Test Price
180 AED✅ Home Collection Available
CA 15.3 Breast Cancer Marker Test in UAE – 180 AED – DHA Licensed
Executive Summary & Core Metrics
- Diagnostic Accuracy: High analytical sensitivity (99.9%) via ISO-certified chemiluminescent immunoassay.
- Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection available daily from 8 AM to 11 PM.
- Post-Test Guidance: Complimentary teleconsultation with a licensed clinician for result interpretation.
- Insurance Support: Direct billing verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The CA 15.3 test quantifies a soluble glycoprotein (MUC-1) shed into the bloodstream by breast cancer cells. It is primarily used for monitoring treatment response and detecting early recurrence in patients with diagnosed breast cancer. This test is not a standalone diagnostic tool and must be interpreted alongside imaging and clinical examination.
| Feature | Our CA 15.3 Test (CMIA) | Alternative CA 27.29 |
|---|---|---|
| Methodology | Chemiluminescent Microparticle Immunoassay (CMIA) | Immunoassay (variable) |
| Precision (CV) | ≤3.5% | ≤5.0% |
| Turnaround | Daily (24h) | 48–72 hours |
| Sample Requirement | 0.5 mL serum (1 SST) | 0.5 mL serum |
Physician Insight & Safety Protocols
Mr. Prabhakar Reddy Kalathoor | Specialist Diagnostic Radiology | DHA Registration ID: 61713011
“As a clinician, I recognize that tumor marker testing can be emotionally demanding. This test is a complementary tool to imaging and physical exams, not a standalone diagnostic. I encourage patients to discuss results holistically with their oncologist.”
Advisory: Medication Caution
⚠ Do not discontinue any prescribed medication without consulting your doctor. The test results should be interpreted in context of your current therapy.
Exclusion Criteria & Emergency Red Flags
- Exclusion: Acute infection, recent surgery, or benign breast conditions may cause transient false‑positive elevations; testing is deferred in such cases.
- Exclusion: Pregnancy or lactation – inform your phlebotomist to contextualise results.
- Emergency Red Flags: If you experience sudden severe bone pain, unexplained shortness of breath, or new‑onset neurological deficits after blood draw, seek emergency care immediately. This test does not replace urgent clinical evaluation.
Patient FAQ & Clinical Guidance
1. What does an elevated CA 15.3 level indicate?
An elevated CA 15.3 result suggests possible breast cancer recurrence or progression, and must be correlated with imaging and clinical findings.
2. How should I prepare for the CA 15.3 test?
Fasting is not required; simply provide a brief clinical history and avoid strenuous exercise 24 hours before collection.
3. Can this replace mammography or biopsy?
No, CA 15.3 is a monitoring serum marker and cannot replace imaging or tissue biopsy for initial diagnosis.
UAE Regulatory & Data Privacy Adherence
Compliance Framework
All laboratory operations are conducted in full compliance 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 data is encrypted and processed solely for clinical purposes. Clinical safety and patient consent adhere to Federal Decree‑Law No. 4 of 2016 on Medical Liability. The facility holds ISO 9001:2015 certification (INT/EGQ/2509DA/3139) and operates under DHA Facility License No. 1143.
Clinical & Logistical Metadata
| Test Name | CA 15.3 Breast Cancer Marker Test |
| Price (AED) | 180 AED |
| Turnaround Time | 24 hours (Daily) |
| Sample Type / Matrix | Serum (0.5 mL, 1 SST) |
| Methodology Used | Chemiluminescent Microparticle Immunoassay (CMIA) |
| ICD-10-CM Code | Z08.0, Z85.3 |
| LOINC Code | 29409-5 |
| DHA Facility License & Laboratory Address | DHA License: 1143 | DNA Labs UAE, Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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