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Epidermal growth factor receptor (EGFR) mutation status in plasma by targeted next-generation sequencing (NGS)

Published: August 9, 2026Updated: August 16, 2026

This test checks for specific genetic changes in a protein called EGFR that may be linked to certain types of lung cancer. These changes can help determine if a targeted cancer treatment might be effective for you.

Quick summary

["Helps guide personalized cancer treatment options based on genetic test results."]

Medically reviewed by WellAlly Editorial TeamLast reviewed August 16, 2026Editorial policy

Key facts at a glance

LOINC
96310-8
Short code
S epidermidis DNA Bld Pos Ql NAA+non-prb
Synonyms
S epidermidis DNA Bld Pos Ql NAA+non-prb
Category
chemistry
Sample
whole-blood
Container
Lavender-top (EDTA)
Units
N/A
Fasting
false
Population
adult
Sex
all
Age range
18–65 years
Method
non-probe-amp-tar
Specimen volume
3 mL
Stability
Room temperature: 4h, Refrigerated: 24h
Hemolysis max
0
Lipemia max
0
Icterus max
0
TAT
4–24 hours
Order
routine

Why This Test Is Done

Your doctor may recommend this test if you have lung cancer and certain genetic markers suggest EGFR mutations. It’s also used in monitoring treatment response or assessing recurrence in patients with known EGFR-positive cancers.

What to Expect Before the Test

A simple blood draw is used to collect plasma. No special preparation is needed, but inform your doctor about any medications or supplements you’re taking, as they may affect results.

How the Test Works

Plasma is analyzed using advanced sequencing technology to detect small genetic changes in EGFR. These changes are compared against a reference database to identify mutations linked to cancer growth.

What the Results Mean

Positive results indicate the presence of EGFR mutations, which may influence treatment choices like targeted therapies or immunotherapy. Negative results mean no detectable mutations in this test.

Clinical interpretation

How abnormal results are interpreted and what conditions they suggest.

Clinical significance: EGFR mutations are actionable targets in about 10–20% of lung cancer cases, particularly in non-small cell lung cancer (NSCLC). These mutations can help tailor treatment to slow or stop cancer progression, but results must be interpreted alongside clinical factors and other genetic tests.

Short name

EGFR Mutation Test (Plasma)

Frequently asked questions

What does a positive result mean for my treatment options?
A positive result suggests EGFR mutations may be present, which could qualify you for targeted therapies like EGFR tyrosine kinase inhibitors (TKIs). Your doctor will discuss these options based on your full medical picture, including other test results and cancer stage.
How long will it take to get my results?
Results typically take 1–3 weeks, depending on lab processing times and whether additional confirmatory testing is needed. Your doctor will contact you once results are available.
Can I stop taking medications before this test?
No special medication changes are required. However, inform your doctor about all current medications, including supplements, as they may affect test accuracy or your treatment plan.
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This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 16, 2026. · Read our editorial policy