Please use this identifier to cite or link to this item: https://doi.org/10.1002/ijc.33822
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dc.titleRisk factors for immune-related adverse events from anti-PD-1 or anti-PD-L1 treatment in an Asian cohort of nonsmall cell lung cancer patients
dc.contributor.authorHuang, Yiqing
dc.contributor.authorSoon, Yu Yang
dc.contributor.authorAminkeng, Folefac
dc.contributor.authorTay, Sen Hee
dc.contributor.authorAng, Yvonne
dc.contributor.authorKee, Adrian CL
dc.contributor.authorGoh, Boon Cher
dc.contributor.authorWong, Alvin SC
dc.contributor.authorSoo, Ross A
dc.date.accessioned2022-12-01T03:13:10Z
dc.date.available2022-12-01T03:13:10Z
dc.date.issued2021-10-13
dc.identifier.citationHuang, Yiqing, Soon, Yu Yang, Aminkeng, Folefac, Tay, Sen Hee, Ang, Yvonne, Kee, Adrian CL, Goh, Boon Cher, Wong, Alvin SC, Soo, Ross A (2021-10-13). Risk factors for immune-related adverse events from anti-PD-1 or anti-PD-L1 treatment in an Asian cohort of nonsmall cell lung cancer patients. INTERNATIONAL JOURNAL OF CANCER 150 (4) : 636-644. ScholarBank@NUS Repository. https://doi.org/10.1002/ijc.33822
dc.identifier.issn0020-7136
dc.identifier.issn1097-0215
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/235038
dc.description.abstractImmune-related adverse events (IrAEs) of immune checkpoint inhibitors (ICIs) can be serious and unpredictable. We examine the incidence rate and risk factors for IrAEs in an Asian cohort of nonsmall cell lung cancer (NSCLC) patients treated with immunotherapy. Between June 2014 and August 2020, we retrospectively analysed IrAEs in NSCLC patients treated with anti-PD-1 or anti-PD-L1 inhibitors at the National University Cancer Institute, Singapore. A Poisson regression model was used to estimate the effect of risk factors on incidence rate of any grade IrAEs. One hundred and forty-one patients were enrolled. Median age was 63. Majority were male (67%) with Eastern Cooperative Oncology Group (ECOG) PS 0-1 (77%). More than half (56%) received pembrolizumab. Eleven percent harboured epidermal growth factor receptor (EGFR) mutation. Eighteen percent received concomitant chemotherapy. Median number of cycles was 4, and median duration of treatment was 2.1 months. IrAEs were seen in 71 (50.4%) patients, with an incidence rate of 99 events per 1000 person-months. Fatigue (25%), rash (10.5%) and pneumonitis (7.9%) were the most common IrAEs. Twenty out of 152 IrAEs (13.2%) were Grade 3 or higher in severity: most common being pneumonitis (5.3%), fatigue (3.3%) and transaminitis (1.3%). Multivariable analysis demonstrated that concomitant chemotherapy use, higher BMI and presence of EGFR mutation are significant predictors for IrAEs (P <.0001; P =.016; P =.007). Our findings can help guide risk stratification and monitoring of IrAEs among NSCLC patients on immunotherapy.
dc.language.isoen
dc.publisherWILEY
dc.sourceElements
dc.subjectScience & Technology
dc.subjectLife Sciences & Biomedicine
dc.subjectOncology
dc.subjectimmune checkpoint inhibitors
dc.subjectimmune-related adverse events
dc.subjectnonsmall cell lung cancer
dc.subjectCHECKPOINT INHIBITORS
dc.subjectCHEMOTHERAPY
dc.subjectPEMBROLIZUMAB
dc.subjectIPILIMUMAB
dc.subjectNIVOLUMAB
dc.subjectTOXICITY
dc.subjectASSOCIATION
dc.subjectCARBOPLATIN
dc.subjectCOMBINATION
dc.subjectBLOCKADE
dc.typeArticle
dc.date.updated2022-11-30T16:04:23Z
dc.contributor.departmentCANCER SCIENCE INSTITUTE OF SINGAPORE
dc.contributor.departmentMEDICINE
dc.description.doi10.1002/ijc.33822
dc.description.sourcetitleINTERNATIONAL JOURNAL OF CANCER
dc.description.volume150
dc.description.issue4
dc.description.page636-644
dc.published.statePublished
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