Evaluation of the CLL-IPI in relapsed and refractory chronic lymphocytic leukemia in idelalisib phase-3 trials.
Jacob D SoumeraiAi NiGuan XingJulie HuangRichard R FurmanJeffrey JonesJeffrey P SharmanMichael HallekAdeboye H AdewoyeRonald DubowyLyndah DreilingAndrew D ZelenetzPublished in: Leukemia & lymphoma (2018)
The CLL-IPI is a risk-weighted prognostic model for previously untreated patients with chronic lymphocytic leukemia (CLL), but has not been evaluated in patients with relapsed CLL or on novel therapies. We evaluated the CLL-IPI in 897 patients with relapsed/refractory CLL in 3 randomized trials testing idelalisib (PI3Kδ inhibitor). The CLL-IPI identified patients as low (2.2%), intermediate (12.8%), high (48.7%), and very high (36.2%) risk and was prognostic for survival (log-rank p < .0001; C-statistic 0.706). Of CLL-IPI factors, age >65, β2-microglobulin >3.5mg/L, unmutated immunoglobulin heavy chain variable region gene, and deletion 17p/TP53 mutation were independently prognostic, but Rai I-IV or Binet B/C was not. The CLL-IPI is prognostic for survival in relapsed CLL and with idelalisib therapy. However, low/intermediate risk is uncommon, and regression parameters of individual factors in this risk-weighted model appear different in relapsed CLL. Reassessment of the weighting of the individual variables might optimize the model in this setting.
Keyphrases
- chronic lymphocytic leukemia
- acute lymphoblastic leukemia
- acute myeloid leukemia
- multiple myeloma
- diffuse large b cell lymphoma
- hodgkin lymphoma
- magnetic resonance
- end stage renal disease
- newly diagnosed
- chronic kidney disease
- stem cells
- magnetic resonance imaging
- dna methylation
- ejection fraction
- mesenchymal stem cells
- bone marrow
- peritoneal dialysis