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Test Price

750 AED

✅ Home Collection Available

DHA-ACCREDITED ISO 9001:2015

Immunohistochemistry (IHC) – Digital Breast Cancer Panel 1 Test in UAE 750 AED

Executive Summary & Core Metrics

  • Accuracy Guarantee: 99.9% diagnostic sensitivity via ISO 9001:2015 accredited processing (Cert: INT/EGQ/2509DA/3139).
  • Premium Logistics: Secure Medical Courier Solid Tissue Specimen Retrieval – temperature-controlled chain of custody for archival FFPE blocks and slides.
  • Clinical Guidance: Complimentary telephonic post-test clinical interpretation by DHA-licensed specialist.
  • Insurance: Direct billing verification via WhatsApp +971 54 548 8731.
Federal Decree-Law No. 45 of 2021 (PDPL) Compliant Federal Law No. 2 of 2019 (Health ICT) Federal Decree-Law No. 4 of 2016 (Medical Liability)

Test Overview & Methodology

The Immunohistochemistry Digital Breast Cancer Panel 1 is a precision diagnostic assay that maps key protein biomarkers (ER, PR, HER2, Ki-67) in breast tumor tissue using digital image analysis with artificial intelligence-assisted scoring. This assay provides objective, quantifiable receptor status and proliferation index, enabling molecular subtyping for personalized oncology decisions.

Feature Our Test (Digital IHC Panel 1) Standard Manual IHC Panel
Methodology Digital IHC with AI-assisted scoring (LC-MS/MS-validated antibodies) Manual light microscopy, subjective scoring
Precision 99.9% inter-operator reproducibility ~90-95%, higher inter-observer variability
Turnaround Block: 5 days | Biopsy: 5 days | Complex: 7 days Often 7–10 days
Guideline Compliance DHA/MOHAP, NCCN, ASCO/CAP aligned May use older ASCO/CAP thresholds

Physician Insight & Safety Protocols

“Every breast cancer journey demands biomarker clarity. This digital IHC Panel provides oncologists and diagnostic radiologists with objective, quantifiable ER/PR/HER2 status, directly influencing personalized therapy decisions. I urge clinicians to correlate these results with full histopathological context and never initiate treatment based on a single test.”

— Mr. Prabhakar Reddy Kalathoor, Specialist Diagnostic Radiology, DHA Lic. 61713011

Important Advisory

This test provides critical diagnostic information but must be interpreted within the full clinical context. Therapy adjustments should only be made under the supervision of your treating oncologist. Digital IHC results complement, not replace, histopathological and radiological assessment.

Exclusion Criteria & Red Flags

  • Sample exclusion: Specimens fixed in non-formalin fixatives (e.g., Bouin’s), insufficient tumour cells (<100 invasive cells), extensive necrosis, decalcified bone biopsies, or samples without matched histopathology report.
  • Patient red flags (seek ER immediately): Sudden severe breast pain, new bloody nipple discharge, rapidly growing mass, or signs of systemic infection post-biopsy.
  • Test limitation: Equivocal HER2 (2+) by IHC will be reflexed to FISH per ASCO/CAP guidelines; this may extend report time.

Patient FAQ & Clinical Guidance

1. What exactly does the Immunohistochemistry Digital Breast Cancer Panel 1 test measure?

The panel quantitatively measures estrogen receptor (ER), progesterone receptor (PR), HER2 oncoprotein, and proliferation marker Ki-67 in breast tumor tissue using advanced digital image analysis—delivering a definitive molecular subtype classification for treatment planning. Read our clinical pathology guide

2. What sample is required and how should it be prepared for the IHC breast panel?

Submit a formalin-fixed paraffin-embedded (FFPE) tumor block or 10% neutral buffered formalin-fixed biopsy tissue at room temperature, always accompanied by a copy of the histopathology report and clinical history to ensure accurate immunohistochemical interpretation. Call for collection kit

3. How should I interpret my breast cancer IHC results and what are the next steps?

Your digital report will show a 0–3+ score for each biomarker; a positive ER/PR (≥1%) and negative HER2 (0–1+) typically indicates an endocrine-responsive tumor, while HER2 3+ or amplified directs anti-HER2 therapy—always discuss with your oncologist before any decision. Download report interpretation guide

UAE Regulatory & Data Privacy Adherence

This laboratory service complies with UAE Federal Decree-Law No. 45 of 2021 on the Protection of Personal Data (PDPL) and Federal Law No. 2 of 2019 concerning the Use of Information and Communication Technology in Health Fields. Patient data is encrypted, access-controlled, and processed exclusively within the Dubai Healthcare City jurisdiction. All clinical procedures adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability, ensuring informed consent and safety standards.

Clinical & Logistical Metadata

Test Name Immunohistochemistry (IHC) – Digital Breast Cancer Panel 1
Price (AED) 750 AED
Turnaround Time 5–7 business days
Sample Type / Matrix FFPE tumor block or 10% formalin-fixed biopsy tissue (archival)
Methodology Used Digital Immunohistochemistry with AI-assisted scoring
ICD-10-CM Code C50.9
LOINC Code 85319-2
DHA Facility License & Laboratory Address License: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE – DNA Labs UAE
Secure Medical Courier Solid Tissue Specimen Retrieval – Temperature-controlled chain of custody WhatsApp Booking

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