Repeatability of 18F-FDG uptake in metastatic bone lesions of breast cancer patients and implications for accrual to clinical trials.

IF 3.1 3区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Mark Muzi, Lanell M Peterson, Jennifer M Specht, Daniel S Hippe, Alena Novakova-Jiresova, Jean H Lee, Brenda F Kurland, David A Mankoff, Nancy Obuchowski, Hannah M Linden, Paul E Kinahan
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引用次数: 0

Abstract

Background: Standard measures of response such as Response Evaluation Criteria in Solid Tumors are ineffective for bone lesions, often making breast cancer patients that have bone-dominant metastases ineligible for clinical trials with potentially helpful therapies. In this study we prospectively evaluated the test-retest uptake variability of 2-deoxy-2-[18F]fluoro-D-glucose (18F-FDG) in a cohort of breast cancer patients with bone-dominant metastases to determine response criteria. The thresholds for 95% specificity of change versus no-change were then applied to a second cohort of breast cancer patients with bone-dominant metastases.

Methods: For this study, nine patients with 38 bone lesions were imaged with 18F-FDG in the same calibrated scanner twice within 14 days. Tumor uptake was quantified by the most commonly used PET parameter, the maximum tumor voxel normalized by dose and body weight (SUVmax) and also by the mean of a 1-cc maximal uptake volume normalized by dose and lean-body-mass (SULpeak). The asymmetric repeatability coefficients with confidence intervals for SUVmax and SULpeak were used to determine the limits of 18F-FDG uptake variability. A second cohort of 28 breast cancer patients with bone-dominant metastases that had 146 metastatic bone lesions was imaged with 18F-FDG before and after standard-of-care therapy for response assessment.

Results: The mean relative difference of SUVmax and SULpeak in 38 bone tumors of the first cohort were 4.3% and 6.7%. The upper and lower asymmetric limits of the repeatability coefficient were 19.4% and - 16.3% for SUVmax, and 21.2% and - 17.5% for SULpeak. 18F-FDG repeatability coefficient confidence intervals resulted in the following patient stratification using SULpeak for the second patient cohort: 11-progressive disease, 5-stable disease, 7-partial response, and 1-complete response with three inevaluable patients. The asymmetric repeatability coefficients response criteria for SULpeak changed the status of 3 patients compared to the standard Positron Emission Tomography Response Criteria in Solid Tumors of ± 30% SULpeak.

Conclusion: In evaluating bone tumor response for breast cancer patients with bone-dominant metastases using 18F-FDG SUVmax, the repeatability coefficients from test-retest studies show that reductions of more than 17% and increases of more than 20% are unlikely to be due to measurement variability. Serial 18F-FDG imaging in clinical trials investigating bone lesions in these patients, such as the ECOG-ACRIN EA1183 trial, benefit from confidence limits that allow interpretation of response.

乳腺癌患者转移性骨病变中 18F-FDG 摄取的重复性及其对临床试验的影响。
背景:实体瘤反应评估标准》等标准反应测量方法对骨质病变无效,这往往使骨转移为主的乳腺癌患者没有资格接受可能有用的疗法的临床试验。在这项研究中,我们前瞻性地评估了一组骨转移乳腺癌患者对 2-脱氧-2-[18F]氟-D-葡萄糖(18F-FDG)的检测-重复摄取变异性,以确定反应标准。然后将变化与不变的 95% 特异性阈值应用于第二批骨转移的乳腺癌患者:在这项研究中,9 名患者的 38 处骨质病变在 14 天内在同一台校准扫描仪上进行了两次 18F-FDG 成像。肿瘤摄取通过最常用的正电子发射计算机断层显像参数--按剂量和体重归一化的最大肿瘤体素(SUVmax)以及按剂量和瘦体重归一化的 1-cc 最大摄取体积的平均值(SULpeak)进行量化。SUVmax和SULpeak的非对称重复性系数及置信区间用于确定18F-FDG摄取变异的界限。在标准治疗前后,用 18F-FDG 对 28 例有骨转移的乳腺癌患者进行了成像,这些患者有 146 个转移性骨病灶:第一组38例骨肿瘤的SUVmax和SULpeak的平均相对差值分别为4.3%和6.7%。SUVmax和SULpeak的重复性系数不对称上下限分别为19.4%和-16.3%,SULpeak为21.2%和-17.5%。18F-FDG 重复性系数置信区间的结果是,使用 SULpeak 对第二个患者队列进行了以下患者分层:11 例疾病进展期患者、5 例疾病稳定期患者、7 例部分反应期患者和 1 例完全反应期患者,其中有 3 例患者无法评估。与标准的实体瘤正电子发射断层扫描反应标准(± 30% SULpeak)相比,SULpeak 的非对称重复性系数反应标准改变了 3 名患者的状态:结论:在使用 18F-FDG SUVmax 评估骨转移的乳腺癌患者的骨肿瘤反应时,测试-再测试研究的重复性系数显示,降低 17% 以上和增加 20% 以上不太可能是由于测量变异造成的。在调查这些患者骨病变的临床试验(如 ECOG-ACRIN EA1183 试验)中,连续的 18F-FDG 成像可从可解释反应的置信区间中获益。
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来源期刊
EJNMMI Research
EJNMMI Research RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING&nb-
CiteScore
5.90
自引率
3.10%
发文量
72
审稿时长
13 weeks
期刊介绍: EJNMMI Research publishes new basic, translational and clinical research in the field of nuclear medicine and molecular imaging. Regular features include original research articles, rapid communication of preliminary data on innovative research, interesting case reports, editorials, and letters to the editor. Educational articles on basic sciences, fundamental aspects and controversy related to pre-clinical and clinical research or ethical aspects of research are also welcome. Timely reviews provide updates on current applications, issues in imaging research and translational aspects of nuclear medicine and molecular imaging technologies. The main emphasis is placed on the development of targeted imaging with radiopharmaceuticals within the broader context of molecular probes to enhance understanding and characterisation of the complex biological processes underlying disease and to develop, test and guide new treatment modalities, including radionuclide therapy.
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