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Medical information Clinical review pending

Cytogenetics

IHC ER-PR HER2NEU

The IHC ER-PR HER2NEU test assesses hormone receptor and HER2 protein status in breast cancer tissue, guiding personalized treatment decisions. Confirm with the laboratory before booking.

General information only: This page is not a diagnosis or personal medical advice. A qualified clinician should decide whether testing is appropriate and interpret results in context.

Review status: No completed medical review is recorded for this page.

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Counselor guidance included Confidential handling Kenya-wide coordination

At a glance

Plan your test

Sample
Formalin-fixed paraffin-embedded (FFPE) breast tissue biopsy or surgical resection specimen. Confirm specific requirements with the laboratory before booking.
Results
Confirm with the laboratory before booking.
Preparation
No specific patient preparation is required for this test. A doctor's prescription is necessary. Confirm with the laboratory before booking.
Test priceKSh 9,000

Payment: M-Pesa and card options can be confirmed during booking.

Insurance & government schemes

Is this test covered for you?

We help you verify whether the IHC ER-PR HER2NEU test can be claimed against your insurer, employer scheme or a Kenyan government health scheme — before you book. Coverage depends on your plan, clinical indication and your provider's rules; final approval always rests with them.

Talk to a claims advisor

Providers & schemes we can help you check

Government & public schemes

SHIF — Social Health Insurance Fund Linda Mama EduAfya NHIF (legacy cards)

Eligibility and benefits follow the current rules of the Social Health Authority (SHA) and applicable government programmes.

Private insurers & employer schemes

Jubilee Health AAR APA Britam CIC Madison Resolution Pioneer Minet Old Mutual GA Life Heritage + other licensed insurers

Names shown for identification only — listing does not imply partnership or guarantee of coverage.

Have these ready when we check

  • Insurer or scheme name & policy / member number
  • A clinician's request / prescription for the test
  • Pre-authorisation letter, if your plan requires one

Free coverage check

Ask us to verify your cover

Send your details and our claims team confirms what documents you need and whether pre-authorisation applies — usually the same working day.

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Used only to process your coverage check — see our Privacy Policy. Verification support is free and does not guarantee your provider will pay.

01

Start with fit

Is this the right test for you?

The best test starts with a clear clinical question. These are common reasons a clinician or family may consider this test.

  • ✓Diagnosis of breast cancer
  • ✓Treatment planning for breast cancer
  • ✓Prognosis assessment in breast cancer
  • ✓Monitoring response to therapy
02

In plain language

What this test helps you understand

This test helps determine the appropriate treatment strategy for breast cancer by identifying the presence of hormone receptors (ER, PR) and the HER2 protein, guiding decisions on hormone therapy and targeted treatments.
The IHC ER-PR HER2NEU test is an immunohistochemical analysis used in the diagnosis and management of breast cancer. It examines breast tissue samples to determine the presence and levels of three key factors: Estrogen Receptors (ER), Progesterone Receptors (PR), and the HER2/neu protein. Understanding these factors is crucial for developing effective treatment plans.

This test measures: - Estrogen Receptors (ER): Helps predict if hormone therapy targeting estrogen might be effective. - Progesterone Receptors (PR): Provides additional information about hormone sensitivity and potential response to hormone therapy. - HER2/neu Protein: Identifies if the cancer cells overexpress this protein, which can indicate a need for targeted therapies like trastuzumab.

This information allows healthcare providers to tailor treatments, including hormone therapy, chemotherapy, and targeted drug therapy, to the specific characteristics of the patient's cancer.
03

Medical review status

Clinical review pending

A completed medical review is not recorded for this page. No clinician has endorsed the information shown here. Please discuss testing decisions with a qualified healthcare professional.

Meet the DNA Labs Kenya medical team →
04

A simple process

What happens next?

You do not have to navigate the test alone. We help you move from question to next step.

1

Speak with us

We check the test and answer your questions before collection.

2

Give your sample

Choose home collection or a coordinated hub visit in Kenya. We explain whether this test uses a cheek swab or blood draw.

3

Understand your report

A counselor helps you understand the result and the next steps.

05

Choose your collection

Home collection or a lab visit

We will explain the sample, preparation, and next steps before anything is collected.

Home collection

Choose a coordinated visit at home or another convenient location. Our team confirms the appointment and sample requirements in advance.

Lab or hub visit

Prefer to visit a coordinated location? We can guide you to the right hub and explain what to expect when you arrive.

Ask about locations →
PreparationNo specific patient preparation is required for this test. A doctor's prescription is necessary. Confirm with the laboratory before booking.
SampleFormalin-fixed paraffin-embedded (FFPE) breast tissue biopsy or surgical resection specimen. Confirm specific requirements with the laboratory before booking.
MethodologyImmunohistochemistry (IHC) using specific antibodies to detect ER, PR, and HER2 protein expression in tissue sections.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
Test results are based on the provided tissue sample. The quality and representativeness of the sample can affect accuracy. This test does not provide information on gene mutations. Confirm with the laboratory before booking.
06

Read your report

What common result terms mean

PositiveA finding was identified. Your clinician or counselor will explain what it means for your care.
NegativeThe specific finding tested for was not identified. It does not rule out every possible cause.
VUSA variant was found, but current evidence is not enough to classify it. Your counselor can explain follow-up.
07

Questions people ask

Frequently asked questions

IHC stands for Immunohistochemistry. ER is Estrogen Receptor, PR is Progesterone Receptor, and HER2NEU is a protein involved in cancer growth. The test checks for these in breast cancer tissue.
It helps doctors understand the specific type of breast cancer and choose the most effective treatments, such as hormone therapy or targeted drugs.
Positive results indicate the presence of the receptor or protein, suggesting certain treatments might be effective. Negative results suggest these treatments may not be suitable, and other options should be considered.
No fasting is required for this test as it is performed on a tissue sample, not blood.
The sample is typically a piece of breast tissue obtained during a biopsy or surgery.
Results are typically provided to the referring physician who ordered the test. They will discuss the results with you.
08

Collaboration

Open for partnership with hospitals, clinics, doctors & researchers

Whether you are referring patients, building a research programme or supporting students, we work as an extension of your team — with responsive communication and clear scientific standards.

Hospitals & clinics

Referral pathways, coordinated sample logistics and shared reporting that fits your clinical workflow.

Doctors & specialists

LOINC-coded reports, ACMG-based variant classification and a direct scientific line for complex cases.

Research institutions

Sanger sequencing, NGS panels and custom assays — with project design support, batch pricing and agreed turnaround commitments.

Students & academic projects

Discounted laboratory services for college, master's and PhD research projects — including proposal guidance and cost-effective batch testing.

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09

Trust & transparency

Sources, standards & how this page is maintained

Standards & references

  • ACMG/AMP technical standards for sequence variant interpretation
  • ClinGen curation and gene–disease validity frameworks where applicable
  • LOINC-coded reporting for interoperable results
  • ISO 9001:2015 quality management; ISO 15189 accreditation in progress

Page provenance

  • Last updated: September 27, 2026
  • Medical review: not yet completed
  • Written for patients & clinicians in Kenya; reviewed periodically against current guidance

Medical disclaimer: this page is general information, not a diagnosis or personal medical advice. Testing decisions and result interpretation should be made with a qualified healthcare professional.

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