Application and Comparison of [68Ga]Ga-FAPI-04 PET, [18F]FDG PET, and Contrast-Enhanced MRI in Predicting Pathological Response to Neoadjuvant Chemotherapy in Breast Cancer Patients

Breast cancer is one of the most common malignancies among women worldwide, with persistently high incidence and mortality rates, posing a serious threat to women's health. With the continuous advancement of treatment strategies, neoadjuvant therapy (NAC) has become increasingly important in the comprehensive management of breast cancer. NAC refers to the use of chemotherapy, targeted therapy, or immunotherapy prior to surgery to reduce tumor size and downstage disease, thereby improving resectability and providing opportunities for breast- or axilla-conserving treatment . This approach is particularly beneficial for patients with HER2-positive and triple-negative breast cancer, in whom NAC has demonstrated significant advantages in improving the rate of pathologic complete response (pCR). Studies have reported that the pCR rate can reach 50%-75% in HER2-positive breast cancer and 40%-65% in triple-negative breast cancer. Achieving pCR not only improves patient prognosis but also reduces the extent of surgery, minimizes complications associated with axillary dissection, and better meets patients' expectations for cosmetic outcomes and quality of life.

Despite these advances, accurate evaluation of treatment response after NAC remains challenging. Conventional imaging modalities, such as ultrasound and MRI, have limited sensitivity and specificity and may not accurately reflect post-treatment tumor changes. Although 18F-FDG PET/CT offers advantages in assessing tumor metabolic activity , its diagnostic performance is susceptible to interference from inflammation and metabolic factors, has limited sensitivity for small lesions, and is relatively costly, which restricts its widespread clinical application. Therefore, the development of more accurate and cost-effective methods for response evaluation remains an urgent need in the field of neoadjuvant therapy for breast cancer.

In recent years, with the rapid development of molecular imaging, fibroblast activation protein (FAP) has emerged as a promising biomarker. FAP is predominantly expressed in carcinoma-associated fibroblasts (CAFs) within the tumor stroma, showing high expression in breast cancer tissues but minimal expression in normal tissues. FAP has been shown to play a crucial role in tumor initiation, progression, and drug resistance by promoting tumor microenvironment formation and immune evasion . Positron emission tomography/magnetic resonance imaging (PET/MRI) using ^68Ga-labeled fibroblast activation protein inhibitors (68Ga-FAPI) enables more precise assessment of tumor burden and provides a novel approach for predicting and evaluating the response to NAC.

In summary, this study utilizes 68Ga-FAPI PET imaging to comparatively evaluate the differences among 18F-FDG PET, 68Ga-FAPI PET, and contrast-enhanced breast MRI before and after treatment in assessing response to NAC in breast cancer. The study aims to compare the value of these three imaging modalities in treatment response evaluation and to explore the role of FAP expression in predicting the efficacy of NAC in patients with axillary lymph node metastasis or locally advanced breast cancer. By integrating the biological characteristics of FAP with 68Ga-FAPI PET imaging, this study is expected to provide new insights into precise response assessment and individualized treatment strategies for breast cancer, thereby advancing the field of breast cancer management.

This is a prospective, single-center cohort study enrolling patients with axillary lymph node-positive or locally advanced breast cancer, consistent with the indications for neoadjuvant therapy in routine clinical practice and as recommended by local guidelines. Different neoadjuvant chemotherapy (NAC) regimens were selected according to breast cancer subtypes. All patients underwent 68Ga-FAPI PET/MRI, 18F-FDG PET/CT, and contrast-enhanced MRI before the initiation of NAC and again after completion of NAC but prior to surgery. Surgical treatment was subsequently performed, and pathologic complete response (pCR) was determined based on postoperative histopathologic findings.