• Written informed consent |
• Declined to participate |
• Female patients with unilateral, stage I-III breast cancer who had undergone standard surgical treatment and confirmed histologically |
• Receipt of neoadjuvant radiotherapy, chemotherapy, or hormonal therapy for breast cancer |
• Available primary tumor samples; Adjacent normal breast tissues selected from an area more than 5 cm from the edge of the tumor |
• Patients had distant metastasis at the time of diagnosis |
• Complete clinicopathological and follow-up information |
• Other concurrent malignant diseases or previous diagnosis of carcinoma |
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• Severe cardiac or cardiovascular disease |
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• Severe cerebrovascular disease |
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• Severe renal failure |
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• Severe respiratory insufficiency |
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• Prior organ transplantation |
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• Pregnancy or lactation |