Comparison of trans-1-amino-3[18F]fluorocyclobutanecarboxylic acid (anti-[18F]FACBC) accumulation in lymph node prostate cancer metastasis and lymphadenitis in rats

被引:13
作者
Kanagawa, Masaru [1 ]
Doi, Yoshihiro [1 ]
Oka, Shuntaro [1 ]
Kobayashi, Ryohei [1 ]
Nakata, Norihito [1 ]
Toyama, Masahito [1 ]
Shirakami, Yoshifumi [1 ]
机构
[1] Nihon Medi Phys Co Ltd, Res Ctr, Chiba 2990266, Japan
关键词
anti-[F-18]FACBC; PET; Prostate cancer metastasis; Lymphadenitis; ANTI-1-AMINO-3-F-18-FLUOROCYCLOBUTANE-1-CARBOXYLIC ACID; CARCINOMA; TRANSPORT; ANTI-F-18-FACBC; MECHANISMS; F-18-NAF; PET/CT;
D O I
10.1016/j.nucmedbio.2014.04.004
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
Introduction: Trans-1-amino-3-[F-18]fluorocyclobutanecarboxylic acid (anti-[F-18]FACBC) is a positron emission tomography (PET) tracer used to visualize prostate cancer (PCa). In this study, we investigated the differences in anti-[F-18]FACBC accumulation between metastatic and inflamed lymph node (LN) lesions. Methods: A PCa LN metastasis (PLM) model was developed by inoculating a rat PCa cell line, MAT-Ly-Lu-B2, into popliteal LNs of Copenhagen rats. Acute lymphadenitis (AL) was induced by injecting concanavalin A (Con A) into the hind footpad, and chronic lymphadenitis (CL) was induced by daily injection of Con A into the tissues surrounding the popliteal LNs for 2 weeks. Main lesions of all animal models were established in lumbar and/or inguinal LNs. Biodistribution and dynamic PET imaging data were acquired after tracer injection. 12-weighted magnetic resonance (MR) images were registered with PET images. Results: In the biodistribution study, the uptake ratios of PLM-to-lymphadenitis in lesional lumbar and inguinal LNs were 0.97 - 1.57 and 1.47 - 2.08 at 15 and 60 min post-anti-[F-18]FACBC injection respectively. In PET imaging, the lesional lumbar LNs of CL and PLM, but not of AL, were visualized on anti[F-18]FACBC-PET/MR fusion images without disturbance from radioactivity from urine, and the rank order of anti-[F-18]FACBC accumulation at 50 - 60 post-injection in lesional lumbar LNs was PLM > CL > AL Conclusions: Anti-[F-18]FACBC accumulation in LNs with PLM was higher than that in inflamed LNs. Advances in knowledge: The study showed that although low but significant levels of anti-[F-18]FACBC uptake by chronic inflamed lesions might cause false-positives in anti-[F-18]FACBC-PET in some PCa patients, uptake of the tracer at acutely inflamed sites was minimal. Implications for patient care: The findings of this study suggest the potential of Anti-[F-18]FACBC for distinguishing between tumors and acute inflammation in clinical practice. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:545 / 551
页数:7
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