Journal
JOURNAL OF NUCLEAR MEDICINE
Volume 63, Issue 2, Pages 212-217Publisher
SOC NUCLEAR MEDICINE INC
DOI: 10.2967/jnumed.121.262134
Keywords
Ga-68-FAPI PET; lymphoma; cancer-associated fibro; cancer-associated fibroblasts; fibroblast activation protein; tumor stroma
Funding
- National Natural Science Foundation of China [82071957]
- Beijing Hospitals Authority Clinical Medicine Development [XMLX202120]
- Capital's Funds for Health Improvement and Research [2018-2-1024]
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This study aimed to profile FAPs in different subtypes of lymphomas and explore the potential utility of Ga-68-FAPI PET/CT in lymphomas. The results showed significantly elevated FAP uptake in Hodgkin lymphoma lesions and aggressive non-Hodgkin lymphoma lesions, while indolent NHL lesions showed weak FAP staining. Ga-68-FAPI imaging can be used to detect FAP expression in lymphoma lesions and may be an alternate method for characterizing lymphoma profiles.
Cancer-associated fibroblasts that overexpress fibroblast activation protein (FAP) are enriched in many epithelial carcinomas and in hematologic neoplasms. PET/CT with radiolabeled FAP inhibitor (FAPI) is a new diagnostic tool for visualizing the tumor stroma. This prospective study aimed to profile FAPs in different subtypes of lymphomas and explore the potential utility of Ga-68-FAPI PET/CT in lymphomas. Methods: In this prospective study, we recruited 73 lymphoma patients who underwent Ga-68-FAPI PET/CT and recorded and measured semiquantitative parameters and ratios of their scan results. FAPI expression was assessed by immunochemistry in samples obtained from 22 of the lymphoma patients. Results: We evaluated 11 patients with Hodgkin lymphoma and 62 with non-Hodgkin lymphoma (NHL). Significantly elevated FAP uptake was observed in Hodgkin lymphoma lesions, correlating with the intensity of FAP immunostaining (score, 3+). A positive association was found between the corresponding clinical classification of NHL and the Ga-68-FAPI uptake activity of the lesion. Aggressive NHL lesions, with moderate to strong FAP immunostaining (score, 2+ to 3+), exhibited intense to moderate Ga-68-FAPI uptake. Indolent NHL lesions showed weak FAP staining and mild to moderate Ga-68-FAPI uptake. No statistically significant correlation emerged between the sum of the product of the diameters and the corresponding SUVmax (P = 0.424). The tumor-to-liver ratios were 6.26 +/- 4.17 in indolent NHL and more than 9 in other subtypes. Conclusion: Ga-68-FAPI imaging can be used to detect FAP expression in lymphoma lesions and may be an alternate method for characterizing lymphoma profiles.
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