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FLT3/ITD Allelic Ratio Test: Booking, Price, and Results

About FLT3/ITD Allelic Ratio Test: Booking, Price, and Results

FieldValue
Also Known AsFLT3 Internal Tandem Duplication Ratio, FLT3-ITD AR, ITD-AR Test, FLT3 Mutation Analysis, FLT3 ITD Mutation DNA Screen/Assay
Sample TypeBone marrow aspirate or peripheral blood (venous)
Fasting RequiredNo
Report Time15 days
Recommended ForAdults diagnosed with or suspected of having acute myeloid leukaemia (AML); all genders
PriceStarting at ₹7,200

What is a FLT3/ITD Allelic Ratio Test?

The FLT3/ITD Allelic Ratio Test is a specialised molecular test that detects and measures a specific genetic mutation in leukaemia cells. It analyses bone marrow or peripheral blood to determine the proportion of mutated FLT3 genes relative to normal ones. Doctors use this test primarily in patients diagnosed with or suspected of having acute myeloid leukaemia (AML). It is also referred to as the FLT3 Internal Tandem Duplication Ratio or ITD-AR Test.

What Does a FLT3/ITD Allelic Ratio Test Measure?

This test uses a method called fragment analysis to detect and quantify a mutation known as an internal tandem duplication (ITD) in the FLT3 gene. The key measurement is the allelic ratio, which compares the amount of mutated FLT3 to the normal (wild-type) FLT3 in the sample.

The table below summarises what the results indicate:

ParameterDescription
ITD Negative (Allelic Ratio = 0)No FLT3-ITD mutation detected in the sample
Low Allelic Ratio (less than 0.5)A smaller proportion of mutated FLT3 genes is present
High Allelic Ratio (0.5 or above)A larger proportion of mutated FLT3 genes is present

Why is a FLT3/ITD Allelic Ratio Test Done?

This test is ordered for patients with newly diagnosed or relapsed AML to guide treatment planning and risk assessment. Here is when it is typically recommended.

Common Symptoms That May Require This Test

Doctors may order the FLT3/ITD Allelic Ratio Test when a patient presents with the following symptoms, which may point to AML:

  • Persistent fatigue or weakness not explained by other causes
  • Shortness of breath even with mild physical activity
  • Unexplained bruising or bleeding
  • Frequent infections due to a weakened immune system
  • Pale skin related to low red blood cell counts
  • Bone pain or tenderness
  • Fever without an obvious cause

Conditions This Test Can Help Detect

The test is specifically used to assess the following:

  • FLT3 internal tandem duplication (FLT3-ITD) mutation, found in approximately 20 to 30% of AML patients
  • Prognostic risk category in AML (to estimate the likely disease outcome)
  • Eligibility for targeted therapy using FLT3 inhibitor drugs
  • Disease status at relapse, where the mutational pattern may have changed

FLT3/ITD Allelic Ratio Test for Chronic Disease Monitoring

The FLT3/ITD Allelic Ratio remains relevant throughout the course of AML treatment. Because FLT3 mutations can be unstable and may change at the time of relapse or disease progression, the test may be repeated to guide decisions about targeted therapy with FLT3 inhibitors. Monitoring the allelic burden over time helps clinicians adapt treatment strategies as the disease evolves.

How to Prepare and What to Expect

No special preparation is needed for the FLT3/ITD Allelic Ratio Test procedure, but there are a few practical points to keep in mind before your appointment.

Do You Need to Fast?

No fasting is required for this test. You can eat and drink normally before your appointment.

Practical Tips Before Your Test

Keep the following in mind before sample collection:

  • Bring a detailed clinical history, including your symptoms, previous test results, and any relevant medical records, as this information is required for the test.
  • Inform your doctor or the collection team about any medications you are currently taking.
  • Let your doctor know if you have had any recent infections or procedures, as these may affect the sample.
  • Bone marrow aspirate is the preferred sample for the most accurate results; peripheral blood may be used if bone marrow cannot be collected.
  • Samples should ideally contain at least 5% tumour cells for reliable detection.

Step-by-Step Procedure

Two types of samples may be collected for this test. Below is what you can expect for each.

Peripheral Blood Collection:

  • A healthcare professional cleans the skin on your arm with an antiseptic wipe.
  • A needle is gently inserted into a vein, usually in the inner elbow, to draw 3 ml of blood.
  • The blood is collected into a lavender-top EDTA tube and labelled with your details.
  • The needle is removed, and light pressure is applied to stop any minor bleeding.

Bone Marrow Aspirate Collection:

  • You will be positioned lying down, and the skin over the collection site (typically the hip bone) is cleaned and numbed with a local anaesthetic.
  • A specialist inserts a thin needle into the bone and withdraws a small amount of liquid bone marrow (approximately 3 ml), collected into a sodium heparin (green-top) tube.
  • The site is cleaned and covered with a small dressing after collection.
  • Both sample types are stored at 2 to 8°C and sent to the laboratory promptly, ideally within 48 hours of collection.
  • In the lab, the sample undergoes fragment analysis, a method that uses polymerase chain reaction (PCR) and capillary electrophoresis to detect and measure the FLT3-ITD mutation.

