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使用氟代脱氧葡萄糖正电子发射断层扫描/计算机断层扫描(FDG-PET/CT)对乳腺癌患者进行小体素重建用于局部区域淋巴结特征分析的诊断意义。

Diagnostic implications of a small-voxel reconstruction for loco-regional lymph node characterization in breast cancer patients using FDG-PET/CT.

作者信息

Koopman Daniëlle, van Dalen Jorn A, Arkies Hester, Oostdijk Ad H J, Francken Anne Brecht, Bart Jos, Slump Cornelis H, Knollema Siert, Jager Pieter L

机构信息

Department of Nuclear Medicine, Isala, Zwolle, the Netherlands.

MIRA Institute for Biomedical Technology and Technical Medicine, University of Twente, Enschede, the Netherlands.

出版信息

EJNMMI Res. 2018 Jan 16;8(1):3. doi: 10.1186/s13550-018-0359-7.

DOI:10.1186/s13550-018-0359-7
PMID:29340798
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5770346/
Abstract

BACKGROUND

We evaluated the diagnostic implications of a small-voxel reconstruction for lymph node characterization in breast cancer patients, using state-of-the-art FDG-PET/CT. We included 69 FDG-PET/CT scans from breast cancer patients. PET data were reconstructed using standard 4 × 4 × 4 mm and small 2 × 2 × 2 mm voxels. Two hundred thirty loco-regional lymph nodes were included, of which 209 nodes were visualised on PET/CT. All nodes were visually scored as benign or malignant, and SUV and TB(=SUV/SUV) were measured. Final diagnosis was based on histological or imaging information. We determined the accuracy, sensitivity and specificity for both reconstruction methods and calculated optimal cut-off values to distinguish benign from malignant nodes.

RESULTS

Sixty-one benign and 169 malignant lymph nodes were included. Visual evaluation accuracy was 73% (sensitivity 67%, specificity 89%) on standard-voxel images and 77% (sensitivity 78%, specificity 74%) on small-voxel images (p = 0.13). Across malignant nodes visualised on PET/CT, the small-voxel score was more often correct compared with the standard-voxel score (89 vs. 76%, p <  0.001). In benign nodes, the standard-voxel score was more often correct (89 vs. 74%, p = 0.04). Quantitative data were based on the 61 benign and 148 malignant lymph nodes visualised on PET/CT. SUVs and TB were on average 3.0 and 1.6 times higher in malignant nodes compared to those in benign nodes (p <  0.001), on standard- and small-voxel PET images respectively. Small-voxel PET showed average increases in SUV and TB of typically 40% over standard-voxel PET. The optimal SUV cut-off using standard-voxels was 1.8 (sensitivity 81%, specificity 95%, accuracy 85%) while for small-voxels, the optimal SUV cut-off was 2.6 (sensitivity 78%, specificity 98%, accuracy 84%). Differences in accuracy were non-significant.

CONCLUSIONS

Small-voxel PET/CT improves the sensitivity of visual lymph node characterization and provides a higher detection rate of malignant lymph nodes. However, small-voxel PET/CT also introduced more false-positive results in benign nodes. Across all nodes, differences in accuracy were non-significant. Quantitatively, small-voxel images require higher cut-off values. Readers have to adapt their reference standards.

摘要

背景

我们使用最先进的氟代脱氧葡萄糖正电子发射断层显像/计算机断层扫描(FDG-PET/CT)评估了小体素重建对乳腺癌患者淋巴结特征的诊断意义。我们纳入了69例乳腺癌患者的FDG-PET/CT扫描图像。PET数据采用标准的4×4×4mm体素和较小的2×2×2mm体素进行重建。共纳入230个局部区域淋巴结,其中209个淋巴结在PET/CT上可见。所有淋巴结均通过视觉评分判定为良性或恶性,并测量了标准化摄取值(SUV)和TB(=SUV/平均本底SUV)。最终诊断基于组织学或影像学信息。我们确定了两种重建方法的准确性、敏感性和特异性,并计算了区分良性和恶性淋巴结的最佳截断值。

结果

共纳入61个良性和169个恶性淋巴结。在标准体素图像上,视觉评估的准确性为73%(敏感性67%,特异性89%),在小体素图像上为77%(敏感性78%,特异性74%)(p = 0.13)。在PET/CT上可见的恶性淋巴结中,与标准体素评分相比,小体素评分更常正确(89%对76%,p < 0.001)。在良性淋巴结中,标准体素评分更常正确(89%对74%,p = 0.04)。定量数据基于PET/CT上可见的61个良性和148个恶性淋巴结。在标准体素和小体素PET图像上,恶性淋巴结的SUV和TB平均分别比良性淋巴结高3.0倍和1.6倍(p < 0.001)。小体素PET显示,与标准体素PET相比,SUV和TB平均通常增加40%。使用标准体素时的最佳SUV截断值为1.8(敏感性81%,特异性95%,准确性85%),而对于小体素,最佳SUV截断值为2.6(敏感性78%,特异性98%,准确性84%)。准确性差异无统计学意义。

结论

小体素PET/CT提高了视觉淋巴结特征的敏感性,并提供了更高的恶性淋巴结检出率。然而,小体素PET/CT也在良性淋巴结中引入了更多假阳性结果。在所有淋巴结中,准确性差异无统计学意义。在定量方面,小体素图像需要更高的截断值。读者必须调整他们的参考标准。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4675/5770346/de3660920b95/13550_2018_359_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4675/5770346/0f33b14b58d1/13550_2018_359_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4675/5770346/8d700926c4fa/13550_2018_359_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4675/5770346/d77690ebccbe/13550_2018_359_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4675/5770346/de3660920b95/13550_2018_359_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4675/5770346/0f33b14b58d1/13550_2018_359_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4675/5770346/8d700926c4fa/13550_2018_359_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4675/5770346/d77690ebccbe/13550_2018_359_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4675/5770346/de3660920b95/13550_2018_359_Fig4_HTML.jpg

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