Volume 5, Issue 2 pp. 169-173
BRIEF REPORT

Docetaxel-based chemotherapy as second-line regimen for advanced thymic carcinoma

Zhengbo Song

Zhengbo Song

Department of Chemotherapy, Zhejiang Cancer Hospital, Hangzhou, China

Key Laboratory Diagnosis and Treatment Technology on Thoracic Oncology, Hangzhou, China

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Xinmin Yu

Xinmin Yu

Department of Chemotherapy, Zhejiang Cancer Hospital, Hangzhou, China

Key Laboratory Diagnosis and Treatment Technology on Thoracic Oncology, Hangzhou, China

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Chunxiao He

Chunxiao He

Department of Chemotherapy, Zhejiang Cancer Hospital, Hangzhou, China

Key Laboratory Diagnosis and Treatment Technology on Thoracic Oncology, Hangzhou, China

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Beibei Zhang

Beibei Zhang

Department of Chemotherapy, Zhejiang Cancer Hospital, Hangzhou, China

Key Laboratory Diagnosis and Treatment Technology on Thoracic Oncology, Hangzhou, China

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Yiping Zhang

Corresponding Author

Yiping Zhang

Department of Chemotherapy, Zhejiang Cancer Hospital, Hangzhou, China

Key Laboratory Diagnosis and Treatment Technology on Thoracic Oncology, Hangzhou, China

Correspondence

Yiping Zhang, Department of Chemotherapy, Zhejiang Cancer Hospital, 38 Guangji Road, 310022, Hangzhou, China.

Tel: +86 57188122182

Fax: +86 57188122188

Email: [email protected]

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First published: 09 July 2013
Citations: 4

Abstract

Thymic carcinoma is an uncommon neoplasm. The efficacy of second-line treatment with docetaxel in advanced thymic carcinoma has not been well studied. Therefore, we conducted a review of the efficacy of docetaxel-based chemotherapy as a second-line regimen for advanced thymic carcinoma. Fifteen patients with advanced thymic carcinoma who received second-line chemotherapy with docetaxel singlet or docetaxel/platinum combination chemotherapy regimens were retrospectively reviewed. There were 11 males and four females, with a median age of 53 years. Squamous cell carcinoma was most common (n = 10), followed by undifferentiated carcinoma (n = 4), and small cell carcinoma (n = 1). Eight patients received docetaxel/platinum combination chemotherapy and seven docetaxel mono-therapy. Four patients showed partial responses, representing a response rate of 26.7%. The median progression-free survival and overall survival in the 15 patients were 4.0 (2.8–5.2) and 22.0 (14.6–29.4) months, respectively. There was no difference in progression-free survival between the docetaxel singlet or docetaxel/platinum combination chemotherapy (3.5 months vs. 4.0 months, P = 0.889). A docetaxel-based regimen could be a potential therapeutic option as a second-line chemotherapy for advanced thymic carcinoma.

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