UMIN ID: UMIN000001540
Registered date:02/12/2008
A Phase I Dose Intensification Study of three dimentional conformal thoracic radiotherapy with concurrent cisplatin and TS-1 for unresectable stage III non-small cell lung cancer
Basic Information
Recruitment status | Complete: follow-up complete |
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Health condition(s) or Problem(s) studied | non-small cell lung cancer |
Date of first enrollment | 2007/09/01 |
Target sample size | 27 |
Countries of recruitment | Japan |
Study type | Interventional |
Intervention(s) | Chemo-Radiotherapy |
Outcome(s)
Primary Outcome | To determin Maximum Torelated Dose and Recommended dose of thoracic radiotherapy for stage III NSCLC. |
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Secondary Outcome | Toxicity, Response rate, Survival |
Key inclusion & exclusion criteria
Age minimum | 20years-old |
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Age maximum | 75years-old |
Gender | Male and Female |
Include criteria | |
Exclude criteria | Interstitial pneumonia. No eligibility for definitive radiotherapy. |
Related Information
Primary Sponsor | Shizuoka Cancer Center, The Cancer Institute Hospital of JFCR |
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Secondary Sponsor | |
Source(s) of Monetary Support | None |
Secondary ID(s) |
Contact
public contact | |
Name | |
Address | Japan |
Telephone | |
h.harada@scchr.jp | |
Affiliation | Shizuoka Cancer Center Radiation Oncology |
scientific contact | |
Name | Hideyuki Harada |
Address | Shimonagakubo 1007, Nagaizumi-cho, Sunto-Gun, Shizuoka, Japan Japan |
Telephone | |
Affiliation | Shizuoka Cancer Center Radiation Oncology |