Per-patient Comparison of [68Ga]-FAPI-46 Versus [18F]FDG as PET Tracers in ER-positive Breast Cancer: Study Design of a Single-centre Prospective Study.

IF 3.4 3区 医学 Q2 ONCOLOGY
Journal of Cancer Pub Date : 2026-09-18 eCollection Date: 2026-01-01 DOI:10.7150/jca.138448
Melissa Lenaerts, Lisa E H W Duijx, Felix M Mottaghy, Matthias Bauwens, Robin M J M van Geel, Vivianne C G Tjan-Heijnen, Philipp Backhaus, Loes F S Kooreman, Patty J Nelemans, Marjolein L Smidt, Joachim E Wildberger, Thiemo J A van Nijnatten
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引用次数: 0

Abstract

Introduction. [18F]FDG can be considered as PET tracer to determine whole-body staging in patients with locally advanced (LABC), metastatic, and recurrent breast cancer. Yet, previous studies demonstrated a lower amount of metabolic accumulation on [18F]FDG PET in case of oestrogen receptor (ER)-positive breast cancer. Consequently, given the lower metabolic accumulation, patients with ER-positive breast cancer might be at risk for underdiagnosis according to [18F]FDG PET. A novel PET tracer, [68Ga]-fibroblast activation protein inhibitor (FAPI)-46, has shown promising results in breast cancer (re)staging. This single-centre prospective pilot study aims to explore the relative diagnostic accuracy of [68Ga]-FAPI-46 compared to [18F]FDG in patients with ER-positive breast cancer and will provide the required information to support sample size calculation for a future validation study. Methods. In this study, 20 patients with ER-positive LABC, metastatic, or recurrent breast cancer will undergo the standard [18F]FDG PET exam and a [68Ga]-FAPI-46 PET/CT and [68Ga]-FAPI-46 PET/MRI exam. Histopathological confirmation will be obtained in cases of discordant or concordant (double-positive) findings, depending on clinical relevance and technical feasibility. The study will provide preliminary estimates of the relative accuracy of [68Ga]-FAPI-46 PET when compared to [18F]FDG PET as well as the proportion of discordant findings and patients in whom a biopsy is feasible. Conclusions. The present single-centre prospective pilot study will characterize the potential of [68Ga]-FAPI-46 PET to identify additional lesions not detected on a [18F]FDG PET exam in patients with ER-positive breast cancer to estimate an adequate sample size for a future validation study. Trial registration. This study was registered prospectively on ClinicalTrials.gov. Trial registration number: NCT06335069; Register date: 28 March 2024.

[68Ga]-FAPI-46与[18F]FDG作为er阳性乳腺癌PET示踪剂的每例患者比较:单中心前瞻性研究的研究设计
介绍。[18F]FDG可作为PET示踪剂用于确定局部晚期(LABC)、转移性和复发性乳腺癌患者的全身分期。然而,先前的研究表明,在雌激素受体(ER)阳性的乳腺癌中,[18F]FDG PET的代谢蓄积量较低。因此,考虑到较低的代谢积累,er阳性乳腺癌患者根据[18F]FDG PET可能存在诊断不足的风险。一种新型PET示踪剂[68Ga]-成纤维细胞活化蛋白抑制剂(FAPI)-46在乳腺癌(再)分期中显示出令人鼓舞的结果。这项单中心前瞻性先导研究旨在探讨[68Ga]-FAPI-46与[18F]FDG在er阳性乳腺癌患者中的相对诊断准确性,并将为未来验证研究提供所需的信息,以支持样本量计算。方法。在本研究中,20例er阳性的LABC、转移性或复发性乳腺癌患者将接受标准的[18F]FDG PET检查和[68Ga]-FAPI-46 PET/CT和[68Ga]-FAPI-46 PET/MRI检查。根据临床相关性和技术可行性,在不一致或一致(双阳性)结果的情况下,将获得组织病理学证实。该研究将提供[68Ga]-FAPI-46 PET与[18F]FDG PET相比的相对准确性的初步估计,以及不一致结果和活检可行患者的比例。结论。目前的单中心前瞻性先导研究将表征[68Ga]-FAPI-46 PET在er阳性乳腺癌患者中识别[18F]FDG PET检查未检测到的其他病变的潜力,以估计足够的样本量,用于未来的验证研究。试验注册。该研究已在ClinicalTrials.gov上注册。试验注册号:NCT06335069;注册日期:2024年3月28日。
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来源期刊
Journal of Cancer
Journal of Cancer ONCOLOGY-
CiteScore
8.10
自引率
2.60%
发文量
333
审稿时长
12 weeks
期刊介绍: Journal of Cancer is an open access, peer-reviewed journal with broad scope covering all areas of cancer research, especially novel concepts, new methods, new regimens, new therapeutic agents, and alternative approaches for early detection and intervention of cancer. The Journal is supported by an international editorial board consisting of a distinguished team of cancer researchers. Journal of Cancer aims at rapid publication of high quality results in cancer research while maintaining rigorous peer-review process.
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