Correlation of 68Ga-FAPi-46 PET Biodistribution with FAP Expression by Immunohistochemistry in Patients with Solid Cancers: Interim Analysis of a Prospective Translational Exploratory Study

被引:89
作者
Mona, Christine E. [1 ,2 ,3 ]
Benz, Matthias R. [1 ,2 ]
Hikmat, Firas [1 ]
Grogan, Tristan R. [4 ]
Lueckerath, Katharina [1 ,2 ,3 ]
Razmaria, Aria [1 ]
Riahi, Rana [5 ]
Slavik, Roger [1 ]
Girgis, Mark D. [6 ]
Carlucci, Giuseppe [1 ,2 ]
Kelly, Kimberly A. [7 ,8 ]
French, Samuel W. [2 ,5 ]
Czernin, Johannes [1 ,2 ,3 ]
Dawson, David W. [2 ,5 ]
Calais, Jeremie [1 ,2 ,3 ]
机构
[1] UCLA, David Geffen Sch Med, Dept Mol & Med Pharmacol, Ahmanson Translat Theranost Div, Los Angeles, CA 90095 USA
[2] UCLA, Jonsson Comprehens Canc Ctr, Los Angeles, CA 90024 USA
[3] UCLA, Inst Urol Oncol, Los Angeles, CA 90095 USA
[4] UCLA, David Geffen Sch Med, Dept Med Stat Core, Los Angeles, CA 90095 USA
[5] UCLA, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA
[6] UCLA, David Geffen Sch Med, Dept Surg, Div Surg Oncol, Los Angeles, CA 90095 USA
[7] Univ Virginia, Sch Engn & Appl Sci, Dept Biomed Engn, Charlottesville, VA USA
[8] Univ Virginia, Sch Med, Robert M Berne Cardiovasc Res Ctr, Charlottesville, VA 22908 USA
关键词
cancer; PET/CT; fibroblast activation protein; immunohistochemistry; Ga-68-FAPi-46; FIBROBLAST ACTIVATION PROTEIN;
D O I
10.2967/jnumed.121.262426
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Fibroblast activation protein (FAP)-expressing cancer-associated fibroblasts confer treatment resistance and promote metastasis and immunosuppression. Because FAP is overexpressed in many cancers, radiolabeled molecules targeting FAP are studied for their use as pan-cancer theranostic agents. This study aimed to establish the spectrum of FAP expression across various cancers by immunohistochemistry and to explore whether Ga-68 FAP inhibitor (FAPi)-46 PET biodistribution faithfully reflects FAP expression from resected cancer and non-cancer specimens. Methods: We conducted a FAP expression screening using immunohistochemistry on a pancancer human tissue microarray (141 patients, 14 different types of cancer) and an interim analysis of a prospective exploratory imaging trial in cancer patients. Volunteer patients underwent 1 whole-body Ga-68-FAPi-46 PET/CT scan and, subsequently, surgical resection of their primary tumor or metastasis. Ga-68-FAPi-46 PET SUVmax and SUVmean was correlated with FAP immunohistochemistry score in cancer and tumor-adjacent non-cancer tissues for each patient. Results: FAP was expressed across all 14 cancer types on tissue microarray with variable intensity and frequency, ranging from 25% to 100% (mean, 76.6% +/- 25.3%). Strong FAP expression was observed in 50%-100% of cancers of the bile duct, bladder, colon, esophagus, stomach, lung, oropharynx, ovary, and pancreas. Fifteen patients with various cancer types (colorectal [n54], head and neck [n53], pancreas [n = 2], breast [n = 2], stomach [n = 1], esophagus [n = 2], and uterus [n = 1]) underwent surgery after their Ga-68-FAPi-46 PET/CT scan within a mean interval of 16.1 +/- 14.4 d. Ga-68-FAPi-46 SUVs and immunohistochemistry scores were higher in cancer than in tumor-adjacent non-cancer tissue: mean SUVmax 7.7 versus 1.6 (P < 0.001), mean SUVmean 6.2 versus 1.0 (P < 0.001), and mean FAP immunohistochemistry score 2.8 versus 0.9 (P < 0.001). FAP immunohistochemistry scores strongly correlated with Ga-68-FAPi 46 SUVmax and SUVmean: r = 0.781 (95% CI, 0.376-0.936; P < 0.001) and r = 0.783 (95% CI, 0.379-0.936; P < 0.001), respectively. Conclusion: In this interim analysis of a prospective exploratory imaging trial, Ga-68-FAPi-46 PET biodistribution across multiple cancers strongly correlated with FAP tissue expression. These findings support further exploration of FAPi PET as a pancancer imaging biomarker for FAP expression and as a stratification tool for FAP-targeted therapies.
引用
收藏
页码:1021 / 1026
页数:6
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