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Clinical Trial Summary

This prospective phase II study is to assess the efficacy and safety of thoracic re-irradiation for locoregionally recurrent non-small cell lung cancer using hypofractionated technique.


Clinical Trial Description

This prospective phase II study is to assess the efficacy and safety of thoracic re-irradiation for locoregionally recurrent non-small cell lung cancer using hypofractionated technique.

1. For peripherally located recurrent tumors, stereotactic body radiation therapy is used at 5000-6000 cGy in 10 fractions.

2. For centrally located recurrent tumors, adaptive hypofractionated radiation is used: Patients are irradiated at 3000-4000cGy in 6-10 daily fractions in the first course. After a four-week interval, patients who have non-progressive disease and an adequate pulmonary function undergo adaptive re-planning, and are irradiated at 2400-3500cGy in 4~7 daily fractions as a boost. Concurrent chemotherapy consists of weekly docetaxel and nedaplatin. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04275687
Study type Interventional
Source Sun Yat-sen University
Contact Bo Qiu, Ph.D
Phone +86-020-87343031
Email qiubo@sysucc.org.cn
Status Recruiting
Phase Phase 2
Start date March 1, 2020
Completion date February 1, 2025