| Literature DB >> 30407886 |
Jacob D Soumerai1,2, Ai Ni2, Guan Xing3, Julie Huang3, Richard R Furman4, Jeffrey Jones5, Jeffrey P Sharman6, Michael Hallek7, Adeboye H Adewoye3, Ronald Dubowy3, Lyndah Dreiling3, Andrew D Zelenetz2.
Abstract
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.Entities:
Keywords: CLL-IPI; Chronic lymphocytic leukemia; idelalisib; leukemia; lymphoma; prognostication
Year: 2018 PMID: 30407886 PMCID: PMC6545166 DOI: 10.1080/10428194.2018.1540782
Source DB: PubMed Journal: Leuk Lymphoma ISSN: 1026-8022