Health Condition 1: null- Patient of Nasopharyngeal Carcinoma
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Informed consent in accordance with local regulations. 2. Age 18 years and above. 3. Histologically confirmed NPC, any WHO subtype UICC 7th Edition Stage III-IVB (i.e. any T3-4 or N2-3, and M0). 4. Primary RT planned with radical intent.
Exclusion criteria
Exclusion criteria: 1. Second primary malignant disease within the past 5 years, other than non melanomatous skin cancer or in situ carcinoma of cervix. 2. Pregnancy. 3. No previous radiotherapy to the head and neck region.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| (I)A national survey on demographic data and RT facilities in participating countries (CRF-I). (II)A cross-sectional study on patient characteristics and patterns of care in participating centres (CRF-II). (III)A comparative study of RT planning and clinical outcomes before (Group A) and after (Group B) an educational intervention and encouragement of local peer review. (CRF-IIIA, B, C, D, E). Timepoint: Progression-Free Survival | — |
Secondary
| Measure | Time frame |
|---|---|
| locoregional failure-free survival (LR-FFS; time to persistence/relapse at primary site and/or regional lymph nodes, censored by death) Distant failure-free survival (D-FFS: time to metastasis at distant sites, censored by death) Timepoint: Clinical outcome at a minimum of 2 years follow up after treatment site and/or regional lymph nodes, censored by death) | — |
Countries
Algeria, Australia, Austria, Canada, Egypt, France, Hong Kong, India, Indonesia, Pakistan, Philippines, Thailand, Tunisia, United Republic of Tanzania, United States of America, Viet Nam
Contacts
Tata Memorial Hospital