Accelerating personalized medicine: Miniaturized patient-derived organoid drug screening for predicting cancer treatment responses and beyond

Read the full article See related articles

Discuss this preprint

Start a discussion What are Sciety discussions?

Listed in

This article is not in any list yet, why not save it to one of your lists.
Log in to save this article

Abstract

Patient-derived-organoids (PDOs) are valuable tools for predicting individual responses to cancer treatments. However, current screening methods require large numbers of PDOs, resulting in long turnaround times and limiting clinical use. This study aimed to streamline the process by automating PDO seeding with the Yamaha Cell Handler™ (YCH). We optimized the YCH to pick and place up to 10 PDOs per well, significantly reducing sample requirements compared to conventional methods. Assay optimization included evaluating seeding densities, devices, readouts, and measurement techniques. We validated the miniaturized assay by comparing it to standard screens and correlating organoid responses with patient outcomes. Our proof-of-concept demonstrated that mCRC PDOs respond to chemotherapy and targeted treatments in a way that closely matches results from traditional assays. This miniaturized automated platform enables efficient, high-quality drug screening with fewer cells, offering promising potential for faster, personalized cancer treatment predictions in clinical settings.

Article activity feed