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Bio B2BCellMax Life 〉NCCN Lung Cancer Panel

NCCN Lung Cancer Panel

NCCN Lung Cancer Panel

1.1st in Taiwan PD-L1 and MSI Testing In Blood.
2.The only NCCN Guideline complete liquid biopsy for targeted and immunotherapy selection. (SNVs / InDels / CNVs/Fusions / Expression / MSI)

Request for Collaboration
Overview
To maximize treatment options for NSCLC patients using a non-invasive and highly sensitive blood test when tissue is not available.
The NCCN Lung Cancer Panel is indicated for NSCLC patients.
  • 1 in 2 PATIENTS EXPECTED TO HAVE AN ALTERATION ASSOCIATED WITH AN FDA-APPROVED TARGETED THERAPY *
  • 1 in 3 PATIENTS EXPECTED TO BE HIGH PD-L1 EXPRESSORS and ELIGIBLE FOR IMMUNOTHERAPY **
* (Based on a population frequency in NSCLC for the following alterations associated with FDA-approved therapies- 35% for EGFR In Asian population, 3-7% ALK fusions,  1% for ROS-1, 1% for RET, 1-3% for BRAF, 2-4% for HER2  and 1-4% for MET  amplifications.) 
Lovly, C., L. Horn, W. Pao. 2016. Molecular Profiling of Lung Cancer. My Cancer Genome 

** (The fraction of patients that had PDL-1 PS of >=50% in KEYNOTE 010 trial for pembrlizumab. Pembrolizumab is FDA-Approved as a 1st line treatment for advanced NSCLC patients with PDL-1 PS>=50%) Grigg et al. 2016. Journal for ImmunoTherapy of Cancer 2016

Testing is done at CellMax laboratories using advanced next-generation sequencing (SMSEQTM) and ultra sensitive CTC capture (CMxTM) platforms.


 
Features




 
Application
The NCCN Lung Cancer Panel is indicated for NSCLC patients.
  • 1 in 2 PATIENTS EXPECTED TO HAVE AN ALTERATION ASSOCIATED WITH AN FDA-APPROVED TARGETED THERAPY *
  • 1 in 3 PATIENTS EXPECTED TO BE HIGH PD-L1 EXPRESSORS and ELIGIBLE FOR IMMUNOTHERAPY **
Collaboration Options
Licensing
Co-development
Marketing & Distribution
Investment
More Information
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