Clinical trial · Interventional
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
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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. For patients with pathologically confirmed axillary lymph node metastasis or locally advanced breast cancer, NAC may reduce TNM stage and even achieve pCR in the breast and/or axilla. This is particularly evident in HER2-positive and triple-negative breast cancer, for which multiple studies have reported pCR rates of approximately 45%-75% and 40%-65%, respectively. NAC may therefore provide opportunities for breast- or axilla-conserving treatment, reducing complications associated with axillary dissection while improving cosmetic outcomes. In addition, NAC enables assessment of tumor sensitivity to systemic therapy. However, accurate and effective methods for evaluating treatment response after NAC remain lacking. Conventional imaging modalities, such as ultrasound and MRI, demonstrate limited sensitivity and specificity. Although 18F-FDG PET/CT can be used to monitor pathologic response after NAC, its diagnostic performance is influenced by inflammation and metabolic factors, shows limited sensitivity for small lesions, and is relatively costly; thus, it is not widely used in clinical practice for response evaluation. Fibroblast activation protein (FAP) is predominantly expressed in cancer-associated fibroblasts (CAFs) within the tumor stroma and promotes tumor growth, invasion, and drug resistance through multiple mechanisms. Under physiologic conditions, FAP expression is low in most adult tissues but is significantly upregulated in breast cancer. Moreover, 68Ga-FAPI has demonstrated superior imaging performance compared with \^18F-FDG in breast cancer. This study aims to evaluate the feasibility and accuracy of 68Ga-FAPI PET/MRI, compared with 18F-FDG PET/CT and contrast-enhanced breast MRI, in assessing response to NAC in breast cancer, thereby providing additional evidence for clinical decision-making. This is a dynamic cohort study that plans to enroll 27 patients with operable or locally advanced breast cancer, tumor size \>5 cm, or lymph node-positive disease. Baseline imaging with 68Ga-FAPI PET/MRI, 18F-FDG PET/CT, and contrast-enhanced breast MRI will be performed within 10 days before initiation of NAC. Patients will then receive standard NAC according to subtype and clinical guidelines. Follow-up imaging with the same modalities will be conducted between 2 weeks after completion of NAC and within 10 days before surgery. Surgery will then be performed, and patients will be classified into pCR and non-pCR groups based on postoperative pathology. Imaging findings from 68Ga-FAPI PET/MRI, 18F-FDG PET/CT, and breast MRI will be compared with histopathologic results to evaluate their ability to predict pCR. Postoperative follow-up will be conducted to assess prognosis, supported by evidence from MRI, CT, ultrasound, and laboratory examinations. The minimum follow-up duration will be ≥12 months.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| 18F-FDG | Drug | — | UNRESOLVED |
| 68Ga-FAPI-04 | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- neoadjuvant chemotherapy
- description
- It is planned to include 27 patients with operable or locally advanced breast cancer, tumor size \>5 cm, or positive lymph nodes. Within ten days before the start of neoadjuvant therapy, baseline examinations including 68Ga-FAPI PET/MRI, 18F-FDG PET/CT, and contrast-enhanced breast MRI will be completed. Subsequently, standard neoadjuvant therapy will be administered according to treatment guidelines based on each subtype. Two weeks after neoadjuvant therapy until ten days before surgery, 68Ga-FAPI PET/MRI, 18F-FDG PET/CT, and contrast-enhanced breast MRI preoperative examinations will be completed, followed by surgical treatment. Finally, based on postoperative pathological results, patients will be divided into the pCR group and non-pCR group, and the results of 68Ga-FAPI PET/MRI, 18F-FDG PET/CT, and breast MRI will be compared with pathological results to evaluate their ability to predict pCR.
- interventionNames
- Drug: 68Ga-FAPI-04
- Drug: 18F-FDG
Primary outcomes (6)
- measure
- 18F-FDG PET analysis
- timeFrame
- Baseline and 21-28 days after the last cycle of neoadjuvant chemotherapy (each cycle is 21days)
- description
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
- Maximum age
- 70 Years
Show eligibility criteria text
Inclusion Criteria: Female, aged 18-70 years Pathologically confirmed primary breast cancer TNM stage T2-4N0M0/T1-4N1-3M0 No prior treatment No severe hematologic, cardiac, pulmonary, hepatic, or renal dysfunction, and no immunodeficiency diseases Patients must have good physical condition, ECOG score of 0-1 Female patients of childbearing potential must agree to use effective contraception during the study Signed written informed consent Exclusion Criteria: Unwilling to undergo 68Ga-FAPI PET/MRI scan Unable to tolerate chemotherapy or surgery Previous history of other malignancies or prior antitumor treatment Evidence of distant metastasis Immunodeficiency or autoimmune disease History of monoclonal antibody allergy Pregnant or breastfeeding women Presence of active infection Patients with mental illness or cognitive impairment
References
Publications (1)
- DERIVEDLuo Y, Zhang X, Li R, Zeng Y, Zhao Y, Li L, Qian B, Xiao Y, Li M, Zhao Y, Xu S, Yang Q, Zhang H, Chen H, Lu C, Lan X, Liu C. Prospective comparison of [68Ga]Ga-FAPI-04 PET/MRI, [18F]FDG PET/CT, and contrast-enhanced MRI for predicting pathologic complete response after neoadjuvant chemotherapy in breast cancer. Eur J Nucl Med Mol Imaging. 2026 Jul 23. doi: 10.1007/s00259-026-08091-y. Online ahead of print. PMID 42489707