Response Monitoring in Metastatic Breast Cancer: A Prospective Study Comparing 18F-FDG PET/CT with Conventional CT

被引:18
作者
Vogsen, Marianne [1 ,2 ,3 ,4 ,5 ]
Harbo, Frederik [6 ]
Jakobsen, Nick M. [2 ]
Nissen, Henriette J. [2 ]
Dahlsgaard-Wallenius, Sara E. [2 ]
Gerke, Oke [2 ,3 ]
Jensen, Jeanette D. [1 ]
Asmussen, Jon T. [6 ]
Jylling, Anne Marie B. [3 ,7 ]
Braad, Poul-Erik [2 ]
Vach, Werner [8 ]
Ewertz, Marianne [3 ]
Hildebrandt, Malene G. [2 ,3 ,5 ,9 ]
机构
[1] Odense Univ Hosp, Dept Oncol, Odense, Denmark
[2] Odense Univ Hosp, Dept Nucl Med, Odense, Denmark
[3] Univ Southern Denmark, Dept Clin Res, Odense, Denmark
[4] Odense Univ Hosp, Odense Patient Data Explorat Network OPEN, Odense, Denmark
[5] Odense Univ Hosp, Ctr Personalized Response Monitoring Oncol PREMIO, Odense, Denmark
[6] Odense Univ Hosp, Dept Radiol, Odense, Denmark
[7] Odense Univ Hosp, Dept Pathol, Odense, Denmark
[8] Basel Acad Qual & Res Med, Basel, Switzerland
[9] Odense Univ Hosp, Ctr Innovat Med Technol, Odense, Denmark
关键词
metastatic breast cancer; response monitoring; 18F-FDG PET; CT; CE-CT; PERCIST; POSITRON-EMISSION-TOMOGRAPHY; F-18-FDG PET/CT; BONE METASTASES; TUMOR RESPONSE; FDG-PET/CT; GUIDELINES; CRITERIA; THERAPY; PERCIST; RECIST;
D O I
10.2967/jnumed.121.263358
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
This study aimed to compare contrast-enhanced CT (CE-CT) and 18F-FDG PET/CT for response monitoring in metastatic breast cancer using the standardized response evaluation criteria RECIST 1.1 and PERCIST. The objective was to examine whether progressive disease was detected systematically earlier by one of the modalities. Methods: Women with biopsy-verified metastatic breast cancer were enrolled prospectively and monitored using combined CE-CT and 18F-FDG PET/CT every 9-12 wk to evaluate response to first-line treatment. CE-CT scans and RECIST 1.1 were used for clinical decision-making without accessing the 18F-FDG PET/CT scans. At study completion, 18F-FDG PET/CT scans were unmasked and assessed according to PERCIST. Visual assessment was used if response criteria could not be applied. The modality-specific time to progression was defined as the time from the baseline scan until the first scan demonstrating pro-gression. Paired comparative analyses for CE-CT versus 18F-FDG PET/CT were applied, and the primary endpoint was earlier detection of progression by one modality. Secondary endpoints were time to detection of progression, response categorization, visualization of changes in response over time, and measurable disease according to RECIST and PERCIST. Results: In total, 87 women were evaluable, with a median of 6 (1-11) follow-up scans. Progression was detected first by 18F-FDG PET/CT in 43 (49.4%) of 87 patients and first by CE-CT in 1 (1.15%) of 87 patients (P, 0.0001). Excluding patients without progression (n 5 32), progression was seen first on 18F-FDG PET/CT in 78.2% (43/55) of patients. The median time from detection of progression by 18F-FDG PET/CT to that of CE-CT was 6 mo (95% CI, 4.3-6.4 mo). At baseline, 76 (87.4%) of 87 patients had measurable disease according to PERCIST and 51 (58.6%) of 87 patients had mea-surable disease according to RECIST 1.1. Moreover, 18F-FDG PET/CT provided improved visualization of changes in response over time, as seen in the graphical abstract. Conclusion: Disease progression was detected earlier by 18F-FDG PET/CT than by CE-CT in most patients, with a potentially clinically relevant median 6-mo delay for CE-CT. More patients had measurable disease according to PERCIST than according to RECIST 1.1. The magnitude of the final benefit for patients is a perspective for future research.
引用
收藏
页码:355 / 361
页数:7
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