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Idelalisib immune-related toxicity is associated with improved treatment response. | LitMetric

AI Article Synopsis

  • Clinical observations indicate that these irAEs may correlate with better survival outcomes, but this connection is less clear in blood cancers compared to solid tumors.
  • A post hoc analysis of trials showed that severe diarrhea/colitis and elevated liver enzymes associated with idelalisib treatment led to higher response rates and longer survival in patients with indolent non-Hodgkin lymphoma and other related conditions.

Article Abstract

Idelalisib is associated with increased occurrence of immune-related adverse events (irAEs). Clinical observations suggest a correlation between immune checkpoint inhibitor-induced irAEs and survival outcomes in patients with solid tumors; however, this relationship in hematologic malignancies is not well understood. In a post hoc analysis of 3 registrational trials, we explored the relationship between Grade ≥3 diarrhea/colitis and alanine/aspartate transaminase (ALT/AST) elevation incidences and efficacy endpoints in patients with indolent non-Hodgkin lymphoma (iNHL), follicular lymphoma (FL), and chronic lymphocytic leukemia treated with idelalisib. Grade ≥3 diarrhea/colitis was associated with higher overall response rate (ORR) and longer progression-free survival (PFS) for all subgroups. Grade ≥3 ALT/AST elevations were associated with improved duration of response and overall survival for all subgroups and improved ORR and PFS for patients with FL or iNHL. Our analysis in hematologic malignancies showed a trend correlating idelalisib-induced Grade ≥3 irAEs with improved efficacy.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9247649PMC
http://dx.doi.org/10.1080/10428194.2021.1948038DOI Listing

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