Addendum and Non-invasive Multiregion, Multisample Tumor Sequencing

Michael Renteln

doi:10.20944/preprints202308.1536.v4

Preprint Review Version 4 Preserved in Portico This version is not peer-reviewed

Version 1 : Received: 21 August 2023 / Approved: 21 August 2023 / Online: 22 August 2023 (07:58:07 CEST)
Version 2 : Received: 5 September 2023 / Approved: 6 September 2023 / Online: 7 September 2023 (02:54:00 CEST)
Version 3 : Received: 31 December 2023 / Approved: 2 January 2024 / Online: 2 January 2024 (10:00:17 CET)
Version 4 : Received: 4 February 2024 / Approved: 5 February 2024 / Online: 5 February 2024 (13:52:59 CET)
Version 5 : Received: 21 March 2024 / Approved: 22 March 2024 / Online: 22 March 2024 (12:06:13 CET)

Recently, I described a novel approach for cancer therapy in an article entitled “Promoting Oncolytic Vector Replication with Switches that Detect Ubiquitous Mutations”. However, there are a few more design details that should potentially be taken into consideration. Also, multiregion, multisample tumor sequencing may be simplified by analyzing cell-free DNA in the blood of patients.

multiregion sequencing; multisample sequencing; targeted cancer therapy; OVERCOME; macrophage magnetotaxis

Medicine and Pharmacology, Oncology and Oncogenics

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Addendum and Non-invasive Multiregion, Multisample Tumor Sequencing

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