Predictive Value of 18F-FDG PET in Patients with Advanced Medullary Thyroid Carcinoma Treated with Vandetanib

被引:25
作者
Werner, Rudolf A. [1 ,2 ]
Schmid, Jan-Stefan [1 ]
Higuchi, Takahiro [1 ,3 ]
Javadi, Mehrbod S. [2 ]
Rowe, Steven P. [2 ]
Maerkl, Bruno [4 ]
Aulmann, Christoph [5 ]
Fassnacht, Martin [6 ,7 ]
Kroiss, Matthias [6 ,7 ]
Reiners, Christoph [1 ]
Buck, Andreas K. [1 ]
Kreissl, Michael C. [8 ,9 ]
Lapa, Constantin [1 ]
机构
[1] Univ Wurzburg, Univ Hosp, Dept Nucl Med, Wurzburg, Germany
[2] Johns Hopkins Univ, Sch Med, Russell H Morgan Dept Radiol & Radiol Sci, Div Nucl Med & Mol Imaging, Baltimore, MD USA
[3] Natl Cardiovasc & Cerebral Res Ctr, Dept Biomed Imaging, Osaka, Japan
[4] Hosp Augsburg, Inst Pathol, Augsburg, Germany
[5] Hosp Augsburg, Med Dept 2, Augsburg, Germany
[6] Univ Wurzburg, Comprehens Canc Ctr Mainfranken, Wurzburg, Germany
[7] Univ Wurzburg, Univ Hosp, Div Endocrinol & Diabet, Dept Internal Med 1, Wurzburg, Germany
[8] Hosp Augsburg, Dept Nucl Med, Augsburg, Germany
[9] Univ Hosp Magdeburg, Dept Radiol & Nucl Med, Magdeburg, Germany
关键词
medullary thyroid carcinoma; tyrosine kinase inhibitor; vandetanib; 2-deoxy-2-(F-18) fluoro-D-glucose; F-18-FDG; positron emission tomography; CANCER; MANAGEMENT; CALCITONIN; SUNITINIB; EFFICACY;
D O I
10.2967/jnumed.117.199778
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
Therapeutic options in advanced medullary thyroid carcinoma (MTC) have markedly improved since the introduction of tyrosine kinase inhibitors (TKIs). We aimed to assess the role of metabolic imaging using F-18-FDG PET/CT shortly before and 3 mo after initiation of TKI treatment. Methods: Eighteen patients with advanced and progressive MTC scheduled for vandetanib treatment underwent baseline F-18-FDG PET/CT before and 3 mo after TKI treatment initiation. During follow-up, CT scans were obtained every 3 mo and analyzed according to RECIST. The predictive value for estimating progression-free survival (PFS) and overall survival (OS) was examined by investigating the F-18-FDG SUVmean/max of the metabolically most active lesion, as well as by analyzing clinical parameters (tumor marker doubling times [calcitonin, carcinoembryonic antigen], prior therapies, rearranged-during-transfection mutational status, and disease type). Results: Within a median follow-up of 5.2 y, 9 patients experienced disease progression after a median interval of 2.1 y, whereas the remainder had ongoing disease control (5 with a partial response and 4 with stable disease). Eight of the 9 patients with progressive disease died from MTC after a median of 3.5 y after TKI initiation. A pretherapeutic SUVmean of more than 4.0 predicted a significantly shorter PFS (1.9 y vs. 5.2 y, P = 0.04). Furthermore, sustained high F-18-FDG uptake at 3 mo with a SUVmean of more than 2.8 tended to portend an unfavorable prognosis, with a PFS of 1.9 y (vs. 3.5 y, P = 0.3). Prolonged carcinoembryonic antigen doubling times were significantly correlated with longer PFS (r = 0.7) and OS (r = 0.76, P < 0.01). None of the other clinical parameters had prognostic significance. Conclusion: Pretherapeutic F-18-FDG PET/CT provides prognostic information in patients with advanced MTC scheduled for treatment with the TKI vandetanib. A low tumor metabolism with an SUVmean of less than 4.0 before treatment predicts a longer PFS.
引用
收藏
页码:756 / 761
页数:6
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