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Updated: Dec 21, 2025

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Measuring Real-time Drug Response in Organotypic Tumor Tissue Slices
Published on: May 2, 2020
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Multiplexed drug testing of tumor slices using a microfluidic platform.
L F Horowitz1,2,3, A D Rodriguez1, Z Dereli-Korkut4
11Department of Bioengineering, University of Washington, Seattle, WA 98195 USA.
NPJ Precision Oncology
|May 22, 2020
Summary
This study presents a new microfluidic platform for rapid, accurate cancer drug testing using patient tumor slices. This approach aids in selecting effective cancer therapies, advancing personalized medicine.
Area of Science:
- Oncology
- Biotechnology
- Microfluidics
Background:
- Current cancer drug response assessments are often inaccurate, slow, or expensive.
- Functional drug testing methods offer a promising alternative for personalized cancer therapy selection.
- Directly assessing patient tumor response to drugs can improve treatment outcomes.
Purpose of the Study:
- To develop and validate a microfluidic platform for multiplexed drug testing of intact human cancer slice cultures.
- To evaluate the platform's ability to rapidly assess drug responses in glioma xenografts and patient tumor biopsies.
- To establish a preclinical tool for improving cancer drug testing and personalized medicine.
Main Methods:
- Development of a digitally manufactured microfluidic device for culturing intact cancer slices.
- Multiplexed drug screening on slice cultures derived from human glioma xenografts and patient tumor biopsies.
- Evaluation of drug response by assessing tissue viability and drug efficacy within days of tissue acquisition.
Main Results:
- The microfluidic platform successfully enabled multiplexed drug testing on intact cancer slice cultures.
- Drug responses were evaluated in human glioma xenografts and patient tumor biopsies.
- The platform provided rapid results, within days of surgery, demonstrating its potential for guiding therapy selection.
Conclusions:
- The developed microfluidic platform is a viable preclinical tool for cancer drug testing and development.
- This approach preserves the tumor microenvironment, offering more accurate drug response assessments.
- The rapid turnaround time has the potential to significantly improve personalized cancer medicine by guiding initial therapy choices.

