To Evaluate the Efficacy and Feasibility of Modified Reduce-volume Target IMRT in the Treatment of Patients With Non-metastatic NPC
Completed
- Conditions
- Nasopharyngeal Carcinoma
- Interventions
- Radiation: modified reduce-volume target IMRT
- Registration Number
- NCT04387266
- Lead Sponsor
- Fujian Cancer Hospital
- Brief Summary
This is a retrospective real-world study to evaluate the efficacy and feasibility of modified reduce-volume target IMRT in the treatment of patients with non-metastatic NPC
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 471
Inclusion Criteria
- Pathologic diagnosis (pathologically confirmed by nasopharyngeal biopsy) was nasopharyngeal carcinoma;
- Newly diagnosed, non-metastatic and treated with modified reduce-volume IMRT;
- Patients with baseline MRI date of nasopharynx and neck, and completed the first course of treatment in our hospital;
- Diagnosis time: November 1, 2014 to December 31 , 2017
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Exclusion Criteria
- Disease progression during IMRT;
- Previous malignancy or other concomitant malignant diseases;
- The evaluation information of tumor efficacy can not be obtained;
- Receive blind treatment in other clinical research.
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Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Modified reduce-volume target IMRT modified reduce-volume target IMRT Patients with newly diagnosed, non-metastatic NPC was given modified reduce-volume target IMRT
- Primary Outcome Measures
Name Time Method Local failure-free survival (LFFS) 60 month The duration of time to LFFS was calculated from the date of histological diagnosis until documented treatment local failure.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Department of radiation oncology, Fujian cancer hospital
🇨🇳Fuzhou, Fujian, China