Thoracic radiotherapy concurrent with chemotherapy stands for the standard regime for limited staged small cell lung cancer. Involved node radiation(INF) replaced elective node irradiation(ENI) as the more popular since several trails compared the two regimes. simultaneous integrated boost IMRT becomes mature with advancing in IMRT and VMAT. The investigator hypothesis that SIB-IMRT can confine the dose for organs at risk to reduce the toxicities compared with routine IMRT in limited disease small-cell lung cancer.
All patients recruited divided into two arms:SIB-IMRT or routine IMRT,in the routine arm,the prescription dose was 60Gy/2Gy/30f,and in the SIB arm ,60Gy was given to the field of the tumor and metastatic lymph nodes,50Gy was given to CR lesion and high-risk prevention. The physical advantages of SIB-IMRT are to reduce the radiation dose of organs that are at risk in the lungs, esophagus, and heart ensuring the adequate dose for tumor area at the same time. The investigators are carrying out this trial to compare the efficacy, safety, side effects, and type of failure of the two radiotherapy techniques, which will provide a new choice and reliable basis for the future dose-segmentation study of limited-stage small-cell lung cancer.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
350
60Gy given to the tumor area,50Gy to the CR lesion or high-risk field at the same time
patients received IMRT or VMAT,with the prescription of 60Gy/2Gy/30F to the planning tumor volume ,concurrent or sequential with EP chemotherapy
Department of Radiation Oncology, Cancer Hospital, Chinese Academy of Medical Sciences
Beijing, Beijing Municipality, China
RECRUITINGprogress-free survival
the rate of patients survival from the treatment to death or progress
Time frame: 2 year
overall survival
rate of patients survival in 2 years
Time frame: 2 year
local control rate
recurrence rate of local field in 2 years
Time frame: 2 year
side-effects
the rate of radiation pneumatic、oesophagitis、haematological toxicity
Time frame: 3-6months after radiation
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