| Literature DB >> 31574022 |
Fausto Petrelli1, Giulia Grizzi2, Michele Ghidini3, Antonio Ghidini4, Margherita Ratti2, Stefano Panni2, Mary Cabiddu1, Mara Ghilardi1, Karen Borgonovo1, Maria C Parati1, Gianluca Tomasello2, Sandro Barni1, Alfredo Berruti5, Matteo Brighenti2.
Abstract
Immune-related adverse events (irAEs) are autoimmune-toxic effects associated with immune checkpoint inhibitors (ICIs) used for the treatment of advanced solid tumors. We performed a systematic review and meta-analysis of the published literature to assess the outcome for cancer patients treated with ICIs who develop irAEs. Two independent reviewers selected prospective or retrospective studies from PubMed, EMBASE, and the Cochrane Library database from their inception to November 2018. Data were pooled using hazard ratios (HRs) for overall survival or progression-free survival or odds ratio for overall response rate of irAEs versus no irAEs according to fixed or random-effect model. HRs for OS (the primary outcome measure) were pooled to provide an aggregate value. A total of 30 studies that included a total of 4324 patients treated with ICIs were selected. Patients who developed irAEs presented a reduced risk of death [HR=0.49, 95% confidence interval (CI): 0.38-0.62; P<0.001]. Similarly, the occurrence of irAEs was associated with a reduced risk of progression (HR=0.51, 95% CI: 0.42-0.64; P<0.001). The odds of response was 4.56 (95% CI: 3.72-5.59; P<0.001). In patients treated with ICIs, irAEs predict survival and response. Although this correlation cannot be fully explained, it may be related to the strongest T-cell activation.Entities:
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Year: 2020 PMID: 31574022 DOI: 10.1097/CJI.0000000000000300
Source DB: PubMed Journal: J Immunother ISSN: 1524-9557 Impact factor: 4.456