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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
  1. Pathologic diagnosis (pathologically confirmed by nasopharyngeal biopsy) was nasopharyngeal carcinoma;
  2. Newly diagnosed, non-metastatic and treated with modified reduce-volume IMRT;
  3. Patients with baseline MRI date of nasopharynx and neck, and completed the first course of treatment in our hospital;
  4. Diagnosis time: November 1, 2014 to December 31 , 2017
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Exclusion Criteria
  1. Disease progression during IMRT;
  2. Previous malignancy or other concomitant malignant diseases;
  3. The evaluation information of tumor efficacy can not be obtained;
  4. Receive blind treatment in other clinical research.
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Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Modified reduce-volume target IMRTmodified reduce-volume target IMRTPatients with newly diagnosed, non-metastatic NPC was given modified reduce-volume target IMRT
Primary Outcome Measures
NameTimeMethod
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
NameTimeMethod

Trial Locations

Locations (1)

Department of radiation oncology, Fujian cancer hospital

🇨🇳

Fuzhou, Fujian, China

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