68Ga-labeled fibroblast activation protein inhibitor (FAPI) PET/CT for locally advanced or recurrent pancreatic cancer staging and restaging after chemoradiotherapy.

IF 12.4 1区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL Theranostics Pub Date : 2024-07-08 eCollection Date: 2024-01-01 DOI:10.7150/thno.95329
Giulia Metzger, Christian Bayerl, Julian Mm Rogasch, Christian Furth, Christoph Wetz, Marcus Beck, Felix Mehrhof, Holger Amthauer, Pirus Ghadjar, Christopher Neumann, Uwe Pelzer, Daniel Zips, Frank Hofheinz, Jane Grabowski, Imke Schatka, Sebastian Zschaeck
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Abstract

Purpose: 68Ga-labeled fibroblast activation protein inhibitor (FAPI) is a novel PET tracer with great potential for staging pancreatic cancer. Data on locally advanced or recurrent disease is sparse, especially on tracer uptake before and after high dose chemoradiotherapy (CRT). The aim of this study was to evaluate [68Ga]Ga-FAPI-46 PET/CT staging in this setting. Methods: Twenty-seven patients with locally recurrent or locally advanced pancreatic adenocarcinoma (LRPAC n = 15, LAPAC n = 12) in stable disease or partial remission after chemotherapy underwent FAPI PET/CT and received consolidation CRT in stage M0 with follow-up FAPI PET/CT every three months until systemic progression. Quantitative PET parameters SUVmax, SUVmean, FAPI-derived tumor volume and total lesion FAPI-uptake were measured in baseline and follow-up PET/CT scans. Contrast-enhanced CT (ceCT) and PET/CT data were evaluated blinded and staged according to TNM classification. Results: FAPI PET/CT modified staging compared to ceCT alone in 23 of 27 patients in baseline, resulting in major treatment alterations in 52% of all patients (30%: target volume adjustment due to N downstaging, 15%: switch to palliative systemic chemotherapy only due to diffuse metastases, 7%: abortion of radiotherapy due to other reasons). Regarding follow-up scans, major treatment alterations after performing FAPI PET/CT were noted in eleven of 24 follow-up scans (46%) with switch to systemic chemotherapy or best supportive care due to M upstaging and ablative radiotherapy of distant lymph node and oligometastasis. Unexpectedly, in more than 90 % of the follow-up scans, radiotherapy did not induce local fibrosis related FAPI uptake. During the first follow-up, all quantitative PET metrics decreased, and irradiated lesions showed significantly lower FAPI uptake in locally controlled disease (SUVmax p = 0.047, SUVmean p = 0.0092) compared to local failure. Conclusion: Compared to ceCT, FAPI PET/CT led to major therapeutic alterations in patients with LRPAC and LAPAC prior to and after radiotherapy, which might help identify patients benefiting from adjustments in every treatment stage. FAPI PET/CT should be considered a useful diagnostic tool in LRPAC or LAPAC before and after CRT.

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68Ga标记的成纤维细胞活化蛋白抑制剂(FAPI)PET/CT用于局部晚期或复发性胰腺癌的分期和化疗放疗后的再分期。
目的:68Ga 标记的成纤维细胞活化蛋白抑制剂(FAPI)是一种新型 PET 示踪剂,在胰腺癌分期方面具有巨大潜力。有关局部晚期或复发疾病的数据很少,尤其是大剂量化放疗(CRT)前后的示踪剂摄取情况。本研究旨在评估[68Ga]Ga-FAPI-46 PET/CT 在这种情况下的分期情况。研究方法27例化疗后病情稳定或部分缓解的局部复发或局部晚期胰腺腺癌(LRPAC n = 15,LAPAC n = 12)患者接受了FAPI PET/CT检查,并在M0期接受了巩固性CRT治疗,每三个月随访一次FAPI PET/CT,直至全身性进展。在基线和随访 PET/CT 扫描中测量 PET 定量参数 SUVmax、SUVmean、FAPI 衍生肿瘤体积和病变 FAPI 总摄取量。对比增强CT(ceCT)和PET/CT数据均经盲法评估,并根据TNM分类进行分期。结果与单纯ceCT相比,27例基线患者中有23例的FAPI PET/CT改变了分期,导致52%的患者的治疗发生重大改变(30%:由于N降期而调整靶体积,15%:由于弥漫转移而仅改用姑息性全身化疗,7%:由于其他原因而放弃放疗)。关于随访扫描,在 24 次随访扫描中,有 11 次(46%)在进行 FAPI PET/CT 扫描后发现治疗方法发生重大改变,其中有 11 次(46%)因 M 上分期和远处淋巴结及少转移灶的消融放疗而改用全身化疗或最佳支持治疗。出乎意料的是,在超过 90% 的随访扫描中,放疗并未引起与局部纤维化相关的 FAPI 摄取。在首次随访期间,所有定量 PET 指标均有所下降,与局部治疗失败相比,局部控制疾病的照射病灶的 FAPI 摄取显著降低(SUVmax p = 0.047,SUVmean p = 0.0092)。结论与ceCT相比,FAPI PET/CT可使LRPAC和LAPAC患者在放疗前后的治疗发生重大改变,这可能有助于识别在每个治疗阶段都能从调整中获益的患者。FAPI PET/CT 应被视为 CRT 前后 LRPAC 或 LAPAC 的有用诊断工具。
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来源期刊
Theranostics
Theranostics MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
25.40
自引率
1.60%
发文量
433
审稿时长
1 months
期刊介绍: Theranostics serves as a pivotal platform for the exchange of clinical and scientific insights within the diagnostic and therapeutic molecular and nanomedicine community, along with allied professions engaged in integrating molecular imaging and therapy. As a multidisciplinary journal, Theranostics showcases innovative research articles spanning fields such as in vitro diagnostics and prognostics, in vivo molecular imaging, molecular therapeutics, image-guided therapy, biosensor technology, nanobiosensors, bioelectronics, system biology, translational medicine, point-of-care applications, and personalized medicine. Encouraging a broad spectrum of biomedical research with potential theranostic applications, the journal rigorously peer-reviews primary research, alongside publishing reviews, news, and commentary that aim to bridge the gap between the laboratory, clinic, and biotechnology industries.
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