PMID- 37187501 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20230517 IS - 1927-1220 (Electronic) IS - 1927-1212 (Print) IS - 1927-1212 (Linking) VI - 12 IP - 2 DP - 2023 Apr TI - Incidence and Risk of Hematological Adverse Events Associated With Immune Checkpoint Inhibitors: A Systematic Literature Review and Meta-Analysis. PG - 66-74 LID - 10.14740/jh1090 [doi] AB - BACKGROUND: Immune checkpoint inhibitors (ICIs) have been a breakthrough in cancer therapy. ICI therapy is generally better tolerated than cytotoxic chemotherapy; however, hematological adverse events (AEs) have not been fully analyzed. Hence, we performed a meta-analysis to evaluate the incidence and risk of ICI-related hematological AEs. METHODS: A systematic literature search was performed using PubMed, EMBASE, Cochrane Library, and the Web of Science Core Collection. Phase III randomized controlled trials (RCTs) involving ICI combination regimens were selected. The experimental group received ICIs with systemic treatment, and the control group received only the same systemic treatment. Odds ratios (ORs) for anemia, neutropenia, and thrombocytopenia were calculated using a random-model meta-analysis. RESULTS: We identified 29 RCTs with 20,033 patients. The estimated incidence rates for anemia of all grades and grades III-V were 36.5% (95% confidence interval (CI) 30.23 - 42.75) and 4.1% (95% CI 3.85 - 4.42), respectively. The incidence of neutropenia (all grades 29.7%, grades III-V 5.3%) and thrombocytopenia (all grades 18.0%, grades III-V 1.6%) was also calculated. CONCLUSION: Treatment with ICIs seemed unlikely to increase the incidence of anemia, neutropenia, and thrombocytopenia in all grades. However, programmed cell death-1 receptor ligand inhibitors significantly increased the risk of grades III-V thrombocytopenia (OR 1.53; 95% CI 1.11 - 2.11). Further research is needed to examine the potential risk factors. CI - Copyright 2023, Ohashi et al. FAU - Ohashi, Takuma AU - Ohashi T AD - Department of Stem Cell and Immune Regulation, Yokohama City University Graduate School of Medicine, Yokohama, Japan. FAU - Takase-Minegishi, Kaoru AU - Takase-Minegishi K AD - Department of Stem Cell and Immune Regulation, Yokohama City University Graduate School of Medicine, Yokohama, Japan. FAU - Maeda, Ayaka AU - Maeda A AD - Department of Stem Cell and Immune Regulation, Yokohama City University Graduate School of Medicine, Yokohama, Japan. FAU - Hamada, Naoki AU - Hamada N AD - Department of Stem Cell and Immune Regulation, Yokohama City University Graduate School of Medicine, Yokohama, Japan. FAU - Yoshimi, Ryusuke AU - Yoshimi R AD - Department of Stem Cell and Immune Regulation, Yokohama City University Graduate School of Medicine, Yokohama, Japan. FAU - Kirino, Yohei AU - Kirino Y AD - Department of Stem Cell and Immune Regulation, Yokohama City University Graduate School of Medicine, Yokohama, Japan. FAU - Teranaka, Hiroshi AU - Teranaka H AD - Department of Stem Cell and Immune Regulation, Yokohama City University Graduate School of Medicine, Yokohama, Japan. FAU - Kunimoto, Hiroyoshi AU - Kunimoto H AD - Department of Stem Cell and Immune Regulation, Yokohama City University Graduate School of Medicine, Yokohama, Japan. FAU - Hagihara, Maki AU - Hagihara M AD - Department of Stem Cell and Immune Regulation, Yokohama City University Graduate School of Medicine, Yokohama, Japan. FAU - Matsumoto, Kenji AU - Matsumoto K AD - Department of Stem Cell and Immune Regulation, Yokohama City University Graduate School of Medicine, Yokohama, Japan. FAU - Namkoong, Ho AU - Namkoong H AD - Department of Infectious Diseases, Keio University School of Medicine, Tokyo, Japan. FAU - Horita, Nobuyuki AU - Horita N AD - Chemotherapy Center, Yokohama City University Hospital, Yokohama, Japan. FAU - Nakajima, Hideaki AU - Nakajima H AD - Department of Stem Cell and Immune Regulation, Yokohama City University Graduate School of Medicine, Yokohama, Japan. LA - eng PT - Journal Article DEP - 20230430 PL - Canada TA - J Hematol JT - Journal of hematology JID - 101635099 PMC - PMC10181326 OTO - NOTNLM OT - Hematological toxicities OT - Immune checkpoint inhibitor OT - Immune-related adverse events OT - Meta-analysis COIS- The authors declare that they have no conflict of interest. EDAT- 2023/05/16 01:09 MHDA- 2023/05/16 01:10 PMCR- 2023/04/30 CRDT- 2023/05/15 19:26 PHST- 2023/02/06 00:00 [received] PHST- 2023/03/25 00:00 [accepted] PHST- 2023/05/16 01:10 [medline] PHST- 2023/05/16 01:09 [pubmed] PHST- 2023/05/15 19:26 [entrez] PHST- 2023/04/30 00:00 [pmc-release] AID - 10.14740/jh1090 [doi] PST - ppublish SO - J Hematol. 2023 Apr;12(2):66-74. doi: 10.14740/jh1090. Epub 2023 Apr 30.