2020
DOI: 10.20892/j.issn.2095-3941.2020.0102
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The mechanism and risk factors for immune checkpoint inhibitor pneumonitis in non-small cell lung cancer patients

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Cited by 62 publications
(62 citation statements)
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“…The definition of CIP is the occurrence of respiratory symptoms/ signs related to a new emerging infiltration viewed on a chest X-ray but excluding new infections tested by sputum and/or bronchoalveolar lavage (BAL) (5). In different tumor types, the overall incidence of CIP varied from 3% to 5% for all grades and ranged from 0.8% to 1.0% for grade ≥ 3 CIP (5,14,25,26). The overall fatality rate of CIP was 10% to 17%.…”
Section: Incidence and Onset Of Cipmentioning
confidence: 99%
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“…The definition of CIP is the occurrence of respiratory symptoms/ signs related to a new emerging infiltration viewed on a chest X-ray but excluding new infections tested by sputum and/or bronchoalveolar lavage (BAL) (5). In different tumor types, the overall incidence of CIP varied from 3% to 5% for all grades and ranged from 0.8% to 1.0% for grade ≥ 3 CIP (5,14,25,26). The overall fatality rate of CIP was 10% to 17%.…”
Section: Incidence and Onset Of Cipmentioning
confidence: 99%
“…In advanced NSCLC, an increasing body of clinical studies suggests that the application of ICIs could achieve significant breakthroughs in PFS and OS (10)(11)(12)(13). Therefore, the US Food and Drug Administration has rapidly incorporated ICIs into firstline therapies for advanced NSCLC (14). In the PACIFIC regimen, durvalumab (a PD-L1 inhibitor) has become the new standard of care after platinum-based chemoradiotherapy for unresectable stage III NSCLC in the United States, Europe, and Japan (15).…”
Section: Introductionmentioning
confidence: 99%
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“…Anti-PD-1 treatment can drive the activation of TILs that have otherwise lost their immunoreactive functionality, thereby restoring their proliferation and cytotoxicity such that the prognosis of treated treatment of NSCLC patients can be significantly improved (102,103). Checkpoint inhibitor pneumonia (CIP) is a particularly dangerous form of immune-related adverse events (IrAE) that can arise in NSCLC patients receiving anti-PD-1/PD-L1 therapy (104,105). Wang et al discovered that the occurrence of CIP changes the proportion of T cell subsets in plasma, thereby promoting increased secretion of IL-35 in plasma and BALF (106).…”
Section: Exploration Of Il-35 and Pd-1/pd-l1 In Cancer Immunotherapymentioning
confidence: 99%