Drug Discovery Testing Compounds in Patient Samples by Automated Flow Cytometry

Pilar Hernández1, Julián Gorrochategui1, Daniel Primo1

  • 11 Vivia Biotech, Tres Cantos, Madrid, Spain.

SLAS Technology
|March 26, 2017
PubMed

Insights

A new automated drug screening platform, PharmaFlow, uses whole patient samples for more reliable ex vivo cancer testing. This approach enhances personalized medicine by predicting treatment response and identifying biomarkers for hematological malignancies.

Area of Science:

  • Oncology
  • Biotechnology
  • Pharmacology

Background:

  • Developing reliable ex vivo assays to predict patient response to anticancer drugs is crucial for personalized cancer treatment.
  • Existing functional assays often lack the ability to capture complex drug mechanisms or the patient's unique microenvironment.

Purpose of the Study:

  • To introduce PharmaFlow, an automated flow cytometry platform for drug screening in hematological malignancies.
  • To evaluate the platform's capability in predicting clinical response and identifying biomarkers using whole patient samples.

Main Methods:

  • Development of an automated flow cytometry platform (PharmaFlow) for high-throughput drug screening.
  • Utilizing peripheral blood or bone marrow samples from patients with hematological malignancies.
  • Employing a robust data analysis system to capture multiple drug endpoints and mechanisms of action.

Main Results:

  • PharmaFlow successfully evaluates multiple drug endpoints and complex mechanisms of action.
  • The platform retains crucial microenvironmental components present in whole patient samples.
  • Identified potential for predicting patient response to existing and novel treatments.

Conclusions:

  • PharmaFlow offers a more clinically relevant and predictive ex vivo assay for personalized medicine in oncology.
  • The platform can aid in preclinical drug discovery and biomarker identification for treatment sensitivity, resistance, and toxicity.
  • This approach better recapitulates the human tumor microenvironment for improved drug response prediction.