Test Price
3,500 AED✅ Home Collection Available
Gastrointestinal Stromal Tumor (GIST) Cancer Targeted Gene Panel Test in UAE | 3500 AED
Executive Summary & Core Metrics
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing, delivering reliable detection of KIT, PDGFRA, and other actionable mutations.
- Premium Logistics: Secure Medical Courier Solid Tissue Specimen Retrieval for archival FFPE tumor blocks; home collection is disabled for safety and specimen integrity.
- Clinical Guidance: Complimentary post‑test telephonic guidance with a DHA‑licensed specialist to interpret your results within the clinical context.
- Insurance Support: Direct billing verification and pre‑authorization assistance via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The Gastrointestinal Stromal Tumor (GIST) Cancer Targeted Gene Panel is a comprehensive next‑generation sequencing (NGS) assay that simultaneously interrogates key oncogenic drivers – primarily KIT and PDGFRA mutations – to guide tyrosine kinase inhibitor therapy. The panel covers all clinically relevant exons of KIT (exons 9, 11, 13, 17) and PDGFRA (exons 12, 14, 18), as well as rare drivers such as BRAF and SDH modifications.
| Feature | Our GIST NGS Panel (ISO‑Accredited) | Standard IHC‑Only Alternative |
|---|---|---|
| Methodology | NGS + Immunohistochemistry + Fragment Analysis | Immunohistochemistry (IHC) only |
| Detection Sensitivity | >99% for clinically actionable mutations | ~70% (limited to protein expression) |
| Turn‑Around Time | 10 Working Days | 7 Working Days |
| Price | 3500 AED | ~1500 AED |
| DHA / MOHAP Compliance | Full – ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139) | Variable |
Physician Insight & Safety Protocols
From Mr. Prabhakar Reddy Kalathoor – Specialist Diagnostic Radiology, DHA Registration ID: 61713011: “As a specialist in diagnostic radiology and oncology imaging, I understand the deep concern that accompanies a GIST diagnosis. This targeted gene panel is a crucial tool to move beyond uncertainty – it precisely identifies the mutation driving your tumour, directly shaping a therapy that is both personalized and effective. All results must be correlated with your full clinical picture and discussed with your treating physician.”
Important Clinical Advisory
⚠️ Important Medication Warning
Do not discontinue any prescribed medication or alter your treatment regimen without a direct consultation with your doctor. Gene panel results inform therapy decisions; they do not replace ongoing clinical management.
Patient Safety & Exclusion Criteria
- Exclusion criteria: Insufficient viable tumour content in the paraffin block (<20% cellularity), decalcified tissue, or specimens fixed in non‑formalin agents. Lack of a fully completed NGS Test Requisition Form (Form 40) and signed informed consent for genetic testing is an absolute exclusion.
- Emergency Red Flags: If you experience sudden severe abdominal pain, persistent vomiting, complete inability to pass stool or gas, or alarming weight loss, seek immediate emergency medical attention. The gene panel is a diagnostic tool, not an emergency intervention.
Patient FAQ & Clinical Guidance
1. What does the GIST cancer targeted gene panel test for?
This advanced NGS panel identifies mutations in KIT, PDGFRA, and other critical genes to guide precision targeted therapy for gastrointestinal stromal tumours. The analysis covers all clinically relevant exons of KIT (exons 9, 11, 13, 17) and PDGFRA (exons 12, 14, 18), as well as rare drivers such as BRAF and SDH modifications. A definitive molecular diagnosis enables oncologists to select the most effective tyrosine kinase inhibitor and avoid therapies unlikely to work.
2. What preparations are needed before sending the sample?
A formalin-fixed paraffin-embedded (FFPE) tissue block with a minimum of 20% tumour cellularity must be provided, along with a fully completed NGS Test Requisition Form (Form 40) and signed informed consent for genetic testing. The block should be shipped at room temperature with complete specimen identification documents. Our team will coordinate Secure Medical Courier Solid Tissue Specimen Retrieval to ensure safe transport under ISO-compliant protocols.
3. How long does it take to receive the results and how are they delivered?
Results are typically reported within 10 working days after sample receipt (Monday before 9 AM), providing rapid, actionable data for treatment planning. Reports are securely delivered via encrypted PDF to the requesting physician and the patient portal. A DHA‑licensed specialist will offer a complimentary post‑telephonic consultation to walk you through the findings, answer questions, and discuss next steps in coordination with your primary oncologist.
UAE Regulatory & Data Privacy Adherence
This service fully complies 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. All genetic testing and patient consent procedures adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability. The laboratory operates under DHA Facility License Number 1143 at Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE. ISO 9001:2015 certification (Cert: INT/EGQ/2509DA/3139) ensures quality management across all processes.
Clinical & Logistical Metadata
| Test Name | Gastrointestinal Stromal Tumor (GIST) Cancer Targeted Gene Panel |
| Price (AED) | 3500 |
| Turnaround Time | 10 Working Days |
| Sample Type / Matrix | Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Block – Archival Specimen |
| Methodology Used | Next-Generation Sequencing (NGS) + Immunohistochemistry + Fragment Analysis |
| ICD-10-CM Code | C26.1 |
| LOINC Code | 100350-6 |
| DHA Facility License & Address | License No. 1143 – Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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