Department of Biomedical Sciences, Humanitas University, Via Rita Levi Montalcini 4Pieve Emanuele, 20090, Milan, Italy.
IRCCS Humanitas Research Hospital, Via Manzoni 56, 20089, Rozzano, Milan, Italy.
Eur J Nucl Med Mol Imaging. 2021 Dec;48(13):4396-4414. doi: 10.1007/s00259-021-05475-0. Epub 2021 Jun 25.
Fibroblast activation protein-α (FAPα) is overexpressed on cancer-associated fibroblasts in approximately 90% of epithelial neoplasms, representing an appealing target for therapeutic and molecular imaging applications. [ Ga]Ga-labelled radiopharmaceuticals-FAP-inhibitors (FAPI)-have been developed for PET. We systematically reviewed and meta-analysed published literature to provide an overview of its clinical role.
The search, limited to January 1st, 2018-March 31st, 2021, was performed on MedLine and Embase databases using all the possible combinations of terms "FAP", "FAPI", "PET/CT", "positron emission tomography", "fibroblast", "cancer-associated fibroblasts", "CAF", "molecular imaging", and "fibroblast imaging". Study quality was assessed using the QUADAS-2 criteria. Patient-based and lesion-based pooled sensitivities/specificities of FAPI PET were computed using a random-effects model directly from the STATA "metaprop" command. Between-study statistical heterogeneity was tested (I-statistics).
Twenty-three studies were selected for systematic review. Investigations on staging or restaging head and neck cancer (n = 2, 29 patients), abdominal malignancies (n = 6, 171 patients), various cancers (n = 2, 143 patients), and radiation treatment planning (n = 4, 56 patients) were included in the meta-analysis. On patient-based analysis, pooled sensitivity was 0.99 (95% CI 0.97-1.00) with negligible heterogeneity; pooled specificity was 0.87 (95% CI 0.62-1.00), with negligible heterogeneity. On lesion-based analysis, sensitivity and specificity had high heterogeneity (I = 88.56% and I = 97.20%, respectively). Pooled sensitivity for the primary tumour was 1.00 (95% CI 0.98-1.00) with negligible heterogeneity. Pooled sensitivity/specificity of nodal metastases had high heterogeneity (I = 89.18% and I = 95.74%, respectively). Pooled sensitivity in distant metastases was good (0.93 with 95% CI 0.88-0.97) with negligible heterogeneity.
FAPI-PET appears promising, especially in imaging cancers unsuitable for [F]FDG imaging, particularly primary lesions and distant metastases. However, high-level evidence is needed to define its role, specifically to identify cancer types, non-oncological diseases, and clinical settings for its applications.
成纤维细胞激活蛋白-α(FAPα)在大约 90%的上皮性肿瘤相关的成纤维细胞中过表达,代表了治疗和分子成像应用的有吸引力的靶点。[Ga]Ga 标记的放射性药物-FAP 抑制剂(FAPI)已被开发用于 PET。我们系统地回顾和荟萃分析了已发表的文献,以提供其临床作用的概述。
搜索仅限于 2018 年 1 月 1 日至 2021 年 3 月 31 日,在 MedLine 和 Embase 数据库中使用所有可能的术语组合“FAP”、“FAPI”、“PET/CT”、“正电子发射断层扫描”、“成纤维细胞”、“肿瘤相关成纤维细胞”、“CAF”、“分子成像”和“成纤维细胞成像”进行搜索。使用 QUADAS-2 标准评估研究质量。使用 STATA“metaprop”命令直接从患者和病变层面计算 FAPI PET 的汇总敏感性/特异性。使用 I 统计量检验研究间的统计异质性。
共选择了 23 项研究进行系统评价。对头颈癌(n=2,29 例患者)、腹部恶性肿瘤(n=6,171 例患者)、各种癌症(n=2,143 例患者)和放射治疗计划(n=4,56 例患者)的分期或重新分期进行了调查。纳入荟萃分析。基于患者的分析,汇总敏感性为 0.99(95%CI 0.97-1.00),异质性可忽略;汇总特异性为 0.87(95%CI 0.62-1.00),异质性可忽略。基于病变的分析,敏感性和特异性具有高度异质性(I=88.56%和 I=97.20%)。原发性肿瘤的汇总敏感性为 1.00(95%CI 0.98-1.00),异质性可忽略。淋巴结转移的汇总敏感性/特异性具有高度异质性(I=89.18%和 I=95.74%)。远处转移的汇总敏感性较好(0.93,95%CI 0.88-0.97),异质性可忽略。
FAPI-PET 似乎很有前景,特别是在成像不适合 [F]FDG 成像的癌症方面,尤其是原发性病变和远处转移。然而,需要高级别的证据来定义其作用,特别是要确定癌症类型、非肿瘤性疾病以及其应用的临床环境。