Nasopharyngeal Carcinoma
Conditions
Brief summary
This phase II trial is studying cisplatin or nedaplatin combine with IMRT to evaluate which one is better efficacy and security in nasopharyngeal carcinoma.
Interventions
DRUGCisplatin
40mg/m2/w
DRUGNedaplatin
40mg/m2/w
Sponsors
Daping Hospital and the Research Institute of Surgery of the Third Military Medical University
Study design
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No
Inclusion criteria
Age≥18,T1-2aN1-3;T2-4NxNPC,VEGFR+,++,KPS\>70,Life expectancy≥6 months, No uncontrolled hypertension,cardiac failure,diabetes,lunacy
Exclusion criteria
Distant metastasis, recurrent disease
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| locoregionally control rate | 3 months | 3 months after treatment |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Survival | 1,3,5 years | 1 year Progress Free Survival,Disease Free Survival,3 years and 5 years Over All Survival,Safety |
Countries
China
Contacts
Primary ContactZhenzhou Yang, Dr.
Outcome results
None listed