Factors That Can Affect Accuracy

The following factors may influence the accuracy of your results:

  • Low tumour cell content in the sample, which can underestimate the true allelic ratio
  • Delays in sample transport or improper storage conditions
  • The proportion of normal versus abnormal cells in the collected sample
  • Laboratory methodology and equipment used for fragment analysis

Understanding Your FLT3/ITD Allelic Ratio Test Results

Results from the FLT3/ITD Allelic Ratio Test must always be reviewed with your haematologist or oncologist, who will consider them alongside your full clinical picture. The table below provides a general guide to interpreting the allelic ratio.

ResultAllelic RatioGeneral Interpretation
Negative0No FLT3-ITD mutation detected
Low Allelic RatioLess than 0.5Lower FLT3-ITD mutant burden
High Allelic Ratio0.5 or aboveHigher FLT3-ITD mutant burden

These ranges are general guidelines. Your doctor will interpret your results based on your age, health history, and other factors. Always consult a qualified healthcare professional for personalised medical advice.

Note: Under the 2022 European LeukemiaNet (ELN) guidelines, all FLT3-ITD-positive patients are now classified as intermediate risk, regardless of allelic ratio or NPM1 status. Your doctor will interpret your results using the most current clinical guidelines.

Results During Special Conditions

Samples that contain a low percentage of leukaemia cells (blasts) may appear to have a lower allelic ratio than the true value, as non-malignant cells dilute the mutant signal. Because FLT3 mutations can change at relapse or after treatment, results obtained at diagnosis may differ from those obtained later in the course of the disease. For this reason, this test is not considered a reliable tool for detecting minimal residual disease.

How to Maintain Healthy Levels

Because this is a genetic mutation test used in cancer diagnosis and monitoring, the concept of "healthy levels" does not apply in the same way as routine blood tests. The following general points may support your overall well-being during treatment:

  • Follow your haematologist's or oncologist's treatment and monitoring plan closely.
  • Attend all scheduled follow-up appointments and repeat testing as advised by your medical team.
  • Maintain a balanced diet and adequate rest to support your body during treatment.

Lupin Diagnostics FLT3/ITD Allelic Ratio Test Price

The FLT3/ITD Allelic Ratio Test cost at Lupin Diagnostics starts at ₹7,200. This test requires a visit to a Lupin Diagnostics centre; home collection is not available for this test due to its specialised sample collection requirements.

CityApproximate Price (₹)
BHOPAL7200
CHENNAI7200
HYDERABAD7200
KOLKATA7200
NAVI MUMBAI7200
PUNE7200

Prices are indicative and may vary by location. Please confirm the current price at the time of booking.

How to Book

Booking your FLT3/ITD Allelic Ratio Test online at Lupin Diagnostics is straightforward:

  • Select the test on the Lupin Diagnostics website.
  • Choose your city and preferred centre location.
  • Visit the centre at your scheduled time for sample collection.
  • Receive your report via email or WhatsApp within the stipulated turnaround time.

Frequently Asked Questions

The FLT3/ITD Allelic Ratio Test measures the proportion of mutated FLT3 genes to normal FLT3 genes in a patient's blood or bone marrow. It is used to determine prognosis and guide treatment decisions in patients with acute myeloid leukaemia (AML). The result helps doctors decide on the most appropriate therapy, including whether targeted FLT3 inhibitor drugs are suitable.

This test is recommended for all patients newly diagnosed with AML, as FLT3-ITD mutations are found in approximately 20 to 30% of cases. It may also be repeated at relapse or disease progression. Your haematologist will advise whether this test is appropriate for your situation.

Bone marrow aspirate is the preferred sample because it provides the most accurate representation of leukaemia cell content. However, peripheral blood can be used if bone marrow cannot be obtained. Your doctor will decide which sample type is most appropriate based on your clinical condition.

A higher allelic ratio indicates a larger proportion of mutated FLT3 genes, which has historically been associated with a less favourable outlook. Patients with a positive FLT3-ITD result may benefit from targeted therapy with FLT3 inhibitor drugs. Your oncologist will explain how your specific result affects your treatment plan.

Under the 2022 European LeukemiaNet guidelines, all FLT3-ITD-positive patients are classified as intermediate risk, regardless of their allelic ratio. This change was made partly due to difficulties in standardising how the allelic ratio is measured across laboratories. The allelic ratio still provides useful information for treatment planning, even if it is no longer the basis for formal risk classification.

At Lupin Diagnostics, the report is typically available within 15 days of sample collection. The specialised nature of fragment analysis means turnaround times are longer than routine blood tests. Your doctor will receive the report and discuss the findings with you.

No fasting or special dietary preparation is needed. However, you must bring a detailed clinical history, including your symptoms, previous test results, and relevant medical records, as this is required for the test. Inform the collection team about any medications you are taking before your appointment.

FLT3/ITD Allelic Ratio Test: Booking, Price, and Results

Price
7,200.00
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