From the Department of Nuclear Medicine (P. Backhaus, W.R., F.B., H.J.B., M.P., M.S.), Clinic for Radiology (M.C.B., S.W., W.H.), and Department of Gynecology and Obstetrics (J.T.), University Hospital Münster, Albert-Schweitzer-Campus 1 A1, 48149 Münster, Germany; European Institute for Molecular Imaging, University of Münster, Münster, Germany (P. Backhaus, F.B., M.S.); and Gerhard-Domagk Institute for Pathology, University of Münster, Münster, Germany (P. Barth).
Radiology. 2022 Jan;302(1):39-47. doi: 10.1148/radiol.2021204677. Epub 2021 Oct 12.
Background Integrated PET/MRI is a promising modality for breast assessment. The most frequently used tracer, fluorine 18 (F) fluorodeoxyglucose (FDG), is applied for whole-body staging in advanced breast cancer but has limited accuracy in evaluating primary breast lesions. The fibroblast-activation protein (FAP) is abundantly expressed in invasive breast cancer. FAP-directed PET tracers have recently become available, but results in primary breast tumors remain lacking. Purpose To evaluate the use of FAP inhibitor (FAPI) breast PET/MRI in assessing breast lesions and of FAPI whole-body scanning for lymph node (LN) and distant staging using the ligand gallium 68 (Ga)-FAPI-46. Materials and Methods In women with histologically confirmed invasive breast cancer, all primary Ga-FAPI-46 breast and whole-body PET/MRI and PET/CT examinations conducted at the authors' center between October 2019 and December 2020 were retrospectively analyzed. MRI lesion characteristics and standardized uptake values (SUVs) were quantified with dedicated software. Mann-Whitney tests were used to compare tumor SUVs across different tumor types. The Pearson correlation coefficient was calculated between SUV and measures of MRI morphologic characteristics. Results Nineteen women (mean age, 49 years ± 9 [standard deviation]) were evaluated-18 to complement initial staging and one for restaging after therapy for distant metastases. Strong tracer accumulation was observed in all 18 untreated primary breast malignancies (mean maximum SUV [SUV] = 13.9 [range, 7.9-29.9]; median lesion diameter = 26 mm [range, 9-155 mm]), resulting in clear tumor delineation across different gradings, receptors, and histologic types. All preoperatively verified LN metastases in 13 women showed strong tracer accumulation (mean SUV= 12.2 [range, 3.3-22.4]; mean diameter = 21 mm [range, 14-35 mm]). Tracer uptake established or supported extra-axillary LN involvement in seven women and affected therapy decisions in three women. Conclusion This retrospective analysis indicates use of Ga fibroblast-activation protein inhibitor tracers for breast cancer diagnosis and staging. © RSNA, 2021 See also the editorial by Mankoff and Sellmyer in this issue.
背景 正电子发射断层扫描/磁共振成像(PET/MRI)一体化是一种很有前途的乳腺评估方式。最常使用的示踪剂氟 18(F)氟脱氧葡萄糖(FDG)用于晚期乳腺癌的全身分期,但在评估原发性乳腺病变方面准确性有限。成纤维细胞活化蛋白(FAP)在浸润性乳腺癌中大量表达。最近已经有 FAP 靶向 PET 示踪剂,但原发性乳腺肿瘤的结果仍然缺乏。目的 评估 FAP 抑制剂(FAPI)在评估乳腺病变中的应用,以及 FAPI 镓 68(Ga)-FAPI-46 用于全身扫描以进行淋巴结(LN)和远处分期。材料与方法 对 2019 年 10 月至 2020 年 12 月在作者所在中心进行的所有经组织学证实的浸润性乳腺癌患者的 Ga-FAPI-46 乳腺和全身 PET/MRI 和 PET/CT 检查进行回顾性分析。使用专用软件对 MRI 病变特征和标准摄取值(SUV)进行定量。采用曼-惠特尼 U 检验比较不同肿瘤类型的肿瘤 SUV。计算 SUV 与 MRI 形态学特征之间的 Pearson 相关系数。结果 19 名女性(平均年龄,49 岁±9[标准差])接受了评估,其中 18 名用于补充初始分期,1 名用于远处转移治疗后再分期。所有未经治疗的原发性乳腺恶性肿瘤(18 例)均有明显的示踪剂摄取(最大 SUV[SUV]平均值为 13.9[范围,7.9-29.9];中位数病变直径为 26mm[范围,9-155mm]),导致不同分级、受体和组织学类型的肿瘤清晰显影。13 名女性中所有术前证实的 LN 转移均显示出明显的示踪剂摄取(SUV 平均值为 12.2[范围,3.3-22.4];平均直径为 21mm[范围,14-35mm])。示踪剂摄取确定或支持 7 名女性的腋窝外 LN 受累,并影响 3 名女性的治疗决策。结论 本回顾性分析表明,镓成纤维细胞活化蛋白抑制剂示踪剂可用于乳腺癌的诊断和分期。