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which cannot be achieved by performing only one type of biopsy, and that the inclusion of ctDNA profiling
should be considered in routine oncology care especially for cancers where targeted therapies are approved
or in development.
DECLARATIONS
Acknowledgments
We thank all the clinicians and patients who provided the biopsy samples used in the study.
Authors’ contributions
Conceived and designed the study: Laes JF
Worked on the acquisition of data, the writing of the article and the analysis and interpretation of data: all
authors
Reviewed and agreed on the manuscript before submission: all authors
Data source and availability
Due to privacy reasons, the data of this study cannot be open for readers. Nonetheless, if a researcher asks
for data, they could be shared upon the signature of a confidentiality agreement.
Financial support and sponsorship
This study was sponsored by OncoDNA SA. The costs associated with the development and publishing of the
manuscript were provided by OncoDNA SA.
Conflicts of interest
All authors are employees of OncoDNA. Ghitti G and Laes JF report ownership of OncoDNA shares.
Patient consent
Patients gave informed consent for their tumor analysis data to be published.
Ethics approval
This study is not approved by IRB; however, all patients signed an informed consent before their samples
underwent molecular profiling according to Belgian law.
Copyright
© The Author(s) 2018.
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