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Medical information Clinical review pending

Genetic Testing

EGFR Mutational Analysis Test

The EGFR Mutational Analysis Test identifies mutations in the EGFR gene, common in non-small cell lung cancer, to guide personalized treatment decisions.

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) tumor tissue block. The block must contain a minimum of 10% tumor cells.
Results
Reports are typically available by Friday or Tuesday, depending on the submission day (Monday or Thursday). Confirm with the laboratory before booking.
Preparation
Ensure the FFPE block is properly labeled. Submit a copy of the Histopathology report and a completed NGS Test Requisition Form (Form 40) with the sample.
Test priceKSh 20,000

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 EGFR Mutational Analysis Test 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.

  • ✓Patients diagnosed with non-small cell lung cancer (NSCLC)
  • ✓Individuals with suspected NSCLC
  • ✓Patients experiencing symptoms suggestive of lung cancer (e.g., persistent cough, chest pain)
  • ✓Patients for whom targeted therapy is being considered
  • ✓Patients with advanced or metastatic NSCLC
02

In plain language

What this test helps you understand

Identifies specific mutations in the EGFR gene associated with non-small cell lung cancer, guiding the selection of targeted therapies and improving treatment outcomes.
The EGFR Mutational Analysis Test is a diagnostic tool used to identify mutations in the epidermal growth factor receptor (EGFR) gene. These mutations are frequently found in non-small cell lung cancer (NSCLC) and can significantly influence treatment choices and patient outcomes. Understanding if these mutations are present helps doctors select the most effective therapies. This test is particularly important for patients diagnosed with cancer, as it provides crucial information for tailoring treatment plans. The test specifically looks for changes in the EGFR gene, which controls cell growth. Mutations can cause cells to grow uncontrollably, leading to cancer. Identifying these mutations allows healthcare providers to determine the best course of action for managing the condition. Patients diagnosed with non-small cell lung cancer, or those experiencing symptoms like a persistent cough, chest pain, or unexplained weight loss, should discuss this test with their doctor. Individuals with risk factors like a history of smoking may also benefit. This test helps create personalized treatment plans, predict how well a patient might respond to specific targeted therapies, and improve overall cancer management by providing oncologists with critical information for informed decision-making. Results indicate whether EGFR mutations are present. A positive result may mean the patient is eligible for targeted therapies, while a negative result helps guide other treatment options. Discussing the results with your oncologist is essential to understand their meaning for your specific treatment plan.
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 →
PreparationEnsure the FFPE block is properly labeled. Submit a copy of the Histopathology report and a completed NGS Test Requisition Form (Form 40) with the sample.
SampleFormalin-fixed paraffin-embedded (FFPE) tumor tissue block. The block must contain a minimum of 10% tumor cells.
MethodologyMolecular genetic testing techniques are used to detect mutations in the EGFR gene.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
The test requires adequate tumor tissue in the FFPE block (minimum 10% tumor cells). Results are specific to the mutations tested. 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

The EGFR gene provides instructions for making a protein called epidermal growth factor receptor. This protein helps cells grow, divide, and reproduce. Mutations in this gene can lead to uncontrolled cell growth, contributing to cancer.
Certain mutations in the EGFR gene are common in non-small cell lung cancer (NSCLC). Identifying these mutations helps doctors determine if a patient might benefit from specific targeted therapies designed to block the mutated EGFR protein.
A formalin-fixed paraffin-embedded (FFPE) block containing tumor tissue is required. The block needs to have at least 10% tumor cells.
Results are typically available by Friday or Tuesday, depending on the submission day (Monday or Thursday). Confirm with the laboratory before booking.
The results will indicate whether specific mutations in the EGFR gene were detected in the tumor sample. Your doctor will interpret these results in the context of your overall health and cancer diagnosis to recommend the best treatment plan.
Insurance coverage varies. Please check with your insurance provider regarding coverage for this specific test.
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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