总病灶糖酵解是胰腺癌术前新辅助化疗患者化疗反应的一个有希望的预测指标。

IF 4.4 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Sooin Byeon, Bridget Abbott, Paul Roach, Dale L Bailey, Angela Chou, Sarah Maloney, Anthony J Gill, Jaswinder Samra, Anubhav Mittal, Sumit Sahni
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引用次数: 0

摘要

背景:在可切除的胰腺导管腺癌(PDAC)患者中,新辅助化疗(NAC)的使用越来越多。[18F]氟-2-脱氧葡萄糖正电子发射断层扫描/计算机断层扫描(FDG-PET/CT)被经常用于确定接受NAC的PDAC患者的治疗反应。最大标准化摄取值(SUVmax)通常被用作FDG-PET/CT参数,但也出现了新的参数,如病灶总糖酵解(TLG),它考虑了平均标准化摄取(SUVmean)和代谢肿瘤体积(MTV)。本研究比较了新兴的FDG-PET/CT参数(即SUVmean, MTV和TLG)与SUVmax相比预测化疗反应的能力。方法:在这项单中心回顾性研究中,招募了nac治疗的PDAC患者(n = 74),他们在nac前后都有FDG-PET/CT扫描。所有扫描被导入到一个单一的分析平台并重新分析。化疗反应是通过评估肿瘤床上存活肿瘤细胞的百分比来确定的。对数据进行统计分析。结果:治疗后FDG-PET/CT扫描参数与肿瘤床内活细胞之间存在显著相关性,其中TLG的相关性较高(r = .3131),高于其他参数(r = .2722-.3008)。TLG的下降百分比(NAC扫描后与NAC扫描前)与肿瘤床上活的癌细胞的相关性最高(r = - 0.3444),并且在NAC应答者(中位数= 80.57)和无应答者(中位数= 65.16)之间具有统计学意义(p = 0.0157)。TLG (nac扫描后与nac扫描前)之间的差异被证明是总体生存的独立预后指标(风险比=。5033, p = .0361)。结论:与所有其他FDG-PET/CT参数相比,在NAC治疗的PDAC患者中,TLG被证明是化疗反应和患者预后的优越预测因子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Total lesion glycolysis is a promising predictor of chemo-response in pancreatic cancer patients treated with neoadjuvant chemotherapy prior to surgery.

Background: There has been increased use of neoadjuvant chemotherapy (NAC) in resectable pancreatic ductal adenocarcinoma (PDAC) patients. [18F]fluoro-2-deoxyglucose positron emission tomography/computed tomography (FDG-PET/CT) scan is being frequently used to determine treatment response in PDAC patients undergoing NAC. Maximum standardized uptake value (SUVmax) is conventionally used as an FDG-PET/CT parameter, but there are emerging parameters, such as total lesion glycolysis (TLG), which take into account mean standardized uptake (SUVmean) and metabolic tumour volume (MTV). This study compared the ability of emerging FDG-PET/CT parameters (i.e. SUVmean, MTV and TLG) to predict chemo-response compared to SUVmax.

Methods: In this single centre, retrospective study, NAC-treated PDAC patients (n = 74) for whom both pre- and post-NAC FDG-PET/CT scans were available were recruited. All scans were imported to a single analysis platform and reanalysed. Chemo-response was determined by the assessment of percentage viable tumour cells in the tumour bed. Statistical analysis was performed on the data.

Results: A significant correlation was observed between post-treatment FDG-PET/CT scan parameters and viable cancer cells in the tumour bed, with TLG showing a higher degree of correlation (r = .3131) compared to all other parameters (r = .2722-.3008). The percentage decrease in the TLG (post-NAC scan vs. pre-NAC scan) demonstrated the highest degree of correlation with viable cancer cells in the tumour bed (r = -.3444) and had a statistically significant (p = .0157) effect between NAC responders (Median = 80.57) and non-responders (Median = 65.16). The difference between TLG (post-NAC scan vs. pre-NAC scan) was shown to be an independent prognostic indicator for overall survival (hazard ratio = .5033, p = .0361).

Conclusion: TLG was shown to be a superior predictor of chemo-response and patient prognosis compared to all other FDG-PET/CT parameters in PDAC patients treated with NAC.

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来源期刊
CiteScore
9.50
自引率
3.60%
发文量
192
审稿时长
1 months
期刊介绍: EJCI considers any original contribution from the most sophisticated basic molecular sciences to applied clinical and translational research and evidence-based medicine across a broad range of subspecialties. The EJCI publishes reports of high-quality research that pertain to the genetic, molecular, cellular, or physiological basis of human biology and disease, as well as research that addresses prevalence, diagnosis, course, treatment, and prevention of disease. We are primarily interested in studies directly pertinent to humans, but submission of robust in vitro and animal work is also encouraged. Interdisciplinary work and research using innovative methods and combinations of laboratory, clinical, and epidemiological methodologies and techniques is of great interest to the journal. Several categories of manuscripts (for detailed description see below) are considered: editorials, original articles (also including randomized clinical trials, systematic reviews and meta-analyses), reviews (narrative reviews), opinion articles (including debates, perspectives and commentaries); and letters to the Editor.
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