All Solid Tumors

Cancer Type

Whole Blood / Pleural Effusion

Specimen Requirements

8 Working Days

Turnaround Time ¹

ACTLiquid™ Lite is an NGS-based liquid biopsy test that analyzes 102 cancer-related genes from whole blood or pleural effusion, providing clinically relevant genomic and treatment-related information to support treatment selection and molecular reassessment at key clinical time points.

Actionable Liquid-based NGS Assay for Treatment Selection and Dynamic Monitoring.

102

Cancer-related Genes

19

Fusion Genes

24

Copy Number Alterations

View Gene List

Hallmarks

Liquid Biopsy When Tissue Is Limited

Uses whole blood or pleural effusion when tumor tissue is limited or unavailable.

102-Gene Genomic Profiling

Profiles 102 cancer-related genes across 96SNVs and InDels, 24 CNAs, 19 fusions and MSI to provide clinically relevant molecular information.

Treatment-related Genomic Information

Integrates clinically relevant variants and biomarkers with corresponding therapeutic information to support evaluation of systemic and targeted therapy options.

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Serial Result Comparison

Supports comparison of molecular findings across serial liquid biopsy tests to help identify changes over the course of treatment.

8 Working Days

Provides professional genomic testing results within 8 working days from receipt of qualified specimens at our CAP-accredited laboratory.

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Summary

Tumor Molecular Profiles May Change DuringTreatment

Tumor molecular profiles may change as cancer progresses and adapts under treatment pressure. Molecular information obtained at an earlier time point may therefore not fully reflect the tumor at later stages of disease. Liquid biopsy provides an approach for molecular reassessment at clinically relevant time points without relying solely on repeat tissue biopsy, helping clinicians obtain updated genomic information when considering subsequent treatment strategies.

Different Clinical Purposes Require Different ctDNA Tests

ctDNA assays are developed for different clinical purposes and therefore require different test designs and analytical sensitivities. ACTLiquid™ Lite is intended for molecular genotyping and treatment-related reassessment in patients with advanced or metastatic so particularly when updated genomic information is needed during disease progression, suspected recurrence or drug resistance.

When to Consider ACTLiquid™ Lite

  • Tumor tissue is limited or unavailable
  • Evaluating systemic or targeted therapy options
  • Monitoring suspected disease progression or recurrence
  • Assessing next-line therapeutic strategies upon drug resistance

Technical Specifications

Next Generation Sequencing

102 cancer-related genes

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Specimen Requirements2

Peripheral Whole Blood: 2 × 8–10 mL (16–20 mL)

Pleural Effusion: 2 × 8–10 mL (16–20 mL)

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Sequencing Mean Depth

~30,000×

Limit of Detection

SNVs/ Indels: 0.25% VAF

CNAs: 2.1-3.0 copies

Fusions: 0.50% VAF

MSI: 3% tumor fraction

Sensitivity3

SNVs/ Indels: 98.9%

CNAs: 100%

Fusions: 100%

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Specificity3

SNV and Indels: >99.9%

CNAs: >99.9%

Fusions: >99.9%

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Documentation

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Gene List

Search
Cancer Type
FDA-approved & NCCN-guided Genes

TSC2

No items found.

SNV / Indel

VHL

Pancreas

SNV / Indel

Full Gene List

SNV / Indel

CNA

Fusion

LGR

*Genes also provide exon-skipping alteration information.

TSC2

SNV / Indel

VHL

SNV / Indel

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Disclaimers / Footnotes

  1. Turnaround time starts from the date of receiptof approved samples at our CAP-accredited laboratory.
  2. Please refer to our specimen instructions.
  3. Analytical performance was established under defined validation conditions.

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