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Test Price

4,500 AED

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Cancer Targeted Gene Panel: Lung with PD‑L1 (DAKO) Test in UAE – 4500 AED

Executive Summary & Core Metrics

Executive Summary

The Cancer Targeted Gene Panel for Lung with PD‑L1 (DAKO) delivers a comprehensive molecular profile combining next-generation sequencing (NGS), fluorescence in situ hybridisation (FISH), and immunohistochemistry (IHC) in a single, clinically actionable report. Designed for non‑small cell lung cancer (NSCLC) patients, the assay identifies >50 key driver mutations, gene rearrangements, and PD‑L1 tumour proportion score (TPS) to guide targeted therapy and immunotherapy decisions.

Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Certified Processing
Secure Logistics: Secure Medical Courier Solid Tissue Specimen Retrieval
Clinical Guidance: Complimentary Telephonic Post‑Test Clinical Result Discussion
Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731

Test Overview & Methodology

The Cancer Targeted Gene Panel: Lung with PD‑L1 (DAKO) integrates three orthogonal platforms – NGS for nucleic acid mutations, FISH for large rearrangements, and DAKO 22C3 pharmDx IHC for PD‑L1 expression. This tri‑modal approach provides a complete genomic and immune landscape essential for optimal NSCLC treatment planning. The assay is performed on archival formalin‑fixed, paraffin‑embedded (FFPE) tissue blocks or biopsy slides, requiring a minimum tumour content of 10%.

Feature Our Test (DNA Labs UAE) Closest Alternative
Precision Tri‑modal: NGS + FISH + IHC (DAKO validated) Single‑modality (NGS only or IHC only)
Methodology LC‑MS/MS quality‑controlled; ISO 15189 aligned Conventional NGS without integrated PD‑L1
Turnaround 10–14 business days from receipt of adequate specimen 14–21 days, highly variable
Coverage >50 key lung cancer genes + PD‑L1 score (TPS) Limited panel, often omitting PD‑L1

Physician Insight & Safety Protocols

Lina Osama Zaki Quteineh | Consultant Medical Genetics | DHA Registration ID: 9294403

“Interpretation of the lung cancer gene panel requires integration of molecular findings with the patient’s complete clinical history. The identification of actionable alterations such as EGFR mutations or PD‑L1 expression offers significant therapeutic opportunities. It is essential that results are reviewed by the treating oncologist to align with the patient’s overall treatment strategy. Our laboratory adheres to rigorous quality controls to ensure every report is clinically reliable.”

Medication Advisory

Do not discontinue or modify any prescribed targeted therapy or immunotherapy without consulting your treating physician. Dose adjustments are only made after expert analysis of these molecular results.

Safety & Exclusion Criteria

  • Sample adequacy: FFPE blocks with less than 10% tumour content cannot be processed; request a re‑biopsy if tumour area is insufficient.
  • Decay: Tissue blocks older than 5 years may yield degraded DNA/RNA – a fresh biopsy is strongly recommended.
  • Drug interference: Any last‑dose of heparin or DNA‑damaging chemotherapy within 48 hours of biopsy should be disclosed.

Patient FAQ & Clinical Guidance

1. What is the cancer targeted gene panel for lung with PD‑L1 test?

It is a comprehensive genomic test identifying key mutations, gene fusions, and PD‑L1 expression to guide personalised lung cancer therapy. The result includes a report of all detected alterations and recommended targeted therapies.

2. How is the test performed and what do I need to provide?

The laboratory uses NGS, FISH and IHC on your existing FFPE tissue block. You must submit a copy of the histopathology report, biopsy site information, clinical history, and a completed NGS requisition form. Our courier will retrieve the specimen securely.

3. What is the cost and can I use insurance?

The price is 4500 AED. We directly verify billing with major insurers – simply message us on WhatsApp at +971 54 548 8731 to initiate the process.

UAE Regulatory & Data Privacy Adherence

Regulatory Compliance & Data Protection

DNA Labs UAE operates under DHA Facility License Number 1143. All clinical data handling, storage, and transmission strictly comply with Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) and Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields. Patient consent and safety protocols are governed by Federal Decree-Law No. 4 of 2016 on Medical Liability.

Clinical & Logistical Metadata

Test Name Cancer Targeted Gene Panel: Lung with PD‑L1 (DAKO)
Price (AED) 4,500
Turnaround Time 10–14 business days from receipt of adequate specimen
Sample Type / Matrix Archival FFPE Tissue Block or Biopsy Slides
Methodology Used Next-Generation Sequencing (NGS), Fluorescence In Situ Hybridization (FISH), Immunohistochemistry (IHC) with DAKO 22C3 pharmDx
ICD-10-CM Code C34.9 (Malignant neoplasm of lung, unspecified)
LOINC Code 96539-6 (Lung cancer somatic mutations panel)
DHA Facility License & Laboratory Address License No. 1143 – Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE

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All reports reviewed by DHA-Certified physicians