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DNA LabsKenya
Medical information Clinical review pending

Cytogenetics

Lung Cancer Panel 1 EGFR ALK1

Detects specific genetic mutations (EGFR, ALK1) in lung cancer tissue to guide personalized treatment options. Essential for patients diagnosed with lung cancer.

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 or unstained slides. Confirm specific requirements with the laboratory before booking.
Results
Confirm with the laboratory before booking.
Preparation
No patient preparation is required for this test. The sample is typically obtained during a biopsy or surgical procedure.
Test priceKSh 36,000

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 Lung Cancer Panel 1 EGFR ALK1 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.

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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.
  • ✓Individuals with advanced or metastatic lung cancer.
  • ✓Patients for whom targeted therapy is being considered.
  • ✓Diagnosis confirmation or treatment guidance for lung cancer.
02

In plain language

What this test helps you understand

This test helps identify specific genetic mutations (EGFR, ALK1) in lung cancer tumors. Detecting these mutations allows doctors to determine if a patient might benefit from targeted therapies designed to address these specific genetic changes, potentially leading to more effective treatment.
The Lung Cancer Panel 1 EGFR ALK1 test is a specialized diagnostic tool used to identify specific genetic mutations linked to lung cancer. This test analyzes tumor tissue for changes in the EGFR (Epidermal Growth Factor Receptor) and ALK1 (Anaplastic Lymphoma Kinase) genes. Understanding these mutations is crucial as they can significantly influence how lung cancer behaves and responds to different treatments. This information helps healthcare providers select the most effective, targeted therapies for individual patients, improving treatment outcomes. This test is particularly important for patients who have been diagnosed with lung cancer, as it can guide personalized treatment strategies.
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 patient preparation is required for this test. The sample is typically obtained during a biopsy or surgical procedure.
SampleFormalin-fixed, paraffin-embedded (FFPE) tumor tissue block or unstained slides. Confirm specific requirements with the laboratory before booking.
MethodologyThis test utilizes molecular techniques, including Fluorescence In Situ Hybridization (FISH) and/or Next Generation Sequencing (NGS) or Sanger Sequencing, to detect specific mutations or rearrangements in the EGFR and ALK1 genes.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test analyzes specific mutations (EGFR, ALK1) and may not detect all possible genetic alterations in lung cancer. Results are based on the quality of the submitted tissue sample. A negative result does not rule out the presence of other mutations or treatment options. 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

This test looks for specific genetic changes (mutations) in the EGFR and ALK1 genes within lung cancer cells. These changes can affect how the cancer grows and responds to treatment.
Identifying these mutations helps doctors choose the most effective treatment plan, particularly targeted therapies that specifically attack cancer cells with these genetic changes.
This test is typically recommended for patients diagnosed with non-small cell lung cancer, especially if targeted therapy is being considered.
The test requires a sample of the tumor tissue, usually obtained from a biopsy or surgery. This is typically formalin-fixed, paraffin-embedded (FFPE) tissue.
Turnaround time varies. Please confirm the current estimated turnaround time with the laboratory before booking.
Yes, this test requires a doctor's prescription or referral.
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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