Neoadjuvant Radiotherapy for Breast Cancer
Not Applicable
Recruiting
- Conditions
- Neoadjuvant RadiotherapyBreast Cancer
- Interventions
- Radiation: adjuvant radiotherapyRadiation: Neoadjuvant radiotherapy
- Registration Number
- NCT06313073
- Lead Sponsor
- Changhai Hospital
- Brief Summary
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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- Female
- Target Recruitment
- 60
Inclusion Criteria
- Female;
- Age range from 18 to 70 years old;
- The pathological diagnosis is invasive cancer, and immunohistochemical examination has been performed to confirm the status of ER, PR, HER2, Ki67, etc;
- Clarify the BRCA gene mutation status;
- Patients who have a baseline stage of T1-3N0-3M0 and meet one of the following conditions and require neoadjuvant therapy: ① mass>5cm; ② Axillary lymph node metastasis; ③ HER-2 positive; ④ Three Yin type; ⑤ Those who have a desire to preserve breast, but have a large ratio of tumor size to breast volume, making it difficult to preserve breast;
- Baseline estimation requires adjuvant radiotherapy, which meets one of the following conditions: ① performing breast conserving surgery; ② T3 or N positive patients after mastectomy and axillary dissection; ③ After mastectomy, sentinel lymph nodes were positive and axillary dissection was not performed;
- KPS score ≥ 80;
- The tumor must be visible in CT scan;
- Patients must undergo magnetic resonance imaging to help determine the contour of the tumor and exclude other lesions. If other lesions are found, biopsy must be performed on these lesions and the result is negative before continuing treatment;
- No history of serious internal medicine diseases or other serious comorbidities, such as a history of mental illness, allergies, etc;
- Sign an informed consent form.
Exclusion Criteria
- Clinical or pathological stage T4 or M1 breast cancer;
- Received preoperative neoadjuvant therapy;
- Pathological confirmation shows that there is no invasive cancer component in DCIS;
- Double breast cancer or previous contralateral breast cancer;
- Imaging examination suggests suspicious malignant lesions in the ipsilateral or contralateral breast, which have not been pathologically confirmed to be benign;
- KPS score ≤ 70;
- There is active infection currently;
- Concomitant with severe heart, liver, kidney, hematopoietic and neurological diseases, psychiatric patients, or estimated survival time<6 months;
- History of malignant tumors in other areas, excluding curable non melanoma skin cancer and cervical cancer in situ;
- History of radiation therapy at the site of previous radiation therapy;
- Pregnancy and lactation period;
- Those with poor compliance or life-threatening conditions who cannot complete treatment.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Adjuvant radiotherapy adjuvant radiotherapy The patient underwent postoperative adjuvant radiotherapy. CTV : 40Gy/15fx/3w, sequential GTV： 8.7-10Gy/3-4 Fx. Neoadjuvant radiotherapy Neoadjuvant radiotherapy The patient received synchronous radiotherapy and chemotherapy before surgery. CTV : 40Gy/15fx/3w, sequential GTV： 8.7-10Gy/3-4 Fx.
- Primary Outcome Measures
Name Time Method pCR up to 3 weeks pathological complete remission
- Secondary Outcome Measures
Name Time Method RCB up to 3 weeks residual cancer burden
Trial Locations
- Locations (1)
Changhai hospital
🇨🇳Shanghai, Shanghai, China