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 NSCLC PDX Models 
A Champions Model Cohort

An extensive bank of  Non-Small Cell Lung Cancer - NSCLC PDX Models directly established from patients with late-stage NSCLC with smoking history, and pretreated patient tumors available for drug development research

 

 

 Clinically Relevant Models

Living & diverse bank of clinically relevant models that correlate with clinical outcomes

Pretreated PDX Models

Established from tumor biopsies from patients pretreated with latest generation therapies

Multi-omic Characterization

Clinical annotations coupled with molecular datasets and in vivo responses 

 

Champions’ Non-Small Cell Lung Cancer NSCLC PDX Models

Champions Oncology offers 179* clinically relevant Non-Small Cell Lung Cancer -NSCLC PDX models for oncology studies and drug development. These models are derived from late-stage NSCLC patients, many with smoking histories and prior treatment with Standard of Care therapies. They encompass a broad range of targetable mutations, including a unique EGFR triple-mutant model (CTG-3970). A significant number of the models have been extensively characterized, with 166* having Whole Exome Sequencing (WES), 158* RNA-seq, and 155* having both, along with in vivo drug response data. This comprehensive dataset enables robust exploration of biomarkers associated with response and non-response in NSCLC. More details on these models can be accessed via Champions’ Model Select®.
(*Model numbers fluctuate as our dataset continuously evolves.)

Champions' leading NSCLC PDX Models cohort showcases primary models, each reflecting key clinical characteristics, mutations, and pretreatment history. 

  • Access to one of the largest  bank of NSCLC PDX models with clinically relevant molecular
    and pathological characteristics on the market. 
  • Access to highly characterized PDX models with High Complexity Flow Cytometry, WES, RNAseq, Proteomics and Phosphoproteomics.
  • Includes models pretreated with advanced therapies like checkpoint inhibitors and EGFR-targeted treatments.