Department of Nuclear Medicine, Ren Ji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200127, China.
Department of Pathology, Ren Ji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200127, China.
Eur J Nucl Med Mol Imaging. 2024 Sep;51(11):3440-3449. doi: 10.1007/s00259-024-06761-3. Epub 2024 May 20.
To compare performance of whole-body [Ga]Ga-FAPI-04 and [F]FDG PET imaging in the detection of Krukenberg tumors (KTs), primary site and extra-ovarian metastases of gastric signet-ring-cell carcinoma (GSRCC), and evaluate the value of [Ga]Ga-FAPI-04 PET/MR imaging strategy and its potential impact on the management of KTs from GSRCC.
Twelve patients with twenty-three KTs from GSRCC, who underwent both [Ga]Ga-FAPI-04 pelvic PET/MR and whole-body [Ga]Ga-FAPI-04 and [F]FDG PET imaging were retrospectively analyzed. [Ga]Ga-FAPI-04 and [F]FDG uptakes were compared by using Wilcoxon signed-rank test or paired t test. McNemar's test was used to compare lesion detectability between two modalities. Two-tailed P<0.05 was considered statistically significant. Immunohistochemistry staining was utilized to analyze the fibroblast activation protein (FAP) expression in KTs.
A total of 12 patients with 23 KTs from GSRCC (8 synchronous and 4 metachronous) were evaluated. [Ga]Ga-FAPI-04 was superior to [F]FDG PET in detecting primary sites of GSRCC (100% [11/11] vs. 18.2% [2/11], p = 0.002), involved lymph nodes (90.9% [10/11] vs. 54.5% [6/11], p = 0.046) and peritoneal metastases (100% [12/12] vs. 41.7% [5/12], p = 0.008), with higher SUVmax and TBR (all p < 0.005). Both tracers had limited value in identifying KTs, with 100% false negative rate on [Ga]Ga-FAPI-04 PET and a low detection rate of 8.7% on [F]FDG PET. Fap immunohistochemistry showed negative or slight FAP expression in neoplastic signet ring cells and ovarian stroma. [Ga]Ga-FAPI-04 PET/MR imaging strategy greatly improved the detection rate of Krukenberg tumors (87%, 20/23). After adding diffusion-weighted imaging (DWI), the detection rate was further improved (87.5% vs. 100%, p = 0.083). [Ga]Ga-FAPI-04 PET/MR imaging strategy either upgraded TNM staging or changed treatment management in twelve patients.
[Ga]Ga-FAPI-04 PET outperformed [F]FDG PET in detecting primary site and most extra-ovarian metastases of GSRCC, but both tracers had limited value in identifying Krukenberg tumors. Pelvis MRI should be applied to compensate the limitation of [Ga]Ga-FAPI-04 PET imaging to identify Krukenberg tumours. The [Ga]Ga-FAPI-04 PET/MR imaging strategy has the potential to impact treatment decisions for GSRCC patients with KTs.
比较全身[Ga]Ga-FAPI-04 和 [F]FDG PET 成像在检测克鲁肯贝格瘤(KTs)、胃印戒细胞癌(GSRCC)原发部位和卵巢外转移,以及评估[Ga]Ga-FAPI-04 PET/MR 成像策略的价值及其对 GSRCC KTs 管理的潜在影响。
回顾性分析了 12 例经[Ga]Ga-FAPI-04 盆腔 PET/MR 和全身[Ga]Ga-FAPI-04 和 [F]FDG PET 成像检查的 23 例 GSRCC 伴 KTs 的患者。采用 Wilcoxon 符号秩检验或配对 t 检验比较 [Ga]Ga-FAPI-04 和 [F]FDG 的摄取情况。采用 McNemar 检验比较两种模态的病变检出率。双侧 P<0.05 为有统计学意义。免疫组化染色分析 KTs 中纤维母细胞激活蛋白(FAP)的表达。
共评估了 12 例 GSRCC 伴 23 例 KTs(8 例同步和 4 例异时)的患者。[Ga]Ga-FAPI-04 在检测 GSRCC 原发部位(100%[11/11] vs. 18.2%[2/11],p=0.002)、受累淋巴结(90.9%[10/11] vs. 54.5%[6/11],p=0.046)和腹膜转移(100%[12/12] vs. 41.7%[5/12],p=0.008)方面优于 [F]FDG PET,具有更高的 SUVmax 和 TBR(均 p<0.005)。两种示踪剂在识别 KTs 方面均价值有限,[Ga]Ga-FAPI-04 PET 的假阴性率为 100%,[F]FDG PET 的检出率为 8.7%。Fap 免疫组化显示肿瘤性印戒细胞和卵巢基质中存在阴性或轻微的 FAP 表达。[Ga]Ga-FAPI-04 PET/MR 成像策略大大提高了 KTs 的检出率(87%,20/23)。添加弥散加权成像(DWI)后,检出率进一步提高(87.5% vs. 100%,p=0.083)。[Ga]Ga-FAPI-04 PET/MR 成像策略在 12 例患者中要么升级了 TNM 分期,要么改变了治疗管理。
[Ga]Ga-FAPI-04 PET 在检测 GSRCC 原发部位和大多数卵巢外转移方面优于 [F]FDG PET,但两种示踪剂在识别 KTs 方面均价值有限。盆腔 MRI 应应用于补偿[Ga]Ga-FAPI-04 PET 成像在识别克鲁肯贝格肿瘤方面的局限性。[Ga]Ga-FAPI-04 PET/MR 成像策略有可能影响 GSRCC 伴 KTs 患者的治疗决策。