Department of Nuclear Medicine, University Hospital Muenster, Albert-Schweitzer-Campus 1, 48149, Münster, Germany.
Clinical Cooperation Unit Nuclear Medicine, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Ann Nucl Med. 2022 Mar;36(3):293-301. doi: 10.1007/s12149-021-01702-8. Epub 2021 Dec 2.
Fibroblast activation protein (FAP) has been recently presented as new imaging target for malignant diseases and offers high contrast to surrounding normal tissue. FAP tracer uptake has been reported in various tumor entities. The aim of this study was to compare FAP and Prostate-specific membrane antigen (PSMA) expression in primary prostate cancer employing histological analyses and PET imaging in two small patient collectives.
Two independent small patient collectives were included in this study. For cohort A, data of 5 prostate cancer patients and 3 patients with benign prostate hyperplasia were included. Patients with prostate cancer were initially referred for PSMA PET staging. Radical prostatectomy was performed in all patients and prostate specimen of patients and biopsies of healthy controls were available for further evaluation. Histological workup included HE and immunohistochemistry using PSMA Ab, FAP Ab. Cohort B consists of 6 Patients with diagnosed mCRPC and available PSMA as well as FAP PET.
Patients with proven prostate cancer infiltration exhibited strong positivity for PSMA in both primary tumors and lymph node metastases while stainings for FAP were found positive in some cases, but not all (2/5). Controls with BPH presented moderate PSMA staining and in one case also with a positive FAP staining (1/3). PET imaging with FAP seemed to result in more precise results in case of low PSMA expression than PSMA-PET.
While PSMA staining intensity is a valid indicator of prostate cancer in both primary tumor and lymph node metastases, the expression of FAP seems to be heterogeneous but not necessarily linked to cancer-associated fibroblasts. It is also present in inflammation-associated myofibroblasts. Therefore, its ultimate role in prostate cancer diagnosis remains a subject of discussion.
成纤维细胞激活蛋白(FAP)最近被提出作为恶性疾病的新成像靶点,与周围正常组织形成高对比。已在各种肿瘤实体中报道了 FAP 示踪剂摄取。本研究的目的是通过组织学分析和在两个小患者群体中的 PET 成像来比较原发性前列腺癌中的 FAP 和前列腺特异性膜抗原(PSMA)表达。
本研究纳入了两个独立的小患者群体。对于队列 A,纳入了 5 例前列腺癌患者和 3 例良性前列腺增生患者的数据。患有前列腺癌的患者最初被转诊进行 PSMA PET 分期。所有患者均接受了根治性前列腺切除术,并且患者的前列腺标本和健康对照者的活检可用于进一步评估。组织学工作包括使用 PSMA Ab、FAP Ab 进行 HE 和免疫组织化学染色。队列 B 由 6 例诊断为 mCRPC 且有 PSMA 和 FAP PET 的患者组成。
具有明确前列腺癌浸润的患者在原发肿瘤和淋巴结转移中均表现出强烈的 PSMA 阳性,而 FAP 染色在某些情况下为阳性,但并非所有情况下均为阳性(2/5)。患有 BPH 的对照者表现出中等强度的 PSMA 染色,在 1 例中也表现出 FAP 染色阳性(1/3)。与 PSMA-PET 相比,FAP PET 似乎在 PSMA 表达较低的情况下产生更精确的结果。
虽然 PSMA 染色强度是原发性肿瘤和淋巴结转移中前列腺癌的有效指标,但 FAP 的表达似乎是异质的,但不一定与癌相关成纤维细胞相关。它也存在于炎症相关的肌纤维母细胞中。因此,它在前列腺癌诊断中的最终作用仍是一个讨论的主题。