Department of Nuclear Medicine, University of Duisburg-Essen and German Cancer Consortium (DKTK)-University Hospital Essen, Hufelandstrasse 55, 45147 Essen, Germany.
Division of Solid Tumor Translational Oncology, DKTK and German Cancer Research Center (DKFZ) Partner Side Essen, Hufelandstrasse 15, 45147, Germany; Bridge Institute of Experimental Tumor Therapy, West German Cancer Center, University Hospital Essen, Hufelandstrasse 55, 45147 Essen, Germany.
PET Clin. 2023 Jul;18(3):409-418. doi: 10.1016/j.cpet.2023.02.006. Epub 2023 Mar 27.
Fibroblast activation protein (FAP)-radioligand therapy might be effective in some patients without being curative. FAP-radioligands deliver ionizing radiation directly to FAP cancer-associated fibroblasts and, in some cancers, to FAP tumor cells; in addition, they indirectly irradiate FAP cells in tumor tissue via cross-fire and bystander effects. Here, we discuss the potential to improve FAP-radioligand therapy through interfering with DNA damage repair, immunotherapy, and co-targeting cancer-associated fibroblasts. As the molecular and cellular effects of FAP-radioligands on the tumor and its microenvironment have not been investigated yet, we call for future research to close this gap in knowledge, which prevents the development of more effective FAP-radioligand therapies.
成纤维细胞激活蛋白 (FAP)-放射性配体疗法可能对一些患者有效,但不能治愈。FAP-放射性配体将电离辐射直接递送至 FAP 癌相关成纤维细胞,并在某些癌症中递送至 FAP 肿瘤细胞;此外,它们还通过交叉火力和旁观者效应间接辐照肿瘤组织中的 FAP 细胞。在这里,我们讨论了通过干扰 DNA 损伤修复、免疫疗法和联合靶向癌相关成纤维细胞来提高 FAP-放射性配体疗法的潜力。由于尚未研究 FAP-放射性配体对肿瘤及其微环境的分子和细胞作用,我们呼吁未来的研究来填补这一知识空白,从而开发出更有效的 FAP-放射性配体疗法。