Understanding Your CLL Genetic Profile: Take Control of Your Treatment Journey
When facing chronic lymphocytic leukaemia, understanding your specific genetic mutations can be the difference between uncertainty and a clear treatment path. Our CLL Mutations Detection Panel 2 provides the comprehensive genetic insights you and your oncologist need to make informed decisions about your care.
What This Test Reveals About Your CLL
This advanced genetic panel examines 10 critical markers that significantly impact your CLL prognosis and treatment response. We analyse specific mutations including SF3B1 K700E, MYD88 L265P, and NOTCH1, along with important chromosomal changes like 11q deletion, 17p deletion, and trisomy 12. These genetic factors help determine how aggressive your CLL might be and which treatments are most likely to be effective.
Who Should Consider This Genetic Testing?
This test is particularly important if you:
- Have recently been diagnosed with CLL and want to understand your prognosis
- Are experiencing symptoms like fatigue, swollen lymph nodes, or frequent infections
- Have a family history of blood cancers or leukaemia
- Are considering treatment options and want genetic guidance
- Have had previous CLL treatment and need updated genetic information
Early genetic profiling can help your oncologist create the most effective treatment strategy from the start.
Why Genetic Testing Matters for Your CLL Journey
Understanding your specific CLL mutations provides several crucial benefits:
- Personalised Treatment: Identifies which therapies will work best for your genetic profile
- Prognostic Clarity: Helps predict disease progression and aggressiveness
- Treatment Timing: Guides decisions about when to start treatment
- Clinical Trial Matching: Opens doors to targeted therapy trials
- Peace of Mind: Reduces uncertainty about your treatment path
Understanding Your Test Results
Our expert team provides clear, comprehensive reports that your oncologist can immediately use in your treatment planning. We explain what each mutation means for your specific situation and provide guidance on next steps. Remember, genetic information is powerful – it helps your medical team create the most effective approach to managing your CLL.
Transparent Pricing – Exceptional Value
| Test Option | Regular Price | Special Price | Savings |
|---|---|---|---|
| CLL Mutations Detection Panel 2 | ZAR 1,700 | ZAR 800 |
This comprehensive genetic analysis represents exceptional value compared to the cost of ineffective treatments or delayed care.
Why Trust Oracle Genomics?
- Nationwide Coverage: Accessible testing centres in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Expert Oncology Team: Specialised genetic counsellors and haematologists
- Advanced Technology: PCR-MLPA methodology for accurate, reliable results
- Fast Turnaround: Sample Monday by 11am, results by Saturday
- Comprehensive Support: Clear result explanations and ongoing guidance
Take the Next Step in Your CLL Journey
Don’t let uncertainty about your genetic profile delay effective treatment. Early detection of these critical mutations can significantly improve your treatment outcomes and quality of life.
Limited Time Offer: Save ZAR 800 on this comprehensive genetic panel. Take control of your CLL treatment journey today.
Test Specifications
Sample Required: 4 mL (2 mL min.) whole blood from 1 Lavender top (EDTA) tube. Ship refrigerated. DO NOT FREEZE.
Mandatory: Duly filled Genomics Clinical Information Requisition Form (Form 20)
Testing Method: PCR – MLPA
Specialty: Oncologist/Haematologist
