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成纤维细胞激活蛋白(FAP)特异性放射性配体可否被视为泛肿瘤药物?

Could Fibroblast Activation Protein (FAP)-Specific Radioligands Be Considered as Pan-Tumor Agents?

机构信息

Nuclear Medicine Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.

Ente Ospedaliero Cantonale, Bellinzona, Switzerland.

出版信息

Contrast Media Mol Imaging. 2022 Feb 22;2022:3948873. doi: 10.1155/2022/3948873. eCollection 2022.

Abstract

BACKGROUND

Cancer-associated fibroblasts (CAFs) can strongly modulate the response to therapy of malignant tumor cells, facilitating their continuous proliferation and invading behaviors. In this context, several efforts were made in identifying the fibroblast activation protein (FAP) as a CAF recognizer and in designing FAP-specific PET radiotracers (as Ga-FAPI) along with FAP-specific therapeutic radioligands. Herein, we review different clinical studies using the various FAP-specific radioligands as novel theranostic agents in a wide range of oncologic and nononcologic indications.

METHODS

A comprehensive systematic search was conducted on the PubMed and Scopus databases to find relevant published articles concerning the FAP-specific PET imaging as well as the FAP-specific radionuclide therapy in patients with oncologic and nononcologic indications. The enrolled studies were dichotomized into oncologic and nononcologic categories, and the required data were extracted by precisely reviewing the whole text of each eligible study. A meta-analysis was also performed comparing the detection rates of Ga-FAPI vs. F-FDG PET/CT using odds ratio (OR) and risk difference as outcome measures.

RESULTS

Of the initial 364 relevant papers, 49 eligible articles (1479 patients) and 55 case reports were enrolled in our systematic review. These studies observed high radiolabeled FAPI avidity as early as 10 minutes after administration in primary sites of various malignant tumors. Based on the meta-analysis which was done on the reported detection rates of the Ga-FAPI and F-FDG PET/CT scans, the highest OR belonged to the primary lesion detection rate of gastrointestinal tumors (OR = 32.079, 95% CI: 4.001-257.212;  = 0.001) with low heterogeneity (I = 0%). The corresponding value of the nodal metastases belonged to hepatobiliary tumors (OR = 11.609, 95% CI: 1.888-71.365;  = 0.008) with low heterogeneity (I = 0%). For distant metastases, the highest estimated OR belonged to nasopharyngeal carcinomas (OR = 77.451, 95% CI: 7.323-819.201; < 0.001) with low heterogeneity (I = 0%).

CONCLUSIONS

The outperformance of Ga-FAPI PET/CT over F-FDG PET/CT in identifying certain primary tumors as well as in detecting their metastatic lesions may open indications for evaluation of cases with inconclusive F-FDG PET/CT findings. What needs to be emphasized is that the false-positive results might be problematic and must be taken into account in Ga-FAPI PET/CT interpretation. More clarification on the role of FAPI radioligands in oncologic imaging, radionuclide therapy, and radiotherapy treatment planning is therefore required.

摘要

背景

癌症相关成纤维细胞 (CAFs) 可强烈调节恶性肿瘤细胞对治疗的反应,促进其持续增殖和侵袭行为。在这种情况下,人们努力鉴定成纤维细胞激活蛋白 (FAP) 作为 CAF 的识别因子,并设计 FAP 特异性 PET 放射性示踪剂(如 Ga-FAPI)以及 FAP 特异性治疗放射性配体。在此,我们回顾了使用各种 FAP 特异性放射性示踪剂作为新型治疗诊断剂在广泛的肿瘤和非肿瘤适应证中的不同临床研究。

方法

在 PubMed 和 Scopus 数据库上进行了全面的系统搜索,以找到有关 FAP 特异性 PET 成像以及 FAP 特异性放射性核素治疗在肿瘤和非肿瘤适应证患者的相关已发表文章。将入组的研究分为肿瘤学和非肿瘤学两类,并通过仔细审查每项合格研究的全文提取所需数据。还使用比值比 (OR) 和风险差异作为结局指标,通过荟萃分析比较了 Ga-FAPI 与 F-FDG PET/CT 的检测率。

结果

最初的 364 篇相关论文中,有 49 篇符合条件的文章(1479 名患者)和 55 篇病例报告被纳入我们的系统综述。这些研究观察到放射性标记的 FAPI 在各种恶性肿瘤的原发部位给药后 10 分钟内即可早期显示出高亲和力。基于对 Ga-FAPI 和 F-FDG PET/CT 扫描检测率的报道进行的荟萃分析,胃肠道肿瘤的原发性病变检测率的最高 OR 值属于胃肠道肿瘤(OR=32.079,95%CI:4.001-257.212;=0.001),异质性低(I=0%)。肝内胆管肿瘤的淋巴结转移的相应值(OR=11.609,95%CI:1.888-71.365;=0.008),异质性低(I=0%)。对于远处转移,鼻咽癌的估计最高 OR 值(OR=77.451,95%CI:7.323-819.201;<0.001),异质性低(I=0%)。

结论

Ga-FAPI PET/CT 在识别某些原发性肿瘤以及检测其转移病灶方面优于 F-FDG PET/CT,这可能为评估 F-FDG PET/CT 结果不确定的病例开辟了适应证。需要强调的是,假阳性结果可能是个问题,必须在 Ga-FAPI PET/CT 解释中考虑到这一点。因此,需要进一步阐明 FAPI 放射性配体在肿瘤成像、放射性核素治疗和放射治疗计划中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cb0/8888077/210ccc33bb39/CMMI2022-3948873.001.jpg

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