 in total

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