Understanding Your CLL Journey: Advanced Genetic Insights for Better Treatment Decisions
When facing a chronic lymphocytic leukaemia diagnosis, uncertainty can feel overwhelming. You deserve clear answers about your specific genetic profile to guide your treatment path. Our comprehensive CLL NGS Panel provides the precise genetic information oncologists need to create personalised treatment strategies that work for your unique condition.
What This Advanced CLL Test Reveals About Your Health
This comprehensive panel combines four critical genetic analyses to give you and your doctor a complete picture of your CLL:
- FISH Analysis: Identifies specific chromosomal abnormalities that affect disease progression
- Karyotyping: Examines your complete chromosome set for structural changes
- IGHV Mutation Status: Determines if your CLL has mutated or unmutated IGHV genes, crucial for prognosis
- TP53 Mutation Analysis: Detects mutations in the TP53 tumour suppressor gene that impact treatment response
Using next-generation sequencing (NGS) technology, we provide the most accurate genetic profiling available in South Africa.
Who Should Consider This Comprehensive CLL Testing?
This test is essential if you’re experiencing:
- Recent CLL diagnosis requiring treatment planning
- Unexplained fatigue, night sweats, or weight loss
- Enlarged lymph nodes or spleen
- Recurrent infections or abnormal blood counts
- Family history of blood cancers
- Need for treatment response monitoring
Early genetic profiling can significantly impact your treatment success and quality of life.
Why Comprehensive Genetic Testing Matters for Your CLL Journey
Understanding your specific genetic profile transforms your treatment experience:
- Personalised Treatment: Match therapies to your genetic markers for better outcomes
- Prognostic Clarity: Understand your disease’s likely progression pattern
- Treatment Selection: Avoid ineffective therapies and potential side effects
- Peace of Mind: Make informed decisions with confidence
- Early Intervention: Identify high-risk features requiring immediate attention
Understanding Your Results: Clear Guidance Every Step
Your comprehensive report will include:
- Clear explanation of all genetic findings in patient-friendly language
- Specific implications for treatment options and prognosis
- Recommendations for discussion with your oncologist
- Follow-up testing suggestions if needed
- Access to our genetic counselling team for questions
We ensure you understand what your results mean for your health journey.
Transparent Pricing – Exceptional Value for Advanced Care
| Test Component | Regular Price | Special Price | Savings |
|---|---|---|---|
| Complete CLL NGS Panel | ZAR 17,350 | ZAR 13,000 | ZAR 4,350 |
Includes: FISH analysis, karyotyping, IGHV mutation status, and TP53 mutation analysis using NGS technology
Turnaround Time: 3 weeks from sample receipt
Sample Required: Peripheral blood + FFPE block
Components: Sodium Heparin Vacutainer (2ml) + EDTA Vacutainer (2ml)
Why South Africans Trust Oracle Genomics for CLL Testing
- Nationwide Coverage: Accessible testing in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise: Specialised oncology genetic testing with gynecologist oversight
- Advanced Technology: Cutting-edge NGS, PCR, and FISH methodologies
- Accuracy Guarantee: Rigorous quality control for reliable results
- Patient Support: Compassionate guidance throughout your testing journey
Take Control of Your CLL Treatment Journey Today
Don’t let uncertainty dictate your treatment path. With comprehensive genetic insights, you and your doctor can make informed decisions that may significantly improve your outcomes.
Important Note: This test requires a doctor’s prescription, except for surgery, pregnancy cases, or international travel planning.
Early genetic profiling can change your treatment trajectory. Book your comprehensive CLL NGS Panel today and gain the clarity you deserve for your health journey.
