Real-life efficacy and safety of idelalisib in 55 double-refractory follicular lymphoma patients

Br J Haematol. 2022 Nov;199(3):339-343. doi: 10.1111/bjh.18426. Epub 2022 Aug 24.

Abstract

Idelalisib, a reversible inhibitor of PI3Kδ (phosphoinositide-3 kinase delta), showed remarkable activity in the phase II DELTA trial, leading to its approval by the European Medicines Agency (EMA) in patients with relapsed/refractory (R/R) follicular lymphoma (FL). However, real-life data on idelalisib are scarce. We treated 55 double-refractory FL patients with idelalisib in a real-life setting. With a median exposure to idelalisib of 10 months (range 1-43), overall response rate was 73%, the highest ever reported. Non-haematological toxicities were mild and manageable. At 12 months, 80% of patients were alive, and 72% disease-free. The efficacy and safety of idelalisib was confirmed in a real-life setting.

Keywords: PI3Kδ; follicular lymphoma; idelalisib; relapsed/refractory.

Publication types

  • Clinical Trial, Phase II
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents* / adverse effects
  • Humans
  • Leukemia, Lymphocytic, Chronic, B-Cell* / drug therapy
  • Lymphoma, Follicular* / drug therapy
  • Phosphatidylinositols / therapeutic use
  • Quinazolinones / adverse effects

Substances

  • Antineoplastic Agents
  • idelalisib
  • Phosphatidylinositols
  • Quinazolinones