TU-A-141-01: Multi Modal PET/CT Imaging for Therapy Response Early Prediction and Therapy Monitoring

2013 ◽  
Vol 40 (6Part25) ◽  
pp. 425-425
Author(s):  
M Hatt ◽  
P Lambin ◽  
P Kinahan
Lung Cancer ◽  
2005 ◽  
Vol 49 ◽  
pp. S33-S35 ◽  
Author(s):  
H.C. Steinert ◽  
M.M. Santos Dellea ◽  
C. Burger ◽  
R. Stahel

2015 ◽  
Vol 42 (7) ◽  
pp. 3979-3991 ◽  
Author(s):  
Christopher Kurz ◽  
Julia Bauer ◽  
Maurizio Conti ◽  
Laura Guérin ◽  
Lars Eriksson ◽  
...  

Author(s):  
Tima DAVIDSON ◽  
Yonatan YAKOBI ◽  
knaana NAYRUZ ◽  
Gabriel LEVIN ◽  
Jacob KORACH ◽  
...  

2020 ◽  
Vol 9 (11) ◽  
pp. 3483
Author(s):  
David Lang ◽  
Gerald Wahl ◽  
Nikolaus Poier ◽  
Sebastian Graf ◽  
David Kiesl ◽  
...  

Cancer immunotherapy using immune-checkpoint inhibitors (ICI) has revolutionized the therapeutic landscape of various malignancies like non-small-cell lung cancer or melanoma. Pre-therapy response prediction and assessment during ICI treatment is challenging due to the lack of reliable biomarkers and the possibility of atypical radiological response patterns. Positron emission tomography/computed tomography (PET/CT) enables the visualization and quantification of metabolic lesion activity additional to conventional CT imaging. Various biomarkers derived from PET/CT have been reported as predictors for response to ICI and may aid to overcome the challenges clinicians currently face in the management of ICI-treated patients. In this narrative review, experts in nuclear medicine, thoracic oncology, dermatooncology, hemato- and internal oncology, urological and head/neck tumors performed literature reviews in their respective field and a joint discussion on the use of PET/CT in the context of ICI treatment. The aims were to give a clinical overview on present standards and evidence, to identify current challenges and fields of research and to enable an outlook to future developments and their possible implications. Multiple promising studies concerning ICI response assessment or prediction using biomarkers derived from PET/CT alone or as composite biomarkers have been identified for various malignancies and disease stages. Of interest, additional major incentives in the field may evolve from novel tracers specifically targeting immune-checkpoint molecules which could allow not only response assessment and prognosis, but also visualization of histological tumor cell properties like programmed death-ligand (PD-L1) expression in vivo. Despite the broad range of existing literature on PET/CT-derived biomarkers in ICI therapy, implications for daily clinical practice remain elusive. High-quality prospective data are urgently warranted to determine whether patients benefit from the application of PET/CT in terms of prognosis. At the moment, the lack of such evidence as well as the absence of standardized imaging methods and biomarkers still precludes PET/CT imaging to be included in the relevant clinical practice guidelines.


2018 ◽  
Vol 2018 ◽  
pp. 1-9 ◽  
Author(s):  
Dongjian Zhang ◽  
Meng Gao ◽  
Nan Yao ◽  
Cuihua Jiang ◽  
Wei Liu ◽  
...  

This study aimed to explore the use of 131I-Hoechst 33258 (131I-H33258) for early prediction of tumor response to vascular-disrupting agents (VDAs) with combretastatin-A4 phosphate (CA4P) as a representative. Necrosis avidity of 131I-H33258 was evaluated in mouse models with muscle necrosis and blocking was used to confirm the tracer specificity. Therapy response was evaluated by 131I-H33258 SPECT/CT imaging 24 h after CA4P therapy in W256 tumor-bearing rats. Radiotracer uptake in tumors was validated ex vivo using γ-counting, autoradiography, and histopathological staining. Results showed that 131I-H33258 had predominant necrosis avidity and could specifically bind to necrotic tissue. SPECT/CT imaging demonstrated that an obvious “hot spot” could be observed in the CA4P-treated tumor. Ex vivo γ-counting revealed 131I-H33258 uptake in tumors was increased 2.8-fold in rats treated with CA4P relative to rats treated with vehicle. Autoradiography and corresponding H&E staining suggested that 131I-H33258 was mainly localized in necrotic tumor area and the higher overall uptake in the treated tumors was attributed to the increased necrosis. These results suggest that 131I-H33258 can be used to image induction of cell necrosis 24 h after CA4P therapy, which support further molecular design of probes based on scaffold H33258 for monitoring of tumor response to VDAs treatment.


PLoS ONE ◽  
2019 ◽  
Vol 14 (6) ◽  
pp. e0218416 ◽  
Author(s):  
Seo Young Kang ◽  
Ji-In Bang ◽  
Keon Wook Kang ◽  
Ho-young Lee ◽  
June-Key Chung

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