Immune checkpoint inhibitors: maximizing benefit whilst minimizing toxicity

被引:2
作者
Fahey, Catherine C. [1 ]
Gracie, Thomas J. [1 ]
Johnson, Douglas B. [1 ,2 ]
机构
[1] Vanderbilt Univ, Dept Med, Med Ctr, Nashville, TN USA
[2] Vanderbilt Univ, Med Ctr, 777 Preston Res Bldg, Nashville, TN 37232 USA
关键词
Biomarkers; immune checkpoint inhibitors; immunotherapy; immune-related adverse events; toxicity; CELL LUNG-CANCER; NIVOLUMAB PLUS IPILIMUMAB; METASTATIC UROTHELIAL CARCINOMA; CUTANEOUS ADVERSE EVENTS; CD8(+) T-CELLS; OPEN-LABEL; 1ST-LINE TREATMENT; GASTROESOPHAGEAL JUNCTION; INTERLEUKIN-6; BLOCKADE; ADJUVANT PEMBROLIZUMAB;
D O I
10.1080/14737140.2023.2215435
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: The advent of immunotherapy has revolutionized the treatment of cancer; anti-tumor efficacy has been observed with immune checkpoint inhibitors (ICI) in similar to 20 different cancer types with durable responses in some cases. However, the risk of toxicity in the form of immune-related adverse events (irAE) partially counterbalances these benefits, and there are no FDA-approved biomarkers to categorize patients by likelihood of response or risk of irAEs. Areas covered: We conducted a thorough review of the literature of clinical studies regarding ICI and their toxicities. In this review, we synthesize the current body of literature about ICI treatment and irAE by summarizing the classes and uses of ICI, how to identify patients at risk for irAE, present the current understanding of irAE development, describe ongoing research into biomarkers of irAE, examine opportunities for irAE prevention, described management of steroid refractory irAE, and highlight future directions for development of prevention and management strategies. Expert opinion: While ongoing biomarker studies are promising, it is unlikely that there will be a 'one-size-fits-all' approach to categorizing irAE risk. In contrast, improved management and irAE prophylaxis are potentially in reach, and ongoing trials will help elucidate best practices.
引用
收藏
页码:673 / 683
页数:11
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