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Medical information Clinical review pending

Genetic Testing

Liquid Biopsy Cancer Therapy Chemo Sensitivity Test

A genetic test using a blood sample to help guide cancer treatment decisions by assessing potential sensitivity to chemotherapy and natural substances.

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
Blood sample (specific volume and tube type to be confirmed with the laboratory).
Results
Confirm with the laboratory before booking. Results are typically available within 10 days.
Preparation
Confirm with the laboratory before booking. Generally, no special preparation is required, but fasting may be requested. Follow any specific instructions provided by the laboratory or your doctor.
Test priceKSh 40,000

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 Biopsy Cancer Therapy Chemo Sensitivity 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 cancer
  • ✓Individuals seeking personalized cancer treatment options
  • ✓Patients exploring chemotherapy sensitivity
  • ✓Patients considering alternative cancer therapies
  • ✓Assisting oncologists in treatment planning
02

In plain language

What this test helps you understand

This test aims to provide information about potential drug sensitivity for cancer patients, assisting clinicians in selecting therapies. It is intended to complement, not replace, standard diagnostic procedures and clinical judgment.
The Liquid Biopsy Cancer Therapy Chemo Sensitivity Test is a diagnostic tool for cancer patients exploring personalized treatment options. It analyzes circulating tumor DNA (ctDNA) from a blood sample to provide insights into how an individual's cancer might respond to various therapies, including chemotherapy and natural substances.

This test evaluates the sensitivity of cancer cells to different drugs. Using advanced Next Generation Sequencing (NGS) DNA sequencing technology, it identifies which therapies may be most effective for the patient, supporting a more personalized approach to cancer treatment.

This test is particularly beneficial for individuals who have a current cancer diagnosis and are seeking more information about personalized treatment options or wish to understand how their cancer cells respond to specific drugs.

Taking this test can provide personalized treatment recommendations based on individual cancer biology. It helps oncologists make informed decisions regarding chemotherapy and alternative therapies, potentially improving treatment outcomes and reducing exposure to ineffective drugs.

Results are typically available within 10 days. Your healthcare provider will explain the findings, indicating which drugs may be most effective for your specific cancer type. This information helps patients and doctors make informed decisions about the treatment journey.
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. Generally, no special preparation is required, but fasting may be requested. Follow any specific instructions provided by the laboratory or your doctor.
SampleBlood sample (specific volume and tube type to be confirmed with the laboratory).
MethodologyNext Generation Sequencing (NGS) DNA sequencing technology is used to analyze circulating tumor DNA (ctDNA) from a blood sample.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test analyzes ctDNA present in the blood, which may not always fully represent the genetic makeup of the primary tumor or metastases. Results indicate potential sensitivity and do not guarantee treatment success or predict side effects. The test's predictive accuracy can vary depending on the cancer type, stage, and the amount of ctDNA in the sample. 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

A liquid biopsy is a test performed on a sample of blood to look for cancer cells or pieces of DNA from tumors that are circulating in the blood.
A sample of your blood will be drawn.
Results are typically available within 10 days, but confirm with the laboratory before booking.
Insurance coverage varies. Please check with your insurance provider regarding coverage for this specific test.
Your doctor or oncologist will interpret the results in the context of your overall health and medical history.
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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