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Medical information Clinical review pending

Diagnostic Testing

Biopsy Breast Modified Radical Mastectomy ER PR HER2 Neu

This test analyzes breast tissue from a modified radical mastectomy to determine hormone receptor status (ER, PR) and HER2/neu protein levels, guiding personalized breast cancer treatment.

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
Tissue sample from the modified radical mastectomy.
Results
Confirm with the laboratory before booking.
Preparation
Confirm with the laboratory before booking. A doctor’s prescription is required.
Test priceKSh 16,500

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 Biopsy Breast Modified Radical Mastectomy ER PR HER2 Neu 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
  • ✓Staging of breast cancer
  • ✓Treatment planning for breast cancer
  • ✓Prognosis assessment in breast cancer
  • ✓Guiding therapy selection (hormone therapy, targeted therapy)
  • ✓Post-mastectomy analysis
02

In plain language

What this test helps you understand

Determines hormone receptor (ER, PR) and HER2/neu status in breast cancer tissue, guiding personalized treatment decisions and predicting response to therapies.
This test is a crucial diagnostic tool used to evaluate breast cancer characteristics after a modified radical mastectomy. It plays a significant role in determining the best treatment options for patients diagnosed with breast cancer. This test is essential for understanding the hormonal and genetic factors involved in breast cancer, allowing for tailored therapeutic approaches.

This test measures the presence of estrogen receptors (ER), progesterone receptors (PR), and HER2/neu protein in breast tissue samples. These components are critical in understanding the biology of the cancer and how it may respond to specific treatments.

Patients who have been diagnosed with breast cancer, particularly those undergoing a modified radical mastectomy, should consider this test. It helps in determining the most effective treatment plan, provides insight into the cancer's behavior and potential response to therapies, allows for personalized medicine approaches, and facilitates better patient outcomes through informed decision-making.

The results indicate whether the cancer is hormone receptor-positive or HER2-positive. This information is vital for oncologists to recommend appropriate therapies, which may include hormone therapy, chemotherapy, or targeted therapies.
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 →
PreparationConfirm with the laboratory before booking. A doctor’s prescription is required.
SampleTissue sample from the modified radical mastectomy.
MethodologyImmunohistochemistry (IHC) is typically used to assess 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.
Results are based on the specific tissue sample provided. Test accuracy depends on proper sample collection and handling. This test does not provide information on all possible genetic mutations associated with breast cancer.
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

This test measures the presence of estrogen receptors (ER), progesterone receptors (PR), and HER2/neu protein in breast tissue.
It helps determine the specific characteristics of breast cancer, guiding doctors in choosing the most effective treatment plan.
A tissue sample obtained during a modified radical mastectomy is required for this test.
Confirm with the laboratory before booking.
The results indicate if the cancer cells have receptors for estrogen or progesterone (ER/PR positive) or overexpress the HER2 protein (HER2 positive), which influences treatment options.
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.

Explore partnerships
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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