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Real-world incidences and risk factors of immune-related adverse events in patients treated with immune checkpoint inhibitors: A nationwide retrospective cohort study
DC Field | Value | Language |
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dc.contributor.author | 김용준 | - |
dc.contributor.author | 신상준 | - |
dc.contributor.author | 이명지 | - |
dc.contributor.author | 이승규 | - |
dc.contributor.author | 이충근 | - |
dc.contributor.author | 정인경 | - |
dc.contributor.author | 홍민희 | - |
dc.date.accessioned | 2024-12-06T03:13:14Z | - |
dc.date.available | 2024-12-06T03:13:14Z | - |
dc.date.issued | 2024-08 | - |
dc.identifier.issn | 0304-3835 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/201013 | - |
dc.description.abstract | Immune-related adverse events (irAEs) caused by immune checkpoint inhibitors (ICIs) are rare but fatal, requiring systemic steroid use. Therefore, to examine the outcomes, incidence, timing, and risk factors of ICI-associated steroid-requiring severe irAEs, we conducted a nationwide, retrospective, cohort study utilizing the Korean Health Insurance and Review Assessment database. We identified 357,010 patients with lung cancer, bladder cancer, or skin melanoma, eligible for ICI reimbursement in Korea between January 2012 to June 2020. Steroid-requiring severe irAEs following ICI treatment or treatment-emergent AEs following cytotoxic chemotherapy were defined as moderate- or high-dose steroid administration for over 2 consecutive days, along with corresponding ICD-10 codes indicating affected organ systems. The ICI-exposed group (N = 10,118) was compared to a matched cohort of 55,436 ICI-unexposed patients treated with cytotoxic chemotherapy. Incidences of acute severe irAEs requiring moderate- and high-dose steroids were higher in the ICI-exposed group (1.95% and 6.42%, respectively). The ICI-exposed group also had a higher risk of developing delayed severe irAEs requiring moderate- and high-dose steroid use (3.89% and 7.39%). Male sex, high comorbidity index, or previously diagnosed autoimmune diseases were associated with an increased risk of severe irAEs. Notably, 27.4–38.8% of the patients experienced recurrent severe irAEs after re-challenge with ICIs following moderate- or high-dose steroid use, with the severity matching the initial episode. Steroid-requiring severe irAEs were significantly more prevalent among patients exposed to ICIs than among those treated with chemotherapy in acute and delayed periods. | - |
dc.description.statementOfResponsibility | restriction | - |
dc.language | English | - |
dc.publisher | Elsevier Science Ireland | - |
dc.relation.isPartOf | CANCER LETTERS | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.subject.MESH | Adult | - |
dc.subject.MESH | Aged | - |
dc.subject.MESH | Drug-Related Side Effects and Adverse Reactions / epidemiology | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Immune Checkpoint Inhibitors* / adverse effects | - |
dc.subject.MESH | Incidence | - |
dc.subject.MESH | Lung Neoplasms / drug therapy | - |
dc.subject.MESH | Lung Neoplasms / immunology | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Melanoma / drug therapy | - |
dc.subject.MESH | Melanoma / immunology | - |
dc.subject.MESH | Middle Aged | - |
dc.subject.MESH | Republic of Korea / epidemiology | - |
dc.subject.MESH | Retrospective Studies | - |
dc.subject.MESH | Risk Factors | - |
dc.subject.MESH | Skin Neoplasms / drug therapy | - |
dc.subject.MESH | Skin Neoplasms / immunology | - |
dc.subject.MESH | Steroids / administration & dosage | - |
dc.subject.MESH | Steroids / therapeutic use | - |
dc.subject.MESH | Urinary Bladder Neoplasms / drug therapy | - |
dc.subject.MESH | Urinary Bladder Neoplasms / immunology | - |
dc.title | Real-world incidences and risk factors of immune-related adverse events in patients treated with immune checkpoint inhibitors: A nationwide retrospective cohort study | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Ophthalmology (안과학교실) | - |
dc.contributor.googleauthor | Yong Joon Kim | - |
dc.contributor.googleauthor | Myeongjee Lee | - |
dc.contributor.googleauthor | Eun Hwa Kim | - |
dc.contributor.googleauthor | Seulkee Lee | - |
dc.contributor.googleauthor | Sejung Park | - |
dc.contributor.googleauthor | Min Hee Hong | - |
dc.contributor.googleauthor | Sang Joon Shin | - |
dc.contributor.googleauthor | Inkyung Jung | - |
dc.contributor.googleauthor | Choong-Kun Lee | - |
dc.contributor.googleauthor | Christopher Seungkyu Lee | - |
dc.identifier.doi | 10.1016/j.canlet.2024.216998 | - |
dc.contributor.localId | A05821 | - |
dc.contributor.localId | A02105 | - |
dc.contributor.localId | A05996 | - |
dc.contributor.localId | A02913 | - |
dc.contributor.localId | A03259 | - |
dc.contributor.localId | A03693 | - |
dc.contributor.localId | A04393 | - |
dc.relation.journalcode | J00448 | - |
dc.identifier.eissn | 1872-7980 | - |
dc.identifier.pmid | 38830470 | - |
dc.identifier.url | https://www.sciencedirect.com/science/article/pii/S0304383524003926 | - |
dc.subject.keyword | Cancer | - |
dc.subject.keyword | Immune-related adverse events | - |
dc.subject.keyword | Immunotherapy | - |
dc.subject.keyword | Nation-wide database | - |
dc.subject.keyword | Toxicity | - |
dc.contributor.alternativeName | Kim, Yong Joon | - |
dc.contributor.affiliatedAuthor | 김용준 | - |
dc.contributor.affiliatedAuthor | 신상준 | - |
dc.contributor.affiliatedAuthor | 이명지 | - |
dc.contributor.affiliatedAuthor | 이승규 | - |
dc.contributor.affiliatedAuthor | 이충근 | - |
dc.contributor.affiliatedAuthor | 정인경 | - |
dc.contributor.affiliatedAuthor | 홍민희 | - |
dc.citation.volume | 596 | - |
dc.citation.startPage | 216998 | - |
dc.identifier.bibliographicCitation | CANCER LETTERS, Vol.596 : 216998, 2024-08 | - |
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