This phase II trial is studying cisplatin or nedaplatin combine with IMRT to evaluate which one is better efficacy and security in nasopharyngeal carcinoma.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
20
40mg/m2/w
40mg/m2/w
Daping Hospital
Chongqing, China
locoregionally control rate
3 months after treatment
Time frame: 3 months
Survival
1 year Progress Free Survival,Disease Free Survival,3 years and 5 years Over All Survival,Safety
Time frame: 1,3,5 years
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