医学
乳腺癌
腋窝淋巴结
化疗
阶段(地层学)
放射科
肿瘤科
前瞻性队列研究
新辅助治疗
间质细胞
完全响应
内科学
原发性肿瘤
淋巴
磁共振成像
乳房磁振造影
节的
实体瘤疗效评价标准
淋巴结
腋窝
临床试验
PET-CT
转移
癌症
乳房外科
作者
Y K Luo,Xiao Zhang,R H Li,Yalan Zeng,Yin Zhao,Li Li,Bei Qian,Yunxiao Xiao,Mengting Li,Yin Zhao,Silin Xu,Qin Yang,Huanwei Zhang,Hengyu Chen,Chong Lu,X L Lan,Chunping Liu
标识
DOI:10.1007/s00259-026-08091-y
摘要
Abstract Purpose Accurate assessment of pathologic complete response (pCR) after neoadjuvant chemotherapy (NAC) remains challenging in breast cancer. This prospective single-center study compared [ 68 Ga]Ga-FAPI-04 PET/MRI, [ 18 F]FDG PET/CT, and contrast-enhanced MRI for predicting pathologic response after NAC. Methods Women with biopsy-confirmed stage II–III breast cancer underwent baseline and post-therapy [ 68 Ga]Ga-FAPI-04 PET/MRI, [ 18 F]FDG PET/CT, and contrast-enhanced MRI before surgery. PET parameters were analyzed for primary tumors and axillary nodes. Selected variables were evaluated using LASSO and receiver-operating-characteristic analyses. Stromal FAP expression was assessed immunohistochemically in paired specimens. Results Twenty-four patients completed the protocol, yielding 25 primary lesions and 44 metastatic lymph nodes across 27 axillary compartments. The pCR rate was 60.00% for primary lesions and 72.73% for axillary nodes. For primary-lesion response, post-therapy [ 68 Ga]Ga-FAPI-04 SUVmax showed the highest performance (AUC, 0.84; sensitivity, specificity, and accuracy, 80.00% each); the best [ 18 F]FDG parameter was ΔTBR% (AUC, 0.747). For nodal response, post-therapy [ 68 Ga]Ga-FAPI-04 SULmean showed the highest performance (AUC, 0.89; sensitivity, 91.67%; specificity, 81.25%; accuracy, 84.09%) and exceeded the best [ 18 F]FDG parameter on DeLong testing. MRI AUCs were 0.733 and 0.770 for primary and nodal disease, respectively. Stromal FAP expression correlated positively with [ 68 Ga]Ga-FAPI-04 SUVmax. Conclusion Post-therapy [ 68 Ga]Ga-FAPI-04 PET may provide useful adjunctive information for response assessment after NAC in breast cancer, particularly for axillary nodal evaluation, potentially supporting more individualized preoperative planning. Trial registration ClinicalTrials.gov, NCT07553741, retrospectively registered.
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