The current project will focus on five main aims:
1. integration of multiplexed cutting-edge sequencing approaches to determine the effect of all tested drug combinations in detail
2. identification of biomarkers that can predict therapy outcome
3. use of microscopic tumor slices rather than less physiological cell suspensions
4. upscaling and simplification of the microfluidic technology to enable routine use by non-specialized staff in the clinic or at third party diagnostic laboratories
5. determining the clinical benefit of the 2nd-generation platform
With ~19 million new diagnoses, 10 million deaths and total economic costs of 1.14 trillion US$ per year, cancer is a major burden for society. One reason for the high mortality and cost is due to the fact that every tumor responds differently to medication. Even worse, tumors rapidly change their response to drugs over time and develop resistances. This leaves patients in the highly uncomfortable position to undergo suboptimal standard therapies with unclear outcome and high mortality. What is needed is a system allowing to rapidly and economically test which drug or drug combination works best on the tumor cells of a given patient, at a given point in time.