Idelalisib immune-related toxicity is associated with improved treatment response Journal Article


Authors: Wagner-Johnston, N. D.; Sharman, J.; Furman, R. R.; Salles, G.; Brown, J. R.; Robak, T.; Gu, L.; Xing, G.; Chan, R. J.; Rajakumaraswamy, N.; Gopal, A. K.
Article Title: Idelalisib immune-related toxicity is associated with improved treatment response
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. © 2021 Informa UK Limited, trading as Taylor & Francis Group.
Keywords: follicular lymphoma; chronic lymphocytic leukemia; indolent non-hodgkin lymphoma; idelalisib; pi3k inhibitor; immune-related adverse event
Journal Title: Leukemia and Lymphoma
Volume: 62
Issue: 12
ISSN: 1042-8194
Publisher: Taylor & Francis Group  
Date Published: 2021-12-01
Start Page: 2915
End Page: 2920
Language: English
DOI: 10.1080/10428194.2021.1948038
PUBMED: 34319205
PROVIDER: scopus
PMCID: PMC9247649
DOI/URL:
Notes: Article -- Export Date: 1 December 2021 -- Source: Scopus
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  1. Gilles Andre Salles
    269 Salles