Department of Radiology and Nuclear Medicine, Amsterdam UMC, Cancer Center Amsterdam, Amsterdam, The Netherlands;
LITO, Inserm, Institut Curie, Orsay, France.
J Nucl Med. 2024 Sep 3;65(9):1343-1348. doi: 10.2967/jnumed.124.267789.
Total metabolic tumor volume (TMTV) is prognostic in lymphoma. However, cutoff values for risk stratification vary markedly, according to the tumor delineation method used. We aimed to create a standardized TMTV benchmark dataset allowing TMTV to be tested and applied as a reproducible biomarker. Sixty baseline F-FDG PET/CT scans were identified with a range of disease distributions (20 follicular, 20 Hodgkin, and 20 diffuse large B-cell lymphoma). TMTV was measured by 12 nuclear medicine experts, each analyzing 20 cases split across subtypes, with each case processed by 3-4 readers. LIFEx or ACCURATE software was chosen according to reader preference. Analysis was performed stepwise: TMTV1 with automated preselection of lesions using an SUV of at least 4 and a volume of at least 3 cm with single-click removal of physiologic uptake; TMTV2 with additional removal of reactive bone marrow and spleen with single clicks; TMTV3 with manual editing to remove other physiologic uptake, if required; and TMTV4 with optional addition of lesions using mouse clicks with an SUV of at least 4 (no volume threshold). The final TMTV (TMTV4) ranged from 8 to 2,288 cm, showing excellent agreement among all readers in 87% of cases (52/60) with a difference of less than 10% or less than 10 cm In 70% of the cases, TMTV4 equaled TMTV1, requiring no additional reader interaction. Differences in the TMTV4 were exclusively related to reader interpretation of lesion inclusion or physiologic high-uptake region removal, not to the choice of software. For 5 cases, large TMTV differences (>25%) were due to disagreement about inclusion of diffuse splenic uptake. The proposed segmentation method enabled highly reproducible TMTV measurements, with minimal reader interaction in 70% of the patients. The inclusion or exclusion of diffuse splenic uptake requires definition of specific criteria according to lymphoma subtype. The publicly available proposed benchmark allows comparison of study results and could serve as a reference to test improvements using other segmentation approaches.
总的代谢肿瘤体积(TMTV)在淋巴瘤中具有预后价值。然而,根据所使用的肿瘤描绘方法,风险分层的截止值差异很大。我们旨在创建一个标准化的 TMTV 基准数据集,以便能够测试和应用 TMTV 作为可重复的生物标志物。
共确定了 60 例基线 F-FDG PET/CT 扫描,涵盖了多种疾病分布(20 例滤泡性,20 例霍奇金,20 例弥漫性大 B 细胞淋巴瘤)。12 名核医学专家分别测量 TMTV,每位专家分析 20 例病例,分为亚型,每个病例由 3-4 位读者进行处理。根据读者偏好选择 LIFEx 或 ACCURATE 软件。分析分步骤进行:TMTV1 使用 SUV 至少为 4、体积至少为 3cm 的自动预选择病变,并使用单次点击去除生理性摄取;TMTV2 使用单次点击去除反应性骨髓和脾脏;TMTV3 如有必要,手动编辑以去除其他生理性摄取;TMTV4 使用鼠标点击选择 SUV 至少为 4(无体积阈值)的病变。最终的 TMTV(TMTV4)范围为 8 至 2,288cm,所有读者在 87%(52/60)的病例中具有极好的一致性,差异小于 10%或小于 10cm。在 70%的病例中,TMTV4 等于 TMTV1,无需额外的读者交互。TMTV4 的差异仅与读者对病变包含或生理性高摄取区域去除的解释有关,与软件的选择无关。对于 5 例,TMTV 差异较大(>25%)是由于对弥漫性脾脏摄取的包含与否存在分歧。
所提出的分割方法能够实现高度可重复的 TMTV 测量,在 70%的患者中仅需最小的读者交互。弥漫性脾脏摄取的包含或排除需要根据淋巴瘤亚型定义特定的标准。公开提供的基准数据集允许比较研究结果,并可作为参考,用于测试使用其他分割方法的改进。