scholarly journals Intra-Patient Heterogeneity of Circulating Tumor Cells and Circulating Tumor DNA in Blood of Melanoma Patients

Cancers ◽  
2019 ◽  
Vol 11 (11) ◽  
pp. 1685 ◽  
Author(s):  
Katharina Gorges ◽  
Lisa Wiltfang ◽  
Tobias Gorges ◽  
Alexander Sartori ◽  
Lina Hildebrandt ◽  
...  

Despite remarkable progress in melanoma therapy, the exceptional heterogeneity of the disease has prevented the development of reliable companion biomarkers for the prediction or monitoring of therapy responses. Here, we show that difficulties in detecting blood-based markers, like circulating tumor cells (CTC), might arise from the translation of the mutational heterogeneity of melanoma cells towards their surface marker expression. We provide a unique method, which enables the molecular characterization of clinically relevant CTC subsets, as well as circulating tumor DNA (ctDNA), from a single blood sample. The study demonstrates the benefit of a combined analysis of ctDNA and CTC counts in melanoma patients, revealing that CTC subsets and ctDNA provide synergistic real-time information on the mutational status, RNA and protein expression of melanoma cells in individual patients, in relation to clinical outcome.

2016 ◽  
Vol 5 (5) ◽  
pp. 466-482 ◽  
Author(s):  
Silvia Calabuig-Fariñas ◽  
Eloísa Jantus-Lewintre ◽  
Alejandro Herreros-Pomares ◽  
Carlos Camps

2018 ◽  
Vol 64 (5) ◽  
pp. 830-842 ◽  
Author(s):  
Verena Haselmann ◽  
Christoffer Gebhardt ◽  
Ingrid Brechtel ◽  
Angelika Duda ◽  
Claudia Czerwinski ◽  
...  

Abstract BACKGROUND The current standard for determining eligibility of patients with metastatic melanoma for BRAF-targeted therapy is tissue-based testing of BRAF mutations. As patients are rarely rebiopsied, detection in blood might be advantageous by enabling a comprehensive assessment of tumor mutational status in real time and thereby representing a noninvasive biomarker for monitoring BRAF therapy. METHODS In all, 634 stage I to IV melanoma patients were enrolled at 2 centers, and 1406 plasma samples were prospectively collected. Patients were assigned to 3 separate study cohorts: study 1 for assessment of circulating tumor DNA (ctDNA) as part of companion diagnostics, study 2 for assessment of ctDNA for patients with low tumor burden and for follow-up, and study 3 for monitoring of resistance to BRAF inhibitor (BRAFi) or mitogen-activated protein kinase inhibitor therapy. RESULTS Overall, a high degree of concordance between plasma and tissue testing results was observed at 90.9% (study 1) and 90.1% (study 2), respectively. Interestingly, discrepant results were in some cases associated with nonresponse to BRAFi (n = 3) or a secondary BRAF-mutant malignancy (n = 5). Importantly, ctDNA results correlated with the clinical course of disease in 95.7% and with response to treatment. Significantly, the detection of BRAF mutant ctDNA preceded relapse assessed by Response Evaluation Criteria in Solid Tumors, and was more specific than serum S100 and lactate dehydrogenase. CONCLUSIONS Blood-based testing compares favorably with standard-of-care tissue-based BRAF mutation testing. Importantly, blood-based BRAF testing correlates with the clinical course, even for early-stage patients, and may be used to predict response to treatment, recurrence, and resistance before radioimaging under BRAFi therapy, thereby enabling considerable improvements in patient treatment.


2015 ◽  
Vol 33 (15_suppl) ◽  
pp. 8570-8570
Author(s):  
David Matthew Kurtz ◽  
Florian Scherer ◽  
Michael Richard Green ◽  
Michael Siavash Khodadoust ◽  
Daniel M. Klass ◽  
...  

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