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Medical information Clinical review pending

Cytogenetics

Liquid Bx Cell Free EGFR T790M L858R Exon 19 Deletion

This non-invasive blood test detects specific EGFR gene mutations (T790M, L858R, Exon 19 deletion) in patients with non-small cell lung cancer, helping guide targeted therapy 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
Peripheral blood sample (typically collected in EDTA tubes). Confirm specific requirements with the laboratory before booking.
Results
Confirm with the laboratory before booking.
Preparation
No special preparation is required for this test. However, confirm with the laboratory for any specific instructions.
Test priceKSh 30,000

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 Liquid Bx Cell Free EGFR T790M L858R Exon 19 Deletion 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).
  • ✓Patients with NSCLC experiencing disease progression during EGFR-targeted therapy.
  • ✓Patients where targeted therapy is being considered.
  • ✓Monitoring treatment response in patients with EGFR-mutated NSCLC.
02

In plain language

What this test helps you understand

This test helps identify specific EGFR gene mutations in non-small cell lung cancer (NSCLC) patients. Detecting these mutations can guide the selection of targeted therapies, monitor treatment response, and inform prognosis.
The Liquid Bx Cell Free EGFR T790M L858R Exon 19 Deletion test is a diagnostic tool used in oncology. It analyzes circulating tumor DNA (ctDNA) from a peripheral blood sample to identify specific genetic mutations associated with non-small cell lung cancer (NSCLC).

This test specifically looks for the presence of EGFR T790M and L858R mutations, as well as Exon 19 deletions. These mutations are important because they can indicate how likely a cancer is to respond to certain targeted therapies, such as tyrosine kinase inhibitors.

Identifying these mutations allows healthcare providers to tailor treatment plans to individual patient needs, potentially improving treatment outcomes and quality of life. This test is particularly useful for patients whose cancer has progressed while on EGFR-targeted therapy.
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 special preparation is required for this test. However, confirm with the laboratory for any specific instructions.
SamplePeripheral blood sample (typically collected in EDTA tubes). Confirm specific requirements with the laboratory before booking.
MethodologyThe test utilizes molecular techniques, such as polymerase chain reaction (PCR) or next-generation sequencing (NGS), to detect specific mutations in cell-free DNA isolated from a blood sample. Confirm with the laboratory before booking.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test detects mutations in circulating tumor DNA (ctDNA). The presence or absence of mutations in ctDNA may not always perfectly reflect the mutations present in the primary tumor tissue. A negative result does not completely rule out the presence of these mutations in the tumor. 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

ctDNA is small fragments of DNA released from tumor cells into the bloodstream. Analyzing ctDNA provides a non-invasive way to learn about the genetic makeup of a tumor.
This test identifies specific mutations in the EGFR gene, which can help doctors choose the most effective treatments, particularly targeted therapies, for non-small cell lung cancer.
No, this test is non-invasive. It requires only a blood sample.
Your doctor will interpret the results in the context of your overall health and medical history. A positive result indicates the presence of specific mutations, which may guide treatment decisions.
Yes, a doctor's prescription is generally required for this test, unless you are planning surgery, pregnancy, or traveling abroad. Please check with the laboratory for specific requirements.
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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