Manohar Poorni M, Peterson Lanell M, Jenkins Isaac C, Wu Qian Vicky, Kurland Brenda F, Novakova-Jiresova Alena, Muzi Mark, Chen Delphine L, Specht Jennifer M, Dintzis Suzanne, Kinahan Paul E, Mankoff David A, Linden Hannah M
University of Washington, Seattle, WA, USA.
Fred Hutchinson Cancer Research Center, FHCC 1144 Eastlake (LG-200), Seattle, WA, 98109-1023, USA.
Mol Imaging Biol. 2025 May 14. doi: 10.1007/s11307-025-02015-2.
This study examines the combination of FES-PET and FDG-PET as complementary imaging for detection of metastatic ILC.
We retrospectively evaluated FES and FDG uptake in patients with metastatic ILC from an estrogen receptor (ER) positive primary tumor. We classified lesions into three categories (FES high/FDG low, FES high/FDG high, FES low/FDG low) using SUVmax cut-off values of 1.5 for FES and 5.0 for FDG. Qualitative evaluation included examination of the difference in the extent of disease between FES and FDG.
Of the 38 patients, 82% had FES uptake in all tumor sites identified by FDG, with 18% lacking FES uptake in at least one lesion. Mean (range) SUVmax for FES and FDG was 4.0 (0.67-10.6) and 4.6 (1.3-12.5), respectively. The majority of ILC patients (25/38), had lesions with FES high/FDG low uptake, consistent with the strongly ER + indolent nature of ILC. Patients with disease classified as FES high/FDG low had longer median overall survival (OS) (3.2 years) and progression-free survival (PFS) (1.5 years) than FES high/FDG high (OS = 2.1 years and PFS = 0.46 years). The median overall OS for all patients was 3.0 years (95% CI 2.5, 4.8) and PFS of 1.3 years (95% CI 0.6, 2.5). 8 patients (21%) had qualitatively more extensive disease by FES-PET.
Our findings suggest that both FES-PET and FDG-PET can identify metastatic ILC and be useful in detecting the pattern and extent of disease. The imaging combination provides additional information for prognosis and clinical decision making, balancing suitability for endocrine therapy and aggressiveness/indolence of disease.
本研究探讨氟雌二醇正电子发射断层扫描(FES-PET)与氟代脱氧葡萄糖正电子发射断层扫描(FDG-PET)联合作为检测转移性浸润性小叶癌(ILC)的补充成像方法。
我们回顾性评估了雌激素受体(ER)阳性原发性肿瘤的转移性ILC患者的FES和FDG摄取情况。我们使用FES的SUVmax临界值1.5和FDG的SUVmax临界值5.0将病变分为三类(FES高/FDG低、FES高/FDG高、FES低/FDG低)。定性评估包括检查FES和FDG之间疾病范围的差异。
在38例患者中,82%在FDG识别的所有肿瘤部位均有FES摄取,18%至少有一个病变缺乏FES摄取。FES和FDG的平均(范围)SUVmax分别为4.0(0.67-10.6)和4.6(1.3-12.5)。大多数ILC患者(25/38)的病变表现为FES高/FDG低摄取,这与ILC强烈的ER+惰性本质一致。疾病分类为FES高/FDG低的患者的中位总生存期(OS)(3.2年)和无进展生存期(PFS)(1.5年)长于FES高/FDG高的患者(OS = 2.1年,PFS = 0.46年)。所有患者的中位总OS为3.0年(95%CI 2.5,4.8),PFS为1.3年(95%CI 0.6,2.5)。8例患者(21%)经FES-PET定性显示疾病范围更广。
我们的研究结果表明,FES-PET和FDG-PET均可识别转移性ILC,并有助于检测疾病的模式和范围。这种成像组合为预后和临床决策提供了额外信息,平衡了内分泌治疗的适用性和疾病的侵袭性/惰性。