Related Experiment Video
Updated: Feb 21, 2026

Gene Regulation and Targeted Therapy in Gastric Cancer Peritoneal Metastasis: Radiological Findings from Dual Energy CT and PET/CT
Published on: January 22, 2018
Predictive Value of 18F-FDG PET in Patients with Advanced Medullary Thyroid Carcinoma Treated with Vandetanib
Rudolf A Werner1,2, Jan-Stefan Schmid1, Takahiro Higuchi1,3
1Department of Nuclear Medicine, University Hospital, University of Würzburg, Würzburg, Germany.
Abstract:
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 18F-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 18F-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 18F-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 18F-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 18F-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.
Insights
Pre-treatment 18F-FDG PET/CT scans can predict outcomes for advanced medullary thyroid carcinoma (MTC) patients receiving tyrosine kinase inhibitors (TKIs). Lower tumor metabolism (SUVmean < 4.0) before treatment indicates a longer progression-free survival.
Area of Science:
- Nuclear Medicine
- Oncology
- Radiology
Background:
- Advanced medullary thyroid carcinoma (MTC) treatment has improved with tyrosine kinase inhibitors (TKIs).
- Assessing treatment response and prognosis in advanced MTC is crucial for optimizing patient care.
- Metabolic imaging with 18F-FDG PET/CT offers a potential tool for evaluating tumor activity.
Purpose of the Study:
- To evaluate the role of 18F-FDG PET/CT in predicting outcomes for advanced MTC patients undergoing TKI therapy.
- To assess the prognostic value of pre-treatment and early post-treatment 18F-FDG PET/CT findings.
- To correlate metabolic imaging parameters with progression-free survival (PFS) and overall survival (OS).
Main Methods:
- Eighteen patients with advanced MTC received vandetanib and underwent baseline 18F-FDG PET/CT before treatment and at 3 months.
- Tumor metabolism was quantified using SUVmean and SUVmax of the most active lesion.
- Progression-free survival (PFS) and overall survival (OS) were analyzed in relation to imaging and clinical parameters (e.g., tumor marker doubling times).
Main Results:
- A pre-treatment SUVmean > 4.0 was associated with significantly shorter PFS (1.9 vs. 5.2 years, P=0.04).
- Sustained high 18F-FDG uptake at 3 months (SUVmean > 2.8) tended towards unfavorable prognosis (PFS 1.9 years).
- Prolonged carcinoembryonic antigen doubling times correlated significantly with longer PFS (r=0.7) and OS (r=0.76, P<0.01).
Conclusions:
- Pre-treatment 18F-FDG PET/CT provides valuable prognostic information in advanced MTC patients treated with vandetanib.
- Lower baseline tumor metabolism (SUVmean < 4.0) predicts longer PFS.
- 18F-FDG PET/CT can aid in stratifying patients and guiding therapeutic decisions in advanced MTC.

