The goal of this clinical trial is to compare the effects of neoadjuvant radiotherapy and adjuvant radiotherapy in patients with breast cancer. The main questions it aims to answer are: * The clinical effect of neoadjuvant radiotherapy for breast cancer was determined according to the postoperative specimens. * Evaluate the acute and late toxicity of preoperative radiotherapy Participants will be randomly divided into two groups: the neoadjuvant radiotherapy group and the adjuvant radiotherapy group.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
60
The patient received synchronous radiotherapy and chemotherapy before surgery. CTV : 40Gy/15fx/3w, sequential GTV: 8.7-10Gy/3-4 Fx.CTV : 40Gy/15fx/3w, sequential GTV: 8.7-10Gy/3-4 Fx.
The patient received radiotherapy after surgery. CTV : 40Gy/15fx/3w, sequential GTV: 8.7-10Gy/3-4 Fx.CTV : 40Gy/15fx/3w, sequential GTV: 8.7-10Gy/3-4 Fx.
Changhai hospital
Shanghai, Shanghai Municipality, China
RECRUITINGpCR
pathological complete remission
Time frame: up to 3 weeks
RCB
residual cancer burden
Time frame: up to 3 weeks
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