无容量
易普利姆玛
医学
联合疗法
不利影响
黑色素瘤
肿瘤科
癌症
临床试验
食品药品监督管理局
内科学
药理学
免疫疗法
癌症研究
作者
Marzieh Nikoo,Fatemeh Rabiee,Hossein Mohebbi,Negar Eghbalifard,Hamid Rajabi,Yalda Yazdani,Delaram Sakhaei,Mohammadreza Khosravifarsani,Reza Akhavan‐Sigari
标识
DOI:10.1016/j.intimp.2023.109881
摘要
Immune checkpoint inhibitors (ICIs) have revolutionized cancer immunotherapy, yielding significant antitumor responses across multiple cancer types. Combination ICI therapy with anti-CTLA-4 and anti-PD-1 antibodies outperforms either antibody alone in terms of clinical efficacy. As a consequence, the U.S. Food and Drug Administration (FDA) approved ipilimumab (anti-CTLA-4) plus nivolumab (anti-PD-1) as the first-ever approved therapies for combined ICI in patients with metastatic melanoma. Despite the success of ICIs, treatment with checkpoint inhibitor combinations poses significant clinical challenges, such as increased rates of immune-related adverse events (irAEs) and drug resistance. Thus, identifying optimal prognostic biomarkers could help to monitor the safety and efficacy of ICIs and identify patients who may benefit the most from these treatments. In this review, we will first go over the fundamentals of the CTLA-4 and PD-1 pathways, as well as the mechanisms of ICI resistance. The results of clinical findings that evaluated the combination of ipilimumab and nivolumab are then summarized to support future research in the field of combination therapy. Finally, the irAEs associated with combined ICI therapy, as well as the underlying biomarkers involved in their management, are discussed.
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