Sysmex Forms Strategic Alliance with QIAGEN to Provide Global Cancer Companion Diagnostics that Uses Ultra-sensitive Liquid Biopsy NGS Technology

On July 1, 2021 Sysmex Corporation (HQ: Kobe, Japan, Chairman and CEO: Hisashi Ietsugu) repored that it has formed a global strategic alliance with QIAGEN N.V. (HQ: Hilden, Germany, CEO: Thierry Bernard) for the development of cancer companion diagnostics (Press release, Sysmex Inostics, JUL 1, 2021, View Source [SID1234586872]).1

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Sysmex is working to strengthen its global relationship with pharmaceutical companies in order to develop companion diagnostics and timely launch them by capitalizing on Plasma-Safe-SeqS technology,2 a liquid biopsy developed by Sysmex using a next-generation sequencer (NGS),3 while leveraging QIAGEN’s experience in developing companion diagnostics.

The effective cancer treatment requires companion diagnostics that identifies drug treatment suitable to patients. For the past few years, growing attention has been focused on companion diagnostics based on blood testing (liquid biopsy testing), which reduces the physical burden on the patients.

Sysmex currently offers the "OncoBEAMTM5 RAS CRC Kit" as companion diagnostics for colorectal cancer. It uses highly-sensitive digital PCR technology, and is regulatory approved and covered by national insurance in Japan. In addition to this, the ultra-sensitive liquid biopsy testing utilizing NGS is also being developed and offered via CRO service for pharmaceutical companies and research use only kits.

Following this, Sysmex has entered into a global strategic alliance with QIAGEN, a company with extensive experience in companion diagnostics in the oncology field. This alliance is intended to promote early clinical implementation of ultra-sensitive liquid biopsy companion diagnostics using Plasma-Safe-SeqS technology by expediting field work with pharmaceutical companies that develop molecularly targeted drugs for cancer.

Sysmex will continue to contribute to the improvement of patients’ quality of life (QOL), the standardization of medical care, and the advancement of personalized medicine by developing and disseminating tests with significant clinical value.

References
1. August 2, 2019 news release: "Sysmex Obtains First Manufacturing and Marketing Approval in Japan for Blood-Based RAS Gene Mutation Testing for Colorectal Cancer" View Source
2. March 5, 2020 news release: "Sysmex Presents Academic Report Related to the Clinical Utility of RAS Gene Mutation Testing for Colorectal Cancer Using Liquid Biopsy" View Source
3. August 3, 2020 news release: "Insurance Coverage Received for Liquid Biopsy RAS Gene Mutation Testing for Colorectal Cancer Using High-Sensitivity Digital PCR" View Source

Terminology
1. Companion diagnostics:
Test to predict the efficacy or risk of side effects of specific drugs before prescription.
2. Plasma-Safe-SeqS technology:
By tagging each molecule of a gene fragment to be analyzed, this technology allows differentiation between true genetic mutations and errors (errors generated in the process of preparing and reading NGS samples). One of the vital issues with traditional NGS is the existence of a certain possibility of error in principle, which always brings doubts to the mutation detection results on whether it is a true mutation or a false positive generated from reading errors. Plasma-Safe-SeqS technology is expected to be the solution to this problem.
3. Liquid biopsy:
A type of biopsy based mainly on the blood. It is designed to impose less burden on the patient, while having the performance equivalent to that of a conventional biopsy collected from solid tissue, such as a tumor dissection.
4. Next-generation sequencer (NGS):
An analyzer capable of simultaneously sequencing large quantities of DNA molecules in parallel.
5. OncoBEAM:
The name of Sysmex’s product to detect minute gene mutations circulating in the blood with a high degree of sensitivity using BEAMing technology. BEAMing technology is a gene analysis method combining digital PCR and flow cytometry technologies for highly sensitive analysis of genetic mutations.