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Haematology A

CLL-IPI (International Prognostic Index for CLL)

Integrates genetic, biological, and clinical factors to predict outcome in CLL. Score 0–10.

Score interpretation

Low Risk 0–1

Low risk. 5-year OS ~93%.

→ Watch and wait. Annual review.

Intermediate Risk 2–3

Intermediate risk. 5-year OS ~79%.

→ Monitoring every 3–6 months. Treat when active disease criteria met.

High Risk 4–6

High risk. 5-year OS ~64%.

→ Consider early treatment in clinical trial. BTK inhibitors or venetoclax-based regimens preferred.

Very High Risk 7–10

Very high risk. 5-year OS ~23%. TP53 dysfunction likely.

→ BTK inhibitor (ibrutinib/acalabrutinib) or venetoclax-obinutuzumab. Allo-SCT if eligible. Clinical trial strongly preferred.

Interpretation bands for the CLL-IPI. Apply clinical judgement and local guidance.

References

Related

Curated clinical cross-links plus same-class fallbacks.

Decision support only — verify against a current formulary, NICE, or your local guideline before clinical use.