Tumor Comprehensive Genomic Profiling Panel Assay
High-Throughput Sequencing
Tumor Comprehensive Genomic Profiling Panel Assay
1200 hot genes of solid tumors, including MSI, TMB, HRR, HLA, immune resistance, hyperprogression and other biomarkers.Provides information for clinically actionable genomic alterations and their associated targeted therapy, both approved and in clinical trials ; TMB / MSI / immunotherapy super progression, positive and negative factors to better inform immunotherapy decisions ; Predicts efficacy and toxicity of chemotherapy based on associated genetic biomarkers; Reveals potential resistance mechanism(s) to current therapies and options for alternative treatments;Indicate some genetic risks by the detection of hereditary cancer-related genes.
BACKGROUND

Tumor initiation and progression are governed by complex mechanisms. While many tumor-associated genes have been discovered, the functions of numerous genes remain to be explored. Large-scale genomic testing comprehensively characterizes tumor genomic profiles and detects rare mutations in key genes. NGS large-panel sequencing guides individualized therapy, helps improve overall survival and offers more therapeutic options and clinical benefits for patients with advanced tumors.


BACKGROUND
DETECTED TARGETS


Covers 1,200 hotspot genes for solid tumors, including biomarkers such as MSI, TMB, HRR, HLA, immunotherapy resistance and hyperprogression, to comprehensively meet clinical testing requirements.


1、162——Targeted therapy-related genes

2、147 ——Hereditary tumor-related genes

3、164 ——MSI loci

4、65 ——Immunotherapy-related genes

5、473——Signaling pathway-related geness

6、53——Chemotherapy drug-related loci

7、TMB——Tumor Mutational Burden (TMB)


PRODUCT INFORMATION
Project Name
Assay Method
Packing Specification
Compatible Platforms
Specimen Material
Tumor Comprehensive Genomic Profiling panel Assay
NGS
24 Tests/ Kit
Platform-agnostic, compatible with Illumina, MGI and more sequencers
Somatic: Tumor tissue samples, cell-free DNA, pleural & ascitic fluid ; Germline: Peripheral blood
APPLICABLE POPULATION

1.Newly diagnosed solid tumor patients: Pre-treatment testing supports treatment planning and prognosis evaluation before targeted, immune or chemotherapy.

2.Solid tumor patients with targeted drug resistance or chemotherapy failure: genomic testing reveals resistance mechanisms and discovers new actionable variants.

3.Persons with family history of tumors needing hereditary cancer risk evaluation.

4.Solid tumor patients with above clinical requirements when pathological tissue is unavailable.

DETECTION SIGNIFICANCE

Targeted Therapy: Provides comprehensive tumor variant profiles including oncogenic pathway genes and rare loci. It interprets tumor pathogenesis, uncovers resistance mechanisms and guides rational targeted drug administration.

Immunotherapy: Comprehensively assesses immunotherapy outcomes based on TMB, MSI status, HLA typing, neoantigen prediction, and genes linked to treatment response and hyperprogression.

Chemotherapy: 53 chemotherapy-associated genes to evaluate efficacy and toxicities and refine chemotherapy strategies.

Hereditary Risk: 147 hereditary cancer genes to evaluate risks of hereditary tumors.

FEATURES & ADVANTAGES
Broad Coverage

Broad Coverage

Covers coding regions of solid tumor hotspots and fusion-related introns

Diverse Variant Detection

Diverse Variant Detection

Supports detection of SNV, CNV, InDel and Gene Fusion.

Comprehensive Therapeutic Targets

Comprehensive Therapeutic Targets

Encompasses all FDA/NMPA-approved targeted therapies

Integrated Immune Profiling

Integrated Immune Profiling

MSI, TMB, MMR and immune regulatory factors are analyzed to evaluate PD-1/PDL1 treatment response

Continuous Database Refresh

Continuous Database Refresh

Regular update and maintenance of gene-drug database

Flexible Customization & Upgrades

Flexible Customization & Upgrades

Sustained upgrade and customization services support diversified research demands

DETECTION PROCESS

01 Nucleic Acid Extraction

02 Library Preparation

03 Sequencing

04 One-stop Data Analysis

05 Report Generation